How Californians are resorting to crowdsourcing to get their Covid-19 vaccine

On Wednesday, under increasing criticism for the state’s slow vaccine rollout, Gov. Gavin Newsom (D) announced that all Californians 65 and older will be eligible for the shot.

But if you were a Californian who wanted to find more information about where to get that shot for yourself or your loved one, you would’ve been out of luck. While the state’s website has been updated to say that individuals 65 or older are eligible, there are no tools to find a nearby location where vaccines are available. The state’s official FAQ answers the question, “How can I get the Covid-19 vaccine?” with, “Most Californians will be vaccinated at community vaccination sites, doctor’s offices, clinics, or pharmacies” — no links, no instructions about how to find one near you.

So, fed-up Californians are taking matters into their own hands: they’re crowdsourcing it. In the last two days, an effort has sprung up to report on where shots are available to the elderly. Volunteers have set up a spreadsheet with a simple premise: One person can call each location every day and ask if vaccines are available, and then publish the information for everyone to see. (There’s a way to submit updates and corrections, too.) Once the team is confident in their two-day-old system, they’ll open up crowdsourcing and reporting, soliciting more help and more publicity so it can reach more Californians.

The crowdsourced list of where Covid-19 vaccines are available, and to whom, is a microcosm of both everything good and everything utterly broken about the United States’ coronavirus response.

Throughout the pandemic, national coordination has been lacking, causing public health tasks to fall to states and counties that vary dramatically in their preparedness to take them on. Coordination tasks that should be the business of government — from ensuring that there’s enough personal protective equipment (PPE) for hospital workers to reporting data on Covid-19 cases to letting people know which clinics offer vaccines — have fallen to hospitals themselves, or even to individuals.

Against that grim backdrop, people have stepped up, over and over, to get things done where our institutions have failed. In Washington State, university researchers studying the flu were among the first to detect the novel coronavirus in the country, while the CDC floundered. In Florida, a lone fired data scientist kept the state’s citizens updated about coronavirus case numbers. Journalists and researchers like Zeynep Tufekci told the public to wear masks and to worry about ventilation long before official organizations like the CDC and WHO recommended that. A group of citizens developed and published a risk points calculator to help people understand the risks of different daily activities.

And now in California, volunteers are trying to figure out which hospitals have enough vaccine supply to vaccinate elderly Americans. Should such a task fall to them? No. But since it has, I’m glad we have them.

How California got an unofficial vaccine availability dashboard overnight

Few US states have done an impressive job of rolling out the desperately needed Covid-19 vaccines in the month since the FDA approved them, but the most populous state, California, is among those having a particularly poor showing. The state with the best vaccination program, West Virginia, has used 78.6 percent of the doses shipped to it; California has used 27 percent, putting it 49th in the country. (Only Alabama, at 21 percent, is doing worse.) Seven percent of West Virginians have been vaccinated; only 2.5 percent of Californians have.

On Wednesday, January 13, Newsom announced that people aged 65 and older could be vaccinated in California, as part of a push to improve the state’s dismal overall vaccination performance. (Newsom’s office has not responded to a request for comment.) Yet California is lacking the infrastructure for vaccine availability reporting that many other states have, though some counties have their own systems. For instance, West Virginia’s vaccination website lists every clinic conducting vaccinations each day, with an address and specific details about how to get a vaccine. Texas has a huge map of vaccination locations across the whole state, with the ones with availability highlighted.

The unofficial California dashboard came together as a result of a call to arms on Twitter from Patrick McKenzie, a well-known tech worker and writer currently at Stripe, a payments company that before the pandemic was based in San Francisco.

McKenzie went on to clarify that he and others would reimburse anyone who spent their own money out of pocket on setting up a system. Californians immediately chimed in with their stories of frustration at trying to get a vaccine:

Having every person in California who needs a vaccine call every doctor’s office until they find one that has availability is, obviously, a terrible way to distribute vaccines; doctors’ offices will be swamped with calls, while at-risk Americans may become dispirited and give up on getting the shot.

So more than 70 volunteers got to work. Ideally, every clinic would get only one call, every day, asking about availability that day; then the information would be made public so eligible residents could figure out where they could get the vaccine without having to make the calls themselves. A Google spreadsheet was linked, then migrated to an AirTable (a spreadsheet/database service with more flexibility than Google Sheets offers). A list of clinics and hospitals and contact information was compiled, and the team got to work calling them.

The reports started flowing in, each one a window into a chaotic vaccination system. “Only doing 75 and older right now, and asked me to call the county public health department at 408 792 5040 to schedule an appointment. That number redirects to 211 at the moment for Coronavirus related concerns and reached a full voicemail box otherwise,” the notes for one report for a hospital read.

Another reads, “says that Yolo county hasn’t had any direction [to start vaccinating elderly Californians], still on [Phase] 1A only.”

“We’re not offering that in LA County yet. I know Orange County’s offering it, but you have to be an Orange County resident,” another caller was told.

There was some good news too. As of January 14, Kaiser, the Oakland-based health care system, has availability for Kaiser patients 65 and older. Sutter Health, another California-based health care system, has availability for Sutter Health patients 75 and older. Ralph’s, the Southern California grocery store, has some slots.

And the site has already been used to get some people vaccinated:

But overall, Newsom’s Wednesday declaration that people 65 and older are eligible to be vaccinated hasn’t translated to policy changes at the vast majority of hospitals in California. Whatever has California so far behind West Virginia, it will take more than an expansion of eligibility — or a crowdsourced tool — to fix.

State and local governments have been put to an extraordinary test over the last year. Many California county health departments have been models of how to handle the pandemic, from their early action declaring an emergency in March to the low death counts all year.

But the vaccination rollout has made it clear that good local governance can’t solve everything. Without good statewide coordination and communication, and without funding, counties simply can’t help everyone eligible for a vaccine arrange to get one. Good county governments and individual/crowdsourced efforts can take over many key government functions, but without state and federal coordination, vaccine distribution will be more chaotic than it should be.

In light of that, perhaps the biggest benefit from a tracking project like this one is accountability. Calling up clinics across California systematically makes it clear that many counties and many hospitals aren’t vaccinating people aged 65 and older, whatever Newsom says. In some areas, clinics are still vaccinating their own health care workers, even though many other states finished vaccinating all willing front-line health care workers earlier this month and moved on to other priority groups.

It makes it clear that many of the state’s most vulnerable citizens are getting shuffled between websites and phone lines, often with no vaccine at the end of the journey — and it cuts through that confusion and mess to find the locations that are getting shots into elderly residents’ arms.

Eventually, maybe Californians will get answers about why the vaccine rollout was botched so badly. In the meantime, though, the answer that can’t wait — which clinics are open — is available online.

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Biden’s plan to fix the Covid-19 vaccine rollout, explained

President-elect Joe Biden announced a plan on Friday for what will likely be his most pressing challenge when he takes the White House next week: fixing America’s messy Covid-19 vaccine rollout.

The plan builds on Biden’s $1.9 trillion economic stimulus proposal, which included a $400 billion Covid-19 plan, announced on Thursday. It seeks more support to states and lower levels of government, a greater expansion of vaccine eligibility, funding for more public health workers, a boost in vaccine production, better communication about the vaccines, an education and awareness campaign, and more. He promises 100 million vaccine doses delivered in his first 100 days in office.

Above all, the plan aims for something that President Donald Trump’s administration didn’t do with Covid-19 more broadly and the vaccine in particular: greater federal involvement. The Trump administration has repeatedly pushed against a bigger federal role — even characterizing more support for states so they can get shots in arms as a “federal invasion.” Biden has rejected that rhetoric, calling for a bigger role by the feds, and cementing it with his plan.

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The stakes are as high as they’ve ever been. The country now averages 240,000 Covid-19 cases and more than 3,300 deaths each day. The American death toll is among the worst in the world, with the country now approaching a total of 400,000 dead. If the US had the same death rate per million people as Canada, over 230,000 more Americans would likely be alive today.

The vaccine is America’s — and the world’s — chance at fixing this mess. Experts say the country must vaccinate at least 70 percent of its population, and possibly more, to reach herd immunity and protect a sufficient amount of the population from the virus. Only then can outbreaks truly be curbed.

But the US has been slow in rolling out a vaccine. The Trump administration overpromised and underdelivered: It promised 40 million doses and 20 million people vaccinated by the end of 2020; two weeks into 2021, only 31 million does have been delivered and just 11 million Americans have received at least the first dose of a vaccine, according to federal data. The country is currently not on track to reach 70-plus percent vaccination rates by the end of the summer.

Biden’s immediate challenge is to clean this all up. His presidency may count on it — his handling of the country’s most pressing crisis will likely be what Americans judge him on over the next year.

More seriously, it’s a matter of life or death: With thousands of people dying each day, ending the epidemic in the US even days or weeks earlier than otherwise could save up to tens or hundreds of thousands of lives.

Here’s how Biden plans to do it.

What Biden’s vaccine plan does

Biden promises to leverage “the full strength of the federal government,” in partnership with state, local, and private organizations, for a truly national vaccine plan. You can read the full proposal here, but these are some of the key points:

  • More federal work to get shots to people: Biden calls for more involvement by the federal government in getting vaccine doses to people. That includes new vaccination centers, mobile vaccination units in underserved communities, reimbursement of states’ National Guard deployments, and expanding vaccine availability in pharmacies. He also promises to target hard-to-reach, marginalized communities with extra support, particularly those that have been hit the hardest by Covid-19.
  • Boost the supply of vaccines: Biden says he’ll make greater use of federal powers, such as the Defense Production Act, to boost the manufacture of vaccines and related supplies. He also says he’ll improve communication with states so they can better understand when and how much vaccine they can expect to get — addressing a big complaint from states today, as the Trump administration has often failed to inform them of even these basic details.
  • Expanded vaccine eligibility: Biden calls for expanding vaccine eligibility to include everyone 65 and older as well as frontline essential workers, including teachers, first responders, and grocery store employees. Several states have already moved in this direction, but Biden promises more support and encouragement toward this objective.
  • Mobilize a larger public health workforce: Building on his stimulus plan, Biden vows to hire and use a larger public health workforce to help deploy the vaccine across the country. He’ll also take other steps, like allowing retired medical professions who aren’t currently licensed under state law to help administer vaccines “with appropriate training.”
  • Launch a national public education campaign: To help convince people to get vaccinated, Biden also plans to launch an education campaign “that addresses vaccine hesitancy and is tailored to meet the needs of local communities.”

All of that is on top of Biden’s broader Covid-19 plan, which promises $400 billion more funds to combat the coronavirus and, specifically, $20 billion more for vaccine efforts.

Biden’s plan hits many of the marks that I’ve heard from experts over the past few weeks as I’ve asked them about what’s going wrong with America’s vaccine rollout.

First, the plan has clear goals to address what supply chain experts call the “last mile” — the path vaccines take from storage to injection in patients — by making sure there’s enough staff, infrastructure, and planning to actually put shots in arms. Second, it takes steps to ensure that supply chain problems are fixed proactively, with careful monitoring and use of federal powers when needed to address bottlenecks. Last, but just as crucially, there’s a public education campaign to ensure that Americans actually want to get vaccinated when it’s their turn.

The question, of course, is if all of this can get implemented properly. As the US response to Covid-19 has floundered, a key question has been how much of the failure is attributable just to Trump versus bigger systemic problems, like the country’s size and sprawl, fractured health care system, and fragmented federalist government.

There’s also the question of whether Biden can get the congressional support needed for all these efforts. Democrats will control both houses of Congress. But more moderate wings of the party may scoff at the high price tag: Biden’s stimulus plan is estimated at $1.9 trillion and the Covid-19 plan alone (which is included in the bigger plan) at $400 billion. The cost of borrowing money is low, and Biden argues that the risk right now is doing too little instead of too much, but it remains to be seen if he gets enough backing in Congress.

If he pulls it off, though, Biden has a chance to show how much of a difference true federal leadership can make — and demonstrate how much the previous administration failed by refusing to embrace a larger role for itself.

Biden wants a federal role that Trump disavowed

At the core of Biden’s plan is a posture of more federal involvement that Trump has resisted at every step throughout the Covid-19 crisis.

This was clear in Biden’s broader Covid-19 plan, too: The ideas in the proposal aren’t at all new. Experts have called for expanding testing, preparing for mass vaccination efforts, supporting schools, providing emergency paid leave, and much more in the past year. Biden himself proposed many of these things last March. You can see many of these ideas in article after article in Vox and elsewhere, dating back to early 2020.

The Trump administration declined more aggressive steps, repeatedly taking a stance that it wasn’t the federal government’s proper role to get hands-on with the Covid-19 response. With protective equipment, Trump resisted using the Defense Production Act to get more masks, gloves, and other gear to health care workers. On testing, the Trump administration left the bulk of the task to local, state, and private actors, describing the federal government as merely a “supplier of last resort.” On tracing, the administration never had anything resembling a plan to make sure the country could track down the sick or exposed and help them isolate or quarantine.

This kind of hands-off, leave-it-to-the-states attitude culminated in the messy vaccine rollout. While there are many factors contributing to America’s slow vaccine efforts — including the country’s size, sprawl, and fragmented health care system — a key contributor is the lack of federal involvement. In effect, the Trump administration purchased tens of millions of doses of the vaccines, shipped them to the states, and then left the states to figure out the rest.

This was clear in the funding numbers. State organizations asked for $8 billion to build up vaccine infrastructure. The Trump administration provided $340 million. Only in December did Congress finally approve $8 billion for vaccine distribution, but experts say that money comes late, given that vaccination efforts are already well underway and the funds could’ve helped in the preparation stages.

When asked about the botched vaccine rollout, the Trump administration has stuck to its anti-federalist stance — arguing that it’s on states and localities to figure out how they can vaccinate more people. Brett Giroir, an administration leader on Covid-19 efforts, argued, “The federal government doesn’t invade Texas or Montana and provide shots to people.”

Characterizing greater federal support for Covid-19 efforts as a federal invasion is of course absurd, but it’s emblematic of the Trump administration’s approach to the crisis.

On vaccines, as with the coronavirus in general, Biden’s promise has long been that he’ll embrace a bigger role for the federal government. With his plan, Biden is putting some specific details to that end. The question now is if he can pull it off — if he gets the support he needs from Congress, and if the feds really can deliver what Biden has promised.

Natural immunity after Covid-19 could last at least 5 months

For the nearly 100 million people around the world who’ve been infected with the coronavirus, new science offers some comfort: Reinfections appear to be rare, and you may be protected from Covid-19 for at least five months.

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The study, the largest of its kind, followed more than 20,000 health workers in the UK, regularly testing them for infection and antibodies. Between June and November, the researchers — from Public Health England (PHE) — found 44 potential reinfections out of the 6,614 participants who had tested positive for antibodies or had a previous positive PCR or antibody test when they joined the study. Meanwhile, of the 14,000-plus people who had tested negative for the virus at the start of the study, there were 409 new infections.

Only two of the 44 potential reinfections were designated “probable” and the rest were considered “possible,” “based on the amount of confirmatory evidence available,” according to the health agency. Fifteen people — or 34 percent — had symptoms.

So if all 44 reinfections are real, that translates to an 83 percent lower risk of reinfection compared to health workers who never had the virus. If only two are confirmed, that rate of protection goes up to 99 percent. Either way, it suggests natural immunity might provide a similar level of protection as the approved Covid-19 vaccines.

But as with the vaccines, it’s not yet clear how long immunity after an infection lasts. Antibodies may fade after five months or last much longer, something the researchers behind the ongoing study, which will run for a total of 12 months, plan to investigate.

“This [new] study does provide some comfort that naturally acquired antibodies are pretty effective in preventing reinfections,” Akiko Iwasaki, an immunobiologist at Yale University, told Vox. The findings also square with another paper on health workers, published in the New England Journal of Medicine in December: Researchers found people who had Covid-19 antibodies were better protected from the virus for six months than people who did not.

Iwasaki added, “You can also interpret these data to mean that protection against reinfection is not complete — especially for people who had Covid during the first wave, say in March-April 2020.”

People who had the virus may still be able to pass it on if reinfected

The good news for individuals who have had Covid-19 also comes with a warning about the risk they can still pose to other people. While antibodies might protect against a second case of Covid-19 in most people, “early evidence from the next stage of the study suggests that some of these individuals carry high levels of virus and could continue to transmit the virus to others,” PHE warned in its press release.

“We now know that most of those who have had the virus, and developed antibodies, are protected from reinfection, but this is not total,” Susan Hopkins, a senior medical adviser at PHE and the study lead, said in a statement, “and we do not yet know how long protection lasts.”

In other words, even if you’ve had Covid-19, while you’re unlikely to get really sick again anytime soon, you should still consider yourself a potential risk of spreading it to others if you catch the virus again and are asymptomatic. That means continuing to take precautions — like mask-wearing and social distancing, Iwasaki added. And it’s one reason why immunologists have said people who’ve already been infected with the virus should still plan to get the vaccine when their turn comes.

So there’s still a lot more to learn about immunity after Covid-19: How will the new coronavirus variants affect it? Lab data from South Africa, where the 501Y.V2 variant has been spreading, suggests it might be able to escape antibodies produced by prior infections in some people.

Who is most likely to have a strong immune response? We do have some evidence that different individuals mount different antibody responses after Covid-19 infections, but the PHE researchers found no statistically significant difference in rates of protection between people who reported symptoms and those who did not. It’s also possible factors like gender and disease severity influence the strength of a person’s immune response.

For now, though, the research suggests that survivors of the virus might just help us get to herd immunity faster — if their immunity lasts long enough. But given the virus has only been known to humans for a little over a year, it may take a while to authoritatively answer the question.

Why the US may not see the next dangerous coronavirus variant coming

There’s a reason why a new, more contagious variant of SARS-CoV-2 appeared first in the UK: The country does a lot of viral genetic sequencing. Since the start of the pandemic, researchers in the UK have uploaded 151,859 individual SARS-CoV-2 sequences to GISAID, an international platform for sharing viral genomic data. That’s the highest number of sequences shared by any country in the world.

If a more contagious strain of SARS-CoV-2 first evolved in the United States, scientists likely would not have noticed so quickly. Despite having a larger population than the UK, a sophisticated biomedical research industry, and tens of millions more cases of Covid-19, to date US labs have only uploaded 69,111 sequences, according to GISAID.

“It’s embarrassing, is all I can say,” Diane Griffin, a microbiologist and immunologist at Johns Hopkins, told Vox.

The US has lagged behind on so many aspects of pandemic response — from an initial lack of testing, to the current strained and clumsy rollout of the Covid-19 vaccines. Lack of genetic surveillance is just another. Without it, we’re kept in the dark: Scientists can’t see, clearly or quickly, how and if the virus is mutating in concerning ways. It also leaves us without another useful tool to deploy in contact tracing studies.

And it’s one this country ought to invest in, and get right, scientists say — at least before the next pandemic strikes.

How the US fails on testing viral genomes

Earlier this year, Griffin was on a committee making recommendations for a recent National Academies of Science report on the state of genomic surveillance in the US. Genomic surveillance is used, routinely, around the world to track flu, and to try to predict which flu vaccine strains will be most effective in a given season. Genetic sequencing tools are not a new technology, and the Academies wanted a report to survey how they were being deployed in the pandemic in the US. Genetic sequencing is of particular import when it comes to coronaviruses because they use RNA as their genetic code, and RNA viruses are known to mutate frequently.

The report, when it was published in July, outlined a bleak landscape of SARS-CoV-2 mutation tracking. It’s not just that the US isn’t collecting enough genome samples of the virus. It’s doing so in an unsystematic, patchwork way.

“Current sources of SARS-CoV-2 genome sequence data … are patchy, typically passive, reactive, uncoordinated, and underfunded in the United States,” the report concluded. And the data that did exist? The report found it was “inadequate to answer many of the pressing questions about the evolution and transmission of the virus.”

Early on in the pandemic — way back in March — the UK government invested £20 million ($27 million) to launch the COVID-19 Genomics UK (COG-UK) consortium, which coordinates the collection of this data from public health labs. The consortium also tracks viral genetic samples from health clinics, university research labs, and public health research facilities, to help generate a close-to-real-time snapshot of how the virus is changing in the country.

It’s what allows researchers to generate maps like this one, which shows how the new, more contagious strain of the virus spread geographically in the country over time.

The rich genetic data, when paired with case reports, also guides researchers to ask and answer crucial questions, such as: Is this new variant more deadly than other ones? Scientists were able to quickly determine the answer is “no.” (That said, a more contagious virus can still end up killing more people than a more virulent one.)

The US Centers for Disease Control and Prevention does have a genetic surveillance program called SPHERES (SARS-CoV-2 Sequencing for Public Health Emergency Response, Epidemiology, and Surveillance), but it’s less well coordinated than the UK effort. Right now labs have to essentially raise their hands and volunteer to contribute. And the funding for their efforts isn’t consistent. That leads to a patchwork of surveillance across the country. “So you might know what’s going on in Boston, or New York City, but have no idea what’s going on in Iowa,” Griffin says.

“In other words,” says Stanford microbiologist David Relman, who also contributed to the National Academies report, “anybody who has the means and interest to engage in genomics is certainly encouraged to do so.” But genomic sequencing, he says, hasn’t been made a “mainstream central pillar of public health efforts.”

What we lose out on when we don’t collect genetic samples of circulating viruses

The National Academies report was published in July. Has the situation gotten much better since? “No,” Griffin says. There has been a little bit of positive movement: Recently, private genomics companies Illumina and Helix have started to help in the detection of new variants in the United States. Even so, James Lu, president of Helix, told MIT Technology Review the US still needs to go from sequencing a few hundred samples a day to around 7,000 per day.

Viral genomics surveillance doesn’t just allow researchers to spot new variants, it helps them learn crucial lessons about how the virus is spreading.

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Scientists take advantage of the fact that viruses are constantly making copies of themselves. And every time they make a copy, they may make a little typo in their genetic code. Most of the time, these mutations are meaningless, but they occur at a regular rate. And that makes it possible to make a family tree of the virus. If one viral sample and another have similar typos, researchers can determine they are more closely related.

This can generate key insights.

“In the beginning of the pandemic, we got our hands on some of the first cases that were identified in Connecticut,” says Mary Petrone, a PhD student who works in a molecular biology lab at Yale. Using genomic data, Petrone and her colleagues were able to figure out whether these cases were introduced from abroad, or came from somewhere in the United States. The genetic data revealed that the viruses more closely resembled those circulating on the West Coast than strains from abroad. “It was telling us: there is actually domestic transmission going on,” she says.

Petrone’s lab delivered a key early insight into understanding the virus’s spread in the US. But it wasn’t like the CDC directed them to do so. “Our lab was actually originally set up to do this type of research for mosquito-borne viruses,” she says. “When the pandemic hit we switched over, because there was an urgent public health need to answer some of these questions. So we just happened to really to be set up to do this type of work.”

Setting up more labs to do this work could also help with contact tracing efforts, overall. “For example, if 10 college students test positive,” Julie Segre, a scientist at the National Human Genome Research Institute, writes in an email, “did they come to school already colonized [i.e. infected] or did they transmit the virus while at school.” Genetic evidence can help answer such a question and help prevent future outbreaks.

What needs to happen: coordination, and money

And it’s not necessarily cheap or easy work to do. While the technology that sequences the viral genomes has become relatively inexpensive in recent years (a plug-in USB sequencer will set you back around $1,500), it still takes a lot of skilled lab work to prep samples for analysis. “You definitely don’t need a PhD to be able to do it,” Petrone says. “But you do need to be pretty well trained in molecular biology in the lab. There are a lot of steps where you can contaminate your samples. It can be quite expensive to do.”

Petrone’s lab can do full genome sequencing; that is, they can read every letter of a virus’s genetic code. But not all labs would need to do that to contribute to a surveillance effort. For instance, Petrone’s group is working on a simpler test that can identify the more contagious B117 variant that first was detected in the UK. “That is something you’d be able to run in a clinic,” she says.

But creating a widespread surveillance network for the new variant would require a lot more coordination than what’s currently taking place.

That’s why the US government needs to be more proactive on this, and help set up a nationwide network for genomic data. And that may be coming. According to STAT, the incoming Biden Administration plans to scale up the country’s genomic sequencing efforts as part of a $415 billion emergency Covid-19 spending package it will ask Congress to approve. (Perhaps also auspicious: Biden has selected Eric Lander, a geneticist who co-led the Human Genome Project, to lead the White House Office of Science and Technology Policy, which will be elevated to a Cabinet-level position.)

For a robust genetic surveillance network to be most useful, it needs to be backed up with other rich datasets too. New variants pop up all the time. What matters is whether those variants are linked to worse health outcomes, more reinfections, or faster spread.

“We would ideally have access to good, consistent data about each sample — at the least, geographical location, but more would be better,” Adam Felsenfeld, director of genome sciences at the National Human Genome Research Institute, writes in an email. If possible, too, “one would need details about the medical record of the patients,” he writes, to try to determine if genetic changes in the virus correspond to different disease courses. Again, this would take coordination, as researchers would need informed consent from people to collect this personal data.

A network of viral genome surveillance isn’t just needed for this pandemic, but for future ones too.

“This won’t be the last pandemic,” Griffin says. “If we could get the infrastructure right and get the approach right, then you have things in place you could activate” … for the next time.

Rich countries are hoarding Covid-19 vaccines

More than 80 million Covid-19 vaccine doses have been distributed around the world so far. Only 55 — 55! — have gone to people in low-income countries. In fact, just one country: Guinea.

Those 55 doses in Guinea don’t even represent “the start of a ‘real’ national vaccination rollout,” said Edouard Mathieu, head of data at Oxford University’s Our World in Data, which has been tracking the global vaccine effort. Rather, a few Guinean public officials were vaccinated at the end of December — with the Russian Sputnik V vaccine — on an experimental basis, the Associated Press reported.

“Then nobody was vaccinated after that,” added Mathieu. (The Guinea health ministry has not responded to Vox’s request for comment.) As a result, Our World in Data stopped tracking Guinea’s rollout.

As the coronavirus continues to spread around the world, with new, dangerous variants picking up pace, the vaccination campaigns in all the world’s poorest countries haven’t even begun. Meanwhile, wealthy nations already vaccinating have pre-purchased access to supplies that can more than cover their populations — about four times over, in the case of the US, according to a December New York Times analysis.

This doesn’t mean there are “warehouses full of extra vaccine doses” sitting around in high-income countries, explained Andrea Taylor, a Duke University researcher who has been analyzing the deals. But the countries with deals have priority manufacturing slots for 2021, “meaning that even if other countries make purchases now, they may have to wait months or even a year for delivery.”

The result: “High-income countries have 16 percent of the world’s population but currently hold 60 percent of the vaccine doses that have been purchased,” Taylor added.

With this kind of vaccine access, the people in rich countries will start to see their epidemics slow down over the next year, and life may regain some of its pre-pandemic rhythm. People in poor countries, meanwhile, may experience no such benefit. In fact, it will likely take years for many low-income countries to even start fully fledged vaccine campaigns, said Agathe Demarais, of the Economist Intelligence Unit, in a recent briefing. “Most developing countries will not have widespread access to the shots before 2023 at the earliest.”

“That’s not just unconscionable,” said Georgetown global health law professor Lawrence Gostin, “but it also is very much against the interests of high-income countries.”

This greed will help the coronavirus continue to spread globally, allowing more opportunity for variants that resist the vaccines to emerge and Covid-19 outbreaks to reignite, including in rich countries. This is a cycle that repeats with just about every disease threat: Rich countries benefit from new health technology first, while poor countries have to wait years, or decades, for it to trickle to them, as the New Yorker’s Michael Specter wrote. But there are growing calls to break the pattern — and Norway is showing the rest of the world how it can be done.

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How rich countries exacerbated the global Covid-19 vaccine scarcity

As of January 27, the majority of the 80.2 million Covid-19 vaccine doses administered worldwide have gone to people in only a handful of high- and middle-income countries and regions (namely, the US, China, the EU, the UK, Israel, and the United Arab Emirates).

Several middle-income countries — the poorest among them include India, Myanmar, Ecuador, and Indonesia — have doled out 2.3 million doses in total. Most — 2.03 million — went to people in India.

But the lowest-income countries — for instance, Zambia, Bolivia, Tajikistan, and Nepal — have not begun vaccinating at all.

So why, in this pandemic, are such disparities allowed? It’s pretty simple: Covid-19 vaccines aren’t a public good. Capital rules who gets access first, and those with capital — rich and middle-income countries — have bought first dibs in the vaccine supply, through lucrative pre-purchase agreements with vaccine developers.

“That’s left a global scarcity and also resulted in a bidding war which has made the prices more expensive,” Gostin said. “As a result, [for] countries themselves which are lower income, there aren’t any doses to buy and they are too expensive.”

Because countries inked deals with manufacturers before clinical trials were complete, betting on which companies might come out with vaccines that work, they each signed multiple agreements, covering their populations many times over.

The pre-purchase agreements “made sense in the world we lived in six months ago, because we didn’t yet know which, if any, of the vaccine candidates would come to market,” said Taylor. But the result was that, by November, high-income countries — along with a few middle-income countries — had already pre-purchased the rights to 3.8 billion vaccine doses, with options for another 5 billion, according to an analysis by Taylor and her colleagues at Duke.

Yes, that’s just about as many doses as there are people in the world.

This vaccine hoarding happened in parallel with an unprecedented multilateral effort to support the development and equitable distribution of 2 billion doses of Covid-19 vaccines to the world’s poorest countries before the end of 2021, called Covax.

The initiative has two parts: a purchasing pool for higher-income countries, and a fundraising effort for poorer countries. By promising to buy a certain number of vaccine doses from manufacturers, countries that join get access to any vaccines that are approved in Covax’s portfolio, while also creating a global market for the shots and driving prices down.

More than 190 countries signed on — including rich ones. But the bilateral deals have undermined Covax. Rich countries “want to have it both ways,” Gostin said. “They join Covax so they could proclaim to be good global citizens, and at the same time rob Covax of its lifeblood, which is vaccine doses.”

How to stop hoarding

In the first quarter of the year, Covax is planning to begin delivering a first batch of 100 million vaccine doses. But vaccine distribution is already lagging in rich countries, where manufacturers have failed to deliver the doses they initially promised, and governments are struggling to set up systems to get millions of people through the door at once.

The emerging disparity has prompted calls for rich countries to stop hoarding vaccines and share their excess supply with poorer countries through Covax. It’s also stirring discussion about how countries and manufacturers can get creative and bolster supplies for the world.

Right now, “the biggest constraint for everyone to get vaccinated is the number of doses,” Nicholas Lusiani, at Oxfam America, told Vox. Instead of fighting over the crumbs, he said, Oxfam has suggested countries build regional vaccine production hubs to churn out vaccines at a lower price in the places they’re needed (and where production costs are lower).

The US, Europe, and other high-income countries could also push companies with effective vaccines to collaborate with other manufacturers on production, sharing their technology, or even waiving intellectual property rights. (AstraZeneca has already done so, sharing information with the Serum Institute in India.)

Then there’s simple donating of vaccines. Gostin and colleagues have called on the US to work with other high-income countries and inoculate only their most vulnerable groups — health workers, older adults — first, then give the excess supply to Covax, which could distribute vaccines to high-risk groups in the rest of the world.

“There’s a certain ethical and political justification for putting your own country first because every government’s first duty is to its own population,” Gostin said. “But that’s to a point.”

Still, Taylor said, “it is complex and there is no easy solution. … It would be a very hard sell for the leader of a rich country to start donating doses to other countries while still vaccinating their own population — this is what needs to happen, but it is hard to imagine.”

Norway has managed to do it. Much like the US, the Nordic country will have access to three times as many vaccines as it needs. “This allows us to redistribute vaccines to other countries,” said Norway’s minister of international development, Dag-Inge Ulstein. “The distribution will be started gradually and in parallel to the current vaccination of the Norwegian population as soon as relevant vaccines are approved.”

The Norwegian government decided it was both ethical and self-interested to ensure people in low-income countries can access effective vaccines as soon as possible. “Otherwise,” Ulstein added, “it will be a long time before these countries are able to vaccinate a sufficiently large proportion of their populations. [And] that would not benefit anyone.” Now it’s time for other countries to follow suit.

4 reasons we’re seeing these worrying coronavirus variants now

Since the start of the pandemic, SARS-CoV-2, the virus that causes Covid-19, has been mutating, its genetic code slowly changing as it spreads from person to person across the globe. For most of that time, the mutations didn’t concern scientists. The genetic changes didn’t seem meaningful in terms of how dangerous the virus is. Mutations are normal. Some even weaken the virus.

Now, things are different.

There are three mutated variants of SARS-CoV-2 of particular concern around the world. Researchers do not have the same level of evidence for each: One is more well understood than the others. But in each case, researchers see a seed of something concerning.

There’s B.1.1.7 (yes, all these variants are clunkily named). This variant was first detected in the UK in September. Scientists strongly suspect it’s more transmissible (i.e., contagious) than past versions of SARS-CoV-2, and there’s some preliminary evidence that it might be slightly more deadly.

Then there’s a pair of variants — one discovered in South Africa in October, and another in Brazil in December — that are less well understood. But scientists are beginning to suspect that they might have evolved ways to evade the human immune system, at least a little bit.

A reasonable question you might be asking: Why now? Why have these three variants of concern popped up in such quick succession? The fact that the virus is mutating isn’t new. It’s been mutating all along.

“We’ve had many, many variants in SARS-CoV-2 for a long time now, and scientists have even been tracking these in fairly detailed ways since the summer of 2020,” Emma Hodcroft, a molecular epidemiologist at the University of Bern, says. “The big difference is that, before December, we hadn’t really seen any variants that seemed to be behaving any differently.” (By “behaving differently” she means that the virus itself didn’t seem at the time to be more infectious, or more dangerous in any intrinsic way.)

Hodcroft and others who study the evolution of viruses provide a few overlapping answers to the question “Why now?” None of them perfectly explain what’s going on.

But thinking through them brings us to another, perhaps even more critical question: How might the coronavirus continue to evolve? Will even more variants emerge that challenge our fight against the virus? And what does that mean for the pandemic?

Overall, experts outlined four reasons we’re seeing these variants now. And it all boils down to one thing: evolution.

Reason 1: The virus’s genetic diversity increases over time

First off, it’s helpful to get a refresher on how evolution works. At its core, evolution requires two things: individual differences and natural selection. Evolution is a nonstop process. Organisms — as a group — accumulate change over time through mutations, and the environment helps determine which changes stick around in a population, and which become less prevalent.

Viruses mutate because they’re constantly making copies of themselves in enormous numbers. If you were writing a draft of something millions of times on a computer, extremely quickly, you’d probably make some typos. This has happened millions and billions of times across the globe. The longer the pandemic rages on, the more chances the virus has to evolve.

In the beginning of the pandemic, the viruses infecting people were really similar to one another, because they weren’t that far removed from the original virus that began the outbreak. But now the virus has been changing genetically over the past year, branching out like a family tree. So many genetic changes have accumulated, in different places.

“We have no evidence that the underlying mutation rate is changing,” Sarah Cobey, an epidemiologist who studies viral evolution at the University of Chicago, says. The virus is still making its typos at the same rate. It’s just that those changes start to accumulate the longer the pandemic continues. If you kept copying a book, over and over, making typos in each copy, you’d end up with a somewhat different book than you started with. Likewise, according to Cobey, you’d expect the genetic diversity of the virus to increase over time.

So that’s one major part of it. The virus has just had a lot of opportunities to become something slightly different.

But that’s not all of it. The increased diversity doesn’t quite explain why we’re seeing these particular — seemingly more concerning — variants at this particular time. “We are seeing evidence of adaptive evolution,” Cobey says. These variants appear to be either getting better at infecting people or possibly evading the immune system, and they are doing so in similar ways.

Genetic diversity alone doesn’t explain that. Natural selection does.

Reason 2: It’s possible the virus is evolving in response to increasing human immunity

The virus’s increasing genetic diversity only explains part of the story. The other part of the story: natural selection.

Some of the virus’s genetic changes provide an advantage, which has led, in some cases, to these variants outperforming older strains of the virus. “Some of those [genetic] substitutions are actually helping the virus replicate better,” Cobey says, which then can lead to the variants infecting an increasingly larger proportion of people compared to other variants.

Both the P.1 variant found in Brazil and the 501Y.V2 variant found in South Africa have a mutation called E484K, which changes the part of the virus that attaches to human cells (it’s also the part that the immune system most readily recognizes after someone is vaccinated). That mutation, Hodcroft says, “might allow reinfection.” In other words, people who have already been infected with SARS-CoV-2 could potentially be a little bit more susceptible to these variants (though this is still not confirmed).

Hodcroft suspects that both the P.1 and 501Y.V2 variants may have evolved in response to human immunity. And she stresses: What follows is mostly speculative at this point.

In the beginning of the pandemic, no human had been exposed to SARS-CoV-2 before. That means everybody’s immune systems were equally bad at recognizing the virus. If there had been a variant that was good at evading the human immune system, it wouldn’t have risen to prominence because it wouldn’t have outperformed its viral peers.

As Hodcroft explains it: “Even if this [E484K] mutation popped up — which we know it did, we can see that it popped up a few times — it might not have been in a place where this was an advantage.”

In many places around the world, there are lots of people who have already been infected and who have developed some level of immunity to the virus.

So now, variants that can evade the immune system have an advantage. They could grow and replicate where other variants cannot. And that variant could quickly become the dominant one.

“I want to be really clear: We aren’t 100 percent sure, scientifically, that this is what’s happened,” Hodcroft says. “But these are the kinds of things to think about when we think about why we might be seeing different variants now. We’ve changed the rules of the game.”

Reason 3: The virus has spread so far that rare things are starting to happen

The longer the pandemic goes on, the more chances there are for rare — and sometimes consequential — things to happen.

The B.1.1.7 variant might be one of these consequences. It appears to have acquired significant genetic changes over a short period — so many that scientists suspect the variant might have emerged in an immunocompromised person.

In most people, Hodcroft explains, the immune system mounts a full-on assault on the virus, eliminating it in a couple of weeks. “In people that have compromised immune systems, though, there’s a very different dynamic,” she says. “So, for one thing, the virus could be in them for months instead of weeks.” That gives the virus more time to evolve, to accumulate mutations that might make it easier to thwart the immune system.

Many things have to happen for this to occur. Not only does an immunocompromised person have to get the virus (and many immunocompromised people are being particularly cautious), the virus would have to acquire mutations, and then the immunocompromised person would have to spread the virus to another person.

“These are all like ‘super-edge cases,’” Hodcroft says. But “by keeping cases so high, you increase the chance that sooner or later, you’re going to hit that jackpot … we keep rolling the die when we keep the cases up so high.”

Reason 4: Some Covid-19 treatments might have instigated some evolution

The rise of these variants “may have something to do with the use of convalescent plasma,” says Michael Worobey, the head of the department of ecology and evolutionary biology at the University of Arizona.

Convalescent plasma treatments are blood plasma transfusions from people who have recovered from SARS-CoV-2. The idea is that along with the transfusion come antibodies that can help someone else with Covid-19 fight off the disease. The problem is that within certain recipients, the plasma could conceivably also create an environment that favors a stronger variant of the virus.

“So there are cases where the identical [mutations] that characterize the UK variant have also evolved in patients who are chronically infected with the virus and were then given convalescent plasma,” Worobey says. “It’s a perfect storm.” The virus has built up genetic diversity in the patient, and then the convalescent plasma acts as a force of natural selection, choosing among those variants one that could evade antibodies in that plasma.

Worobey is not saying that this definitely happened with the B.1.1.7 variant, just that it’s possible. (A similar thing, he says, could have happened with using monoclonal antibodies — synthetic antibodies produced as a Covid-19 treatment — on immunocompromised patients.)

It’s not that these treatments never should have been used. In many cases, they may have helped save lives when there are few treatment options for Covid-19. But in the case of using convalescent plasma on immunocompromised people, Worobey says, it may have been “a bit irresponsible.”

The virus will keep evolving. Vaccinations need to happen quickly, and cases need to decrease.

The virus will keep changing, and there will be more variants. Not all will be variants of concern, though.

“I think one thing that we definitely have to keep in mind, particularly in the next few weeks and months, is that a lot of people are now very interested in doing [viral genetic] sequencing and looking for variants,” Hodcroft says. “And that’s fantastic. This is exactly what I’ve been kind of begging for for a long time — for more countries to really dedicate resources to this.” But with the increased vigilance, she says, “we’re going to see a lot of false alarm variants.”

But there also might be more variants of concern in the near future, as the virus is about to get hit by another big selection pressure: vaccines.

If, due to random mutations, there’s a strain of the virus that is just a little bit better at evading the immunity provided by vaccines, it could spread.

That’s why these viral evolution experts want vaccination to happen as fast as possible. Just as partial immunity in a single immunocompromised person can act as a selection pressure for evolution, partial immunity in the population at large can as well.

“What we don’t want is for there to be high levels of virus circulating and spending a lot of time with a partially vaccinated population,” Hodcroft says. “We want to keep case numbers while we’re vaccinating as low as we can.”

That’s because “once you vaccinate hundreds of millions of people, the virus is going to be under really quite intense pressure to evolve [immune] escape variants,” Worobey says. Some of these variants, he warns, “may already be in existence” among the public but have not yet been detected — or may soon form as the pandemic continues. “And those variants, I think, we can expect to sweep up to much higher frequency once vaccination provides this huge selective force.”

Evolution happens when there’s a lot of genetic diversity, which then meets a selection pressure. This is what’s happening as the pandemic continues during a vaccination campaign.

The good news is that, for now, it appears the existing vaccines will still be broadly effective against the variants, and that it’s possible to update the vaccines to account for future changes. But how can we stop more viral evolution from happening in the first place?

“The best way to avoid it is to go back in time and not allow the pandemic to spin so out of control,” Worobey says. “If we had done that, and then vaccinated, then we would have been in a much less dangerous situation.”

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Insulted, ignored, persevering: AFL is home to great Irish sporting stories

THEY WERE THE days of their lives. At least that is what his father often tells him. Regularly they gather and reminisce about that famous summer. In 2014, Darragh Joyce captained Kilkenny to All-Ireland minor glory against a Limerick team that included Sean Finn, Cian Lynch, Barry Nash, Peter Casey and Seamus Flanagan.

Afterwards, Tipperary and Kilkenny played out a thrilling draw in the senior final. Still giddy from success, a few weeks later Joyce and his team-mates boarded the bus to Dublin and journeyed to Hill 16. From there he watched his older brother Kieran, who didn’t play the first day, put in a man-of-the-match performance as the Cats claimed the Liam MacCarthy Cup.

Source: Cathal Noonan/INPHO

Darragh won a minor title with the club in 2013.  A year later his older brothers, Kieran and Conor, played for Rower-Inistioge as they won the All-Ireland intermediate championship in Croke Park. On the rise and triumphant in the heartland of hurling. All the road signs pointed one way. A path firmly mapped out.

Until he veered off course. Fast forward two years. Joyce has accepted a rookie contract with AFL outfit St Kilda. Pursing a chance as a professional athlete in a world he knew little about. He landed and found himself scrambling to get organised. The teenager agonised over the decision, discussing it at length with local legends like Eddie Brennan.

This was a double-barrelled transition, to a new sport and a new realm. Any presumptions about the pervasive luxuries of a professional environment quickly proved wide of the mark. Routinely, the Irish Down Under point at our proximity to the UK football scene as the cause of so much misconception. The average salary in the AFL for an established player is around €240,000. The average in the Premier League is 10 times that. These planets are in separate solar systems.

Joyce had to figure it all out for himself. Before he’d even received his first paycheck, he had to organise a loan so he could buy a second-hand car. Imagine the pain when his new pride and joy broke down with engine issues shortly after. 

In every club, the Irish recruit starts at the bottom of the ladder. Number 45 on a list of 44. The smallest fish in a sizeable pond.

At the start, Joyce was mistakenly called ‘Daryl’ more than once and the centre of attention as the Irish novelty. A few months in and he was dropped. Not from the seniors, from the reserves. Down to a league he scarily knew existed. It doesn’t anymore. The development league. ‘Two’s twos.’

Source: Ryan Byrne/INPHO

Togging out at 10 in the morning to play as a curtain-raiser for the VFL as dogwalkers and recoiling Saturday night partygoers passed by obliviously.   

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Every day, Joyce would trek home from training. On the way, he’d pass a travel agent. Quickly he developed a routine. Head in and the same refrain: ‘I was just wondering how much flights to Ireland are today? Two routes loomed large on his horizon. Fight or flight. Returning home was the understandable one. The route the majority would opt for.

Joyce elected for a different approach. He dug in. Persevered. Persisted. Transformed his body and his attitude. Bottled all his frustration. As a key defender, he will never have 30 possessions. It is about shutting your opposite man out. Daily physicality and tenacity. He started embracing rather than dreading every weight and skin fold test. 88kg of puppy fat became 96kg of sheer brawn. All the while, channelling any slight to create an arsenal of aggression, unleashed in every single practice match.  

“Around 2018 he wasn’t getting a look, but I always found him a really tough opponent and defender,” recalls star AFL goalkicker Joshua Bruce. Bruce has 150 AFL appearances. He was St Kilda’s leading goalkicker in 2015 and the Western Bulldogs’ leading goalkicker in 2021. He and Joyce were regular training opponents. 

“His bodywork and strength and speed were really good for that lockdown defender role. It felt like he obviously still needed to work on his game sense, but I kept telling the coaches that he was a bloody hard match-up. I think I kept using the phrase ‘best defender we’ve got’ to force it home.”

Eventually, the message registered with the selection committee and they took his advice on board. Darragh Joyce debuted in July 2018.  

“Turns out they actually listened and did give him a few games,” says Bruce. “I think physically he’s bloody annoying to play on which is always a good sign as a key defender!”

Source: AAP/PA Images

Since then, Joyce has played 10 games for the club. He was set for his first prolonged stint in the first team last year until fate dealt another cruel blow. Three concussions in 12 months and a Covid contact scare after attending a rugby international severely hampered his campaign. Despite serious interest from one other club, he signed a new deal with the Melbourne outfit ahead of a crucial 2022. 

St Kilda are looking to kick on from a disappointing season and have recruited another Irishman to help them do it. Cavan native Nicholas Walsh was recently appointed high-performance manager of the club. The same Walsh that was once told he wasn’t capable of coaching football because he was Irish and wouldn’t understand the technicalities of the game.

These are just some of the remarkable Irish in Australia yarns. In some ways, it seems a shame they aren’t given due recognition. Coverage closer to home struggles to scratch the surface. Basic details like statistics, achievements or the clubs they play for are often wrong. Not everyone opts for the Stuart Magee approach and actually calls up to correct the record.

As a child, Magee and his family boarded a boat in Belfast and docked in Williamstown weeks later. He went on to amass 216 appearances for South Melbourne and Footscray. So, you can imagine his reaction when he opened the paper to read about Zach Tuohy’s big milestone.

“It said, ‘The second Irishman after Jim Stynes to reach that milestone,’” Magee recalled last year.

“We got the paper here and I was looking at it thinking, ‘I came over in a boat. I lived in a hostel, and we put up with some of the worst things. I travelled all over Melbourne to play. Do I not count?’

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“What happened to me? That is why I rang the bloke from the paper. I said, ‘my name is Stuart Magee, I was born in Belfast in 1952. I travelled to Australia and played for South Melbourne. I captained the Western Bulldogs.’”

For the current crop Down Under, the scars from how the media treated Conor McKenna after his Covid case still linger. And in Ireland, such missteps are understandable. Australia is, after all, on the other side of the globe. Gaelic football and AFL are similar sports but also, totally different. It is a near-impossible task to understand a different sporting history and contextualise foreign achievements within that sphere.

Source: Tommy Dickson/INPHO

65 GAA converts have made the move since Sean Wight in 1982. Five of them have played over 150 games. The vast majority return after a few years. Still, recruiters maintain that it is a promising strike rate when compared to the AFL draft. There any prospect picked outside the top 20 is doing extremely well to come anywhere close to 100 games. Outside of the top 50 picks, the average appearance is less than 50.

At the end of last year, Luke Towey and Stefan Okunbor’s stints with the Gold Coast Suns and Geelong respectively came to an end. Mark Keane and Anton Tohill voluntarily elected to leave Collingwood and return home. Oisin Mullin also turned down the opportunity to join Geelong.

Any fears that this would prompt clubs to reconsider Irish recruitment have proven to be ill-founded. Clubs continue to utilise a rich and varied scouting network. Discussions about a return of the combine, perhaps in a joint capacity for males and females, are ongoing. A few more will make the move over the next few years and attempt to scale an arduous mountain.  

This season, Joyce, Hawthorn’s rejuvenated Conor Nash, Sydney Swans stalwart Colin O’Riordan and Brisbane flyer James Madden will all hope for regular game time. Zach Tuohy and Mark O’Connor aspire to be leading lights as Geelong chase an elusive Premiership. Callum Brown looks to kick on with GWS Giants. Sydney’s Barry O’Connor and Essendon’s Cian McBride want to debut and put the chaos of two Covid-compromised years behind them. At Brisbane, Deividas Uosis will continue his development. Fionn O’Hara is just starting out on his career with Hawthorn.  

All striving to defy the odds and make their mark. Continuing to produce chapters in a great Irish sporting story. 

Ireland internationals Devin Toner and Lindsay Peat were our guests for The Front Row’s special live event, in partnership with Guinness, this week. The panel chats through Ireland’s championship chances ahead of the final round of Guinness Six Nations matches, and members of the Emerald Warriors – Ireland’s first LGBT+ inclusive rugby team – also join us to talk about breaking down barriers in rugby. Click here to subscribe or listen below:

The evidence that Covid-19 vaccines are safe and effective in pregnancy is growing

People who are pregnant are now eligible to get the coronavirus vaccine in more than 40 states — typically ahead of their lower-risk peers. And more than 60,000 of them have already rolled up their sleeves, according to the Centers for Disease Control and Prevention.

Although the Covid-19 vaccines authorized in the US were not studied in pregnancy, early data is now starting to emerge suggesting — as researchers expected — that the vaccines are likely safe during pregnancy and confer protection not only to the recipient but also, potentially, the baby.

“It’s all very positive,” says Stephanie Gaw, a maternal-fetal medicine specialist at the University of California San Francisco Medical Center, of the findings so far.

There have been many reasons to suspect the vaccines should be safe in pregnancy, including the lack of major adverse events reported so far, solid studies in animals, and a good understanding of how the vaccines work in the body (they don’t contain live virus, and they are quickly broken down). “The data that we’re collecting on it so far has no red flags,” Anthony Fauci, the top US infectious disease doctor, said in February.

Meanwhile, new research, published March 25 in the American Journal of Obstetrics and Gynecology, found that the vaccines offer strong immune protection for people who are pregnant, just like their non-pregnant peers.

Preliminary research also suggests vaccines might provide some protection to newborns, who are unlikely to have their own approved Covid-19 vaccine anytime soon (and are also vulnerable to more severe illness). The new AJOG paper joins other early findings that antibodies to Covid-19 generated by pregnant mothers after receiving their vaccines were passed through the placenta to the fetus.

But Covid-19 vaccine rollout to the pregnant population has been inconsistent around the globe.

For months, the US and many national medical groups — including the American College of Obstetrics and Gynecology, the Society for Maternal-Fetal Medicine, and the Academy of Breastfeeding Medicine — say the vaccine should be offered to this group, in large part because there’s strong evidence that pregnancy elevates the risk for severe Covid-19 and death. (Given this data, the American Society for Reproductive Medicine goes so far as to say the vaccine is “recommended” for those who are pregnant or considering pregnancy.)

“If a pregnant patient gets infected during pregnancy, her risk of intensive care admission is around 5 percent,” says David Baud, chief of obstetrics at Le Centre hospitalier universitaire vaudois in Switzerland, where he studies infections during pregnancy. “I do not know of any disease that put a 30-year-old woman at such high risk to be admitted to the ICU.” Furthermore, if the infection happens late in pregnancy, it increases the risk of preterm birth and the baby needing intensive care.

Israel went as far as adding pregnant women to its vaccine priority list in January. But other countries, such as the UK and Germany, and the World Health Organization are still saying most people who are pregnant should wait.

Why the disagreement? The clinical trials of the new Covid-19 vaccines explicitly excluded pregnant people, and we don’t yet have enough follow-up data from individuals who have opted to get the shots to say for sure they are safe for everyone during pregnancy.

Add to this muddled landscape the persistent misinformation swirling around the Covid-19 vaccines and pregnancy and fertility, and it is little wonder some people are still confused or worried. And most organizations still stop short of advising all pregnant people to definitely get the vaccine.

Thankfully, these information gaps are starting to fill in. Numerous studies are underway following the outcomes of pregnant and breastfeeding people and their offspring after immunization. And a handful of them are now starting to report early, reassuring results.

In the meantime, however, a growing number of people have had to come to their own decision, with the optional help of their care provider, with some uncertainty. And no one needs an extra thing to stress about during a pandemic pregnancy.

So more information about the coronavirus vaccines in pregnancy can’t come soon enough.

4 reasons the coronavirus vaccine should be okay to get while pregnant — but why not everyone is recommending it yet

One of the big reasons why, despite Covid-19’s known risks in pregnancy, not everyone has unequivocally recommended the vaccines that currently have emergency approval in the US for pregnant people is that the way they work is fairly new. But we do have some key pieces of information already:

1) These vaccines don’t contain live coronavirus. The only types of vaccines that are contraindicated in pregnancy contain live virus that has been weakened, such as the chickenpox vaccine. (Even fewer immunizations, such as the smallpox vaccine, are not recommended during lactation.) While these vaccines don’t pose a risk to most people, there is a small, theoretical chance they could cross the placenta and infect the fetus.

The Pfizer/BioNTech and Moderna vaccines, on the other hand, contain just a fragment of genetic material, called messenger RNA, that can tell human cells to build a tiny part of the virus’s outer shell, which the immune system learns to recognize and fight off. The Johnson & Johnson vaccine uses a different method, known as a viral vector (the same platform as the already-used Zika and Ebola vaccines), to get the body to build part of the virus’s shell.

In either case, there is no way the vaccine can cause a Covid-19 infection.

2) The main coronavirus vaccines are very fragile. Once the mRNA enters the body, it likely only reaches local arm muscle cells before the body breaks it down. This means it is unlikely to enter the bloodstream, and even less likely to make it as far as the placenta. Even if it does get that far, “one of the placenta’s main functions is to be an immune barrier to the fetus,” which adds another layer of protection, says Gaw. And although it contains genetic material, it doesn’t enter our cells’ nuclei, meaning that it can’t cause any mutations to our cells — or those of a developing fetus. This mRNA is so fragile, vaccine developers had to wrap it in nanolipids (which are also presumed to be safe for pregnancy) just to keep it intact long enough to reach muscle cells in the arm.

Experts also expect it is unlikely for the mRNA to make its way intact into breast milk. Preliminary research from Gaw and her team, which is in the process of being peer-reviewed, found no trace of the vaccine itself in breast milk samples from hours and days post-vaccination. And even if a small amount of it were to be transferred to a feeding baby, researchers say it (and any lipid nanoparticles) would get broken down by the baby’s stomach acids.

3) Animal studies look promising. Before any shots were given to pregnant humans, vaccine companies gathered safety data in other pregnant mammals. None of these developmental and reproductive toxicity (DART) studies from Pfizer/BioNTech, Moderna, or Johnson & Johnson suggest any safety concerns for use during pregnancy.

Rats, of course, are not humans, and DART study results do not always translate identically into humans. “Some results are similar to humans, and some are very different,“ Gaw says. Nevertheless, they are a good starting point — when combined with strong safety data in the clinical trials and public vaccinations so far.

4) We haven’t seen adverse events in pregnant people who have gotten it so far. For the Covid-19 vaccine trials, those of “childbearing potential” were screened for pregnancy before each shot, and those with positive tests were removed from the studies. However, a handful of people (12 who got the vaccine in Pfizer/BioNTech’s study and six who got the vaccine in Moderna’s study) ended up having been pregnant at the time of vaccination — and companies haven’t reported any negative outcomes from these individuals.

A newer and much larger data set is emerging from the Centers for Disease Control and Prevention, which is following pregnant people who sign up for its tracking platform V-safe after being vaccinated — and allowing them to sign up for a more targeted pregnancy-specific vaccine registry.

At the beginning of March, the CDC reported data from more than 1,800 pregnant people in the registry who had received Covid-19 vaccines. Among these individuals, there was not a statistically significant increase in adverse pregnancy or birth outcomes. Nor have they found any significant differences in side effects from the vaccine (such as fatigue or fever).

“From a scientific perspective, there’s no specific reason to think that pregnant individuals would have more adverse reactions to the vaccine or that there would be a risk to the fetus with the vaccine, while we know that there is risk with the Covid infection,” says Alisa Kachikis, an assistant professor of obstetrics and gynecology at the University of Washington.

A January study published in JAMA Internal Medicine, for example, analyzed the outcomes of more than 406,000 people who gave birth in hospitals between April and November 2020 and found that a significantly higher rate of those with Covid-19 had major complications. “The higher rates of preterm birth, preeclampsia, thrombotic [blood clotting] events, and death in women giving birth with Covid-19 highlight the need for strategies to minimize risk,” noted the authors.

So why are some, such as the WHO and the UK, still saying most pregnant people should not get the coronavirus vaccine yet? They are waiting for more data.

There are also, of course, other types of coronavirus vaccines in the works, such as protein-based vaccines (which is the basis for Novavax’s shots). This model of shot has been used for years — including for pertussis and hepatitis B — “and we are very comfortable with [their] safety profile,” Gaw says. Viral vector vaccines (which is how the Johnson & Johnson and AstraZeneca/Oxford shots work) have also been used safely in pregnancy, such as for the Ebola and Zika vaccines, although there is less historical data on these.

So, says Kachikis, if what’s hanging people up about getting a Covid-19 vaccine in pregnancy is mostly the novelty of the mRNA vaccines, having other types to choose from — as long as they’re just as effective — could be a good option.

What studies are happening, and what will they help us learn about the Covid-19 vaccine in pregnancy?

The CDC continues to monitor for any adverse outcomes and side effects through its V-safe program — and related pregnancy registry (which will check in with participants in each trimester, after delivery, and when the baby is 3 months old).

Pfizer/BioNTech started giving vaccine doses in their pregnancy-focused, placebo-controlled clinical trial this February. They are first running a smaller safety study of just 350 healthy pregnant participants before scaling up to give the vaccine to a total of about 4,000 people who are at between 24 and 34 weeks gestation. (This study design, however, will still leave some questions about the safety and efficacy of the vaccine, especially earlier in pregnancy.)

Moderna has created a registry that people can sign up for after receiving their vaccine while pregnant. For its part, Johnson & Johnson plans to conduct trials of its vaccine in pregnant participants later (likely after it studies the vaccine in children).

In the meantime, other researchers are racing to collect and study data from the natural experiment that started in December, when many pregnant people began electing to get vaccines as they became eligible because of their high-risk work in hospitals or long-term care centers.

At the University of Washington, Kachikis is leading a study to also follow vaccination in people who are pregnant. Thousands of people from around the US and the world who have received the vaccine while pregnant have already signed up for the registry, she says. (People who are pregnant or lactating but have not yet gotten vaccinated can also sign up, as can people who are considering becoming pregnant within the next two years.) This research will help them track any adverse outcomes, as well as gather additional data, such as whether any vaccinated individuals (or their newborns) later get Covid-19.

An additional large-scale clinical trial, which has not started enrolling participants, aims to track 5,000 women and their offspring over the course of 21 months. Other smaller studies are in the works as well, such as one at Duke University.

At UCSF, Gaw and her team are in the midst of separate observational studies. They will more closely follow a smaller group of participants — 100 or so of whom are pregnant and roughly 50 of whom are lactating — “to determine whether the Covid vaccines are equally effective in pregnant and lactating women, how long antibody responses last, and whether immunity is transferred to the baby,” Gaw explains.

Other vaccines are routinely given in pregnancy, such as pertussis, in large part to provide protective antibodies to the fetus and protect the newborn until they are old enough to get the vaccine themselves.

Covid-19 antibodies have been shown to transfer across the placenta in women who were positive for the virus at delivery. The new AJOG study found that even higher levels of antibodies were present in the umbilical cord after Covid-19 vaccination than after natural infection. “The research shows really promising results,” Kachikis says.

If these antibodies prove to be protective, it could be especially helpful, as newborns and infants will likely be among the last to have an authorized vaccine — and have the highest rates for complications and death from the virus among children. “There is still a lot of data that needs to be assessed, but for individuals who are thinking of ways that the vaccine may benefit their newborn, this is really encouraging,” Kachikis says.

More nuanced research might also eventually help advise on optimal timing for the Covid-19 vaccine during pregnancy. For example, Gaw notes, “there needs to be sufficient time for the mom to develop a robust antibody response, and then pass [this] to the baby.” After extensive research, the Tdap vaccine is recommended around 27 weeks of gestation so as to provide the best protection for the infant after birth. Without such information for the Covid-19 vaccine, many experts are recommending that those who decide to get the shot treat it like the flu shot — getting it as soon as it’s available to them, regardless of where they are in their pregnancy.

People who are lactating were also excluded from the vaccine trials. So researchers at a number of institutions are now working to study how the vaccine might impact breast milk contents and a nursing child. A study from October 2020 showed that most people who had recovered from Covid-19, as well as those suspected of being infected, passed on antibodies to the virus in their breast milk.

The recently released AJOG paper found a high level of antibodies in breast milk from women who had received the Covid-19 vaccine. Gaw’s team also has new findings, which are currently in peer review, that show a solid dose of Covid-19 antibodies in breast milk samples after vaccination. This, they hope, will provide some protection from the virus for babies.

“It’s all reassuring,” Gaw says. But “all the studies have been small…[so] we can’t 100 percent determine safety until a lot more people have been vaccinated and it’s been reported on.”

Wait, why weren’t pregnant people included in the early research to begin with?

Pregnancy has, for decades, been considered a “vulnerable” condition when it comes to researching new medical treatments and preventions, meaning people who are pregnant have been excluded from general trials in much the same way as have those who are unable to give informed consent, like children and those with severe mental disabilities.

Part of the reason for this might be due to the damaging legacy of thalidomide. This drug was given to pregnant women around the world starting in the 1950s as a way to ease nausea (although it was never approved specifically for use in pregnancy in the US). Soon, thousands of these babies were being born with devastating birth defects. This hammered home for scientists and the public that, when it comes to pregnant women and their fetuses, much more care ought to be taken in giving medications or vaccines.

But this conclusion, many are now saying, has it backward, as the oft-repeated phrase indicates: Protect pregnant people “through research, not from research.” If thalidomide had been carefully and systematically studied for pregnancy, it likely never would have been approved for use (or used unofficially) in this population, preventing the majority of these tragic outcomes.

“It can’t be emphasized enough that pregnant women should be included in vaccine trials from the get-go,” Kachikis says.

Gaw agrees: “We actually cause harm by not including [pregnant people] in early research, as they have to wait longer for good data to be published.”

So when will we have more data about the coronavirus vaccine in pregnancy and lactation?

One big challenge with researching anything to do with pregnancy is that it takes a long time: nine months, plus follow-up time to monitor infant outcomes. And subsequent study during lactation while you’re at it, and maybe preconception research, too.

Consider that it took vaccine makers just 10 months to develop the Covid-19 vaccines and ensure they were safe and effective in adults. But with formal studies in pregnant people just getting underway (and with many having not yet started, and others, like Pfizer’s, currently limited to late pregnancy), it could be late 2021 or beyond until we have comprehensive, robust safety data for all stages of pregnancy. And even later to assess long-term outcomes for babies.

Follow-up to the early work Gaw and colleagues are doing at UCSF will take “at least six to nine months, as we have to wait for a sufficient number of babies to deliver,” Gaw says.

Kachikis and her team at the University of Washington plan to follow the outcomes of people who sign up for their list for about a year, with hopes to continue more long-term follow-up. For example, they plan to test babies months after birth to see how long antibodies from vaccines given during gestation persist — and if these antibodies are equally as effective at fighting off the coronavirus as those found in the vaccinated adults.

But they aren’t waiting that long to start sharing what they learn. “The focus is on getting any data out,” Kachikis says. And “if multiple groups can get some data out, that will be better than having absolutely nothing,” which has been the situation, she notes.

For now, much of the official guidance in the US stresses the need for people to conduct their own analysis of the known increased risks of Covid-19 in pregnancy with the remaining unknowns of the vaccine. And this calculus is not the same for everyone.

“As more evidence is coming out, it’s tilting to more benefit of getting the vaccine,” Gaw says. “But every individual has a different level of risk they’re willing to take” — as well as the amount of risk they might have of contracting the virus or getting extremely sick from it. The bottom line, based on the latest Covid-19 vaccine research in pregnancy, she says, is that “it’s looking more and more like it does work, it does pass antibodies to the baby (although we don’t know yet how protective they are), and there doesn’t look like there’s any harm at this moment.”

Additionally, even those who are reluctant to advocate the vaccine for all pregnant people just yet, such as the WHO, do suggest it should be available to those at high risk of exposure to the virus or underlying health conditions that increase their risk of severe Covid-19.

And some might elect to wait until there is more solid data. So to help move along the plodding process, people who are pregnant and have gotten the vaccine — or are considering it — can contribute to getting more and better guidance sooner by opting in to registries and studies.

Katherine Harmon Courage is a freelance science journalist and author of Cultured and and Octopus! Find her on Twitter at @KHCourage.

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Biden now promises 200 million vaccine shots in 100 days. The US is already on track for that.

President Joe Biden on Thursday set a new goal for Covid-19 vaccines in the US: 200 million shots in his first 100 days in office. That’s up from Biden’s original goal of 100 million in 100 days. “I know it is ambitious — twice our original goal,” Biden said.

But the goal of 200 million shots in 100 days is really not that ambitious; it’s achievable if absolutely nothing changes with America’s current vaccine rollout.

That’s a testament to how much America’s vaccine campaign has improved since Biden took office. Before Inauguration Day, the country administered less than 1 million shots a day. Today, the US is at 2.5 million shots a day, on average.

At the current rate, the country could hit Biden’s goal of 200 million shots in 100 days — hitting the goal as soon as April 28, a couple days before Biden’s 100th day in office.

Things stand to improve beyond the current rate. As vaccine manufacturers ramp up production, they’ve already made deals with the federal government to deliver enough vaccines for every adult in the summer. At the very least, that should address questions about the supply of vaccines, though not about distribution or willingness to take them.

Biden previously pledged that the US will have enough vaccines for every adult in the US by the end of May. Getting all of those vaccines into arms will require a distribution boost: At the current rate of 2.5 million shots a day, only about 180 million adults, of roughly 255 million, will be fully vaccinated by the end of May. The US has to do more than 4 million shots a day, on average, by then to fully vaccinate every adult in the US before June.

That will be a challenge, with lots of potential factors involved: whether drug companies can ramping up manufacturing, whether the federal government can ship those vaccines out, whether local and state governments can turn those doses into shots in arms, and whether vaccine hesitancy is sufficiently addressed to get all adults to want the vaccine.

That’s a lot that could go wrong. Biden, for his part, has vowed to get ahead of these issues, dedicating more money to vaccine distribution and public education and awareness efforts, funded in part by the recently enacted Covid-19 relief package.

Now Americans waiting for a shot will have to wait and see if Biden can turn those promises into reality.

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Prisons have already failed to contain Covid-19. What happens when the new variants arrive?

The rapid spread of new variants of the coronavirus, some of which seem to be more contagious than older versions, has experts in the US calling for stricter social distancing and better masking to avoid yet another big surge of new Covid-19 cases and deaths.

Health advocates and epidemiologists are particularly concerned about what will happen once the new variants find their way into prisons, jails, and immigration detention facilities.

Across the US, at least one in five incarcerated individuals has already been infected with Covid-19, and a disproportionate number of them have died. One study found that the 2.3 million Americans living behind bars have twice the risk of dying from Covid-19 as a similar person who is not.

Jaimie Meyer is an associate professor at Yale School of Medicine and a researcher and clinician who specializes in the spread of infectious diseases behind bars. The pandemic “has laid bare [and] exposed the issues around conditions in confinement,” she told Vox, including how difficult or impossible it is to truly safeguard those held behind bars. In its quest to survive, Covid-19 will find “all of the holes [in our public health strategy] … all of the weaknesses, and pressure test them” she added. “If facilities have not done something to keep people safe, a more highly transmissible strain will spread like wildfire.”

An epidemiological nightmare

Prisoners are at an increased risk of Covid-19 for a simple reason: how the virus spreads. Scientists now know that the illness is mostly passed from person to person through respiratory droplets and sometimes through the air, which is why being in sustained, close proximity to others is so risky — and why crowded prisons and jails are especially dangerous. Contagion also frequently happens even before someone has symptoms, making it impossible to know who to isolate without frequent, rapid, near-universal testing.

“Congregate settings in general, and prisons in particular, are places where physical distancing is impossible,” said Meyer. Moreover, she added, people in prisons are more likely to have certain medical conditions, including obesity and diabetes, that put them at greater risk of infectious diseases.

The epidemiological realities of Covid-19 have been exacerbated by the failures of elected officials and institutions whose job it is to protect those who are incarcerated. Chris Beyrer, a professor of public health and human rights at Johns Hopkins, has been a vocal critic of Maryland’s approach to managing the crisis. In December, cases of the virus in the state’s prisons more than doubled.

“The single most important thing you have to do to deal with Covid in prison is to [reduce] overcrowding,” he told Vox. “We failed at that.” Although prison and jail populations dropped at the outset of the pandemic — mostly because fewer people entered the system due to virus concerns, rather than early release pushes — these populations are now on the rise again.

The second most important thing is to implement policies that can stem the spread of the disease, including social distancing and giving prisoners and staff masks and other essential supplies. “That, too, has been slow, inadequate, and insufficient,” Beyrer said. The Maryland Department of Corrections, he told Vox, isn’t providing free, unlimited bars of soap to people locked up in the state, leaving prisoners unable to do something as fundamental as wash their hands.

And the concerns don’t stop there. In facilities across the country, incarcerated people have reported a range of serious safety issues during the pandemic: correctional officers who refuse, or are not required, to wear masks; insufficient or failed efforts to test staff and incarcerated people; and the creation of new outbreaks by transferring Covid-positive prisoners to new facilities.

Meanwhile, vaccination has not even begun in most of the country’s prisons and jails, while those in other congregate settings — including nursing homes and homeless shelters — have been among the first in line to receive the shot.

“We are living through the failure of the basics of Covid prevention,” said Beyrer.

With all of these systemic shortcomings, many are extremely worried prisons and jails will be even harder hit when more contagious strains breach their walls. Early research has indicated that people infected with the new strain may carry higher viral loads, meaning that engaging in the same conduct — spending extended periods of time indoors without distancing — poses an even greater risk of spreading the virus than it did previously. For prisoners, that means that the worst outbreaks may be yet to come.

“A more infectious virus is only going to infect more people,” Beyrer said. “If more people are going to get infected, more people are going to die.”

“Scared as hell”

With so few resources to protect themselves and, in most places, no vaccine in sight, many prisoners are worried about the future. Jabriel Lewis is incarcerated at Allenwood federal prison in Pennsylvania. “That new strain got everybody in here scared as hell,” he said. “[I]f it gets into the federal institutions it could possibly mean a death sentence.”

For Michelle Angelina, a woman locked up in New Jersey’s Edna Mann facility, the threat posed by the new variants isn’t limited to the virus. The steps the prison system has taken to protect prisoners — shutting down all visitation, ending academic and substance abuse programming, and canceling religious services — will only be extended even further. “It’s putting an immense strain on all of us.”

Her concerns were echoed by Shebri Dillon, a woman incarcerated at Fluvanna Correctional Center at Virginia, who described the difficulty of spending “hours upon hours in a concrete cage, without seeing or hugging our children and family.”

“This new variant means an extension of all that pains us,” Dillon told Vox. “It is not a matter of if it will get in, but when.”

A matter of equity and public health

There are basic ways, however, to protect this large, vulnerable segment of the population — and the rest of the public at the same time.

For epidemiologists, advocates, and incarcerated people, the answer is to implement the policies they’ve recommended all along. “The implications of a more rapidly spreading Covid-19 variant in jails are clear,” said Robert Cohen, a physician who previously worked on Rikers Island and now serves on the Board of Corrections that oversees New York City’s jails. In addition to providing better access to basic PPE, sanitizing supplies, and testing, as many people as possible need to be released from prisons, jails, and other detention facilities, stressed Cohen, and all remaining incarcerated people and staff must be inoculated against the virus sooner rather than later.

In a handful of states, including Massachusetts and California, the vaccinations of prisoners have already begun — but in many places, including New York, they aren’t being prioritized for the vaccine.

Advocates say this reality is just another example of the inequitable impact of the virus on poor people and people of color, given that Black and Latinx individuals are locked up at many times the rate of their white peers. “Despite calling for equity in vaccine distribution, [New York’s] Gov. Cuomo has neglected incarcerated people even while rolling out vaccines to other congregate settings,” including homeless shelters, said Katie Schaffer, director of advocacy and organizing at Center for Community Alternatives, which provides programming and policy work to reduce incarceration across New York state.

While many incarcerated individuals are eager to be inoculated, vaccine hesitancy does exist inside prisons and jails, in no small part due to the long history of medical experimentation inside these facilities. Some agencies are providing incentives to encourage prisoners to participate, including video visits with family members and slightly shortened sentences, while outside initiatives have sought to educate prisoners about the vaccine and its safety. Since the two coronavirus vaccines in the US currently only have emergency approval from the FDA, it’s likely unlawful for correctional authorities to mandate that prisoners or staff receive the shot.

Releasing more prisoners and accelerating the vaccination of those left inside is not only a matter of human rights, say public health officials — it’s also a necessary step to protect the public at large.

There are indications that widespread infection inside these sorts of facilities easily spreads to the community and beyond. One study found that the March outbreak in Chicago’s Cook County jail contributed to about one in seven of the state’s total cases in the following month. Prisons have also incubated especially deadly variants of other illnesses, including strains of multi-drug-resistant tuberculosis.

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“This is part of our public health,” said Meyer. “We should all want people who are in any congregate setting to have the best chance of preventing exposure and infection” — for their own health and safety as well as that of everyone else in the country.

Aviva Stahl is an award-winning investigative reporter who writes about how health care policy and scientific debates play out in the prison context. She’s written for a variety of outlets including Vox, the Guardian, and the New York Times, and can be followed at @stahlidarity.