Category: Covid-19 Vaccine

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COVID-19 vaccine appointments canceled due to severe weather, Austin health officials say – Austin American-Statesman

February 16, 2021

Heather Osbourne|Austin American-Statesman

Editor's note:This story about winter weather is free for everyone to view as a public service. If you already subscribe, thank you. If not, please do so today using the blue "Subscribe" button in the top right corner of this page.

Austin Public Health officials on Monday canceled all coronavirus vaccine and testing appointments scheduled for Tuesday because of thesevere winter weather affectingmost of Texas.

Austin-area residents on Monday were urged to stay indoors and avoid driving in dangerous road conditions, which ultimately led Austin Public Health to cancel vaccination appointments for the fourth day in a row.

Austin Public Health had canceled all vaccination appointments Saturday when roads began to ice over, leading to multiple vehicle crashes across Central Texas. ByMonday, Travis County's icy roads were covered in powdery snow as temperatures dipped into the single digits.

More: Take a drone tour over Austin after snowfall amid freezing temperatures

Dr. Mark Escott, interim Austin-Travis County health authority, and Austin Public Health Director Stephanie Hayden-Howard on Fridaysaid their staffs would work with individuals to reschedulevaccination appointments onceweather conditions improved.

Austin Public Health officials again on Monday afternoon said the power outages did not affect the vaccine doses and that they will not expire beforelater this week when appointments are rescheduled.

Before Saturday, Austin Public Health was working to administer 12,000 first doses and 12,000 second doses it received from the state last week. It's unclear when the Texas Department of State Health Services willdeliver more doses to Central Texas because of the road conditions.

Austin-Travis County residentssuch as 77-year-old Jerry Griffin on Monday said they werealready struggling to sign up for a first doseof the coronavirus vaccine even before the winter stormrolled into Austin.

More: Who is next for COVID vaccine in Texas? Abbott advisor says maybe middle-aged people

Those who currently qualify for a coronavirus vaccine, many of whom are 65 and older, have remained frustrated and confusedabout Austin Public Health's distribution efforts, including problems with its registration website. SinceAustin Public Health receives only about 12,000 first doses everyMonday, vaccineappointments bookquickly.

Griffin said he wasn't surprised that Austin Public Health pushed back appointments because of the snowstorm, but he just hoped it wouldn't delay doses for him and his wifetoo long.

"My wife and I are both still struggling," Griffin said. "We are registered at a couple of places. I really want to receive a vaccine, but every time someone gets a shot it helps.

"We tend to shut down pretty quickly around here when we have weather conditions like this. We'll just hangin there, keeping our fingers crossed and hoping for the best."

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COVID-19 vaccine appointments canceled due to severe weather, Austin health officials say - Austin American-Statesman

Japan formally approves its first COVID-19 vaccine – The Associated Press

February 16, 2021

TOKYO (AP) Japan on Sunday formally approved its first COVID-19 vaccine and said it would start nationwide inoculations within days, but months behind the U.S. and many other countries.

Japans health ministry said it had approved the vaccine co-developed and supplied by Pfizer Inc.

The announcement comes after a government panel on Friday confirmed that final results of clinical testing done in Japan showed that the vaccine had an efficacy similar to what overseas tests showed.

Many countries began vaccinating their citizens late last year, and Pfizers vaccine has been used elsewhere since December.

Under the current plan, about 20,000 front-line medical workers at hospitals in Japan will get their first shots beginning around Wednesday. About 3.7 million other medical workers will be next, followed by elderly people, who are expected to get their shots in April. By June, its expected that all others will be eligible.

Health ministry official Yuta Yamashita said inoculations can start as soon as a ministry panel on vaccination logistics gives the go-ahead.

The approval was granted in a special fast-track process for emergency use. It took two months compared to the usual one year in a country known for cautious and slow-moving approval processes.

Still, the rollout in Japan is months behind many other countries because the government had asked for clinical testing at home in addition to the multinational tests Pfizer conducted on more than 40,000 people from July to November. Many countries accepted Pfizers results and moved ahead.

In a country where many people are skeptical about vaccines, Japan sought additional tests to address safety concerns. But the tests were conducted on only 160 people, and some question whether it was worth it to delay the rollout.

Vaccines are considered key to holding the delayed Tokyo Olympics this summer. Japan is expected to receive 144 million doses from Pfizer, 120 million from AstraZeneca and about 50 million from Moderna before the end of this year, enough to cover its population.

Vaccines being developed by Japan are still in the early stages, so the country must rely on imports. AstraZeneca applied for approval in Japan only recently, while Moderna hasnt applied yet. Japans reliance on the imports, many of them subject to EU export controls, is also causing concerns about supplies.

Shigeru Omi, the head of the government coronavirus task force, earlier this month cited a lack of global competitiveness of Japanese pharmaceuticals as a reason for the delayed rollout.

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Follow Mari Yamaguchi on Twitter at https://www.twitrer.com/mariyamaguchi

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Japan formally approves its first COVID-19 vaccine - The Associated Press

DHEC sends letter to Horry County over reports of COVID-19 vaccines given to ineligible individuals – WBTW

February 16, 2021

HORRY COUNTY, S.C. (WBTW) The South Carolina Department of Health and Environmental Control (DHEC) sent a letter to Horry County over reports of ineligible people receiving COVID-19 vaccines.

The letter was sent Sunday after DHEC said it received reports of people outside of the Phase 1a group receiving vaccines from Horry County Fire Rescue. The letter asks for a record of who has been vaccinated by the program in Horry County as well as how the distribution was planned.

DHEC is asking whether or not Horry County Fire Rescue vaccinated county employees not part of the 1a group.

DHEC said 1,818 first doses and 123 second doses have been administered by Horry County Fire Rescue as of Sunday.

A county government can register its EMS to be a vaccine provider. Horry County Fire Rescue is one of three EMS groups in the state approved to administer vaccines. The other two are Clarendon County Fire and Rescue and Cherokee County Fire and Rescue, according to DHEC.

DHEC said it continues to monitor reports of providers vaccinating people outside of the 1a group.

News13 obtained the letter Horry County Fire Rescue sent to DHEC in response. In the letter, Horry County Fire Rescue said it spoke with Alexandra Hayes and Donna McNeil of DHEC before any vaccines were administered and were told to vaccinate people as quickly as possible and with as little waste as possible.

In consideration with that guidance, employees who opted to receive the vaccine were granted a designee to also receive a vaccine with an emphasis on those who met Phase 1a criteria, the letter says. We recognize and appreciate the criteria system and will continue to assist the state in this critical mission.

Horry County Fire Rescue said it is committed to working with DHEC and partner agencies in the vaccination rollout and said it is willing to discuss the matter further with DHEC.

Read the full letter below:

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DHEC sends letter to Horry County over reports of COVID-19 vaccines given to ineligible individuals - WBTW

Winter weather cancels drive-thru COVID-19 vaccine clinic in Mount Vernon – knoxpages.com

February 16, 2021

MOUNT VERNON Winter weather has once again forced local public health officials in Knox County to change the date for a COVID-19 vaccination clinic for more than 700 people.

Tuesday's drive-thru clinic at Cooper Progress Park (the former Siemens Energy campus), sponsored by Knox Public Health, has been canceled due to the impending winter storm expected in central Ohio.

The second-dose clinic has been rescheduled as a walk-in clinic on Sunday, Feb. 21 from 10 a.m. to 4 p.m. at the Mount Vernon High School Energy Fieldhouse (101 Yellow Jacket Dr.). This is the same site as the first-dose clinic. There are no appointments, and attendees can come anytime from 10 a.m. to 4 p.m.

Clinic participants are being notified by phone with a pre-recorded message from the Knox County alert system. Clinic details are also posted on the Knox Public Health website, knoxhealth.com, and social media.

Originally scheduled for Feb. 13, the new date for the second-dose clinic extends the normal 21-day period between the first and second doses for the Pfizer-BioNTech COVID-19 vaccine. However, public health officials indicate this will not affect the window of opportunity for the vaccine to be fully effective.

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Winter weather cancels drive-thru COVID-19 vaccine clinic in Mount Vernon - knoxpages.com

Chinas Covid-19 Vaccine Diplomacy Boosts Its Influence in Europe – The Wall Street Journal

February 14, 2021

Some small European governments are turning to China for Covid-19 vaccines as European Union procurement stumbles and Western vaccine makers production hiccups hamper the continents fight against the pandemic.

The trend could increase Chinas influence in the region as it campaigns to present itself as a reliable ally in fighting the coronavirus that was first detected on its soil.

The European Union, which buys vaccines on behalf of its 27 member states, has authorized three shots developed in Germany, the U.S. and the U.K. But the bloc was slow to sign contracts and authorize the shots, while manufacturers have struggled to deliver the doses promised. Shortages have been even worse in non-EU countries in Europe.

So far, it is mainly small nations on the blocs margins that have turned to Beijing for help. Yet as voters frustrations mount, larger members are now considering Chinas two vaccines and another developed in Russia.

On Jan. 31, German Health Minister Jens Spahn called on the EU to approve the shot made by Chinas Sinopharm Group if it were found to be safe and effective. Then, Austrian Chancellor Sebastian Kurz said the company should manufacture its shots in his country.

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Chinas Covid-19 Vaccine Diplomacy Boosts Its Influence in Europe - The Wall Street Journal

Bill Gates’ daughter jokes on social media about getting COVID-19 vaccine – Fox Business

February 14, 2021

Microsoft co-founder Bill Gates, chair and the Bill & Melinda Gates Foundation, joins Chris Wallace on 'Fox News Sunday.'

Bill Gates daughter told her social media followers that the first dose of the COVID-19 did NOT implant my genius father into my brain.

BILLIONAIRE BILL GATES SAYS LOCKDOWNS OF BARS, RESTAURANTS ARE 'APPROPRIATE' AS COVID-19 CASES SURGE

Jennifer Gates, 24, made the joke to dispel wild conspiracy theories that the billionaire Microsoft founder was somehow using the vaccine to get inside peoples minds and track their movements, according to a report.

Jennifer Gates is a second-year medical student at New Yorks Icahn School of Medicine at Mount Sinai.

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I am beyond privileged to receive my first dose of mRNA to teach my cells to mount a protective immune response to this virus. As a medical student and aspiring physician, I am grateful it will give me protection and safety for my future practice, she told her more than 357,000 Instagram followers Friday.

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Bill Gates' daughter jokes on social media about getting COVID-19 vaccine - Fox Business

COVID-19 vaccines can adapt to new variants. Heres what it will take – PBS NewsHour

February 14, 2021

Researchers have unlocked vaccines for coronavirus at an unprecedented pace, but COVID-19 has managed to stay a step ahead.

On Jan. 29, pharmaceutical giant Johnson & Johnson unveiled a vaccine that is less difficult to distribute than others. It is a single shot that only needs a normal refrigerator practically roughing it compared to the elaborate cold-chain technology that Pfizers two-dose vaccine demanded a month earlier.

This latest vaccine underwent trials with nearly 44,000 people in the United States, Latin America and South Africa, all places where the virus had run wild for months and easily transmissible variants had been detected. In the U.S., the new vaccine was 72 percent effective, but in South Africa, where a more potent variant had taken shape, researchers found the same vaccine prevented infections in a smaller percentage of volunteers 57.6 percent during clinical trials. The data raised alarm bells about how much protection these new vaccines might afford and what else might need to be done.

Drugmakers are exploring how to tailor vaccines more narrowly to these mutants, but modifying existing vaccines is not as easy as flipping a switch. The decision sets into motion questions and concerns about manufacturing logistics, regulatory hurdles and distribution bottlenecks that have stymied the United States response throughout the COVID-19 pandemic.

Viruses mutate to stay alive. The more times a virus spreads or replicates the more opportunities there are for random evolutionary accidents in its genome. Any change could either doom the virus or play to its advantage, said Dr. Angela Rasmussen, a virologist at the Georgetown University Center for Global Health and Security.

READ MORE: Why new coronavirus variants emerge, and what that means for you

Right now, three notable COVID-19 variants appear to be transmitted more easily than other strains of virus, and threaten to frustrate efforts to contain the pandemic and get life back to normal. The Centers for Disease Control and Prevention has confirmed that cases of B.1.1.7 from the United Kingdom, B.1.351 from South Africa and P.1 from Brazil have have all been found in the U.S., and it is likely that more variants exist but havent been detected yet, CDC Director Rochelle Walensky said during a recent White House COVID-19 briefing.

Scientists say its far better to be vaccinated and have evidence-based protection against the virus than to skip your turn and gamble with your health. But so far, the nations efforts to monitor the virus remain woefully inadequate when it comes to capturing the true volume of new infections and tracing exactly how the new variants are moving within the population lingering consequences from the Trump administrations disorganized response to the pandemic. Vaccine distribution has also lagged, though it is picking up pace, according to Tim Manning, the national supply chain coordinator for the White House COVID-19 Response Team. But while experts figure out how to catch up to the virus and the country waits, there are already steps being taken right now to buy more time.

Public service workers help people to check in at a drive-through COVID-19 vaccination site in Robstown, Texas, U.S. February 9, 2021. REUTERS/Go Nakamura

According to the CDC, more than 59 million doses of the approved vaccines have been distributed, and roughly 42 million doses have been administered almost 13 percent of the U.S. population, without taking into account that no vaccine yet has been approved for pediatric use. Experts estimated that if about 70 percent of the country gets vaccinated or immunized against the virus, then it may be possible to slow or stop its spread

The vaccines from Pfizer and Moderna that are currently being used around the country were shown in clinical trials to be more than 90-percent effective in preventing infection, according to data the companies submitted. Those trials wrapped up before the most recent variants revealed how much of a threat they could become, so theres not enough data (yet) to determine the vaccines effectiveness against these variants.

READ MORE: Trust in COVID-19 vaccines is vital to control the pandemic. Why are some hesitant?

These vaccines can be quickly tweaked, said Dr. Drew Weissman, a physician and infectious disease expert at the University of Pennsylvania. The genome for SARS-COV-2 maps out the sequence of proteins that form the virus. The mRNA vaccines are short segments of the viral genome, so if the virus changes at all, researchers can swap out proteins to mimic those evolutionary adaptations. For 15 years, Weissman worked with biochemist Katalin Kariko to develop the research and technology for the mRNA vaccines, which have been vital in fighting the virus.

It would take six weeks for researchers to go from plugging new variants into the vaccine to make a new vaccine ready to go into people, he said, but that does not account for the time it would take to have a drug approved. Weissman compared the process to the way the vaccines for the seasonal influenza are modified each time it circumnavigates the globe.

But while that analogy might work in terms of the science, the regulatory process is not likely to be the same. Flu vaccines have been used for more than four decades on hundreds of millions of people and they dont require full-scale clinical trials to earn FDA approval each year. We dont have that kind of history with coronavirus vaccines yet, said Dr. Jesse Goodman, former chief scientist at the FDA and professor of medicine and infectious disease at Georgetown University.

But Goodman said he thinks the FDA can find a pathway. The way he sees it, there are at least three options:

The two vaccines that already received FDA authorization have already undergone pretty rigorous trials, Goodman said. In the months since they were permitted for emergency use, both of those vaccines have been tracked closely and regulators appear to be increasingly comfortable with what they have seen so far, he said. He said that one approach could include designing a vaccine that targets a particular variant and gathering data on its effect on several hundreds of people in a study that is comparable to the phase 1 or phase 2 clinical trials. If granted an EUA, Goodman said, You could envision them being rolled out, and perhaps more data being collected.

You want to make sure that if you do give it to people, its going to be protective, he said.

Based on how the mRNA vaccines are designed, the process of changing them is much more straightforward than using a weakened version of a virus to trigger and train up the bodys immune response, as is the case with vaccines for measles and chickenpox, said Dr. James Hildreth, president of Meharry Medical College, who sits on the FDAs committee that has reviewed data on COVID-19 vaccine safety, effectiveness and appropriate use. But the bigger question is whether or not the FDA will require new rounds of clinical trials after these changes are made to authorize updated vaccines for public use.

Theres no reason to expect that the safety profiles would be different for the two (EUA vaccines) if the modifications are minor, if there are one or two changes in the sequence, Hildreth said.

But he said the sequence would still be a new one, and without data documenting its safety and efficacy, he said it would be hard to be definitive in knowing how the human body might respond once injected with any modified vaccines. Data from earlier trials might be helpful in figuring out how to safely tweak already approved vaccinations to better combat variants, Hildreth said.

AstraZenecas two-dose vaccine does not use mRNA, and it has not yet been approved for use in the U.S. On Sunday, South Africa paused its plan to begin vaccinations because the AstraZeneca vaccine was not found to offer minimal protection against mild and moderate cases of the virus, BBC reported, which added that the new variant accounts for almost all new COVID-19 infections in the country. The pharmaceutical company has said it will develop a modified version, but that wont be ready until autumn, according to company officials.

Dr. Tom Frieden, former CDC director, said that new regulatory pathways outside of an EUA must be considered and must be thought through openly to avoid fracturing public trust about the process. Especially in communities of color, a history of systemic racism and abuse in health care have fueled distrust of the medical community. Public health needs to lean on trusted messengers to promote the continued need for vaccination, Hildreth said.

As more people get the vaccine, some of those who are hesitant are realizing its OK, he said.

Considering how vaccines may need to adapt to COVID-19, Weissman urged the public and researchers to take a long-term perspective and strategy. Over the past two decades, he said the world has hosted three (far smaller) coronavirus epidemics.

You have to assume theres going to be more, he said. Once were done with COVID-19, theres going to be some other coronavirus epidemic at some point in time.

Rather than let the globe be caught off guard all over again, Weissman said researchers should explore more comprehensive strategies to beat back runaway viruses. He said he is working with a team of researchers to develop a pan-coronavirus vaccine. If that can be created and ready the next time a viral outbreak is detected, Weissman said, We can stop the pandemic before it starts.

At a Boys and Girls Club in Reading, Pennsylvania, students to come and do their remote learning with desks setup and spaced apart in the clubs gym. Photo by Ben Hasty/MediaNews Group/Reading Eagle via Getty Images

To Rasmussen, this moment serves as a warning about letting COVID-19 spread out of control and a reminder to approach the pandemic more aggressively.

It doesnt mean vaccines are hopeless, and were doomed to an eternal pandemic, she said. Its even more important to vaccinate as many people as quickly as possible.

But Vaccination alone is not going to get us out of this, Frieden said.

Months before any vaccines were available to the public, New Zealand squashed the coronavirus by supporting scientists to guide the nations response, entering lockdown for several weeks. and using contact tracing as cases shrank.

Even with the emergence of variants, that success is still possible in the U.S., Rasmussen said. While more transmissible, the variants rely on the same methods to infect new hosts. That means we already have the tools we need to stop them, she said, like masks, avoiding crowded spaces and getting tested and isolating if you feel sick.

This is the home stretch, she said. If people can just grit their teeth and get through this, the sooner more people do that, the sooner were going to be able to relax and cross the finish line.

This is going to take months to turn around, not days.

During his first days in office, President Joe Biden signed several executive orders to strengthen the nations collective response to the virus, giving state and local health departments more support to fight the pandemic and offering more public transparency through regular press briefings. On Tuesday, Andy Slavitt, the White Houses senior adviser to the COVID-19 response team, tweeted that the Biden administration increased vaccine shipments to states by 28 percent after three weeks in office.

Another option is for the Biden administration to more fully deploy the Defense Production Act, a way to prioritize supplies and resources needed to ramp up enough testing materials, personal protective equipment and vaccines, he said. One benefit of using this tool could allow Pfizer to accelerate vaccine production, Slavitt said.

The Biden administrations all-of-the-above approach of encouraging more face masks, less travel, better access to testing and faster distribution of vaccines is needed right now because the U.S. has languished during the pandemic for so long, Frieden said. But these new variants are the pandemics wild card, he said. To keep them at bay, all of these strategies must be ratcheted up.

This is going to take months to turn around, not days, Frieden said.

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COVID-19 vaccines can adapt to new variants. Heres what it will take - PBS NewsHour

Three Men Are Accused in Scheme to Sell Covid-19 Vaccines – The New York Times

February 14, 2021

Three Baltimore men have been accused by federal prosecutors of putting up a fake website to sell Covid-19 vaccines for $30 a dose, prosecutors say.

The men, Olakitan Oluwalade, 22, and Odunayo Baba Oluwalade, 25, who are cousins, and Kelly Lamont Williams, 22, each face a charge of conspiracy to commit wire fraud, the United States Attorneys Office for the District of Maryland said on Thursday.

Prosecutors said the men created a website that resembled that of Moderna, the biotechnology company based in Cambridge, Mass., that in December won federal approval to distribute its Covid-19 vaccine.

The genuine website is modernatx.com, and the website created by the men, which the authorities have since seized, was modernatx.shop. Prosecutors said the source code of the fake domain showed that its creator had used a tool to copy the real Moderna website.

The logo, markings, colors and texts on the fake domain were visually similar to the companys actual home page, officials said in a statement. But prosecutors said the fake website had an addition: YOU MAY BE ABLE TO BUY A COVID-19 VACCINE AHEAD OF TIME, with a link to Contact us.

The men were caught after an undercover agent contacted the number on the fake website on Jan. 11 and set up a transaction for 200 doses of the vaccine for $6,000, according to the statement. Officials said the three men never actually had any doses.

The agent was instructed to transfer half of the funds to Mr. Williamss account at the Navy Federal Credit Union, and by Jan. 15 agents had seized the fake domain and searched Mr. Williamss home.

Investigators found texts between Mr. Williams and the cousins discussing the scheme, according to court documents.

An agent used Mr. Williamss phone to send a message to Odunayo Baba Oluwalade and sent some of the money from the exchange to the cousins, prosecutors said. Both of their homes were soon searched, too.

It was unclear how much money the men defrauded people of. A spokeswoman for the U.S. attorneys office said Friday that she could not provide more details about the charges beyond what was in the statement.

A representative for Moderna could not be immediately reached on Friday.

A lawyer, Richard Bardos, said he had been assigned to Odunayo Baba Oluwalades case but declined to comment further, citing a Maryland law that prohibits lawyers from speaking about ongoing cases.

Jonathan Van Hoven, a lawyer for Mr. Williams, declined to comment. The Office of the Federal Public Defender for the District of Maryland said Olakitan Oluwalade had not yet been assigned a lawyer.

As the public seeks vaccines to protect themselves and their families from Covid-19, fraudsters are waiting to take advantage of their desperation, said James R. Mancuso, a special agent from Homeland Security Investigations. We want to remind the public to exercise extreme caution online, especially when it comes to Covid-19 vaccines, treatments and protective equipment.

Link:

Three Men Are Accused in Scheme to Sell Covid-19 Vaccines - The New York Times

Vaccine efficacy – When covid-19 vaccines meet the new variants of the virus | Briefing – The Economist

February 14, 2021

Feb 13th 2021

ON FEBRUARY 1ST researchers around the world saw the tweet for which they had been waiting: We say with caution, the magic has started. Eran Segal, a scientist at the Weizmann Institute, had been posting regular updates on the course of Israels covid-19 epidemic since its mass vaccination campaign had begun six weeks earlier. By February 1st he was seeing the number of hospitalisations dropping significantly among the over-60sa cohort in which the number vaccinated had reached 70%, seen as a crucial level, three weeks before. After an expected but still somewhat nail-biting lag, the vaccine was doing its thing.

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By February 6th about 85% of the over-60s in Israeland 40% of the general populationhad received at least one dose of the Pfizer/BioNTech mRNA vaccine (or in a few cases the Moderna mRNA vaccine) and 75% of the over-60s had received their second dose, too. In that age group hospital admissions for covid-19 were about two-thirds what they had been at their peak in January and still falling (see chart 1). At the same time, the country as a whole was seeing its caseload rise.

The vaccine was not the only thing which arrived in Israel late last year. So did B.1.1.7, a highly contagious variant of SARS-CoV-2, the virus responsible for covid-19, which was first identified in Britain in September. It set about filling up hospital wards in Israel just as it has done in Britain, Ireland and Portugal. Despite an extended lockdown it is still doing so.

It is no surprise that SARS-CoV-2 has evolved new biological tricks over a year spent infecting more than 100m people. But the near simultaneous arrival of not just B.1.1.7 but also B.1.351, which is now the dominant strain in South Africa, and P.1, a variant first seen in Brazil, is making the roll-out of mass vaccination more complicated and more confusing than might have been hoped when the first evidence of safe, effective vaccines became available last November. How fast the various new variants can spread, how well todays vaccines work against them and how soon new vaccines better attuned to themand to the other variants which will turn up over timebecome available will determine the course of the pandemic.

As of February 10th at least nine vaccines had been authorised for use in one or more countries. The Pfizer/BioNTech vaccine, first out of the gate, has now been authorised for use in 61, as well as for emergency use by the WHO. The number of doses administered, 148m, now exceeds the number of confirmed covid-19 cases recorded over the entire course of the pandemic. All of the vaccines appear very good at preventing severe cases of covid-19 of the sort that lead to hospitalisation and/or death; in trials which compared the vaccinated with control groups the efficacy with which the various vaccines prevented these outcomes was 85-100%.

Their efficacy against all symptomatic cases of the disease found in trials has been lower, ranging between 66% and 95%. Some of that range is down to intrinsic differences between the vaccines. Some is down to trials being done according to different protocols and in different populations, sometimes against different variants of the virus. It is hard to disentangle such effects. The general message, though, is fairly clear. The vaccines make serious cases of all sorts very rare, and mild-to-moderate cases caused by the original strain of the virus a lot rarer than they would be otherwise.

That is undoubtedly good news; it lessens the death toll, the suffering and the strain on hospitals. But the situation is not perfect. For one thing mild and moderate cases can be worse than they sound. Many cases of long covid, a debilitating form of the disease in which some effects last for months, follow original infections that were not severe enough to require hospital admission. It is not yet clear whether long covid is less likely in people who have been vaccinated.

What is more, this pattern of effects does not reveal what the vaccines are doing about transmission. As Natalie Dean, a biostatistician at the University of Florida, points out, there are two ways one can imagine a vaccine bringing about the pattern of protection the covid-19 vaccines have been seen to provide (see chart 2). In one of them the same number of infections occurs as would occur otherwise, but the consequences of these infections are systematically downgraded. Thus almost all of the infections which would lead to severe cases lead to moderate or mild cases, and many of the infections that would have led to moderate or mild cases produce no symptoms at all.

The alternative is that the total number of infections is being reduced, but the ratio of severe to mild to asymptomatic cases stays roughly the same. The already low number of deaths and hospitalisations shrinks to something hardly there. The number of mild cases is similarly deflated (although, since bigger, remains palpable). And so is the number of asymptomatic cases. Indeed, the main difference between the two scenarios is that in one the asymptomatic cases rise, and in the other they fall.

In the real world there is almost certainly a bit of both going on: lower infections overall and a lessening of the symptoms that follow, with different vaccines offering different profiles. But considering the two extremes is still instructive. Vaccines which do little more than downgrade the symptoms will be doing relatively little to stop the spread of the virus. Honey-I-shrank-the-infections vaccines, on the other hand, will be making a big dent in the epidemics now infamous R numberthe number of new infections to which each infection gives rise. If you imagine reducing what are known as non pharmaceutical interventionsmasks, social distancing, shelter at home orders and the likethat difference would begin to matter a lot.

Some people will not be vaccinated, either because of pre-existing conditions which make it dangerous for them, because there isnt enough vaccine for everyone, or because they choose not to (see article). If the vaccines are basically downgrading symptoms, then these unvaccinated people will be at risk. If they are making the virus less transmissible that risk will be lessened.

A covid-19 vaccine that is highly effective in preventing transmission will, therefore, be particularly useful. According to a model by Imperial College London, all other things being equal, a vaccine that blocks 40% of infections and thus prevents 40% of disease would have a similar impact on the number of covid-19 deaths as a vaccine that got rid of 80% of disease but left infection untouched.

Epidemiologists are waiting with bated breath for results that will tell them how good existing vaccines are at reducing asymptomatic infections and infectiousness. Data from Israel suggest that the viral load in swabs from infected individuals is lower if they have been vaccinated. Clinical trials of the Oxford/AstraZeneca vaccine suggest that the jab may halve infections as detected by PCR tests. Such results suggest that covid-19 vaccines are likely to reduce overall transmission of the virus. But understanding quite how much transmission is blockedand the degree to which some vaccines are better at blocking transmission than otherswill take months.

And then there is the further complication of the new variants. Vaccines seem to have no particular problem with B.1.1.7. It just complicates things by running through the unimmunised parts of the population that bit faster. B.1.351, which has now been found in more than 30 countries, is of greater concern. At least three vaccinesthose from Oxford/AstraZeneca, J&J and Novavaxhave been found to be less effective at stopping it from causing disease than they are against variants elsewhere. There is increasing evidence that P.1, now also reported in a number of countries beyond Brazil, also appears to be better at avoiding immunity created by prior infection and by some vaccines.

Countries that have already vaccinated a lot of people could be brought back to square one by the spread of such variants. Britain, where 13m people had been vaccinated as of February 10th, and millions more have been infected and thus have some immunity (British studies have found reinfection very rare for at least five months), is trying hard to keep B.1.351 from making inroads in the population. Health authorities are mass-testing neighbourhoods where cases of B.1.351 have been spotted and are doing particularly meticulous contact tracing when a case is found. Border controls have been tightened.

Not all such new variants can be spotted and stopped at borders. Mutations can arise anywheresometimes the phone call is coming from inside the house. But there may be a limited range of mutations about which people need to worry. The new variants all differ from the original virus and from each other in various ways. But P.1 and B.1.351 both share a particular mutational quirktechnically called E484K but mercifully nicknamed Eric or Eekwhich makes a specific change to the spike protein on the outside of the virus. Eek has now been found in some isolates of B.1.1.7. too. Researchers are beginning to think that the change Eek represents is what allows those variants to infect people even if they have been vaccinated or previously infected.

It would be great if there were no vaccine-resistant strains. But given that there are, the possibility that they are all using the same trick offers a bit of comfort. It suggests that Eek may be the best way for new variants to avoid immune responses capable of dealing with the original strain, or at least the way evolution can most easily find. If the variants have all converged on the same trick, tweaking vaccines to protect against one may protect against alland against any later variants to which natural selection teaches the same ruse. If the virus had found a whole panoply of ways by which to avoid existing immune responses things would look a lot worse.

Whether or not Eek turns out to be crucial, new ways of broadening immunity are on their way. Some vaccine-makers are developing booster shots designed to help people vaccinated with earlier versions of their jabs deal with new variants. Others are developing vaccines intended to work for multiple SARS-CoV-2 variants straight away. On February 3rd GlaxoSmithKline and CureVac, a German biotech company with an mRNA vaccine in late-stage clinical trials, added their names to those developing such multivalent vaccines.

Tweaked covid-19 vaccines will not be required to go through large scale clinical trials to prove their efficacy, any more than updated seasonal flu shots do; small trials that look for markers of immunity in the blood may suffice. Britains National Health Service, which should be able to vaccinate all adults who choose to be jabbed by the end of the summer, is already starting to make plans for a round of covid-19 booster shots aimed at new variants in the autumn. Increased surveillance may yet provide advance warning of which variants need to be dealt with by subsequent tweaks. It will take luck, diligence and hard work, but the magic that started at the beginning of this year may be made to last for many years to come.

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All our stories relating to the pandemic and the vaccines can be found on our coronavirus hub. You can also listen to The Jab, our new podcast on the race between injections and infections, and find trackers showing the global roll-out of vaccines, excess deaths by country and the viruss spread across Europe and America.

This article appeared in the Briefing section of the print edition under the headline "Obstacle course"

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Vaccine efficacy - When covid-19 vaccines meet the new variants of the virus | Briefing - The Economist

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