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    <title>Massive Science - Vaccines</title>
    <description>This is a collection of our articles about vaccines, full of real facts (and clear explanations) from scientists. We cover how vaccines are developed, why immunization is important, and where vaccine ingredients come from.


Wondering about different COVID-19 vaccines? How vaccines work? You&#39;re in the right place.</description>
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<guid isPermaLink="true">https://massivesci.com/articles/kids-covid19-vaccines-clinical-trials-pediatrician/</guid>
<link>https://massivesci.com/articles/kids-covid19-vaccines-clinical-trials-pediatrician/</link>
<pubDate>Tue, 06 Apr 2021 23:05:02 EST</pubDate>
<title>When can kids get the COVID-19 vaccine? A pediatrician answers parent questions</title>
<description>Hang in there, parents – vaccines for children are in the works</description>

<media:content url="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/b319f77e-498b-430f-af15-a9c4cb4797e7/atoms-rxa9YlunVlY-unsplash.jpg?auto=compress%2Cformat&amp;crop=faces&amp;fit=crop&amp;fm=jpg&amp;h=600&amp;q=75&amp;w=900" type="image/jpeg">
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  <dc:creator><![CDATA[James B. Wood]]></dc:creator>
  <atom:author>
    <atom:name>James B. Wood</atom:name>
    <atom:uri>https://massivesci.com/people/james-b-wood/</atom:uri>
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  <content:encoded><![CDATA[
    <p><em>A big question among parents and teachers as more schools reopen is when their kids will be vaccinated against COVID-19. Some have wondered whether the vaccine is even necessary for children. There is news on that front. In a press release </em><a href="https://www.pfizer.com/news/press-release/press-release-detail/pfizer-biontech-announce-positive-topline-results-pivotal"><em>on March 31, 2021</em></a><em>, vaccine maker Pfizer suggested its vaccine is as effective in children ages 12-15 as it is in young adults. However the results of Pfizer’s vaccine trials in adolescents have not been fully released or reviewed by the Food and Drug Administration, and that will take several weeks.</em>&nbsp;</p>
<p><a href="https://news.iu.edu/iu-experts/profile/m/1046/wood-james"><em>Dr. James Wood</em></a><em>, a pediatrician and assistant professor of pediatric infectious diseases, explains what doctors know today about the risk children face of getting and spreading the coronavirus and when vaccines might be available.</em></p>
<h2 id="do-kids-really-need-to-get-the-covid-19-vaccine">Do kids really need to get the COVID-19 vaccine?</h2>
<p>The short answer is yes. A lot of studies have shown that COVID-19 <a href="https://www.cdc.gov/coronavirus/2019-ncov/covid-data/investigations-discovery/hospitalization-death-by-age.html">isn’t as severe in children</a>, particularly younger kids – but that doesn’t mean kids aren’t at risk of getting infected and potentially <a href="https://doi.org/10.5694/mja2.50823">spreading the virus</a>.&nbsp;</p>
<p>Children under 12 who get COVID-19 do tend to have mild illnesses or no symptoms, while teenagers seem to have responses somewhere between what adults and younger kids have experienced. The Centers for Disease Control and Prevention found that <a href="https://www.cdc.gov/mmwr/volumes/69/wr/mm6939e2.htm?s_cid=mm6939e2_w">teens were about twice as likely</a> to be diagnosed with COVID-19 as children ages 5-11.&nbsp;</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/notes/covid-pandemic-children-school-masks/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Fnotes%2Fcovid-pandemic-children-school-masks%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>Researchers are still trying to understand why we’re seeing these differences between older and younger kids. Behavior probably plays a part. Teenagers are more likely to engage in social or group activities, and they may or may not be wearing masks. <a href="http://doi.org/10.1126/scitranslmed.abd5487">Immune differences</a> and <a href="http://jamanetwork.com/article.aspx?doi=10.1001/jama.2020.8707">biologic factors</a> may also play a role. Non-SARS-CoV-2 coronaviruses are <a href="https://doi.org/10.1128/jcm.00636-10">common in children</a>, often resulting in upper respiratory infection. Is their frequent exposure to other coronaviruses helping protect them from severe COVID-19? That is one hypothesis. We know younger kids’ immune responses in general are different from adults, and likely play a role in protection.&nbsp;</p>
<p>It’s important to remember that while most children get only mild symptoms, they still face risks. At least <a href="https://www.cdc.gov/nchs/nvss/vsrr/covid_weekly/index.htm#AgeAndSex">226 U.S. children</a> with COVID-19 have died, and <a href="https://services.aap.org/en/pages/2019-novel-coronavirus-covid-19-infections/children-and-covid-19-state-level-data-report/">thousands have been hospitalized</a>.</p>
<p>The key to minimizing the risk is to make sure kids eventually get vaccinated, follow social distancing recommendations and wear masks.</p>
<h2 id="are-kids-spreading-the-virus">Are kids spreading the virus?</h2>
<p>In a setting like a school where mask-wearing and social distancing are enforced, young kids seem to not spread the virus very much when the rules and guidelines are being followed. One CDC review found <a href="https://www.cdc.gov/mmwr/volumes/70/wr/mm7003e1.htm">little difference in community cases</a> in counties with elementary schools open and those with remote learning.</p>
<p>If precautions aren’t being taken, children infected with the coronavirus very well could <a href="https://www.cidrap.umn.edu/news-perspective/2020/12/study-kids-adults-equally-susceptible-home-covid-19-spread">spread it to adults</a>. What isn’t clear yet is how great that risk is.</p>
<p>To keep schools as safe as possible, continuing schoolwide mask and social distancing policies will be important. With teenagers in particular, mask rules can’t hinge on whether the person has been vaccinated or not. Until <a href="https://www.nature.com/articles/d41586-021-00728-2">herd immunity</a> within the whole community is at a good level, social distancing and masking is still going to be the recommendation.</p>
<figure class="center large"><img alt="a girl reading a book while wearing a mask" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/a434be03-2ffd-4661-b263-0007f065348d/kelly-sikkema-r2hTBxEkgWQ-unsplash.jpg"/><figcaption> <span class="credit"><p>Photo by <a href="https://unsplash.com/@kellysikkema?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Kelly Sikkema</a> on <a href="https://unsplash.com/s/photos/kids-covid?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Unsplash</a> &nbsp;</p></span></figcaption></figure>
<h3 id="so-when-can-kids-get-vaccinated">So, when can kids get vaccinated?</h3>
<p>Right now, the Pfizer vaccine is the only one in the U.S. authorized for teenagers <a href="https://www.fda.gov/media/144412/download">as young as 16</a>. &nbsp;Before kids under 16 can be vaccinated, clinical trials need to be completed in thousands of young volunteers to assess the vaccines’ safety and efficacy, and the results must be fully reviewed and then authorized by the Food and Drug Administration.</p>
<p>Pfizer said it expects to submit results from its adolescent trials <a href="https://www.pfizer.com/news/press-release/press-release-detail/pfizer-biontech-announce-positive-topline-results-pivotal">for review soon</a>. Vaccine manufacturer <a href="https://www.cdc.gov/coronavirus/2019-ncov/vaccines/different-vaccines/Moderna.html">Moderna</a> also has <a href="https://clinicaltrials.gov/ct2/show/NCT04368728">trials underway with adolescents</a>. &nbsp;If their vaccines are shown to be safe and effective and regulators authorize them, kids 12 and up could be vaccinated before school starts in the fall.</p>
<p>Realistically, young children probably won’t be eligible for the vaccine until late fall or winter at the earliest. Moderna announced in mid-March that it had started testing its vaccine <a href="https://investors.modernatx.com/news-releases/news-release-details/moderna-announces-first-participants-dosed-phase-23-study-0">in children ages 6 months to 11 years</a>. Pfizer said it is <a href="https://www.businesswire.com/news/home/20210331005503/en/">also starting testing</a> in young children, but these trials take time.</p>
<h2 id="whats-different-about-the-vaccines-kids-will-get">What’s different about the vaccines kids will get?</h2>
<p>The composition of the COVID-19 vaccines for children is the same as used in adults – the difference is that children may require a different &nbsp;dose.</p>
<p>The first step in vaccine trials is to figure out the right dose. The &nbsp;companies want to find the lowest possible dose that is both safe and produces a target level of antibodies. For example, Moderna uses a 100-microgram dose in adults. It is testing three different doses for children under age 2 – 25, 50 and 100 micrograms – and two doses for children over age 2, at 50 and 100 micrograms.&nbsp;</p>
<p>Once the company determines the optimal dose, it will launch a placebo-controlled trial to test its effectiveness, in which some children will get a placebo and some will get the vaccine.</p>
<p>A rigorous system for pediatric vaccine trials is <a href="https://doi.org/10.1203/01.PDR.0000106317.36875.6A">well established</a> in the U.S. These trials are key to assessing the safety and efficacy of vaccines in children, which can differ from adults.&nbsp;</p>
<p>I am optimistic that a safe and effective vaccine will be available for children. Thus far, there have not been any safety signals from &nbsp;either the adult or adolescent studies that have been worrying to me as a pediatrician, but the studies still need to be done in children.</p>
<figure class="right medium"><img alt="a woman holding a young boy who is wearing a mask and looking at the camera" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/2bdd1062-80fa-4172-a70e-225f312156dc/taylor-brandon-jYI7L4zLFkM-unsplash.jpg"/><figcaption> <span class="credit"><p>Photo by <a href="https://unsplash.com/@house_42?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Taylor Brandon</a> on <a href="https://unsplash.com/s/photos/kids-covid?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Unsplash</a> &nbsp;</p></span></figcaption></figure>
<h3 id="how-can-parents-create-safe-playdates-for-kids">How can parents create safe playdates for kids?</h3>
<p>When I talk to parents, I explain that it’s a risk-versus-benefit question. Each family has a different tolerance.</p>
<p>From a medical standpoint, the mental health of kids and having them play with other kids is an important part of childhood.</p>
<p>I would say that unvaccinated kids playing indoors without masks on is still not a great idea. The risk is just too high at this point. As weather warms up, I would encourage kids to play outside. Ride bikes, play and socialize – just do it in a safe manner.</p>
<p>We all have pandemic fatigue, including medical professionals. As the weather gets warmer, I think everyone just wants to get back to normal. The worst thing we can do, right as we <a href="https://covid.cdc.gov/covid-data-tracker/#trends_dailytrendscases">start to see a light at the end</a>, is fall backward again – because that would just make it that much longer for everyone.</p>
    


<p><em><a href="https://massivesci.com/people/james-b-wood/">James B. Wood</a> studies 

<p class="mb0">

<span class="scientist__field">Pediatrics</span>

</p>

 at 

<p class="mb0 o7">

<span class="scientist__institution">Indiana University School of Medicine</span>

</p>

.</p>



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<guid isPermaLink="true">https://massivesci.com/articles/veev-biological-weapons-vaccine-decoy-molecule/</guid>
<link>https://massivesci.com/articles/veev-biological-weapons-vaccine-decoy-molecule/</link>
<pubDate>Thu, 25 Mar 2021 22:33:27 EST</pubDate>
<title>A decoy may be the key to developing a vaccine against a deadly bioweapon</title>
<description>New research shows how Venezuelan equine encephalitis virus attaches to cells, paving the way for a vaccine</description>

<media:content url="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/b3cd7fcf-74f0-4e63-9840-2a4de7553618/scott-rodgerson-6tiytXTQ3Yg-unsplash.jpg?auto=compress%2Cformat&amp;crop=faces&amp;fit=crop&amp;fm=jpg&amp;h=600&amp;q=75&amp;w=900" type="image/jpeg">
  <media:title>gas mask</media:title>
  <media:description>a gas mask staring at the camera and sitting in a pile of leaves</media:description>
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  <dc:creator><![CDATA[Amanda Rossillo]]></dc:creator>
  <atom:author>
    <atom:name>Amanda Rossillo</atom:name>
    <atom:uri>https://massivesci.com/people/amanda-rossillo/</atom:uri>
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  <content:encoded><![CDATA[
    <p>Though the international <a href="https://wayback.archive-it.org/all/20140803040358/http:/www.unog.ch/80256EE600585943/(httpPages)/04FBBDD6315AC720C1257180004B1B2F?OpenDocument">Biological and Toxin Weapons Convention</a> prohibited biological warfare and the development of bioweapons in 1975, the knowledge gained from previous research and testing didn’t just disappear. This, combined with a <a href="https://www.nti.org/learn/treaties-and-regimes/convention-prohibition-development-production-and-stockpiling-bacteriological-biological-and-toxin-weapons-btwc/">lack of means to enforce</a> the agreement and subsequent <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1326439/" target="_blank">flagrant violations</a>, has prompted some nations to attempt to develop vaccines against known bioweapons as a precaution.</p>
<p>One such bioweapon is <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5691631/" target="_blank">Venezuelan equine encephalitis virus</a> (VEEV), which is naturally found as far north as Florida and south through Mexico, Central America, and South America. It is transmitted to humans through mosquitos or through <a href="https://pubmed.ncbi.nlm.nih.gov/30282570/" target="_blank">aerosols</a> from infected horses and donkeys. VEEV targets the nervous system, and can be fatal if it enters the brain. Though VEEV is not usually deadly in humans, it causes symptoms in <a href="https://www.sciencedirect.com/topics/medicine-and-dentistry/venezuelan-equine-encephalitis">nearly 100 percent of those infected</a>, including fever, severe headache, vomiting, and diarrhea, and may cause neurological complications.</p>
<p>VEEV was <a href="https://onlinelibrary.wiley.com/doi/abs/10.1002/0471686786.ebd0047.pub2" target="_blank">developed as a biological weapon</a> by the United States and Soviet Union during the Cold War. It was manufactured as an <a href="https://www.sciencedirect.com/science/article/pii/B9780128001592000075" target="_blank">incapacitating agent</a>, designed to cause severe symptoms that would not only weaken the opposing military, but also require valuable resources to contain and treat.&nbsp;</p>
<p>Though it has never actually been used in warfare, VEEV has <a href="https://www.aphis.usda.gov/animal_health/emergency_management/downloads/sop/sop_vee_e-e.pdf" target="_blank">many characteristics</a> that make it a powerful potential bioweapon. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134406/">Its symptoms resemble other viruses</a> like dengue and it requires specialized tests to diagnose. It is relatively easy to produce and store, and there are multiple dangerous strains. To make matters worse, it’s also extremely infectious — at least 20 staff became ill when in 1959 <a href="https://www.globalsecurity.org/wmd/intro/bio_vee.htm">a small vial was dropped</a> in a laboratory stairwell in the former Soviet Union.&nbsp;</p>
<aside class="pullquote"><blockquote>...researchers created a “decoy” protein and injected it into living mice in an effort to trick the virus</blockquote></aside>
<p>Most VEEV strains are under highly restricted access in the United States, and there is no vaccine available for the public; a live-virus vaccine does exist for the <a href="https://www.healio.com/news/infectious-disease/20170428/us-army-awards-sri-international-47-million-to-manufacture-test-encephalitis-vaccine" target="_blank">military</a> and at-risk laboratory personnel. However, this vaccine often causes adverse side effects, requires multiple booster shots, and may even be able to <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3134406/" target="_blank">revert back to its infectious form</a> once inside the body.</p>
<p><a href="https://www.nature.com/articles/s41586-020-2915-3">In a recent study published in <em>Nature</em></a>, scientists used CRISPR gene editing technology to determine how VEEV enters cells. Because they could not access the most dangerous strains of VEEV, they created a hybrid virus using genes from a milder VEEV strain and a related virus. This hybrid infected cells in the same way as the most dangerous VEEV strains while being safe to handle.</p>
<p>They then deleted genes from mice brain cells and exposed the cells to the modified version of VEEV. They found that when a little-studied gene called <em>Ldlrad3</em> was removed, the virus could not enter these cells. Conversely, when <em>Ldlrad3</em> was added to different types of cells that are usually naturally resistant to VEEV infection, VEEV was able to enter. Notably, when study co-author William Klimstra <a href="https://www.eurekalert.org/pub_releases/2020-11/wuso-lbi111720.php" target="_blank">repeated these tests</a> using human cells and a dangerous, restricted strain of VEEV, they observed the same results.</p>
<p><em>Ldlrad3</em> codes for a protein that’s found on the surface of neurons, and the researchers believe it to be the main “handle” that the virus uses to attach to the cell (in the same way that <a href="https://www.nature.com/articles/s41586-020-2180-5" target="_blank">ACE2 is the entry point</a> of SARS-CoV-2 into cells). However, since this gene is naturally present in our bodies, it can’t just be deleted to prevent infection.</p>
<figure class="center large"><img alt="three donkeys looking through a wire fence" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/6d371e66-e8d4-43e6-8495-c0e11bfca4b9/tim-mossholder-LdWlt-MivHI-unsplash.jpg"/><figcaption><span class="caption"><p>VEEV is spread to humans by mosquitoes as well as aerosols from horses, donkeys, and mules</p></span> <span class="credit"><p>Photo by <a href="https://unsplash.com/@timmossholder?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Tim Mossholder</a> on <a href="https://unsplash.com/s/photos/donkey?utm_source=unsplash&amp;utm_medium=referral&amp;utm_content=creditCopyText">Unsplash</a> &nbsp;</p></span></figcaption></figure>
<p>To circumvent this issue, these researchers created a “decoy” protein and injected it into living mice in an effort to trick the virus. The idea is that a VEEV virus attaches to a decoy, which blocks it from latching on to the protein LDLRAD3 (made by the gene <em>Ldlrad3)</em>, much like how having your hands full keeps you from picking up something new. This would mean that VEEV viruses would be unable to enter the cells, preventing infection. For this experiment, the team was able to access one of the restricted VEEV strains.</p>
<p>The mice were injected with the decoy protein six hours before and 24 hours after exposure to VEEV. All of the mice who were infected with VEEV without the decoy protein died, while all of those who received the decoy survived. Even when VEEV was injected directly into their brains, eight of the ten mice who received the decoy survived.</p>
<p>While the decoy hasn’t yet been tested in humans or other susceptible animals, researchers hope that it could be developed into a vaccine to be used during outbreaks.</p>
<p>Outbreaks are particularly devastating in regions that rely on equines (horses, donkeys, and mules) for agriculture and transportation. Not only do equines commonly spread the disease to humans, but they are also much <a href="https://ann-clinmicrob.biomedcentral.com/articles/10.1186/s12941-020-00360-4">more likely to die</a> from the virus. Though some equine VEEV vaccines have been used in the past, they unknowingly contained the activated, infectious virus and are thought to have actually <a href="https://www.annualreviews.org/doi/10.1146/annurev.ento.49.061802.123422">caused most, if not all, outbreaks</a> prior to 1970. A new and improved vaccine that could be given to both farm animals and humans could slow the spread of the virus, minimizing the health and economic impacts of outbreaks.</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/articles/chemical-weapon-sarin-polymer-membrane-ppe-smart-fabric/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Farticles%2Fchemical-weapon-sarin-polymer-membrane-ppe-smart-fabric%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>These same regions are also home to the mosquito vectors of VEEV. These mosquitos prefer warm, wet habitats, and more recent outbreaks have been recorded after <a href="https://ann-clinmicrob.biomedcentral.com/articles/10.1186/s12941-020-00360-4">particularly heavy rains and floods</a>. As global warming accelerates, VEEV-carrying mosquitos may <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5557581/" target="_blank">expand further north</a> into North America, putting even more people at risk of contracting this pathogen even in the absence of an act of war.&nbsp;</p>
<p>VEEV is just one of many potentially lethal bioweapons without a satisfactory vaccine. The vaccine for anthrax must be administered in <a href="https://www.cdc.gov/vaccines/vpd/anthrax/public/index.html" target="_blank">five separate doses</a> over the course of 18 months, with booster shots needed each year. Vaccines for botulism, caused by one of <a href="https://www.who.int/news-room/fact-sheets/detail/botulism" target="_blank">the deadliest known toxins</a>, also exist, but their actual effectiveness is unknown and <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5618201/" target="_blank">none are FDA-approved</a>.</p>
<p>Though more testing is needed to evaluate the decoy protein's potential as a new vaccine for VEEV, its preliminary success may pave the way for improved vaccines for other bioweapons in the future.</p>
<p>And while VEEV is (hopefully) not an imminent security threat to the United States, we may sleep a little easier knowing that a vaccine is in the works to prevent another pandemic.</p>
    


<p><em><a href="https://massivesci.com/people/amanda-rossillo/">Amanda Rossillo</a> studies 

<p class="mb0">

<span class="scientist__field">Evolutionary Anthropology</span>

</p>

 at 

<p class="mb0 o7">

<span class="scientist__institution">Duke University</span>

</p>

.</p>



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<guid isPermaLink="true">https://massivesci.com/articles/immunocompromised-covid19-vaccination/</guid>
<link>https://massivesci.com/articles/immunocompromised-covid19-vaccination/</link>
<pubDate>Sun, 07 Mar 2021 22:16:04 EST</pubDate>
<title>Immunocompromised people must be a priority in the COVID-19 vaccination effort</title>
<description>Vaccinating immunocompromised people will both protect their health and slow viral evolution</description>

<media:content url="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/4284ee00-5b0a-42ed-a480-ad8d4447ba6a/mehmet-turgut-kirkgoz-KiqRtq8LhXY-unsplash.jpg?auto=compress%2Cformat&amp;crop=faces&amp;fit=crop&amp;fm=jpg&amp;h=600&amp;q=75&amp;w=900" type="image/jpeg">
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  <media:description>a woman&#39;s hand holding a vial of vaccine against a sky backdrop</media:description>
</media:content>


  
  <dc:creator><![CDATA[Francesco Zangari]]></dc:creator>
  <atom:author>
    <atom:name>Francesco Zangari</atom:name>
    <atom:uri>https://massivesci.com/people/francesco-zangari/</atom:uri>
  </atom:author>


  
  <content:encoded><![CDATA[
    <p><a href="https://www.kff.org/policy-watch/how-are-states-prioritizing-who-will-get-the-covid-19-vaccine-first/" target="_blank">Vaccine prioritization</a> is both necessary and important, with a demand for coronavirus vaccines much greater than supply. These policies assure the most at-risk populations are protected from COVID-19. This has included front-line workers (ie. patient-facing nurses and doctors), the elderly, and those with serious health complications. Other non-healthcare priorities are those employed in firefighting, retail, public transport and logistics.</p>
<p>We have needed these phased distribution efforts to ensure a compassionate framework for high-risk populations. These initial plans were adequate, but findings from two case studies of immunocompromised people highlight a new priority for vaccination. These emerging data highlight two poignant facts — immunocompromised people lack the ability to fight COVID-19, rendering poor health outcomes while also serving as an unintended launching pad for SARS-CoV-2 evolution.&nbsp;</p>
<p>Immunocompromised people have weakened immune systems, so the virus sticks around longer and <a href="https://www.sciencedirect.com/science/article/pii/S1201971220325741" target="_blank">copies itself</a> to a high degree. Through this process, the virus adapts to its human cellular environment faster than normal, <a href="https://jamanetwork.com/journals/jama/fullarticle/2775006" target="_blank">promoting mutations</a> and potentially the formation of more transmissible variants. This is in some ways analogous to how incorrect or inconsistent dosing of antibiotics can cause the rise of antibiotic-resistant bacteria.&nbsp;</p>
<p>The first evidence for enhanced SARS-CoV-2 evolution within immunocompromised individuals was <a href="https://www.nejm.org/doi/full/10.1056/NEJMc2031364" target="_blank">reported in the <em>New England Journal of Medicine</em> in late December 2020</a>, from a 45-year-old man with an autoimmune disorder called <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3836378/" target="_blank">catastrophic antiphospholipid syndrome</a> (CAPS) who had contracted COVD-19. People with CAPS are often treated using combination therapy that suppresses the immune system to repress autoimmunity. The man battled the virus successfully at first and lowered levels of viral load were seen approximately 39 days after infection. One month later, however, he was hospitalized with symptoms of COVID-19 and again tested positive, one of three recurrences. &nbsp;</p>
<aside class="pullquote"><blockquote>...the rapid evolution of the virus points to an urgent need to prioritize vaccinations for immunosuppressed patients</blockquote></aside>
<p>Over his 154-day battle with COVID-19, the research team continued taking samples from the patient to characterize the virus's evolution. Using sequencing technology, researchers monitored the viral genome through infection. The results were striking – they saw that the virus in his body had evolved substantially compared to existing strains in circulation at the time. Some strains contained the same mutations later found in <a href="https://www.cdc.gov/coronavirus/2019-ncov/more/science-and-research/scientific-brief-emerging-variants.html">circulating COVID-19 variants like E484K and N501Y</a> that are associated with increased transmission.</p>
<p><a href="https://doi.org/10.1038/s41586-021-03291-y">A secondary piece of evidence for accelerated COVID-19 evolution was reported in early February 2021</a>. A person undergoing chemotherapy for B cell lymphoma was in an immunocompromised state when they also contracted COVID-19. Through similar methods to the first study, researchers took samples from the person to assess how SARS-CoV-2 was evolving in their body.&nbsp;</p>
<p>Once again, they saw significant evolution of the virus. They detected many viral variants unique to this person through the 102 days of testing. One dominant viral variant in the population included deletion of amino acids 69/70, mutations also seen in <a href="https://www.cdc.gov/coronavirus/2019-ncov/more/science-and-research/scientific-brief-emerging-variants.html" target="_blank">circulating variants</a>.&nbsp;</p>
<p>Further investigation showed the danger of these variants, as they were better able to avoid detection by antibodies known to neutralize original SARS-CoV-2. With mutations being concentrated in the spike region and thought to change the architecture of the spike, the rapid evolution of the virus points to an urgent need to prioritize vaccinations for immunosuppressed patients.&nbsp;</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/notes/moderna-vaccine-b117-covid19-variant/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Fnotes%2Fmoderna-vaccine-b117-covid19-variant%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>Despite this evidence, the urgency of prioritizing immunosuppressed people for vaccination has not been translated into public health plans. In the <a href="https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations.html">US</a> and <a href="https://www.canada.ca/en/public-health/services/immunization/national-advisory-committee-on-immunization-naci/guidance-prioritization-key-populations-covid-19-vaccination.html#a3">Canada</a>, there has been mention to prioritize “those with underlying medical conditions,” but no focus on specifically targeting immunocompromised patients. The <a href="https://ec.europa.eu/commission/presscorner/detail/en/qanda_20_2467">European Union and the UK’s focus </a>is similar as well. Vaccination efforts remain focused on healthcare personnel and the elderly, although in some US states vaccine availability has rapidly expanded and other categories of people are now eligible.&nbsp;</p>
<p>Policymakers need to consider emerging data from the scientific community. A pivot towards vaccinating immunocompromised people could still use the existing framework of focusing on the most elderly and at-risk populations, requiring a minor deviation from current plans.</p>
<p>The generosity of the immunocompromised people who gave their samples for research – both of whom died from COVID-19 – cannot be understated. The samples taken throughout their treatments illuminated an overlooked aspect for more compassionate patient treatment. Even disregarding the public health perspective, immunocompromised people should be prioritized for COVID-19 vaccination to avoid serious health complications.&nbsp;</p>
<p>By drastically changing course and prioritizing immunocompromised people for vaccination, we can achieve two important goals by addressing public health concerns by limiting opportunity for viral evolution and protecting this group of more vulnerable people from serious COVID-19 complications.&nbsp;</p>
    


<p><em><a href="https://massivesci.com/people/francesco-zangari/">Francesco Zangari</a> studies 

<p class="mb0">

<span class="scientist__field">Molecular Biology</span>

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<span class="scientist__institution">University of Toronto</span>

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<guid isPermaLink="true">https://massivesci.com/articles/covid19-vaccine-moderna-pfizer-rollout/</guid>
<link>https://massivesci.com/articles/covid19-vaccine-moderna-pfizer-rollout/</link>
<pubDate>Tue, 22 Dec 2020 13:10:56 EST</pubDate>
<title>How the COVID-19 vaccine is distributed determines how the pandemic will end</title>
<description>National health care systems will make things more organized, but the US is still finding its footing</description>

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  <dc:creator><![CDATA[Sara May Bergstresser ]]></dc:creator>
  <atom:author>
    <atom:name>Sara May Bergstresser </atom:name>
    <atom:uri>https://massivesci.com/people/sara-may-bergstresser/</atom:uri>
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    <p>The news is now full of pictures of the first vaccinations for COVID-19. In the UK, 90-year-old <a href="https://www.standard.co.uk/news/uk/first-person-covid-pfizer-vaccine-margaret-keenan-b216271.html" rel="noopener noreferrer" target="_blank">Margaret Keenan</a> was the first to get her “jab," and in the US, the first vaccines have been given to health care workers including <a href="https://www.washingtonpost.com/nation/2020/12/14/first-covid-vaccines-new-york/" rel="noopener noreferrer" target="_blank">New York nurse Sandra Lindsay</a>.&nbsp;</p>
<p>In both the UK and the US, the COVID response over the past nine months has been haphazard, with many failed policies, soaring case numbers and deaths, controversy, and widespread social and economic disruption. The vaccine rollout represents a much needed promise of hope for the future, but it is important to remember that a lot more still needs to happen before the pandemic can be controlled. Not even the vaccine stories for Margaret Keenan and Sandra Lindsay are complete, since for full protection they will both need to take the <a href="https://www.cdc.gov/vaccines/covid-19/info-by-product/pfizer/clinical-considerations.html" rel="noopener noreferrer" target="_blank">second dose of the Pfizer/BioNTech vaccine</a> after about three weeks.</p>
<p>On the surface, it may look like an organized global rollout process is getting underway, but there are still many uncertainties surrounding vaccine distribution internationally and within each country. How quickly vaccines can become widely available and who receives early priority are determined by national purchasing power, available supply, logistics, national priorities, and variations in health regulations and laws.&nbsp;</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/articles/pfizer-moderna-vaccine-covid-coronavirus/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Farticles%2Fpfizer-moderna-vaccine-covid-coronavirus%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>Countries with national health systems such as the UK and Canada have the opportunity to use existing care provision frameworks and facilities to help organize efficient population-wide vaccine initiatives. The US, on the other hand, does not have the same type of health system infrastructure, which means vaccine distribution may vary wildly from state to state. National priorities also dictate the order in which people will be able to receive the vaccine, and national policymakers must <a href="https://massivesci.com/articles/pfizer-moderna-vaccine-covid-coronavirus/" rel="noopener noreferrer" target="_blank">decide whether to focus</a> on direct protection for vulnerable individuals or to prioritize those who are most likely to spread the disease to others.&nbsp;</p>
<p>The CDC has put out <a href="https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations.html" rel="noopener noreferrer" target="_blank">recommendations</a> about which groups should get early vaccine priority. These recommendations were based on the Advisory Committee on Immunization Practices (ACIP) <a href="https://www.cdc.gov/mmwr/volumes/69/wr/mm695152e1.htm?s_cid=mm695152e1_w" rel="noopener noreferrer" target="_blank">Interim Recommendation</a> for Allocating Initial Supplies of COVID-19 Vaccine. The CDC cites its main goals to be: “Decrease death and serious disease as much as possible,” “Preserve functioning of society,” and “Reduce the extra burden COVID-19 is having on people already facing disparities.” Based on this, the two main groups recommended for early vaccination are <a href="https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/hcp.html" rel="noopener noreferrer" target="_blank">Healthcare Personnel</a> and residents of nursing homes (“<a href="https://www.cdc.gov/coronavirus/2019-ncov/vaccines/recommendations/LTCF-residents.html" rel="noopener noreferrer" target="_blank">Long Term Care Facilities</a>”). After that, an approximate sense of where others may be in the queue can be calculated <a href="https://www.nytimes.com/interactive/2020/12/03/opinion/covid-19-vaccine-timeline.html" rel="noopener noreferrer" target="_blank">here</a>. Nevertheless, recent history has shown that public health recommendations are not always followed in the US, and individual states may choose to allocate differently from ACIP recommendations.&nbsp;</p>
<p>Finally, as is typical for new pharmaceutical products, <a href="https://jamanetwork.com/journals/jama/fullarticle/2772137" rel="noopener noreferrer" target="_blank">safety monitoring </a>must continue after its rollout. This is even more important for COVID vaccines, because they were developed rapidly under atypical circumstances, and <a href="https://www.nejm.org/doi/full/10.1056/NEJMp2026393" rel="noopener noreferrer" target="_blank">problems of public trust remain</a>. <a href="https://www.cdc.gov/mmwr/volumes/69/wr/mm695152e1.htm?s_cid=mm695152e1_w" rel="noopener noreferrer" target="_blank">ACIP and the CDC also recommend</a> that any adverse events should be reported to the <a href="https://vaers.hhs.gov/index.html" rel="noopener noreferrer" target="_blank">Vaccine Adverse Events Reporting System (VAERS)</a>, even if it is not clear that a vaccine caused the event. Vaccine data is difficult to track in the US due to its uneven health practices and regulations, so a new <a href="https://www.hhs.gov/cto/initiatives/public-health-innovation/immunization-gateway/index.html" rel="noopener noreferrer" target="_blank">nationwide system</a> is starting up to aid in that effort.&nbsp;</p>
<aside class="pullquote"><blockquote>It is important to remember that health policy must account for human behavior in addition to the predictions of epidemiological models</blockquote></aside>
<p>In the UK, a more <a href="https://www.gov.uk/government/publications/priority-groups-for-coronavirus-covid-19-vaccination-advice-from-the-jcvi-2-december-2020/priority-groups-for-coronavirus-covid-19-vaccination-advice-from-the-jcvi-2-december-2020#vaccine-priority-groups-advice-on-2-december-2020" rel="noopener noreferrer" target="_blank">comprehensive plan for allocation</a> has been released, with the explicit intent to inform future policy. These recommendations also prioritize older adults and healthcare providers, but they go on to elaborate on many subsequent priority categories based on age and risk due to underlying health conditions. The UK, due to its existing national health infrastructure and decision to purchase <a href="https://www.bloomberg.com/news/articles/2020-12-09/which-countries-have-reserved-the-most-covid-19-vaccines-u-s-is-32nd-on-list" rel="noopener noreferrer" target="_blank">sufficient vaccine doses</a> for its population, is starting its rollout efficiently so far.&nbsp;</p>
<p>In the US, director of the National Institute of Allergy and Infectious Diseases Anthony Fauci, predicts that a return to <a href="https://news.harvard.edu/gazette/story/2020/12/anthony-fauci-offers-a-timeline-for-ending-covid-19-pandemic/" rel="noopener noreferrer" target="_blank">something close to normal </a>can be achieved by the end of 2021, as long as the vaccination rollout goes well and 75-80% of the population are vaccinated by that time. There are a number of issues that may complicate this optimistic timeline including past health communication missteps, public mistrust, and <a href="https://www.tandfonline.com/doi/full/10.1080/10410236.2020.1838096" rel="noopener noreferrer" target="_blank">vaccine hesitancy</a>, <a href="https://www.vice.com/en/article/4ad43m/the-trump-administrations-covid-vaccine-rollout-is-pure-chaos" rel="noopener noreferrer" target="_blank">states receiving fewer doses</a> than promised, problems with Pfizer vaccine cold storage requirements in <a href="https://www.statnews.com/2020/11/11/rural-hospitals-cant-afford-freezers-to-store-pfizer-covid19-vaccine/" rel="noopener noreferrer" target="_blank">rural areas</a>, and confusion over packaging leading to <a href="https://www.statnews.com/2020/12/16/labeling-confusion-led-to-wasted-doses-of-pfizer-covid-19-vaccine-in-first-days-of-rollout" rel="noopener noreferrer" target="_blank">wasted doses</a>. If these limitations cannot be overcome, the process will take longer than hoped.&nbsp;</p>
<p>There are also tensions between implementing some numerically sound strategies for stopping the spread of disease and the need to increase public trust. For example, <a href="https://theconversation.com/why-covid-19-vaccines-need-to-prioritize-superspreaders-145232" rel="noopener noreferrer" target="_blank">some health economists and policy experts argue </a>that people most likely to become “superspreaders” be prioritized over the more vulnerable, but this would mean that young people who are more likely to have asymptomatic or mild cases would be vaccinated before the elderly, those with preexisting health risks, and other vulnerable and underserved populations. It is important to remember that health policy must account for human behavior in addition to the predictions of epidemiological models; for communities at high risk whose members have disproportionately become infected and died, watching healthy college students at spring break parties after getting their vaccines first would likely further diminish trust in the public health system and its recommendations.</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/articles/covid19-mrna-vaccine-cold-chain/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Farticles%2Fcovid19-mrna-vaccine-cold-chain%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>One main lesson that should be permanently learned from COVID is that infectious diseases that start anywhere across the globe can fast become global pandemics. It is a priority of ethics and justice that humans should have access to vaccines regardless of whether they live in economically powerful countries. Right now, wealthy countries are buying up most of the available doses, meaning that “nine out of 10 people in 70 low-income countries are <a href="https://www.theguardian.com/society/2020/dec/09/nine-out-of-10-in-poor-nations-to-miss-out-on-inoculation-as-west-buys-up-covid-vaccines" rel="noopener noreferrer" target="_blank">unlikely to be vaccinated</a> against COVID-19 next year.” Many people in low-income countries <a href="https://www.nature.com/articles/d41586-020-03370-6" rel="noopener noreferrer" target="_blank">might have to wait until 2023 or 2024</a> for vaccination. In an attempt to counter this trend towards severe inequality, WHO has <a href="https://www.who.int/publications/m/item/fair-allocation-mechanism-for-covid-19-vaccines-through-the-covax-facility" rel="noopener noreferrer" target="_blank">a plan</a> to ensure equitable allocation, but it faces many implementation <a href="https://www.sciencemag.org/news/2020/09/who-unveils-global-plan-fairly-distribute-covid-19-vaccine-challenges-await" rel="noopener noreferrer" target="_blank">challenges</a>. The arrival of vaccines from additional manufacturers is also promising for fairness in distribution because they have fewer technical limitations. The impending release of the <a href="https://endpts.com/in-historic-vote-mrna-vaccines-go-2-and-0-as-fda-experts-unanimously-back-modernas-covid-19-vaccine" rel="noopener noreferrer" target="_blank">Moderna vaccine</a> is notable because it has less stringent <a href="https://www.scientificamerican.com/article/the-covid-cold-chain-how-a-vaccine-will-get-to-you/" rel="noopener noreferrer" target="_blank">cold chain requirements</a>, and the Oxford–AstraZeneca vaccine is specifically aiming for “<a href="https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)32623-4/fulltext" rel="noopener noreferrer" target="_blank">global supply, equity, and commitment</a> to low-income and middle-income countries” and should be ready for use <a href="https://www.bloomberg.com/news/articles/2020-12-16/u-k-hopes-oxford-astra-vaccine-will-be-ready-by-early-new-year" rel="noopener noreferrer" target="_blank">in 2021</a>.</p>
<p>Finally, a second important lesson that must be learned is that for public health plans to succeed, it is not sufficient for scientists to work fast. Countries must design and implement sound public health policies, people must follow these policies, and the idea of vaccine as “<a href="https://www.bangkokpost.com/world/2030543/who-warns-vaccine-no-magic-bullet" rel="noopener noreferrer" target="_blank">magic bullet</a>" must be replaced with a more nuanced understanding of the complexities of Covid and its spread. This means that preventative public health practices like social distancing and mask wearing must be continued throughout the vaccine process. Some of these health behaviors might even be here to stay within certain risky contexts, since coronaviruses may continue as <a href="https://academic.oup.com/jid/article/222/5/719/5860444" rel="noopener noreferrer" target="_blank">seasonal outbreaks</a> like influenzas, and <a href="https://pubmed.ncbi.nlm.nih.gov/8604175/" rel="noopener noreferrer" target="_blank">new infections </a>will continue to emerge into the human population.</p>
    


<p><em><a href="https://massivesci.com/people/sara-may-bergstresser/">Sara May Bergstresser </a> studies 

<p class="mb0">

<span class="scientist__field">Bioethics</span>, 

<span class="scientist__field">Public Health</span>, 

and <span class="scientist__field">Biochemistry</span>

</p>

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<span class="scientist__institution">Columbia University</span>

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<guid isPermaLink="true">https://massivesci.com/articles/covid19-vaccine-hesitancy-scicomm/</guid>
<link>https://massivesci.com/articles/covid19-vaccine-hesitancy-scicomm/</link>
<pubDate>Mon, 21 Dec 2020 11:31:08 EST</pubDate>
<title>Empathy is key to overcoming COVID-19 vaccine hesitancy</title>
<description>COVID-19 vaccines are an enormous feat. Their use will hinge on explaining how it was done</description>

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  <dc:creator><![CDATA[Shelby Bradford]]></dc:creator>
  <atom:author>
    <atom:name>Shelby Bradford</atom:name>
    <atom:uri>https://massivesci.com/people/shelby-bradford/</atom:uri>
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    <p>Following promising phase III clinical trials, the UK and Canada have approved Pfizer's novel vaccine against COVID-19. In the U.S., the FDA has given <a href="https://www.reuters.com/article/us-health-coronavirus-fda-pfizer/u-s-fda-authorizes-pfizer-covid-19-vaccine-for-emergency-use-idUSKBN28L1IG" rel="noopener noreferrer" target="_blank">emergency use authorization</a> (EUA) for the Pfizer vaccine and the <a href="https://www.nbcnews.com/news/world/covid-d-day-arrives-vaccine-set-arrive-all-50-states-n1251074" rel="noopener noreferrer" target="_blank">first doses</a> were administered on December 14. These are collectively tremendous accomplishments and suggest that the virus causing COVID-19 can be contained through an immunization program. However, that hinges on these vaccines actually getting administered to people. This may be an unanticipated hurdle to relief from the pandemic.&nbsp;</p>
<p>A poll from the <a href="https://www.pewresearch.org/science/2020/12/03/intent-to-get-a-covid-19-vaccine-rises-to-60-as-confidence-in-research-and-development-process-increases/" rel="noopener noreferrer" target="_blank">Pew Research Center </a>in mid-November shows that about 60 percent of Americans would get an approved COVID-19 vaccine. While this is up from <a href="https://www.pewresearch.org/science/2020/09/17/u-s-public-now-divided-over-whether-to-get-covid-19-vaccine/" rel="noopener noreferrer" target="_blank">September polls</a> and a <a href="https://news.gallup.com/poll/323378/new-experiment-shows-boost-covid-vaccine-acceptance.aspx" rel="noopener noreferrer" target="_blank">Gallup</a> poll in October, which indicated only about 50 percent of Americans were planning to get a vaccine against COVID-19, this would be below the 70 percent of the population the FDA estimates would need to be immunized in order to meaningfully reduce spread of the virus.&nbsp;</p>
<p>Many of these people who have reservations about getting immunized, sometimes called "vaccine hesitant," are concerned about how safe and how effective a vaccine which has been produced so quickly can be. These concerns were reflected in a <a href="https://jamanetwork.com/journals/jamanetworkopen/fullarticle/10.1001/jamanetworkopen.2020.25594?utm_source=For_The_Media&amp;utm_medium=referral&amp;utm_campaign=ftm_links&amp;utm_term=102020" rel="noopener noreferrer" target="_blank">JAMA</a> paper in published in October, where there was survey subjects indicated lowered faith in a vaccine licensed under an EUA from the FDA than one which went through the standard approval process. Furthermore, some groups, such as Black individuals, can be distrustful of American public health institutions because of historical <a href="https://www.washingtonpost.com/opinions/black-people-are-justifiably-wary-of-a-vaccine-their-trust-must-be-earned/2020/12/09/4cf5f18c-3a36-11eb-9276-ae0ca72729be_story.html" rel="noopener noreferrer" target="_blank">abuses</a> in medical science and maintained <a href="https://www.aamc.org/news-insights/how-we-fail-black-patients-pain" rel="noopener noreferrer" target="_blank">biases</a> that impact health outcomes today. This highlights a need to strategize communication efforts amongst scientists and public health officials to address these specific concerns so people understand and trust the science behind these vaccines.&nbsp;</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/articles/pfizer-moderna-vaccine-covid-coronavirus/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Farticles%2Fpfizer-moderna-vaccine-covid-coronavirus%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>Most of us are not familiar with the details of clinical trials, but we understand that they are designed to ensure new medicine works and is safe. If we know anything else, it is that clinical trials usually take a long time. In the absence of good communication and transparency about how these trials are being accelerated, many people can become concerned that corners were cut or scientists don’t fully know if these vaccines are safe and effective. It is not enough to say “this is safe” as reason to accept a vaccine, nor will data transparency alone be helpful in convincing people of safety or efficacy. The data released will likely be densely laden with jargon and statistics most people can’t decipher.&nbsp;</p>
<p>Instead, a thorough network of public health officials, physicians, and the scientific community should take the advice outlined in a <a href="https://www.centerforhealthsecurity.org/our-work/publications/the-publics-role-in-covid-19-vaccination" rel="noopener noreferrer" target="_blank">report</a> jointly from the Center for Health Safety and the International Access Center. The report recommends the development of an approach centered on communicating these vaccines safety, risks, benefits, and availability to the public in a non-partisan and empathetic manner to the general public.&nbsp;</p>
<div class="oembed"><iframe width="200" height="113" src="https://www.youtube.com/embed/ddDiyIKUP0M?feature=oembed" frameborder="0" allow="accelerometer; autoplay; clipboard-write; encrypted-media; gyroscope; picture-in-picture" allowfullscreen></iframe></div>
<p>Examples, such as <a href="https://www.youtube.com/watch?v=ddDiyIKUP0M&amp;feature=emb_logo&amp;ab_channel=UniversityofOxford" rel="noopener noreferrer" target="_blank">this video</a> from University of Oxford, about how the process was sped up, that are condensed into convenient and understandable formats could be one tool to communicate how scientific integrity was maintained while meeting urgent needs for a product. Content which illustrates how the ability of the vaccine to prevent disease was assessed in clinical trials, and how it will continue to be monitored, would assure individuals of scientists’ basis for confidence in these vaccines. While recommendations from leading public health experts from the FDA, CDC, and WHO would boost confidence and trust as well, these come after or in association with seeing proof of these vaccines safety and efficacy to most individuals.</p>
<p>A widespread campaign to address concerns and provide clear information would establish trust between science bodies and communities, giving individuals the power to make their own informed decisions. Conversely, <a href="https://www.nejm.org/doi/full/10.1056/NEJMp2020926" rel="noopener noreferrer" target="_blank">mandates</a> that enforce immunization, which have been suggested as a way to boost vaccine compliance <a href="https://www.nature.com/articles/s41591-020-1124-9" rel="noopener noreferrer" target="_blank">lowered</a> acceptance of a COVID vaccine: 44 percent of a study group agreed they would take a vaccine proven safe and effective, but only 14 percent agreed when asked if they would take the vaccine were their employer to recommend or require it.&nbsp;</p>
<p>One rationale this study cited for this is that, while mandates are effective at ensuring vaccine compliance, these are more likely to lower actual confidence and trust in public health measures, <a href="https://www.nejm.org/doi/full/10.1056/nejmp1113008" rel="noopener noreferrer" target="_blank">driving</a> concerned individuals toward seeking healthcare providers willing to overlook vaccine recommendations and pursue exemptions in school and work. This is observed in <a href="https://www.medicine.wisc.edu/sites/default/files/overcoming_challenges_to_childhood_immuno_conway.pdf" rel="noopener noreferrer" target="_blank">childhood vaccination</a> rates, where school requirements often improve immunization status unless medical and non-medical exemptions are available that vaccine-hesitant parents seek.&nbsp;</p>
<p>In these instances, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6016709/" rel="noopener noreferrer" target="_blank">educating</a><a href="https://www.medicine.wisc.edu/sites/default/files/overcoming_challenges_to_childhood_immuno_conway.pdf" rel="noopener noreferrer" target="_blank"> </a>parents on vaccine safety and benefits and disease severity was shown to significantly increase immunization for MMR and DTaP, by 5.1 percent and 4.5 percent respectively, and reduce medical exemptions. However, where non-medical exemptions were permitted, immunization coverage was not affected by state interventions or mandates. This demonstrates the importance of not only communicating vaccine safety and importance, but also to listen to the specific concerns of the individual patient or group and cultivate an open dialogue to establish trust.</p>
<aside class="pullquote"><blockquote>At the end of the day, even the most protective vaccine will not matter if not enough people take it</blockquote></aside>
<p>Individual demographics are a vital consideration in any communication strategy. It is not without reason, as has been <a href="https://www.washingtonpost.com/opinions/black-people-are-justifiably-wary-of-a-vaccine-their-trust-must-be-earned/2020/12/09/4cf5f18c-3a36-11eb-9276-ae0ca72729be_story.html" rel="noopener noreferrer" target="_blank">discussed</a>, that greater hesitation to vaccination may be highly prevalent among Black people. This is despite the fact that this demographic has experienced cases, hospitalizations, and deaths at a <a href="https://www.cdc.gov/coronavirus/2019-ncov/covid-data/investigations-discovery/hospitalization-death-by-race-ethnicity.html" rel="noopener noreferrer" target="_blank">greater incidence</a> than white, non-Hispanic individuals. Communication efforts must address the specific concerns people have and provide the trust that they will be protected throughout their acceptance of these vaccines.&nbsp;</p>
<p>At the end of the day, even the most protective vaccine will not matter if not enough people take it. Widespread vaccination can be achieved by organized efforts on the part of public health officials, physicians, and science communicators, to illustrate how scientists have still assessed safety and protection in these products even on this accelerated timeline. People want to understand how there is so much certainty in these vaccines; many are suggesting waiting until “they see the evidence." Scientists have the evidence, it is just a matter of communicating it.&nbsp;</p>
    


<p><em><a href="https://massivesci.com/people/shelby-bradford/">Shelby Bradford</a> studies 

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<span class="scientist__field">Immunology</span>

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<span class="scientist__institution">West Virginia University</span>

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<guid isPermaLink="true">https://massivesci.com/articles/covid19-mrna-vaccine-cold-chain/</guid>
<link>https://massivesci.com/articles/covid19-mrna-vaccine-cold-chain/</link>
<pubDate>Sat, 19 Dec 2020 13:11:26 EST</pubDate>
<title>Why do the COVID-19 mRNA vaccines need to be kept so cold?</title>
<description>The Pfizer and Moderna vaccine cold chains, explained</description>

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  <dc:creator><![CDATA[Joshua Peters]]></dc:creator>
  <atom:author>
    <atom:name>Joshua Peters</atom:name>
    <atom:uri>https://massivesci.com/people/joshua-peters/</atom:uri>
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    <p>Monday, December 14th, marked the first public vaccinations of the Pfizer-BioNTech vaccine in the US. It came 339 days after the release of the SARS-CoV-2 genome and months of clinical trials involving more than 43,000 people during a raging pandemic that has infected 73,600,000 and killed 1,640,000 people worldwide. Pfizer-BioNTech’s vaccine is among<a href="https://www.nytimes.com/interactive/2020/science/coronavirus-vaccine-tracker.html"><ins> 23 vaccines</ins></a> in the final stages of testing and approval – phase 3 and/or nearing approval. In the United States, Moderna’s vaccine is expected to be distributed soon, after <a href="https://www.nytimes.com/2020/12/17/health/covid-vaccine-fda-moderna.html"><ins>endorsement</ins></a> by an FDA panel, and emergency approval <a href="https://www.usatoday.com/story/news/nation/2020/12/19/covid-update-moderna-vaccine-authorized-biden-vaccinated/3962420001/"><ins>received</ins></a>, with similar efficacy results to Pfizer-BioNTech’s vaccine.</p>
<p>Both of these vaccines are <a href="https://massivesci.com/articles/mrna-vaccine-covid19-coronavirus-moderna/"><ins>RNA-based</ins></a>. Instead of priming the immune system with a dead virus or a piece of a virus, as vaccines in the past have done, these vaccines deliver a template – RNA – for our cells to make a single protein from SARS-CoV-2. The body creates the protein, generates a protective immune response, then throws away the RNA&nbsp;– much like kids passing notes in class, then crumpling them up and tossing them in the trash.&nbsp;</p>
<p>Each vaccine consists of two doses, given a few weeks apart. Manufacturing is expected to produce close to 2 billion doses in 2021 (up to <a href="https://www.pfizer.com/news/press-release/press-release-detail/pfizer-and-biontech-announce-vaccine-candidate-against"><ins>1.3 billion</ins></a> for Pfizer-BioNTech, up to <a href="https://investors.modernatx.com/news-releases/news-release-details/moderna-announces-primary-efficacy-analysis-phase-3-cove-study"><ins>1 billion</ins></a> for Moderna), enough for almost 15% of the world’s population if these companies reach their maximum output. Despite unprecedented success in the development of these new vaccines, their extensive testing, and scaling up manufacturing, there remains another hill to climb before these vaccines can help protect people. These RNA vaccines require extremely cold temperatures.&nbsp;</p>
<figure class="right medium"><img alt="A common ultracold freezer found in a lab. It stands upright, with a temperature readout on the bottom" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/d497ebfe-4ea2-4f0c-9fc1-448d9dd09c4e/Revco_-80_freezer_pl.jpg"/><figcaption><span class="caption"><p>A common ultracold freezer found in a lab. These types of freezers can cost $10,000 or more</p></span> <span class="credit"><p><a href="https://commons.wikimedia.org/wiki/User:Pleple2000" title="User:Pleple2000">Pleple2000</a> via Wikimedia</p></span></figcaption></figure>
<p>Pfizer-BioNTech’s vaccine requires -70°C (-94°F), colder than the South Pole, and only lasts around 5 days once placed in a refrigerator. Moderna’s vaccine is a bit more forgiving, shipped at -20°C (-4°F) and good for a month in a refrigerator. For comparison, inactivated or live attenuated vaccines (like the <a href="https://www.cdc.gov/h1n1flu/vaccination/storage_handling_qa.htm" target="_blank">flu</a> vaccine) are stored at typical refrigerator temperatures, about 2-8°C (46°F). While the Sputnik V <a href="https://weather.com/en-IN/india/coronavirus/news/2020-11-26-covid-19-vaccine-race-all-you-need-to-know-about-cold-storage" target="_blank">vaccine</a> also needs freezer-like temperatures, we can expect emerging vaccines from Novavax (NVX-CoV2373), AstraZeneca-University of Oxford (AZD1222), Johnson &amp; Johnson (Ad26.COV2.S), and others to require only refrigerator temperatures.&nbsp;</p>
<p>RNA is notorious for its instability. Before working with RNA, it’s common for scientists working with it in a lab to clean their workspace of “RNases” or ubiquitous environmental enzymes that break down RNA quickly. Unlike DNA, which typically consists of two strands and contains a submolecule called deoxyribose (hence “<em>D</em>NA”), RNA is single-stranded and contains ribose (hence “<em>R</em>NA”), which makes RNA molecules more susceptible to degradation. Despite the chemical modifications and packaging these companies use to make it more resistant, it still suffers compared to DNA or protein.&nbsp;</p>
<p>The extreme temperatures slow down chemical and enzymatic degradation, allowing the RNA vaccines to maintain their efficacy from manufacturing to injection. RNA’s instability is good for our cells: many copies of RNA are transcribed from DNA templates, which are then used to create proteins. But as the proteins required by the cell are made, the instructions are degraded away.&nbsp;</p>
<p>These companies define these temperatures through testing the vaccine across a range of temperatures and storage durations. Protein vaccines have their own requirements as well. While they are typically stored in a refrigerator, freezing them can disfigure the proteins, rendering them ineffective. Pfizer-BioNTech has mentioned <a href="https://www.npr.org/sections/health-shots/2020/11/17/935563377/why-does-pfizers-covid-19-vaccine-need-to-be-kept-colder-than-antarctica"><ins>ongoing studies</ins></a> on storage conditions, but for now, ultracold transportation with GPS tracking it is.&nbsp;</p>
<figure class="right medium"><img alt="A diagram showing a five sided sugar molecule from RNA on the left and one from DNA on the right. The sugar from RNA has an extra oxygen that DNA is missing" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/f584229e-0d37-41c1-8227-3e4f220b5f70/The_difference_between_ribose_and_deoxyribose.png"/><figcaption><span class="caption"><p>The only chemical difference between RNA and DNA is the presence of a single oxygen atom (RNA carries a ribose, left, highlighted in red) that is missing in DNA, which carries a deoxyribose (right)</p></span> <span class="credit"><p><a href="https://commons.wikimedia.org/w/index.php?title=User:Miranda19983$!&amp;action=edit&amp;redlink=1" title="User:Miranda19983$! (page does not exist)"><ins>Miranda19983$!</ins></a> via Wikimedia</p></span></figcaption></figure>
<p>The transport of vaccines, and cold items more broadly, from a manufacturing site to a recipient is known as the <a href="https://www.nytimes.com/interactive/2020/12/10/us/covid-vaccine-distribution.html"><ins>cold chain</ins></a>. The cold chain can be divided into different temperature requirements, such as freezer temperatures (about -20°C) that the Moderna vaccine requires or ultracold temperatures for Pfizer-BioNTech’s, or even cryogenic temperatures which can reach -150°C (-238°F) for shipping biological materials. Over the course of the first week, 636 sites were expected to receive the vaccine through the Fedex and UPS shipping networks. Pfizer’s shipping containers can stay cold enough for 10 days unopened. After receiving these precious vaccines, sites need to maintain these temperatures in ultra-low freezers (good for six months), which cost well over $10,000 with enormous energy consumption, in the original shipping container by refilling with dry ice (-79°C, -109°F, good for 30 days) or storing in a refrigerator, where the vaccines must be used within 5 days.</p>
<p>This extreme cold chain has sprouted intense investment and <a href="https://www.reuters.com/article/us-health-coronavirus-vaccines-distribut/why-pfizers-ultra-cold-covid-19-vaccine-will-not-be-at-the-local-pharmacy-any-time-soon-idUKKBN27P2VI"><ins>concern</ins></a>. Perhaps most notably, India has <a href="https://timesofindia.indiatimes.com/india/india-needs-5-2m-11m-cold-chain-equipment-to-handle-vaccine-govt-projects/articleshow/79748757.cms"><ins>projected needing millions of additional equipment</ins></a> to handle these various vaccines. The dramatic need for cold chain solutions across the globe has grabbed <a href="https://www.nytimes.com/2020/12/15/business/cold-storage-covid-vaccine.html"><ins>Wall Street’s attention</ins></a>, driving investment in one company, Cryoport, up over 200% year to date. Given the challenges in countries with developed healthcare infrastructures, it’s not hard to imagine the additional challenges in less developed countries. There’s some <a href="https://www.nytimes.com/2020/12/15/us/coronavirus-vaccine-doses-reserved.html"><ins>precedent</ins></a> before with the Ebola vaccine, but the scale of these infections are vastly different. Despite these challenges, perhaps the first issue is the <a href="https://www.nytimes.com/2020/12/15/us/coronavirus-vaccine-doses-reserved.html"><ins>availability</ins></a> of these vaccines, which was quickly cleared by Western countries.</p>
<p>The cold chain required for vaccines is not a new challenge. The WHO and <a href="https://www.path.org/articles/vaccine-cold-chain-q/"><ins>PATH</ins></a>, among others, have been focusing on supply chain issues for decades, developing new technology like solar-powered refrigerators and <a href="https://www.who.int/immunization/call-to-action_ipac-iscl.pdf"><ins>calling for action</ins></a> in 2014. The overwhelming <a href="https://www.visualcapitalist.com/history-of-pandemics-deadliest/"><ins>scale</ins></a> of COVID-19 and mass vaccination campaigns mixed with subfreezer temperatures is a new challenge. As we end 2020, we can hope more efficacious vaccines are approved early in 2021, allowing more people from more walks of life to have access to protection against COVID-19, ending the pandemic.</p>
    


<p><em><a href="https://massivesci.com/people/joshua-peters/">Joshua Peters</a> studies 

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<span class="scientist__field">Biological Engineering</span>

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<span class="scientist__institution">Massachusetts Institute of Technology</span>

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<guid isPermaLink="true">https://massivesci.com/articles/pfizer-moderna-vaccine-covid-coronavirus/</guid>
<link>https://massivesci.com/articles/pfizer-moderna-vaccine-covid-coronavirus/</link>
<pubDate>Sun, 22 Nov 2020 13:37:11 EST</pubDate>
<title>How should a COVID-19 vaccine be distributed?</title>
<description>With Pfizer and Moderna vaccines proving effective, how should a population get vaccinated?</description>

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  <dc:creator><![CDATA[Jill Neimark]]></dc:creator>
  <atom:author>
    <atom:name>Jill Neimark</atom:name>
    <atom:uri>https://massivesci.com/people/jill-neimark/</atom:uri>
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    <p>If the book of nature is written in the language of mathematics, as Galileo once declared, the Covid-19 pandemic has brought that truth home for the world’s mathematicians, who have been galvanized by the rapid spread of the coronavirus.</p>
<p>So far this year, they have been involved in everything from revealing <a href="https://labblog.uofmhealth.org/rounds/how-scientists-quantify-intensity-of-an-outbreak-like-covid-19"><ins>how contagious</ins></a> the novel coronavirus is, how <a href="https://www.thelancet.com/journals/lancet/article/PIIS0140-6736(20)31142-9/fulltext"><ins>far we should stand</ins></a> from each other, how long an infected person <a href="https://www.cdc.gov/coronavirus/2019-ncov/hcp/duration-isolation.html"><ins>might shed</ins></a> the virus, how a single strain <a href="https://www.nytimes.com/2020/04/08/science/new-york-coronavirus-cases-europe-genomes.html"><ins>spread from Europe to New York</ins></a> and then <a href="https://www.nytimes.com/2020/05/07/us/new-york-city-coronavirus-outbreak.html"><ins>burst across America</ins></a>, and how to ‘’<a href="https://www.weforum.org/agenda/2020/05/covid-19-coronavirus-models-data-behaviour-infection-death-rate-flatten-curve-policy/"><ins>flatten the curve’</ins></a>‘ to save hundreds of thousands of lives. Modeling also helped persuade the Centers for Disease Control and Prevention that the virus <a href="https://www.nytimes.com/2020/10/05/health/cdc-coronavirus-airborne-indoor-air.html"><ins>can be airborne</ins></a> and transmitted by <a href="https://science.sciencemag.org/content/early/2020/10/02/science.abf0521?rss=1"><ins>aerosols that stay aloft</ins></a> for hours.</p>
<p>And at the moment many are grappling with a particularly urgent — and thorny — area of research: modeling the optimal rollout of a vaccine. Because vaccine supply will be limited at first, the decisions about who gets those first doses could save tens of thousands of lives. This is critical now that promising early results are coming in about two vaccine candidates — one <a href="https://www.statnews.com/2020/11/09/covid-19-vaccine-from-pfizer-and-biontech-is-strongly-effective-early-data-from-large-trial-indicate/"><ins>from Pfizer and BioNTech</ins></a> and one <a href="https://www.nytimes.com/2020/11/16/health/Covid-moderna-vaccine.html"><ins>from Moderna</ins></a> — that may be highly effective and for which the companies may apply for emergency authorization from the Food and Drug Administration.</p>
<p>But figuring out how to allocate vaccines — there are close to 50 in clinical trials on humans — to the right groups at the right time is “a very complex problem,” says <a href="https://www.isye.gatech.edu/users/eva-lee"><ins>Eva Lee</ins></a>, director of the Center for Operations Research in Medicine and Health Care at the&nbsp;<a href="https://www.gatech.edu/"><ins>Georgia Institute of Technology</ins></a>. Lee has <a href="https://sites.google.com/view/evaklee/realopt"><ins>modeled</ins></a> dispensing strategies for vaccines and medical supplies for Zika, Ebola, and <a href="https://pubsonline.informs.org/doi/full/10.1287/inte.2015.0814"><ins>influenza</ins></a>, and is now working on Covid-19. The coronavirus is “so infectious and so much more deadly than influenza,” she says. “We have never been challenged like that by a virus.”</p>
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<p><a href="https://som.yale.edu/faculty/howard-p-forman"><ins>Howard Forman</ins></a>, a public health professor at Yale University, says “the last time we did mass vaccination with completely new vaccines,” was with smallpox and polio. “We are treading into an area we are not used to.” All the other vaccines of the last decades have either been tested for years or were introduced very slowly, he says.</p>
<p>Because Covid-19 is especially lethal for those over 65 and those with other health problems such as obesity, diabetes, or asthma, and yet is spread rapidly and widely by healthy young adults who are more likely to recover, mathematicians are faced with two conflicting priorities when modeling for vaccines: Should they prevent deaths or slow transmission?</p>
<p>The consensus among most modelers is that if the main goal is to slash mortality rates, officials must prioritize vaccinating those who are older, and if they want to slow transmission, they must target younger adults.</p>
<p>“Almost no matter what, you get the same answer,” says Harvard epidemiologist <a href="https://www.hsph.harvard.edu/marc-lipsitch/"><ins>Marc Lipsitch</ins></a>. Vaccinate the elderly first to prevent deaths, he says, and then move on to other, healthier groups or the general population. One recent study modeled how Covid-19 is likely to spread in six countries — the U.S., India, Spain, Zimbabwe, Brazil, and Belgium — and concluded that if the primary goal is to reduce mortality rates, adults over 60 should be prioritized for direct vaccination. The study, by <a href="https://www.colorado.edu/cs/daniel-larremore"><ins>Daniel Larremore</ins></a> and <a href="https://www.colorado.edu/certificate/iqbiology/kate-bubar"><ins>Kate Bubar</ins></a> of the University of Colorado Boulder, Lipsitch, and their colleagues, has been published as a <a href="https://www.medrxiv.org/content/10.1101/2020.09.08.20190629v1.article-metrics"><ins>preprint</ins></a>, meaning it has not yet been peer reviewed. Of course, when considering Covid-19’s outsized impact on minorities — especially Black and Latino communities — additional considerations for prioritization come into play.</p>
<p>Most modelers agree that “everything is changing with coronavirus at the speed of light,” as applied mathematician <a href="https://research.fhcrc.org/halloran/en/members.html"><ins>Laura Matrajt</ins></a>, a research associate at the Fred Hutchinson Cancer Research Center in Seattle, put it in an email. That includes our understanding of how the virus spreads, how it attacks the body, how having another disease at the same time might raise the risk, and what leads to super-spreader events.</p>
<p>So far, the research has yielded some surprising results. While children are usually prioritized for flu vaccine, for example, experts say the very young should be a lower priority for Covid-19 vaccines in the United States, because thus far young adults have been primary drivers of transmission. (This is not necessarily true across the globe; in India, for instance, where multiple generations often live together in smaller spaces, new research shows both <a href="https://science.sciencemag.org/content/early/2020/09/29/science.abd7672"><ins>children and young adults</ins></a> are spreading much of the virus in the two states studied.)</p>
<p>In addition, several models suggest that significant headway can be made against the pandemic even with lower deployment of a vaccine that is only partly effective. And several others emphasize the importance of local infection and transmission rates. According to Lee, whose early assessments of the pandemic’s origin, virulence, and probable global trajectory proved to be <a href="https://undark.org/2020/04/09/eva-lee-georgia-tech-fraud-covid-19/"><ins>strikingly accurate</ins></a>, New York could potentially contain the virus if about 40 percent of the population were vaccinated, because local transmission of the virus is <a href="https://www1.nyc.gov/site/doh/covid/covid-19-data.page"><ins>fairly low</ins></a> (a positivity rate of a little below 3 percent as of Nov. 16), and around 20 percent have already been infected.</p>
<p>“The higher the fraction of people in the population who already have antibodies, the more bang for your buck,” says Larremore, because you can prioritize giving vaccines to those who don’t have antibodies.</p>
<p>All these findings are important because, “at the end of the day, you will never have enough vaccines for the entire population,” says Lee — and not all Americans will take it. In fact, the World Health Organization recently predicted that healthy young adults may not even be able to get a vaccine until 2022, after the elderly, health care workers, and other high-risk groups are vaccinated.</p>
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<p>To model the rollout of vaccines, mathematicians must build formulas that reflect the starburst of human life and our complex interactions, using data like housing and socioeconomic status, daily habits, age, and health risks. But first they establish how contagious the virus is — its reproductive rate, or “R-naught.” This represents the number of people that one infected person can be expected to transmit the infection to.</p>
<p>When some fraction (depending on R-naught) of people are immune (either by recovering from natural infection, if that grants immunity, or through vaccination), herd immunity has been achieved. That means that while small outbreaks may still occur, the pandemic will not take off globally again. Given the R-naught of SARS-CoV-2, the virus that causes Covid-19, the World Health Organization has estimated that 65 percent to 70 percent of the population needs to be immune before this can be achieved.</p>
<figure class="center large"><img alt="Vaccine rollout scenarios developed by Bubar et al. include five different ways of distributing the first doses of vaccines, presented in the left panel. The scenarios show the same pattern: to prevent deaths, vaccinate the elderly first, and then move on to other, healthier groups or the general population." src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/10b82fc8-f01d-460c-8946-31e43babdb98/lipstich-preprint-fig-1-edit-scaled-e1605647583986.jpg"/><figcaption><span class="caption"><p>Vaccine rollout scenarios developed by Bubar et al. include five different ways of distributing the first doses of vaccines, presented in the left panel. The scenarios show the same pattern: to prevent deaths, vaccinate the elderly first, and then move on to other, healthier groups or the general population.</p></span> <span class="credit"><p><a href="https://www.medrxiv.org/content/10.1101/2020.09.08.20190629v1.full.pdf+html" target="_blank"><ins><em>Bubar et al. / MedRxiv</em></ins></a></p></span></figcaption></figure>
<p>Modeling vaccine rollout requires a complex acrobatics, and while the models to flatten the curve that mesmerized the public last spring took weeks to craft, vaccine distribution models take many months. There are innumerable practical challenges facing modelers. For one thing, many of the vaccines currently in the pipeline — including the two candidates from <a href="https://www.nytimes.com/2020/11/12/business/pfizer-covid-vaccine-coronavirus.html"><ins>Pfizer and BioNTech</ins></a> and <a href="https://www.sciencemag.org/news/2020/11/just-beautiful-another-covid-19-vaccine-newcomer-moderna-succeeds-large-scale-trial"><ins>Moderna</ins></a> — require two shots, several weeks apart, which involve registries and follow-up to ensure that people get the second, critical booster shot. And as The New York Times <a href="https://www.nytimes.com/2020/09/18/business/coronavirus-covid-vaccine-cold-frozen-logistics.html"><ins>noted in late September</ins></a>, “Companies may have to transport tiny glass vials thousands of miles while keeping them as cold as the South Pole in the depths of winter.”</p>
<p>There is also the question of vaccine efficacy. Will a given vaccine provide robust immunity, and in all groups? Or will it primarily shorten duration of infection and lessen symptoms, which would still be of great value in reducing mortality as well as transmission? And what if a vaccine is less effective among the elderly, as is often the case? At the moment, vaccines using <a href="https://www.statnews.com/2020/10/26/mrna-vaccines-face-their-first-test-in-the-fight-against-covid-19-how-do-they-work/"><ins>messenger RNA</ins></a> (including those produced by Moderna and Pfizer and BioNTech) are “looking pretty good in older adults,” according to <a href="https://www.medschool.umaryland.edu/profiles/Neuzil-Kathleen/"><ins>Kathleen Neuzil</ins></a>, director of the Center for Vaccine Development and Global Health at the University of Maryland School of Medicine. Preliminary analyses of both vaccine candidates show that they may be more than 90 percent effective.</p>
<p>Finally, there is also the vexing question of how long immunity might last after infection. For some viruses, such as the varicella-zoster virus that causes chickenpox, immunity can last for decades. For others, such as the family of coronaviruses that includes SARS-CoV-2 and the common cold, the virus has a relatively high mutation rate that <a href="https://www.nature.com/articles/s41467-017-01706-x"><ins>may protect novel strains</ins></a> from our antibodies. That uncertainty is difficult to model precisely, so many modelers assume that, for the time being at least, those who have been infected are immune.</p>
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<p>Matrajt, of the Fred Hutchinson Cancer Center in Seattle, remembers vividly how hard it was to begin to construct a model out of thin air when she began working with colleagues on a vaccination model this past April. There were “so many uncertainties,” she recalls. Together, the researchers developed algorithms based on an astonishing 440 or so combinations of parameters, from transmission to immunity to age groups and mortality. Their computers spent nearly 9,000 hours running equations, and their model, <a href="https://www.medrxiv.org/content/10.1101/2020.08.14.20175257v1"><ins>published</ins></a> in August as a preprint, shows that if there is only a low supply of vaccine at first, older adults should be prioritized if the goal is to reduce deaths.</p>
<p>But for vaccines that are at least 60 percent effective, once there is enough to cover at least half the population, switching to target healthy individuals ages 20 to 50 as well as children would minimize deaths. The model also predicts how many deaths can be averted with different amounts of vaccine coverage. For instance, if 20 percent of the population has already been infected and is immune, deaths could be halved by vaccinating just 35 percent of the remainder, if the vaccine is at least 50 percent effective.</p>
<p>In the model by Matrajt and her colleagues, herd immunity is achieved once 60 percent of the population is immune. “It is completely normal that different models will give different numbers,” she says, explaining why her estimate varies slightly from the WHO figure of 65 percent.</p>
<p>The model does “a really nice job looking at a large number of plausible cases,” says <a href="https://springborn.faculty.ucdavis.edu/"><ins>Michael Springborn</ins></a>, an environmental and resource economist at the University of California, Davis, who just finished his own model with <a href="http://www.des.ucdavis.edu/faculty/baskett/research/studentsPostdocs.html"><ins>Jack Buckner</ins></a>, a colleague at UC Davis, and <a href="https://publichealth.gsu.edu/profile/gerardo-chowell/"><ins>Gerardo Chowell</ins></a>, a mathematical epidemiologist at Georgia State University. Their <a href="https://www.medrxiv.org/content/10.1101/2020.09.22.20199174v3.full.pdf"><ins>study</ins></a>, released in preprint, also suggests the power of careful initial targeting in reducing deaths.</p>
<p>The models suggest that even a partially-effective vaccine given to just part of the population, says Springborn, “can go a really long way to reducing infections and reducing deaths.”</p>
<figure class="center large"><img alt="A vaccine rollout model shows how availability and efficacy of the vaccine affects infections and deaths due to Covid-19. " src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/664c0b26-c3d1-43f2-9d04-66207348ec5b/matrajt-vaccine-figure-no-letters-top-only-1.jpg"/><figcaption><span class="caption"><p>A vaccine rollout model by Matrajt and her colleagues shows how availability and efficacy of the vaccine affects infections and deaths due to Covid-19.&nbsp;</p></span> <span class="credit"><p><a href="https://www.medrxiv.org/content/10.1101/2020.08.14.20175257v2" target="_blank"><ins><em>Matrajt et al. / medRxiv</em></ins></a></p></span></figcaption></figure>
<p>Lee’s modeling, created with <a href="https://www.realopt.gatech.edu/"><ins>software</ins></a> she first developed in 2003, in conjunction with the CDC, for dispensing of supplies in natural disasters and pandemics, analyzes how the disease might be contained in areas with different infection rates and initially scarce vaccine supplies. In New York City, which was hit so hard in the spring, her model predicts that roughly 60 percent of the population may need immunity to contain the pandemic. Assuming 20 percent are already infected, about 40 percent would need to be vaccinated. In San Diego, however, where infection rates have been lower, Lee’s model suggests that 65 percent will need to achieve immunity through infection or vaccination. In Houston, the figure may be as high as 73 percent because the infection has persisted at a “slow burn” and because of the city’s large, vulnerable Latino and African American populations, who have borne disproportionate risk.</p>
<p>Lee cautions that these results do not mean you can suddenly go to a football game in Houston or Broadway show in New York, but it does mean that with ongoing precautions, the virus might well be contained with the percentages given in her models, until more vaccine arrives.</p>
<p>Though their results vary, most models agree that certain factors are critical, notably age group, which changes the risk of contracting, spreading, and dying from a virus. It’s not always predictable: The swine flu, for instance, <a href="https://www.wired.com/2009/06/old-people-may-be-immune-to-swine-flu/"><ins>spared older adults</ins></a> to some degree, while SARS-CoV-2 has severely affected those over 65. Adults 65 and older compose 16 percent of the U.S. population but account for about <a href="https://www.kff.org/coronavirus-covid-19/issue-brief/what-share-of-people-who-have-died-of-covid-19-are-65-and-older-and-how-does-it-vary-by-state/"><ins>80 percent of Covid-19 deaths</ins></a>.</p>
<p>In addition, age indirectly influences transmission patterns. In 2009, Yale epidemiologists Alison Galvani and Jan Medlock published a mathematical model in <a href="https://pubmed.ncbi.nlm.nih.gov/19696313/"><ins>Science</ins></a>, showing that targeting flu vaccines to children and young adults (in addition to the elderly) could have slashed swine flu infections from 59 million to 44 million; and for seasonal influenza, 83 million infections could plunge to 44 million. Children, it turns out, drive a disproportionate amount of flu transmission, and protecting them protects society at large.</p>
<p>The study, and others like it, inspired a change in CDC policy to prioritize vaccinating children. “It was a revolution in how we think about vaccines,” says Larremore. Vaccination models now routinely consider the power of indirect protection of the most vulnerable by vaccinating those most responsible for spread.</p>
<p>Age also intersects, in complex ways, with social connectivity in different regions. For instance, African American and Latino communities in the United States have been disproportionately hit by Covid-19, in part because of the prevalence of <a href="https://www.samhsa.gov/sites/default/files/covid19-behavioral-health-disparities-black-latino-communities.pdf"><ins>multiple generations living together</ins></a>: Older individuals are much more exposed to the young adults who might be the likeliest carriers of infection.</p>
<p>Modeling connectivity requires drawing grids that represent how we live and move among each other. In 2008, <a href="https://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.0050074"><ins>a landmark paper</ins></a> built a grid that epidemiologists everywhere still use today. It stratified people into groups based on age, from birth to 70 years old and up. In the study, more than 7,000 individuals kept a diary of their contacts — nearly 98,000 of them — over the course of one day. Contacts were sorted by place (home, school, work, leisure) and by nature (physical or nonphysical, brief or longer lasting). The model found that 5- to 19-year-olds tend to experience the highest incidence of infection when a new pathogen begins to spread in a completely susceptible population, possibly because of their more frequent and physical contact with others. It also showed how profoundly a society’s grids of connection influence transmission.</p>
<p>The model was <a href="https://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1005697"><ins>expanded globally in 2017</ins></a>, with contact rates for 152 countries. “It’s what we all use,” says Matrajt, “because it’s the best thing we have to identify how people contact each other.” She incorporated the contact grid into her model.</p>
<p>For example, “if kids are really the hubs around which society is built,” Larremore says, “so that if you vaccinate the kids, you fragment that transmission network, then that’s going to give us a totally different way of rolling out this vaccine.”</p>
<p>The original grid relied on diaries. Today, our ability to gather data through real time cellphone and online activity may be even greater.</p>
<p>When social distancing became widespread this past spring, it dramatically altered the input into the typical transmission model, says Springborn. Data from the Institute for Health Metrics and Evaluation at the University of Washington <a href="https://covid19.healthdata.org/united-states-of-america?view=social-distancing&amp;tab=trend"><ins>shows the power</ins></a> of social distancing in reducing transmission. The contact grids in previous studies are “from pre-pandemic times,” Springborn wrote in an email. “We know that contact rates are very different under social distancing and we want to account for that. And we expect social distancing to soften as the number of infections falls. Human nature: As risk falls, so does risk-mitigating behavior.”</p>
<p>That needs to be modeled as well. And it will influence the expectations for a vaccine’s rollout and success. In fact, Lee maintains, if we had 90 percent compliance with face masks and social distancing right now, we could contain the virus without a vaccine.</p>
<p>In the study by Springborn, Buckner, and Chowell, social distancing is modeled by creating age-stratified categories for both essential and nonessential workers. Essential workers — health care workers, grocery workers, and many schoolteachers, among others — are at high risk for infection because they cannot socially distance. This model finds that deaths, as well as total years of life lost, are dramatically decreased when essential workers are prioritized to receive the vaccine. Older essential workers between 40 and 59 should be prioritized first if the goal is to minimize deaths, the authors maintain.</p>
<p>With no vaccine, about 179,000 people may die in the first six months of 2021, Springborn says. His team’s model suggests that deaths could decline to about 88,000 simply by introducing a vaccine gradually, giving it to 10 percent of the population each month, and distributing it uniformly without prioritizing any groups. But distributing vaccines in a targeted way, based on people’s ages and whether they are essential workers, could save another 7,000 to 37,000 lives, depending on the situation.</p>
<p>There are other methods of teasing out social connectivity beyond diaries and cellphone data. Census and other data reflect age, profession, and socioeconomic status, and Lee includes them in her models. “The zip code gives you a huge amount of information,” she says. Public health data on disease prevalence and hospitalizations can tease out the other unrelated diseases that Covid-19 patients have, as well as vulnerabilities in a given area. Even information on a city’s housing, whether skyscrapers or single-family homes, can give a clue to how closely people are packed together and how likely they are to interact. Inputting this kind of data allows for a vaccine rollout that is sensitive to local conditions. Lee would need to model about 500 representative cities around the U.S., she says, to cover the country accurately.</p>
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<p>As powerful as the models can be, they are an imperfect guide. Inevitably they intersect with deep and broad social concerns. The pandemic has disproportionately harmed and killed minorities and those with lower incomes. For that reason, various groups are looking into the ethical principles that should frame vaccine allocation, according to <a href="https://www.who.int/immunization/sage/members/bio_nohynek/en/"><ins>Hanna Nohynek</ins></a>, deputy head of the Infectious Diseases Control and Vaccinations Unit at the Finnish Institute for Health and Welfare, and a member of the WHO’s SAGE Working Group on Covid-19 vaccines.</p>
<p>In the U.S., the National Academies of Sciences, Engineering, and Medicine has <a href="https://www.nap.edu/catalog/25914/discussion-draft-of-the-preliminary-framework-for-equitable-allocation-of-covid-19-vaccine"><ins>begun to model</ins></a> an equitable allocation of a vaccine. In addition, two other important models have emerged, <a href="https://science.sciencemag.org/content/369/6509/1309.abstract"><ins>one associated</ins></a> with University of Pennsylvania School of Medicine, and <a href="https://www.centerforhealthsecurity.org/our-work/publications/interim-framework-for-covid-19-vaccine-allocation-and-distribution-in-the-us"><ins>the other</ins></a> with Johns Hopkins University. Both are guided by concerns about ethics, fairness, maximizing benefits, building trust and the greater public good.</p>
<p>But building trust can be challenging in practice. For instance, it’s widely acknowledged that Black people have experienced hospitalization and death at disproportionately high rates compared to White people. Yet when ethicists begin to talk about prioritizing Black people for vaccines, it can be perceived as an intent to experiment on them by pushing them to the head of the line. If there is concern among African Americans, it’s a logical reaction to “a vast history of centuries of abuse of African Americans in the medical sphere,” says medical ethicist Harriet Washington, author of “<a href="https://www.penguinrandomhouse.com/authors/32502/harriet-a-washington"><ins>Medical Apartheid</ins></a>.”</p>
<p>Ultimately, both ethical and mathematical models have to face real-world practicalities. “It’s hard because math essentially boils down to a utilitarian calculus,” says Lipsitch, the Harvard epidemiologist.</p>
<p>Nonetheless, says Larremore, the models will help guide us in the uncertain early days. “Vaccines take a while to roll out,” he says. “We can’t let our foot off the gas the moment a vaccine is announced.”</p>
    


<p><em><a href="https://massivesci.com/people/jill-neimark/">Jill Neimark</a> studies 

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<span class="scientist__field">Science Journalism</span>

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<link>https://massivesci.com/articles/covid-19-vaccine-medicago-vlp-tobacco-plant/</link>
<pubDate>Tue, 13 Oct 2020 22:47:41 EST</pubDate>
<title>A virus-like COVID-19 vaccine is being grown in tobacco plants</title>
<description>The &quot;virus-like particle&quot; produced by the Canadian company Medicago is the only vaccine in clinical trials made in plants</description>

<media:content url="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/95c6f7ab-fa0c-420b-a57a-0f848a3e730f/39794577754_ef230d251a_k.jpg?auto=compress%2Cformat&amp;crop=faces&amp;fit=crop&amp;fm=jpg&amp;h=600&amp;q=75&amp;w=900" type="image/jpeg">
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  <dc:creator><![CDATA[Hayley McKay ]]></dc:creator>
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    <atom:name>Hayley McKay </atom:name>
    <atom:uri>https://massivesci.com/people/hayley-mckay/</atom:uri>
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    <p>Currently, there are close to <a href="https://www.who.int/publications/m/item/draft-landscape-of-covid-19-candidate-vaccines" rel="noopener noreferrer" target="_blank">two hundred coronavirus vaccine candidates in development, 42 </a>of which have entered clinical trials.</p>
<p>Out of these 42 candidates, one is unique: it is the only one to be produced in a plant. The Quebec City-based biopharmaceutical company, Medicago, has harnessed the speed and efficiency of plants to produce a virus-like protein (VLP) SARS-CoV-2 vaccine candidate. A VLP is like a virus. It has a similar outer shell but lacks a genome, which makes it completely harmless. It's like a water balloon with nothing in it. On July 14, it was the first SARS-CoV-2 vaccine candidate to <a href="https://www.theglobeandmail.com/canada/article-first-canadian-clinical-trial-of-any-covid-19-vaccine-is-launched-in/" rel="noopener noreferrer" target="_blank">enter clinical trials in Canada</a>.&nbsp;</p>
<p>Plants can be used to quickly and ethically produce safe and effective vaccines, reducing the reliance on traditional chicken egg vaccine production technology. Flexible and versatile, this technology has the ability to adapt to fast changing virus landscapes and create new vaccines for emerging diseases, including SARS-CoV-2.&nbsp;</p>
<aside class="pullquote"><blockquote>VLPs mimic the outer structure of viruses, which allows them to be easily recognized by the immune system</blockquote></aside>
<p>“Creating a sufficient supply of COVID-19 vaccines within the next year is a challenge which will require multiple approaches, with different technologies,” said Dr. Bruce Clark, president and CEO of Medicago in a <a href="https://www.medicago.com/en/newsroom/medicago-begins-phase-i-clinical-trials-for-its-covid-19-vaccine-candidate/">release</a>. “Our proven plant-based technology is capable of contributing to the collective solution to this public health emergency.”</p>
<h6 id="which-is-faster-the-chicken-egg-or-the-plant"><strong>Which is faster, the chicken egg or the plant?</strong></h6>
<p>Normally, vaccines take years to progress through development pipelines before they are approved for use. Many of the vaccines we use today were created more than 50 years ago using old technology. It is only in the past 20 years that scientists have begun working to harness the power of plants in order to produce vaccines and other pharmaceutical products – like <a href="https://doi.org/10.1016/j.bcmd.2016.10.005" rel="noopener noreferrer" target="_blank">enzyme replacement therapies</a>, <a href="https://doi.org/10.1155/2020/3038564" rel="noopener noreferrer" target="_blank">antibodies,</a> <a href="https://doi.org/10.1046/j.1432-1033.2003.03716.x" rel="noopener noreferrer" target="_blank">proteins</a>, and <a href="https://www.google.com/url?sa=t&amp;rct=j&amp;q=&amp;esrc=s&amp;source=web&amp;cd=&amp;cad=rja&amp;uact=8&amp;ved=2ahUKEwjVhLrGpaHsAhXFmuAKHQ0IDo0QFjAAegQIAxAC&amp;url=https%3A%2F%2Fwww.jscimedcentral.com%2FDrugDesign%2Fdrugdesign-4-1052.pdf&amp;usg=AOvVaw0tVfKlzxgsPgZJDqKJwXGv" rel="noopener noreferrer" target="_blank">biosimilar drugs</a> – to treat a variety of diseases.&nbsp;</p>
<p>Historically, vaccines targeting viruses like <a href="https://www.cdc.gov/flu/prevent/how-fluvaccine-made.htm" rel="noopener noreferrer" target="_blank">influenza</a> are produced by injecting the virus of interest into fertilized chicken eggs, where it replicates for a couple of days. Fluid from the egg is then harvested to isolate the viral particles, which are used to make the vaccine. Huge amounts of eggs are required for this type of vaccine production: each vaccine dose needs at least one egg. More recently, other organisms have also been used to produce vaccine components, including <a href="https://doi.org/10.1136/esmoopen-2018-000481" rel="noopener noreferrer" target="_blank">cultured mammalian cells</a>, <a href="https://doi.org/10.18388/abp.2014_1878" rel="noopener noreferrer" target="_blank">bacteria</a>, and <a href="https://doi.org/10.1093/femsyr/foz007" rel="noopener noreferrer" target="_blank">yeast</a>. Vaccines can also be produced without organisms at all – <a href="https://doi.org/10.4161/rna.22269" rel="noopener noreferrer" target="_blank">mRNA vaccines</a> can be entirely synthesized in a test tube.&nbsp;</p>
<p>Producing VLP vaccines in plants is a complex process, but it may be surprising that it’s much quicker than the <a href="https://www.who.int/csr/disease/swineflu/notes/h1n1_vaccine_20090806/en/" rel="noopener noreferrer" target="_blank">six months</a> it takes to produce a vaccine in a chicken egg. It also eliminates ethical concerns surrounding reliance on animal products.</p>
<aside class="pullquote"><blockquote>...once the plant is infected by the <em>Agrobacterium</em>, it will reliably produce the virus-like particles</blockquote></aside>
<p>With a six-to-eight week time-frame, Medicago’s plant produced vaccine technology, “seems to be a viable alternative for making vaccines,” says Dr. Daphne Goring, a professor at the University of Toronto who studies signal transduction in plants, and is not involved with Medicago.</p>
<p>In addition to their SARS-CoV-2 vaccine candidate, Medicago has used their plant produced VLP vaccine technology to create candidates for <a href="https://www.medicago.com/en/pipeline/#we-re-growing-a-robust-development-and-clinical-program" rel="noopener noreferrer" target="_blank">influenza, norovirus and rotavirus as well</a>.</p>
<p>VLPs mimic the outer structure of viruses, which allows them to be easily recognized by the immune system. Unlike a real virus, VLPs do not contain genetic material, which means they cannot reproduce and spread inside the body. Without genetic material, it is impossible for VLPs to cause infection. But, they can still teach the immune system how to fight a real infection, leading to immunity against the virus.&nbsp;</p>
<figure class="right medium"><img alt="Nicotiana benthamiana being agroinfiltrated, injected with Agrobacterium" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/077a705c-14b6-4676-a2fb-c656b53af247/Agroinfiltration.jpg"/><figcaption><span class="caption"><p><em>Nicotiana benthamiana</em> being injected with <em>Agrobacterium</em></p></span> <span class="credit"><p>Via <a href="https://commons.wikimedia.org/wiki/File:Agroinfiltration.jpg" target="_blank">Wikimedia</a></p></span></figcaption></figure>
<p>In order to produce a VLP vaccine in a plant, scientists at Medicago have genetically engineered a special plant-infiltrating bacterium called <em>Agrobacterium</em> to turn plants into miniature VLP 'factories.' Specific sequences of viral DNA which produce the coronavirus’ outer structure proteins are inserted into the <em>Agrobacterium</em> genome. Then, <em>Agrobacterium</em> is allowed to infect the plant. Once inside the plant’s cells, the genetically modified <em>Agrobacterium</em> delivers the inserted viral DNA to the plant so it can use it as a template to produce the virus-like particle.</p>
<p>This system is very robust – once the plant is infected by the <em>Agrobacterium</em>, it will reliably produce the virus-like particles. All that’s left is harvesting the plant and purifying the VLPs from its tissue.</p>
<p>“It seems to be a very efficient system,” says Goring, “once they have a sequence, they can produce [the vaccine] very quickly.”</p>
<p>Medicago claims to produce a clinically viable vaccine in two months or less, similar to the estimated time-frame of <a href="https://www.modernatx.com/modernas-work-potential-vaccine-against-covid-19" rel="noopener noreferrer" target="_blank">Moderna's mRNA vaccine</a>. Medicago's plant of choice, a relative of tobacco called <em>Nicotiana benthamiana</em>, grows quickly and easily and is highly susceptible to <em>Agrobacterium </em>infiltration.</p>
<aside class="pullquote"><blockquote>In vast, bright growth rooms, thousands of plants are cultivated and exposed to cultures of <em>Agrobacterium</em></blockquote></aside>
<p>In vast, bright growth rooms, thousands of plants are cultivated and exposed to cultures of <em>Agrobacterium</em> (in vacuums which helps the plants absorb as much bacteria as possible). Of the six to eight weeks spent developing the vaccine, the infected plants take about one week to produce VLPs inside their cells, after which their tissue is harvested. Then, the VLPs are purified from the harvested tissue and are subjected to quality control and safety steps to ensure they are safe and efficient for preventing viral infection.&nbsp;</p>
<h6 id="silver-linings-"><strong>Silver Linings&nbsp;</strong></h6>
<p>If all goes well in clinical trials, Medicago’s VLP vaccine will be able to contribute to the other coronavirus vaccines already in production. The best-case scenario for eliminating, or at least controlling COVID-19, will be <a href="https://www.nature.com/articles/d41591-020-00029-7" rel="noopener noreferrer" target="_blank">successfully generating multiple vaccines</a> that can be administered on a global scale.</p>
<p>Medicago’s vaccine has the potential to be the first plant produced vaccine to combat not only SARS-CoV-2, but many other time-sensitive viral diseases as well. Currently, none of the vaccines developed by Medicago or any other plant-based company have been approved for human use, despite successful clinical trial results. But Moderna is in the same boat: while they have also developed innovative mRNA vaccine technology, <a href="https://www.modernatx.com/pipeline" rel="noopener noreferrer" target="_blank">none</a> of their therapies have been approved for human use.&nbsp;</p>
<figure><img alt="The SARS-CoV-2 virus" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/1ae4c7e8-94ec-461c-9d48-3b080d3962ca/49655855721_0ed2931742_o.jpg"/><figcaption><span class="caption"><p>The SARS-CoV-2 virus. A virus-like particle mimics the outside envelope but does not contain the genome within</p></span> <span class="credit"><p>Via <a href="https://www.flickr.com/photos/nihgov/49655855721/in/album-72157713108522106/" target="_blank">NIH</a></p></span></figcaption></figure>
<p>Medicago's seasonal flu vaccine, which has completed <a href="https://clinicaltrials.gov/ct2/show/NCT03301051" rel="noopener noreferrer" target="_blank">phase three clinical trials</a>, has the potential to adapt to the ever-changing seasonal influenza strain with their plant production technology.</p>
<p>“Each year they’ve got to come up with a new vaccine,” remarks Goring, “and with their system, they can do it quickly.”</p>
<p>Speed is of the essence when it comes to vaccine production, especially for combating influenza, a rapidly mutating virus. Once up to date viral target sequences are deciphered, plants can manufacture vaccines to fight them at a surprisingly rapid pace. Due to the proprietary nature of the vaccine production industry, there is currently not enough publicly available data to determine if plants definitively hold the title of fastest vaccine production platform. However, the two month time-frame is most certainly quicker than chicken egg vaccine production, and likely means plant-based vaccine production platforms are among the speediest.&nbsp;</p>
<p>In addition to speed, there's scalability. Vaccine platforms involving plants are <a href="https://doi.org/10.1016/j.biotechadv.2017.03.011" rel="noopener noreferrer" target="_blank">less expensive</a> than cell-based and are almost infinitely <a href="https://doi.org/10.1016/j.biotechadv.2020.107519" rel="noopener noreferrer" target="_blank">scalable</a>: simply sow more seeds to increase yield. While mRNA vaccine production times are similar to plant based production, they are not as easy to scale. Although still uncertain, Medicago has <a href="https://www.medicago.com/en/newsroom/medicago-begins-phase-i-clinical-trials-for-its-covid-19-vaccine-candidate/" rel="noopener noreferrer" target="_blank">estimated</a> it could produce up to one billion doses of their SARS-CoV-2 vaccine annually, compared to <a href="https://bioprocessintl.com/bioprocess-insider/facilities-capacity/moderna-on-1-3bn-manufacturing-scale-up-of-mrna-covid-vaccine/" rel="noopener noreferrer" target="_blank">Moderna's estimate</a> at only half as much.&nbsp;</p>
<p>Another benefit of plant produced biopharmaceutical systems is <a href="https://doi.org/10.1016/j.biotechadv.2020.107519" rel="noopener noreferrer" target="_blank">decreased susceptibility of contamination from harmful viruses</a> compared to platforms which use mammalian cells. While mammalian cells can play host to viruses that can also infect humans, plants have intrinsically different cellular architecture which doesn't allow a human virus to infect them. This means the plants and their biopharmaceutical products cannot pass on these unwanted viruses to the humans who use them.&nbsp;</p>
    


<p><em><a href="https://massivesci.com/people/hayley-mckay/">Hayley McKay </a> studies 

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<span class="scientist__field">Genetics</span>

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<span class="scientist__institution">University of Toronto</span>

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<guid isPermaLink="true">https://massivesci.com/articles/covid-19-coronavirus-herd-immunity-r0-testing-vaccines-reinfection/</guid>
<link>https://massivesci.com/articles/covid-19-coronavirus-herd-immunity-r0-testing-vaccines-reinfection/</link>
<pubDate>Fri, 28 Aug 2020 10:04:46 EST</pubDate>
<title>Don&#39;t bank on herd immunity to save us from COVID-19</title>
<description>The best way forward is to use quality research to shape policy</description>

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  <dc:creator><![CDATA[Sara May Bergstresser ]]></dc:creator>
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    <atom:name>Sara May Bergstresser </atom:name>
    <atom:uri>https://massivesci.com/people/sara-may-bergstresser/</atom:uri>
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  <content:encoded><![CDATA[
    <p>There has recently been some <a href="https://www.nytimes.com/2020/08/17/health/coronavirus-herd-immunity.html" rel="noopener noreferrer" target="_blank">speculation</a> that the human population, or at least some segments of it, may already have had sufficient COVID-19 infections to achieve the protective effect of “herd immunity.” There are also <a href="https://science.sciencemag.org/content/369/6505/846" rel="noopener noreferrer" target="_blank">new</a> <a href="https://www.medrxiv.org/content/10.1101/2020.04.27.20081893v3" rel="noopener noreferrer" target="_blank">studies</a> using computational modeling that suggest that the population levels of immunity needed for broad protection are lower&nbsp;than the most common estimates of 60-66% immune. While these new and hypothetical constructs of infection-acquired herd immunity show useful directions for the future of public health research for both COVID-19 and other infectious diseases, there are still too many unknowns to use these numbers to design active health policy.</p>
<p>As I <a href="https://massivesci.com/answers/coronavirus-covid-19/#herd-immunity-coronavirus-covid19" rel="noopener noreferrer" target="_blank">wrote earlier this year</a>:</p>
<blockquote><em>Herd immunity refers to the protection that an at-risk individual can gain by being surrounded by others who are already immune to a disease. It relies on a proportion of individuals within a population already having immunity to an infection, but the exact proportion of individuals needed for herd immunity depends on the characteristics of each particular</em> <a href="https://www.sciencemediacentre.org/expert-comments-about-herd-immunity/" rel="noopener noreferrer" target="_blank"><em>infection</em></a><em>. In addition, the understanding of the concept has been developed mainly as related to vaccination, where immunity is produced in a person by giving a vaccine, rather than that person having to develop and recover from the disease.</em><br>
</blockquote>
<p>Many hard hit communities, such as the Hasidic community in the Borough Park neighborhood of <a href="https://www.jta.org/2020/07/08/health/brooklyns-hasidic-jews-are-acting-like-they-have-herd-immunity-could-they-be-right" rel="noopener noreferrer" target="_blank">Brooklyn</a>&nbsp;and other urban neighborhoods in <a href="https://www.nytimes.com/2020/08/17/health/coronavirus-herd-immunity.html" rel="noopener noreferrer" target="_blank">London</a> and <a href="https://www.bloomberg.com/news/newsletters/2020-08-23/herd-immunity-in-india" rel="noopener noreferrer" target="_blank">Mumbai</a>, have already had a substantial number of infections within distinct spatially contained groups, leading people to speculate that they may have established a protective level of immunity within these areas. In addition, many researchers have developed mathematical models of the outbreak and have come up with values lower than the typical estimates of the population needed for herd immunity for COVID-19, ranging from <a href="https://science.sciencemag.org/content/369/6505/846" rel="noopener noreferrer" target="_blank">about 43%</a> to as low as <a href="https://www.medrxiv.org/content/10.1101/2020.07.23.20160762v1" rel="noopener noreferrer" target="_blank">10-20%</a>.</p>
<aside class="pullquote"><blockquote>Our current knowledge about SARS-CoV-2 (the virus that causes COVID-19) is incomplete, including a lack of information about how we may develop immunity and how long immunity will typically last.</blockquote></aside>
<p>The classical calculation of herd immunity is based on the infectivity of the virus in question, <a href="https://academic.oup.com/cid/article/52/7/911/299077" rel="noopener noreferrer" target="_blank">defined</a>&nbsp;by the mathematical expression, <em>1-(1/R0</em>). R0 (“R-naught”) is the “basic reproductive number” of the virus, which is an indicator of how easily an infection is transmitted. This is an estimate of the number of secondary cases generated by an infectious individual at the start of a novel outbreak, when the rest of the population is susceptible. There are <a href="https://www.nytimes.com/2020/04/23/world/europe/coronavirus-R0-explainer.html" rel="noopener noreferrer" target="_blank">many difficulties</a> in estimating R0 during an <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073717/" rel="noopener noreferrer" target="_blank">active outbreak</a>, resulting in some <a href="https://wwwnc.cdc.gov/eid/article/25/1/17-1901_article" rel="noopener noreferrer" target="_blank">wide variations</a> in estimates over time and&nbsp;data coming from different geographic locations. Early WHO estimates turned out to be <a href="https://academic.oup.com/jtm/article/27/2/taaa021/5735319" rel="noopener noreferrer" target="_blank">too low</a>, but the <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7074654/" rel="noopener noreferrer" target="_blank">most</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7073717/" rel="noopener noreferrer" target="_blank">widely</a> <a href="https://wwwnc.cdc.gov/eid/article/26/6/20-0495_article" rel="noopener noreferrer" target="_blank">used</a> estimates R0 for SARS-CoV-2 now remain at around 2.5 to 3, meaning that one infectious person will infect 2.5 to 3 others. The calculated estimate based on an R0 of 2.5 to 3 results in 60-66% percent of people needing to have immunity before there is any “herd” immunity effect for the population.</p>
<figure class="center medium"><img alt="graphic showing the difference between disease transmission when there is herd immunity versus without it" title="herd immunity" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/10e2929d-0456-4fe5-a7b5-196c7931d624/50116011672_92bd9ce2f7_b.jpg"/><figcaption><span class="caption"><p>Herd immunity helps reduce the likelihood of disease transmission from infected individuals to non-immune individuals. Immunity can be acquired from vaccines or, in many cases, previous infection and recovery from the infection.</p></span> <span class="credit"><p>&nbsp;U.S. Government Accountability Office on <a href="https://www.flickr.com/photos/usgao/50116011672" target="_blank">Flickr</a>.</p></span></figcaption></figure>
<p>A mathematical model <a href="https://science.sciencemag.org/content/369/6505/846" rel="noopener noreferrer" target="_blank">recently published</a> by Tom Britton and colleagues in <em>Science</em> suggests that because population groups vary by factors including age and rates of social activity and contact, herd immunity could be established through illness and recovery with only around 43% of the population,&nbsp;instead of the 60% required using a classical model assuming an R0 of 2.5.</p>
<p>While this type of mathematical model for herd immunity is theoretically interesting since it attempts to capture contextual factors and elements of population heterogeneity, it is still too early to be directly applied to public policy. Our current knowledge about SARS-CoV-2 (the virus that causes COVID-19) is incomplete, including a lack of information about how we may develop immunity and how long immunity will typically last.&nbsp;Mathematical modeling is&nbsp;also based on broad assumptions that are often untested in the real world. Much more research is needed before we know if these new ideas about herd immunity should be applied to public health interventions and planning.</p>
<figure class="center large"><img alt="graphic with disease transmission path, from susceptible to exposed to infectious to recovered." title="mechanistic modeling" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/04fbdabf-4cf4-4793-832e-c56da2c955eb/50215237238_39949d00fb_b.jpg"/><figcaption><span class="caption"><p>There are generally two broad categories of infectious disease models: mechanistic models, which use scientific understanding of disease dynamics and human behavior, and statistical models, which rely only on patterns in the data</p></span> <span class="credit"><p>U.S. Government Accountability Office on <a href="https://www.flickr.com/photos/usgao/50215237238/" target="_blank">Flickr</a>.</p></span></figcaption></figure>
<p>The most striking example of how fast our understanding can change is the recent confirmation of reinfection with a second case of COVID-19 after four and a half months <a href="https://www.scmp.com/news/hong-kong/health-environment/article/3098551/hong-kongs-third-wave-losing-momentum-city" rel="noopener noreferrer" target="_blank">in Hong Kong</a>.&nbsp;Unlike earlier reports of reinfection, which were mainly anecdotal, this case was confirmed based on <a href="https://academic.oup.com/cid/advance-article/doi/10.1093/cid/ciaa1275/5897019" rel="noopener noreferrer" target="_blank">viral genome sequencing</a>, showing that the second infection was from a <a href="https://www.nature.com/articles/d41586-020-00502-w" rel="noopener noreferrer" target="_blank">genetically distinct strain</a>. This suggests that reinfection is an important possibility and that immunity acquired through illness and recovery may last only months. This new case adds additional elements of uncertainty to <a href="https://science.sciencemag.org/content/369/6505/846" rel="noopener noreferrer" target="_blank">Britton and colleagues’ model</a>, since the authors state that their current model was designed based on the assumption that “infection with and subsequent clearance of the virus leads to immunity against further infection for an extended period of time.”&nbsp;</p>
<p>Reinfection and the typical duration of immunity are not the only uncertainties. It also remains unclear to what degree immunity is <a href="https://www.bmj.com/content/370/bmj.m3018" rel="noopener noreferrer" target="_blank">antibody-mediated versus cell-mediated</a>, which&nbsp;kinds of <a href="https://www.nih.gov/news-events/nih-research-matters/potent-antibodies-found-people-recovered-covid-19" rel="noopener noreferrer" target="_blank">antibodies</a> are most important, whether immunity might prevent future disease or only make reinfections less severe, and whether prior exposure to <a href="https://www.nature.com/articles/s41577-020-0389-z" rel="noopener noreferrer" target="_blank">common cold coronaviruses</a> offer any protection. The immune response also may depend on characteristics beyond age, including <a href="http://nature.com/articles/s41586-020-2700-3" rel="noopener noreferrer" target="_blank">biological sex</a> and <a href="https://www.scientificamerican.com/article/do-your-genes-predispose-you-to-covid-19/" rel="noopener noreferrer" target="_blank">individual genetic variation</a>, and <a href="https://www.quantamagazine.org/the-tricky-math-of-covid-19-herd-immunity-20200630/" rel="noopener noreferrer" target="_blank">other factors</a>. The data available is often incomplete, meaning that mathematical models may be based on biased samples; <a href="https://science.sciencemag.org/content/368/6490/489" rel="noopener noreferrer" target="_blank">underreporting</a> of data has been high, and areas <a href="https://www.statnews.com/2020/04/27/coronavirus-many-states-short-of-testing-levels-needed-for-safe-reopening/" rel="noopener noreferrer" target="_blank">without sufficient testing</a>&nbsp;do not provide adequate data.</p>
<p>There are also a number of <a href="https://www.the-scientist.com/features/why-r0-is-problematic-for-predicting-covid-19-spread-67690" rel="noopener noreferrer" target="_blank">difficulties</a> inherent in using the basic reproductive rate to predict disease spread, and it is difficult to disentangle the basic rate R0 from the actual transmission rate (Rt), which is impacted by <a href="https://monitor.pubs.asahq.org/article.aspx?articleid=2766288" rel="noopener noreferrer" target="_blank">changes</a> in behavior and in population immunity over time. If done properly, all of the measures meant to control the virus, including lockdowns, social distancing, business closures, travel bans, mask-wearing, and contact tracing, will reduce the transmission. While this is a good thing for the public’s health, it makes the data collected ambiguous: has disease transmission has been slowed by public health measures, or is it waning naturally?</p>
<figure class="right medium"><img alt="A cartoon of an infected person moving through a crowd of uninfected people." title="Current estimates suggest that a person infected with COVID-19 will, on average, pass the virus to 2-3 other people." src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/1353ab6d-fb68-4a4a-a816-04659a05eef6/united-nations-covid-19-response-lbWcHW6KAyI-unsplash.jpg"/><figcaption><span class="caption"><p>Current estimates suggest that a person infected with COVID-19 will, on average, pass the virus to 2-3 other people.</p></span> <span class="credit"><p>United Nations COVID-19 Response on <a href="https://unsplash.com/photos/lbWcHW6KAyI" target="_blank">Unsplash</a>.</p></span></figcaption></figure>
<p>There are also speculations that the amount of virus a person contacts impacts the severity of illness (this is known as&nbsp;<a href="https://www.medrxiv.org/content/10.1101/2020.06.26.20140624v1" rel="noopener noreferrer" target="_blank">a dose-response relationship</a>), potentially explaining why masking is effective. It is still unclear to what degree <a href="https://jamanetwork.com/journals/jamanetworkopen/fullarticle/2767010" rel="noopener noreferrer" target="_blank">seasonality</a> plays a role in transmission, and more research is needed on the <a href="https://www.scientificamerican.com/article/how-coronavirus-spreads-through-the-air-what-we-know-so-far1/" rel="noopener noreferrer" target="_blank">exact mechanisms</a> of virus spread and persistence in the air and the role of <a href="https://www.epa.gov/coronavirus/indoor-air-and-coronavirus-covid-19#:~:text=In%20addition%20to%20close%20contact,encouraged%20by%20social%20distancing%20recommendations." rel="noopener noreferrer" target="_blank">indoor conditions</a> such as humidity, temperature, and ventilation. Finally, once a vaccine becomes available, it will impact herd immunity, though the results will depend both on the effectiveness and the distribution of any future vaccines as well as whether people are <a href="https://www.sciencemag.org/news/2020/06/just-50-americans-plan-get-covid-19-vaccine-here-s-how-win-over-rest" rel="noopener noreferrer" target="_blank">willing to get the vaccine at all</a>.</p>
<aside class="pullquote"><blockquote>Throughout this pandemic, the concept of herd immunity has been frequent fodder for wishful thinking.&nbsp;</blockquote></aside>
<p>Throughout this pandemic, the concept of herd immunity has been frequent fodder for wishful thinking. Some countries, including Britain and Sweden, attempted to rely on herd immunity rather than implementing broad control measures. Now Britain has <a href="https://www.bbc.com/news/uk-52012432" rel="noopener noreferrer" target="_blank">reconsidered</a> this plan, and Sweden has sustained <a href="https://theconversation.com/coronavirus-why-the-nordics-are-our-best-bet-for-comparing-strategies-135344" rel="noopener noreferrer" target="_blank">much larger spread</a> of the disease and greater <a href="https://newsroom.uvahealth.com/2020/07/03/covid-19-deaths-in-sweden/" rel="noopener noreferrer" target="_blank">number of deaths</a> than its neighbors.</p>
<p>In the United States, wishful thinking about the <a href="https://www.axios.com/trump-coronavirus-disappear-cac3b50f-14f5-435a-932b-32e61f448554.html" rel="noopener noreferrer" target="_blank">virus disappearing on its own</a>&nbsp;has <a href="https://www.publichealth.columbia.edu/public-health-now/news/covid-19-projections-delayed-response-rebound-would-cost-lives" rel="noopener noreferrer" target="_blank">delayed needed intervention</a> and prompted <a href="https://www.usatoday.com/story/news/education/2020/08/17/unc-chapel-hill-covid-cases-fall-semester-online-classes/3383874001/" rel="noopener noreferrer" target="_blank">premature reopening</a>. Pandemic control measures have many unpleasant side effects, and herd immunity can be an appealing concept for those who seek reassurance that the world will eventually return to normal, but our best way forward requires an understanding that conducting quality research and applying it effectively to policy take time and a great deal of work.</p>
    


<p><em><a href="https://massivesci.com/people/sara-may-bergstresser/">Sara May Bergstresser </a> studies 

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<span class="scientist__field">Bioethics</span>, 

<span class="scientist__field">Public Health</span>, 

and <span class="scientist__field">Biochemistry</span>

</p>

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<span class="scientist__institution">Columbia University</span>

</p>

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<guid isPermaLink="true">https://massivesci.com/articles/mrna-vaccine-covid19-coronavirus-moderna/</guid>
<link>https://massivesci.com/articles/mrna-vaccine-covid19-coronavirus-moderna/</link>
<pubDate>Thu, 02 Jul 2020 11:57:52 EST</pubDate>
<title>What are the advantages of an mRNA vaccine for COVID-19?</title>
<description>They&#39;re easier to manufacture than traditional vaccines, but scientifically their history is checkered</description>

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  <media:description>A woman gets a vaccine injection in her arm</media:description>
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  <dc:creator><![CDATA[Joshua Peters]]></dc:creator>
  <atom:author>
    <atom:name>Joshua Peters</atom:name>
    <atom:uri>https://massivesci.com/people/joshua-peters/</atom:uri>
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    <p>Most human medicines, including vaccines, are small molecules or proteins. A decade ago, a company called Moderna started on the premise of messenger RNA (mRNA) as a therapy. Only two RNA-based therapies have been <a href="https://massivesci.com/articles/rna-therapy-treatments/"><ins>approved</ins></a>, neither being <em>messenger </em>RNA. While it’s not the only company focused on mRNA, it’s the front runner by far. Within eight years, it became the most valued biotechnology company before breaking a public offering record. Their stock has <a href="https://finance.yahoo.com/quote/MRNA/history/"><ins>tripled</ins></a> to over $60 a share as the pandemic swept across the world.</p>
<p>A quick look at their drugs in <a href="https://www.modernatx.com/pipeline"><ins>development</ins></a> reveals a laundry list of therapies for rare metabolic disorders, cancers, heart failure, and a host of pathogens like Zika virus, Epstein-Barr virus, and the novel coronavirus SARS-CoV-2. It is the mRNA technology itself enabling them to tackle such diverse diseases with a single platform.</p>
<aside class="pullquote"><blockquote>After delivery, a person's cells act as the factory, no virus necessary</blockquote></aside>
<p>The premise of any vaccine is to induce a long-lived immune “memory” in the form of B and T cells. Upon any encounter with a pathogen (which can be bacteria or viruses), these cells will recognize the danger and fight it off by destroying the pathogen and pathogen-infected cells. The danger signal takes the form of an antigen, a molecule that notifies the immune system of a pathogen. For SARS-CoV-2, the antigen targeted by B and T cells is usually a <a href="https://www.economist.com/briefing/2020/03/12/understanding-sars-cov-2-and-the-drugs-that-might-lessen-its-power"><ins>protruding spike protein</ins></a> on the surface of the virus. The challenge in vaccination is inducing this response without, which requires a handshake between an antigen-presenting cell and a specific type of T cell, without getting people sick. It’s the antigen peptide (smaller sections of antigen molecule) presented in this interaction that determines the target of the immune response.&nbsp;</p>
<p>Common vaccines are weakened or inactivated versions of the virus, like the yearly flu or the polio vaccine children receive 2 months after birth. A huge variety of antigens, some useful and some not, can be presented since cells are receiving the entirety of the virus. Newer vaccines utilize other engineered, well-studied doses containing specific regions of the target pathogen to create specific immune reactions. Moderna’s challenger in the race for a COVID-19 vaccine is based on this concept. <a href="https://www.astrazeneca.com/media-centre/press-releases/2020/astrazeneca-advances-response-to-global-covid-19-challenge-as-it-receives-first-commitments-for-oxfords-potential-new-vaccine.html"><ins>Astra Zeneca’s</ins></a> vaccine candidate is a nonreplicating, weakened version of the common cold virus that contains the SARS-CoV-2 spike protein. This approach has been successful before as the first Ebola vaccine. Other approaches simply inject the proteins researchers want the body to recognize as a danger, along with other molecules to raise the alarm initially for the vaccine response. For SARS-CoV-2, the surface spike protein is the most common target to be tested for vaccines.</p>
<figure class="center large"><img alt="A diagram of an mRNA vaccine in action. It shows a synthetic mRNA being translated by a ribosome into individual proteins from SARS-CoV-2, which induce an immune response." src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/4bb5c265-7340-423c-b627-119c3f8c4ff1/mrna_vaccine_conversation.jpg"/><figcaption><span class="caption"><p>An mRNA vaccine provides a patient's cells with the mRNA to create proteins from SARS-CoV-2, which cause an immune response</p></span> <span class="credit"><p>Courtesy of <a href="https://theconversation.com/what-the-phase-1-trials-of-the-first-covid-19-vaccine-really-mean-139020" target="_blank">The Conversation</a></p></span></figcaption></figure>
<p>The mRNA vaccine belongs in the last potential category for a vaccine to prevent COVID-19. Moderna’s vaccine candidate inserts mRNA into cells, which is translated into the exact protein antigens researchers design for the immune response. Instead of manufacturing inactivated virus, viral carriers, or proteins, Moderna manufactures these RNA sequences. After delivery, a person's cells act as the factory, no virus necessary. By enabling the cells to generate the antigens, it avoids the costly, difficult purification of proteins and equips the proteins with typical features viral proteins have, like surface sugars and the correct 3D shape. The flexibility of this platform stems from the ease of working with genomic sequences. Inject the diligently-defined sequence of A’s, T’s, C’s, and G’s and voilà, the cells do the rest. They are easy to design, produce, and test once the sequence of the pathogen is known. Others cite <a href="https://www.nature.com/articles/nrd.2017.243#Sec17"><ins>safety and efficacy benefits</ins></a>, which may be theoretically true, but as with every medicine, will need to be fully tested. Many of these benefits are similarly shared with DNA vaccines, which are slightly different in their design and delivery and are used in veterinary <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4425421/"><ins>medicine</ins></a>.</p>
<p>Do mRNA vaccines have advantages over traditional protein vaccines? Scientifically, it’s still unclear. Early <a href="https://www.nature.com/articles/s41541-020-0159-8"><ins>studies</ins></a> showed underwhelming results, but the molecular design and delivery of these vaccines has quickly progressed. Beyond manufacturing <a href="https://www.nature.com/articles/s41541-020-0159-8"><ins>benefits</ins></a>, some have suggested that, in theory, they may require less <a href="https://pubmed.ncbi.nlm.nih.gov/27269061/"><ins>adjuvant</ins></a> (a bolstering second molecule that signals “danger!” to our immune system ) because the mRNA itself is inherently stimulating to our immune systems. Considering the novelty of mRNA vaccines clinically, there isn't great data regarding protein vs. mRNA vaccines directly. While there may be theoretical benefits to this type of vaccine, it comes down to the tested efficacy and safety of a candidate and, perhaps more importantly in any therapeutic race, who is willing to invest the eight to nine figures required to see any return on their research.</p>
<aside class="pullquote"><blockquote>The preliminary nature of these data can’t be overemphasized, but we can be hopeful</blockquote></aside>
<p>COVID-19 was identified on December 31st, 2019. Five days later, the full sequence of the viral genome was obtained. Eight days after that, the frontrunner vaccine candidate for COVID-19 was finalized at Moderna: mRNA-1273. Within 63 days, Moderna administered their first dose in an NIH-led phase 1 study. Considering the “average” timeline to develop a vaccine is 10-15 <a href="https://www.historyofvaccines.org/content/articles/vaccine-development-testing-and-regulation"><ins>years</ins></a>, this is lightspeed acceleration through the scientific and regulatory gauntlet. Moderna doesn’t have a single FDA-approved medicine, making their COVID-19 vaccine candidate extremely high stakes for their platform – not to mention the stakes for all the lives continually at risk for the virus and its socioeconomic upheaval.</p>
<p>With a Phase 3 protocol finalized, so far, so good for mRNA-1273. Initial data from the Phase 1 study highlighted safe and well-tolerated responses across the dosages, although some worrisome reactions were <a href="https://www.statnews.com/2020/05/26/moderna-vaccine-candidate-trial-participant-severe-reaction/"><ins>noted</ins></a>. Moderna also mentioned, “neutralizing antibody titer level... reaching or exceeding neutralizing antibody titers generally seen in convalescent sera,” meaning some volunteer study participants had antibodies that could inactivate the virus at levels higher than patients with COVID-19. Although scientists are eagerly awaiting the final, complete Phase 1 data, this short statement is exciting.</p>
<p>In a <a href="https://www.biorxiv.org/content/10.1101/2020.06.11.145920v1"><ins>study</ins></a> released to the preprint server bioRxiv, Kizzmekia Corbett, Darin Edwards, and Sarah Leist lead a team centered at the NIH’s Vaccine Research Center profiling mRNA-1273 in mice. The results continue the promising trend, showing mice vaccinated with mRNA-1273 are protected from the virus, have neutralizing antibody responses, and harbor fewer virions in the airways of the mice. This is exactly the type of immune response vaccines need to elicit. Phase 2, now underway, includes 600 patients receiving two doses.&nbsp;</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/notes/pfizer-covid-vaccine-90-percent-effective-mrna-rna-bnt162b2/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Fnotes%2Fpfizer-covid-vaccine-90-percent-effective-mrna-rna-bnt162b2%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>The preliminary nature of these data can’t be overemphasized, but we can be hopeful. Questions remain as to the scale and cost of vaccinating the global population, but Moderna highlights their partnership with Lonza, a biotechnology manufacturing company, to supply 500 million to 1 billion doses <a href="https://www.reuters.com/article/us-health-coronavirus-vaccine-lonza-excl/exclusive-lonza-sets-new-goal-to-make-moderna-covid-19-vaccine-ingredients-idUSKBN2392C4"><ins>annually</ins></a>. The messenger RNA platform in the works for more than a decade by Moderna has been subbed in during the 9th inning with bases loaded. While it will take many more months to gather all the safety and efficacy data to properly assess this vaccine (and others), the progress thus far has been record-breaking in every measure.&nbsp;</p>
    


<p><em><a href="https://massivesci.com/people/joshua-peters/">Joshua Peters</a> studies 

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<span class="scientist__field">Biological Engineering</span>

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<span class="scientist__institution">Massachusetts Institute of Technology</span>

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<guid isPermaLink="true">https://massivesci.com/articles/malaria-spit-vaccine/</guid>
<link>https://massivesci.com/articles/malaria-spit-vaccine/</link>
<pubDate>Thu, 20 Dec 2018 09:50:00 EST</pubDate>
<title>Saliva is just what we needed to create a new malaria vaccine</title>
<description>The mistake mosquitos made? Leaving their spit behind</description>

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  <dc:creator><![CDATA[Hannah Thomasy]]></dc:creator>
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    <atom:name>Hannah Thomasy</atom:name>
    <atom:uri>https://massivesci.com/people/hannah-thomasy/</atom:uri>
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    <p>Malaria is one of the <a href="http://www.who.int/en/news-room/fact-sheets/detail/children-reducing-mortality" target="_blank">leading killers of children under 5</a>. There's a vaccine <a href="https://afro.who.int/news/historic-launch-malaria-vaccine-pilots-africa" target="_blank">currently available in three African countries</a>, the RTS,S vaccine, and it is undoubtedly a massive step forward. But, it’s still only partially effective: in a large clinical trial, the vaccine only prevented about <a href="http://www.who.int/malaria/media/rtss-phase-3-trial-qa/en/#What%20were%20the%20vaccine%20efficacy%20trial%20results?" target="_blank">30% of cases of severe malaria</a>. The fight against malaria is far from over.</p>
<p>Researchers have been working on malaria vaccines since the <a href="http://www.jimmunol.org/content/53/1/113" target="_blank">1940s</a>, with limited success. These previous conventional vaccines attempted to help the human immune system recognize the parasites that cause malaria (called <em>Plasmodium</em>), but this has proved to be an extremely difficult task.</p>
<aside class="pullquote"><blockquote>Constantly changing, it skillfully evades the immune system of its host.</blockquote></aside>
<p>Although there have been issues with limited funding, much of this difficulty&nbsp;in creating an effective vaccine has come from the incredible complexity of the&nbsp;<em>Plasmodium</em> parasite. Its genome is made up of <a href="http://journals.plos.org/plosmedicine/article?id=10.1371/journal.pmed.0040116" target="_blank">23 million base pairs</a>. While that’s <a href="https://www.genome.gov/11006943/human-genome-project-completion-frequently-asked-questions/" target="_blank">130 times fewer base pairs than a human</a>, it’s <a href="http://www.cidrap.umn.edu/infectious-disease-topics/smallpox" target="_blank">115 times more base pairs than, say, the smallpox virus</a>. <em>Plasmodium</em> has a <a href="https://www.ncbi.nlm.nih.gov/pubmed/?term=Mackinnon+MJ%2C+Marsh+K.+The+selection+landscape+of+malaria+parasites.+Science+2010%3B+328%3A+866%E2%80%9371." target="_blank">complex life cycle</a> – progressing through multiple tissues in two different host species <em>and</em> undergoing ten morphological changes over the course of its life. Constantly changing, it skillfully evades the immune system of its host.</p>
<p>But now researchers at Yale are coming at the problem from a different angle. Since the <a href="https://www.cdc.gov/malaria/about/faqs.html" target="_blank">vast majority of malaria infections occur when a person is bitten by a mosquito</a>&nbsp;which transmits the&nbsp;<em>Plasmodium </em>parasite, what if we didn’t need the immune system to recognize the parasite itself? What if we just needed to recognize the mosquito?</p>
<figure class="right medium"><img alt="This thin film blood smear photomicrograph depicts an immature, Plasmodium malariae schizont, which contains three chromatin masses, a light cytoplasm, and a dark pigment." title="Plasmodium" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/92e613e9-c174-4fd7-9a4f-8c9523342c5d/plasmodium.tif"/><figcaption><span class="caption"><p>This is what <em>Plasmodium</em> looks like, just in case.</p></span> <span class="credit"><p>&nbsp;CDC/ Dr. Mae Melvin&nbsp;</p></span></figcaption></figure>
<p>They gave it a go. The researchers at Yale have created a vaccine not against the parasite itself, but <a href="https://www.cell.com/cell-host-microbe/fulltext/S1931-3128(18)30137-9" target="_blank">against the mosquito saliva</a> that carries the parasite into the human body. Yes, mosquito spit.</p>
<p>More specifically, the vaccine teaches the immune system to recognize a protein in mosquito spit called AgTRIO. To do this, they created a vaccine containing the AgTRIO protein itself and an adjuvant (a substance designed to heighten the immune response). Mice who received the AgTRIO vaccine before being exposed to infected mosquitoes ended up with significantly fewer parasites in their blood compared to their counterparts who had received an inactive vaccine.</p>
<p>Unfortunately, it didn’t provide complete protection – some of the immunized mice still had parasites. So researchers wondered what would happen if this partially effective strategy was combined with another partially effective strategy, like the more conventional RTS,S vaccine. RTS,S teaches the body to recognize a <em>Plasmodium</em> protein called circumsporozoite protein, or CSP.</p>
<aside class="pullquote"><blockquote>As weird as it seems, spit actually seems to play a big role in how blood-sucking bugs transmit infections to humans (or other animals) that they feed on.</blockquote></aside>
<p>When researchers gave mice vaccines against both AgTRIO and CSP, they were almost completely free of parasites – a much stronger result than either vaccine administered alone. Thus, researchers believe that an AgTRIO vaccine might be able to act synergistically with the RTS,S vaccine – a combo that could provide much more effective protection against malaria.</p>
<p>But how does this work? Why does immunizing against spit help protect against a parasite? As weird as it seems, spit actually seems to play a big role in how blood-sucking bugs transmit infections to humans (or other animals) that they feed on. For example, tick saliva may increase the infectiousness of the bacteria that causes Lyme disease by <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3747359/pdf/fcimb-03-00043.pdf" target="_blank">altering responses of the host immune system</a>. So it’s possible (although still controversial) that <em>Plasmodium</em> is getting a boost from mosquito spit. Interestingly, <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5998332/" target="_blank">researchers still don’t know what AgTRIO does</a> – so they’re not sure exactly how the vaccine against it helps to protect against <em>Plasmodium</em>. They <em>do</em> know that the AgTRIO vaccine caused the parasites to move more slowly through the skin of the host, which perhaps impeded their ability to cause a full-blown infection.</p>
<figure class="right medium"><img alt="A crowd gathers around Crown Fountain in Chicago&#39;s Millenium Park, where a fountain appears to &quot;spit&quot; water on visitors." title="Crown Fountain" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/78ede949-5415-4424-83be-cf3b0e485962/Chicago_-_Crown_Fountain_-_Millennium_Park_(2713868085).jpg"/><figcaption><span class="caption"><p>Spit: pretty good and fun actually.</p></span> <span class="credit"><p>Serge Melki via Wikimedia Commons</p></span></figcaption></figure>
<p>Immunizing against spit has other advantages too. The currently approved malaria vaccine only protects against infection by one species – <em>Plasmodium falciparum</em>. There are over a hundred species of <em>Plasmodium</em> and <a href="https://www.cdc.gov/malaria/about/biology/parasites.html" target="_blank">at least five of them cause disease in humans</a>. Since the fifth – <a href="https://www.clinicalmicrobiologyandinfection.com/article/S1198-743X(15)00381-X/fulltext" target="_blank"><em>Plasmodium knowlesi</em></a> – was only discovered to commonly infect humans in 2004, it’s possible that there could be more species infecting us that we have yet to discover. However, since all the <em>Plasmodium</em> species are accompanied by mosquitoes and their saliva, a spit vaccine could potentially provide much broader protection. It's possible that it could even provide protection against other diseases (<a href="https://www.ncbi.nlm.nih.gov/pubmed/29695682" target="_blank">like the O’nyong nyong virus</a>, <a href="https://www.tandfonline.com/doi/full/10.1080/20477724.2017.1355431" target="_blank">which infects people in East Africa</a>) that are carried by <em>Anopheles</em> mosquitoes, although this has not yet been proven.</p>
<p>There’s still a lot of work to be done before the AgTRIO vaccine is ready to be tested on humans, but this study is potentially an important step in developing a more effective malaria vaccine that could save hundreds of thousands of lives. And with the rise of <a href="https://www.cdc.gov/malaria/resources/pdf/drug_resistance/bloland_who2001.pdf" target="_blank">drug-resistant malaria</a>, vaccines are needed more than ever.</p>
    


<p><em><a href="https://massivesci.com/people/hannah-thomasy/">Hannah Thomasy</a> studies 

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<span class="scientist__field">Neuroscience</span>

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<span class="scientist__institution">University of Washington</span>

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<guid isPermaLink="true">https://massivesci.com/articles/cmv-vaccine-siv-hiv/</guid>
<link>https://massivesci.com/articles/cmv-vaccine-siv-hiv/</link>
<pubDate>Tue, 18 Dec 2018 09:18:00 EST</pubDate>
<title>Humanity&#39;s viral stowaway is now a defense against our greatest diseases</title>
<description>Engineered viruses may be the key to HIV and tuberculosis vaccines</description>

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  <dc:creator><![CDATA[Joshua Peters]]></dc:creator>
  <atom:author>
    <atom:name>Joshua Peters</atom:name>
    <atom:uri>https://massivesci.com/people/joshua-peters/</atom:uri>
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    <p>Chances are you are infected with it. Cytomegalovirus (CMV) is a nearly ubiquitous, but rarely discussed, virus affecting a third of children by age five and half of adults by age 40. Except in the case of pregnancy, it typically causes no harm. <a href="https://www.ncbi.nlm.nih.gov/pubmed/18087722" target="_blank">Named after the first observation of abnormally swelling cells the virus&nbsp;causes</a>, CMV has been evolving in humanity’s blood for millions of years. And, once infected, CMV stays in the body.&nbsp;'Til death do human and CMV&nbsp;part.</p>
<p>As much as CMV may like us, our bodies&nbsp;don't like CMV. CMV&nbsp;causes a dramatic immune response. A flood of antibodies and T cells will quickly control the infection, pushing the virus into a dormant state. As CMV attempts to reactivate during our lifetime, we respond again and again with vigor.&nbsp;</p>
<aside class="pullquote"><blockquote>This is some trippy version of The Lion King where there are multiple Rafikis holding up multiple Simbas on Pride Rock.&nbsp;</blockquote></aside>
<p>In <a href="https://www.nature.com/articles/nature10003" target="_blank">2011</a>, scientists led by Louis Picker of Oregon Health and Science University published groundbreaking work on a CMV vaccine. It wasn’t a vaccine <em>against</em> CMV, but rather a new vaccine <em>with</em> CMV, but targeted against SIV (the non-human primate version of HIV). Since a successful vaccine hinges on a strong, robust reaction, they realized that the immunogenic effects of CMV could be used to design a new vaccine. By re-engineering the virus, the researchers turned CMV into a double-agent.&nbsp;</p>
<p>In monkeys (rhesus macaques), a vaccine containing modified CMV with proteins from SIV – the HIV analog in monkeys – on its surface immunized about 50% of monkeys against SIV. For HIV vaccine research at the time, this was a tremendous result which still holds against other efforts today. By exploiting CMV’s ability to vigorously provoke an immune response, CD8+ T cells, which recognize infected cells and remove them, moved in after the initial infection to control SIV.</p>
<figure class="right small"><img alt="A small macaque with bright orange eyes and pursed lips." title="Rheseus macaque" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/5e847b06-6c1e-4cab-97b4-79dad0400baf/macaque.jpg"/><figcaption><span class="caption"><p>Is 50% vaccination something to sneeze at?</p></span> <span class="credit"><p>Mike Wawro via Flickr</p></span></figcaption></figure>
<p>“People were very excited about it. That was the first iteration, you thought, 50%, well that’s fantastic. Maybe you’ll get better than that,” says Dr. Bruce Walker, Director of the Ragon Institute of Massachusetts General Hospital, MIT, and Harvard.</p>
<p>After the results were published, the field, including Picker’s own group, wanted more answers about how CMV provokes an immune response. Was there something fundamentally different about how CMV signaled our body’s SWAT team?</p>
<p>In the following years, contrary to typical behavior, it was discovered that these CD8+ T cells were recognizing a diversity of MHC class I and II proteins.&nbsp;MHC proteins signal "DANGER!" to the immune system by displaying small proteins on the surface of an infected cell. These signals are specific to each pathogen and provoke T cells developed to recognize that specific signal. In this case, CD8+ T cells were not following the rules. The T cells responding to CMV recognized different MHC proteins with a variety of signals, instead of just one particular signal. This breadth of recognition by T cells is thought to be behind the success of the CMV-based vaccine. Imagine&nbsp;Rafiki holding up Simba, if Rafiki was an infected cell, Simba a pathogen, and all the animals of the savanna your T cells. This is some trippy version of The Lion King where there are multiple Rafikis holding up multiple Simbas on Pride Rock.&nbsp;</p>
<p><br></p>
<figure class="right medium"><a href="https://www.flickr.com/photos/indibos/4884651814/in/photolist-8rD7NJ-dycepr-kJ3iLi-o3YiXw-VboGM-daG8zX-oWabGU-BwbFxj-gKoJpm-96CQoG-95vt9p-dMEkRK-Q89tno-8aoiVL-bsATiu-rmF6hs-6uu7DF-aBYwst-s84vAd-axJxU3-azf8y6-q4bcou-kWrTRo-a1EY9T-dJ6xcF-dHUhFQ-oM2n2B-gPvd5Y-nKdCja-aikzbc-rRQjxb-a1Fnjv-98BoBF-SbmU21-7Dakxo-aCMFpq-bFvR3a-qsxkWJ-c91RPL-5rektG-7Qazxn-Xq9eBw-hPuHjb-dTdQMs-dUgCjw-SKY6Qj-818WhE-dA31qD-ecKmzu-kWqmDB"><img alt="A pride of lions with a few cubs all staring menacingly at something off camera." title="Pride of lions" src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/8ea7b503-d981-47cb-8cd6-7435d14f6538/pride%20of%20lions.jpg"/></a><figcaption><span class="caption"><p>Many Simbas.</p></span> <span class="credit"><p>John via Flickr</p></span></figcaption></figure>
<p>Interestingly, by changing the proteins within the CMV virus, different responses could be elicited, and in different tissues. This unconventional response to the CMV-based vaccine may have serious advantages in HIV, where subtypes have emerged, in the same way that there are many different types of influenza. This diversity has been a major challenge in the field.</p>
<p>“Pressure has been applied on HIV through certain immune responses that has resulted in diversification of the virus,” says Dr. Walker, who focuses on immune control in HIV. “[The] CMV vector induces responses to epitopes [immune response signals] that are not under selection pressure.” This may be advantageous for creating a broadly effective vaccine.</p>
<p>Nearly seven years later, <a href="http://www.sciencemag.org/news/2018/03/monkeys-reveal-new-clues-toward-elusive-hiv-vaccine-and-cure" target="_blank">new results</a> continue to build upon new understanding of when, why, and how our T cells respond to a re-engineered vaccine vector-like CMV. Questions still remain though, as Dr. Walker points out. “In terms of mechanistically, we still don’t know what the effector mechanism responsible for control is.”</p>
<p>Dr. Walker raises another point. “Would a vaccine that gives 50% protection, but nothing in the other individuals, be a solution?” It has been over seven years since Louis Picker published his&nbsp;50% effective&nbsp;CMV-based SIV vaccine. Considering the time it took to conduct and publish the study and the planning of the first human trials, we are looking at a decade with no human results yet. Dan Barouch, a Professor at Harvard Medical School and member of the Ragon Institute, has been working on&nbsp;an&nbsp;<a href="https://hms.harvard.edu/news/hiv-vaccine-takes-big-step" target="_blank">HIV vaccine</a> for nearly 15 years now. “How do you iterate in making vaccines if it takes that long and it’s that expensive?” asks Dr. Walker.</p>
<aside class="pullquote"><blockquote>Even now, our first-line treatment of bladder cancer is an injection of <em>Mycobacterium bovis</em>, a mostly harmless relative of <em>Mycobacterium tuberculosis</em>.</blockquote></aside>
<p>Other targets have emerged as well. In&nbsp;<a href="https://www.nature.com/articles/nm.4473" target="_blank">January</a>, Picker and an armada of scientists published more promising results on tuberculosis (TB)–the deadliest pathogen ever. Picker and the team prevented infection&nbsp;by the TB pathogen&nbsp;<em>Mycobacterium tuberculosis </em>with a CMV-based vaccine&nbsp;in over 40% of vaccinated monkeys. Michael Jarvis and his team, from the University of Plymouth, UK, added <a href="https://www.sciencedirect.com/science/article/pii/S0264410X1500328X" target="_blank">Ebola</a> to the list of CMV targets.</p>
<p>Cancer could be a target too.&nbsp;The benefit of immunogenicity in cancer&nbsp;treatment has been a theme in research for some time – perhaps before we even truly understood it. Even now, <a href="https://www.cancer.org/cancer/bladder-cancer/treating/intravesical-therapy.html" target="_blank">our first-line treatment of bladder cancer</a> is an injection of <em>Mycobacterium bovis</em>, a mostly harmless relative of <em>Mycobacterium tuberculosis</em>. The bacteria cause our immune system to invade the bladder and attack both bacteria and cancer alike. <a href="http://cancerimmunolres.aacrjournals.org/content/3/5/536" target="_blank">Vaccinating against cancer with CMV</a> in mice caused a robust CD8+ T cell response, which both prevented the growth of newly implanted tumor cells and killed off established tumors.</p>
<p>Taken together, CMV may be both foe and friend. In that,&nbsp;CMV is not alone: adenovirus (Ad), <a href="https://www.ncbi.nlm.nih.gov/pubmed/22808149" target="_blank">an engineered vector commonly used for gene therapy</a>, is another virus with <a href="https://www.nature.com/articles/s41467-018-04859-5.pdf" target="_blank">potential utility in vaccine design</a>. Whereas CMV-based vaccines controlled the viral infection, Ad-based vaccines are known to boost&nbsp;preventative&nbsp;protection against catching the infection in the first place.</p>
<p>Clinical trials are underway for adenovirus-based vaccines, like Dr. Barouch’s <a href="https://www.imbokodo.org.za/" target="_blank">above-mentioned HIV vaccine</a>. Over 2,600 women will be enrolled to test this vaccine. CMV-based vaccine trials, specifically for tuberculosis, are beginning soon, led&nbsp;by Vir Biotechnology, a company co-founded by Louis Picker.</p>
<p>Cytomegalovirus continues to ride in the sidecar during humans' evolutionary journey, infecting and persisting in an enormous fraction of the population. Now, its extraordinary ability to provoke and train our immune systems has redefined what we know about effective vaccination and, <em>perhaps,</em> holds promise in being part of an effective vaccine against human’s greatest foes.</p>
    


<p><em><a href="https://massivesci.com/people/joshua-peters/">Joshua Peters</a> studies 

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<span class="scientist__field">Biological Engineering</span>

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<p class="mb0 o7">

<span class="scientist__institution">Massachusetts Institute of Technology</span>

</p>

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<guid isPermaLink="true">https://massivesci.com/articles/rna-therapy-treatments/</guid>
<link>https://massivesci.com/articles/rna-therapy-treatments/</link>
<pubDate>Fri, 31 Aug 2018 13:47:36 EST</pubDate>
<title>Haven&#39;t heard of RNA therapy yet? You will</title>
<description>After a decade of painstaking progress​, the underdog is on the brink of treating a broad range of diseases</description>

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  <dc:creator><![CDATA[Joshua Peters]]></dc:creator>
  <atom:author>
    <atom:name>Joshua Peters</atom:name>
    <atom:uri>https://massivesci.com/people/joshua-peters/</atom:uri>
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    <p>Although you may have heard of gene therapy, you probably haven't heard of RNA therapy. Unlike gene therapy, which provides new DNA to cells, RNA therapy modifies or provides ribonucleic acid (RNA) to patients' cells. Despite the overwhelming popularity of gene-editing technologies like CRISPR, new advancements in RNA therapy are poised to address some of their serious limitations. RNA therapy now has the potential to treat a wide variety of diseases, including cardiovascular disease, hemophilia, and cancer.</p>
<aside class="pullquote"><blockquote>RNA therapy and gene therapy are often lumped together</blockquote></aside>
<p>RNA therapy and gene therapy are often lumped together, but they're actually distinct classes of treatment known as nucleic acid therapies. They're related through the central dogma of molecular biology, an <a href="https://wellcomelibrary.org/item/b18174139#?c=0&amp;m=0&amp;s=0&amp;cv=0&amp;z=-0.1615%2C0.3574%2C1.6387%2C0.8806">elegantly simple foundation</a> for all living organisms. Outlined by Francis Crick in 1953, the theory states that genetic information flows from DNA to RNA to proteins, in that order. Generally, to transfer information, DNA’s string of chemical units, known as nucleobases (adenine, thymine, cytosine, and guanine), are transcribed to RNA’s nucleobases (adenine, uracil, cytosine, and guanine). A type of RNA called messenger RNA (mRNA) is then translated into protein by a <a href="https://sciencetrends.com/codon-chart-table-the-nucleotides-within-dna-and-rna/">biological cipher</a>, which converts three nucleic acids to one amino acid.</p>
<p>But in the last six decades, we've learned that this transfer of information is actually much, much more complicated. While Crick's diagram suggested RNA's role was limited to carrying genetic information, we now know RNA is an animated, powerful commander of our cells’ machinery. Researchers have identified types of RNA responsible for several important activities, including coding and organizing protein creation, modifying how instructions for DNA are transmitted, destroying other RNAs, and preventing rearrangement of genomes.</p>
<div class="oembed"><div class="iframely-embed"><div class="iframely-responsive" style="height: 140px; padding-bottom: 0;"><a href="https://massivesci.com/videos/nhgri-human-pangenome-film/" data-iframely-url="https://cdn.iframe.ly/api/iframe?url=https%3A%2F%2Fmassivesci.com%2Fvideos%2Fnhgri-human-pangenome-film%2F&amp;key=a91f6c63822d2172297a7435cae7a9eb"></a></div></div><script async src="https://cdn.iframe.ly/embed.js" charset="utf-8"></script></div>
<p>By focusing directly on what many refer to as the software of the cell, RNA therapies have direct biological targets: a specifically engineered strand of RNA is delivered to interact or produce specific functions within the cell. And simply tweaking the nucleobase code can adjust what the therapy impacts.&nbsp;</p>
<p>“You simply change the sequence and you’re hitting another indication,” says Professor Paula Hammond, head of MIT’s Department of Chemical Engineering and a member of the Scientific Advisory Board of Moderna Therapeutics. “If the platform works once, it multiplies.”&nbsp;</p>
<p>This makes RNA therapy more targeted <em>and</em> more versatile than conventional treatments, like immunotherapy, or even aspirin or insulin. (In comparison, we still don't know how many drugs — including <a href="https://www.washingtonpost.com/news/wonk/wp/2015/07/23/one-big-myth-about-medicine-we-know-how-drugs-work/?utm_term=.e44fe851804c">Tylenol </a>— actually work.)</p>
<p>There are two main types of RNA therapy, antisense –&nbsp;which degrades dysfunctional or harmful proteins in the cell –&nbsp;and mRNA, which produces functional proteins.&nbsp;</p>
<p>Currently, antisense therapy is more common, though more complicated. Numerous mechanisms and classes of RNA are considered antisense, but all focus on the complementary pairing of RNA strands. (For example, a strand of AUCG binds with a strand UAGC; A binds with U, and C binds with G.)</p>
<p>Several RNA <a href="https://doi-org.libproxy.mit.edu/10.1016/j.cmet.2018.03.004">antisense therapies</a> already exist to improve kidney transplant outcomes, treat hemophilia, and lower LDL-cholesterol. One such mechanism called RNAi, was a <a href="https://www.nobelprize.org/nobel_prizes/medicine/laureates/2006/">2006 Nobel Prize-winning discovery</a>, and offers the basis for a <a href="https://labiotech.eu/rnai-infographic/">plethora of exciting new therapies</a>. RNAi employs special types of short RNA that act as specific instructions to the cell. A protein complex uses these instructions to destroy mRNA that are creating dysfunctional proteins. Alnylam Pharmaceuticals is preparing to launch the <a href="http://investors.alnylam.com/news-releases/news-release-details/alnylam-announces-2018-corporate-goals">first siRNA drug this year</a>, targeting an inherited disease called ATTR amyloidosis, and numerous other companies are <a href="https://www.ncbi.nlm.nih.gov/pubmed/28389707">racing to</a>develop RNAi therapies.</p>
<p>The second kind of RNA therapy focuses on replacing mRNA. Cystic fibrosis patients, for example, fail to make a functional protein called CFTR in their cell membranes. Scientists hope to have patients inhale particles containing healthy mRNA, replacing the dysfunctional CFTR protein in the lung. Translate Bio will start selling an mRNA candidate to treat patients with cystic fibrosis within the <a href="https://cysticfibrosisnewstoday.com/2018/04/17/translate-bio-readies-first0clinical-trial-of-mrt5005-potential-cystic-fibrosis-treatment/">next several months</a>, and another company, Moderna Therapeutics, is also developing a treatment for <a href="https://www.bostonglobe.com/business/2017/06/05/vertex-goes-all-its-effort-conquer-cystic-fibrosis/sIUBpbtItPoiyKDsyGcxRP/story.html">cystic fibrosis</a>. Despite not having a single drug on the market, Moderna is valued at over $7.5 billion –demonstrating the enthusiasm for these strategies.</p>
<p>A lot of this interest in RNA therapy is driven by the possibilities of better vaccines. Researchers are working on using RNA-encoding proteins from pathogens, like influenza, rabies, or Zika to develop vaccines. After receiving the new mRNA, cells translate the strands into protein, stimulating the immune system to produce a response specific to the exact strain of the pathogen.&nbsp;</p>
<p><br></p>
<p>This would eliminate current vaccines' need for an injection of live, dead, or weakened pathogens. Some researchers are even now applying this concept to <a href="https://www.modernatx.com/newsroom/press-releases/moderna-and-merck-expand-mrna-cancer-vaccines-collaboration">cancer</a>. Like viruses, tumors have specific signatures, called neoepitopes, that immune cells can recognize and then fight. Initial cancer treatments using mRNA to target neoepitopes have shown some <a href="https://www.nature.com/articles/nature23003">clinical success</a>, and at least <a href="https://www.nature.com/articles/nrd.2017.243#main">six companies</a> have been founded to pursue this approach.</p>
<p>The short, specific arrangement of nucleic acids make RNAi easier to manufacture than more complicated protein-based therapies, like immunotherapies. Longer strands, like mRNA, are slightly harder, but the <a href="https://www.bostonglobe.com/business/2016/09/21/moderna-build-million-drug-plant-norwood/Ahsb6Pg2rdkfIkpXwXN0IN/story.html">investment in their manufacturing</a> is not scarce.&nbsp;</p>
<p>This means RNA therapy will likely be cheaper, more stable, and more accessible than complicated, personalized gene-based treatments.&nbsp;</p>
<p>“If we can stimulate the immune system efficiently <em>in vivo</em>, that would have huge value in lowering cost,” says Hammond. (And Moderna’s mRNA cancer vaccine candidates are aiming to do just that.)</p>
<figure class="left small"><img alt="A patient gets vaccinated." src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/87c07acf-35d1-4ff4-bed3-92206d51fcd4/AC-12-1_immunization.jpg"/><figcaption> <span class="credit"><p>Heather Hazzan,&nbsp;<em>SELF&nbsp;Magazine</em>&nbsp;</p></span></figcaption></figure>
<p>Of course, there are still a few challenges to be worked out: as in gene therapy, delivery remains a primary issue. Both RNA and gene therapy need to be delivered into the cell, through one of many <a href="https://www.nature.com/articles/natrevmats201756">potential solutions</a>. (So far, virus vectors and lipid nanoparticles — a ball of fat-like molecules –&nbsp;remain frontrunners.) There's a growing variety of delivery strategies — with <a href="https://www.bostonglobe.com/business/2018/04/16/tradesecrets/1fe4vZ3jQUWd6cLX4XYYvJ/story.html">patent battles unfolding</a>. For the field, this is a confident sign that profitable, proven methods will be found to deliver RNA to the cell.&nbsp;</p>
<p>“Having all of these [therapies] out in the market at once will accelerate the use of all of them. They are going to synergize each other,” says Hammond.</p>
<p>But after a decade of painstaking progress, RNA therapies are finally poised to become a widely-applicable approach.&nbsp;</p>
<p>“We can now move back and forth along the central dogma to tackle diseases,” says James Kaczmarek, a senior PhD candidate in the Anderson Lab at MIT who has <a href="https://genomemedicine.biomedcentral.com/articles/10.1186/s13073-017-0450-0">chronicled RNA therapies extensively</a>. “Engineering efforts over the past decade have brought the field to clinical reality."&nbsp;</p>
<p>It's difficult to overstate the potential impacts for medicine.</p>
    


<p><em><a href="https://massivesci.com/people/joshua-peters/">Joshua Peters</a> studies 

<p class="mb0">

<span class="scientist__field">Biological Engineering</span>

</p>

 at 

<p class="mb0 o7">

<span class="scientist__institution">Massachusetts Institute of Technology</span>

</p>

.</p>



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<guid isPermaLink="true">https://massivesci.com/articles/can-scientists-learn-from-the-stock-market-to-eradicate-hiv/</guid>
<link>https://massivesci.com/articles/can-scientists-learn-from-the-stock-market-to-eradicate-hiv/</link>
<pubDate>Thu, 06 Jul 2017 15:33:05 EST</pubDate>
<title>Can scientists learn from the stock market to eradicate HIV?</title>
<description>HIV is tricky to fight because the virus changes so much. That reminded researchers of something else that fluctuates frequently.</description>

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  <dc:creator><![CDATA[Kasra Zarei]]></dc:creator>
  <atom:author>
    <atom:name>Kasra Zarei</atom:name>
    <atom:uri>https://massivesci.com/people/kasra-zarei/</atom:uri>
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    <p>Scientists have been trying for decades to develop an HIV vaccine. But the virus changes so fast that it's hard to design a treatment that can keep up with it. That property has a group of scientists trying something new by drawing inspiration from a different hard-to-predict structure: the stock market. If the approach shows promise, it could bring us one step closer to finally stopping and eliminating the disease.</p>
<h3 id="fast-moving-virus">Fast-moving virus</h3>
<p>According to the World Health Organization, more than 70 million people worldwide have been infected with HIV since the epidemic officially began in 1981. To date, about 35 million people have died of HIV and another 36.7 million infected people are still living today. Millions of dollars have poured into HIV research, and scientists have developed antiviral drugs that make the disease more manageable. So far, however, no effective vaccine exists.&nbsp;</p>
<p>“Like Polio, we hope to one day eradicate HIV and AIDS. However, one of the major problems with HIV vaccine design is the diversity of the highly dynamic virus,” says Hiffel Haim, of the University of Iowa.</p>
<p>HIV is a deadly message encased in a protective envelope. On the surface of the envelope is a coat of spiky structures called Env proteins. The virus works by first docking on host cells using these punctuating spines, and then later infecting them. That mechanism is fairly straightforward, but there's a catch: the surface proteins are the part of the virus that changes rapidly. That's a big problem for anyone trying to develop treatments, because Env proteins are the only target for vaccines on the surface of HIV molecules.</p>
<figure><img src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/1fefbb3b-ff76-4ed7-9940-d0defcf61678/HI-virion-structure_en.svg.png"/><figcaption><span class="caption"><p>A diagram of the HIV virus, showing the spiky Env proteins on the surface.</p></span> <span class="credit"><p>Illustration by <a href="https://commons.wikimedia.org/wiki/User:Splette" rel="noopener noreferrer" title="https://commons.wikimedia.org/wiki/User:Splette">Thomas Splettstoesser </a>via <a href="https://commons.wikimedia.org/wiki/File:HI-virion-structure_en.svg" target="_blank">Wikimedia Commons</a></p></span></figcaption></figure>
<p>“Compared to other viruses, the diversity of HIV is staggering. Two samples collected from the same exact HIV-affected individual at the same time are at least 10 percent different in the composition of their Env proteins,” Haim said.</p>
<p>Because the HIV virus mutates so quickly, there are many different types of the virus out there, making designing a catch-all vaccine incredibly difficult.</p>
<p>“To make a vaccine that will continue to match the virus over time, vaccine makers need to know what Env variants are currently circulating in the patient population and also be able to predict how these proteins will change,” Haim said.</p>
<h3 id="market-based-solutions">Market-based solutions</h3>
<p>That's where the stock market comes in. While the stock market is complex, we've been able to build models that examine the structure and change in a stock's price over time and predict its future prices, with varying levels of success. These models typically consist of a long-term representation of the stock market over time, and make use of a concept called <em>volatility</em>.</p>
<p>In the stock market, volatility is a measure of how much a stock's price tends to fluctuate over time. Individual stocks often have a characteristic volatility, almost like a signature, which allows us to predict how they'll move over time. Like stocks, the amount of fluctuation in individual properties of the HIV virus seems to be characteristic. For some properties, the fluctuation is characteristically small, and for others, the fluctuation is large.</p>
<figure><img src="https://images.takeshape.io/fd194db7-7b25-4b5a-8cc7-da7f31fab475/dev/83fab99c-f7f4-457f-b8bb-995182a9a96c/HIV-budding-BW-detail(2).jpg"/><figcaption><span class="caption"><p>Scanning electron micrograph image of HIV virions attached to the surface of a lymphocyte.</p></span> <span class="credit"><p>Photo by C. Goldsmith via <a href="https://commons.wikimedia.org/wiki/File:HIV-budding-BW-detail(2).jpg" target="_blank">Wikimedia Commons</a></p></span></figcaption></figure>
<p>That's the similarity Haim explored in <a href="https://www.ncbi.nlm.nih.gov/pubmed/28384158">his new study</a>, which took the same tools used to predict stock prices and applied them to one of the world's largest banks of HIV blood samples, collected by Jack Stapleton, one of Haim's colleagues at the University of Iowa. Haim and his team found that measures of volatility from HIV patients in the 1980s can be used to accurately predict how different properties of HIV Env proteins evolved in the population of Iowa in the course of 30 years.</p>
<p>Interestingly, stock price prediction models might be even better at predicting viruses than they are at forecasting the very thing they were designed to predict. Financial models can’t seem to account for everything that happens in the stock market, since random, day-to-day events on the global scale can have small to large effects on the market.</p>
<p>“Compared to stock prices, fewer elements affect HIV and its evolution in an individual and a population. It’s so much more predictable, and the predictions of changes in HIV that we have shown are so much more accurate,” Haim said.</p>
<h3 id="predicting-the-future-of-the-vaccine">Predicting the future of the vaccine</h3>
<p>Haim’s study provides a framework for other computational biologists to build on. And Haim hopes his work can apply beyond HIV, including improving the design of seasonal flu vaccines.</p>
<p>But there's still plenty to be done. While mathematical models can predict the evolution of HIV properties over time, additional work will be needed to translate the predicted properties into a preventative vaccine. We have to create structures from the predicted HIV properties, and see if introducing them to the human body in small amounts helps build the body's immune response. While we’ll have to wait for this exciting continuation, we’re one step closer to eradicating HIV/AIDS.</p>
    


<p><em><a href="https://massivesci.com/people/kasra-zarei/">Kasra Zarei</a> studies 

<p class="mb0">

<span class="scientist__field">Biomedical Sciences</span>

</p>

 at 

<p class="mb0 o7">

<span class="scientist__institution">University of Iowa</span>

</p>

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