In desperate times, there are many ways to stretch vaccines and speed up inoculation campaigns, according to experts who have done it.
Splitting doses, delaying second shots, injecting into the skin instead of the muscle and employing roving vaccination teams have all saved lives — when the circumstances were right.
During cholera outbreaks in war zones, Doctors Without Borders has even used “takeaway” vaccination, in which the recipient is given the first dose on the spot and handed the second to self-administer later.
Unfortunately, experts said, it would be difficult to try most of those techniques in the United States right now, even though vaccines against the coronavirus are rolling out far more slowly than had been hoped.
Those novel strategies have worked with vaccines against yellow fever, polio, measles, cholera and Ebola; most of those vaccines were invented decades ago or are easier to administer because they are oral or can be stored in a typical refrigerator.
The new mRNA-based coronavirus vaccines approved thus far are too fragile, experts said, and too little is known about how much immunity they confer.
The incoming Biden administration should focus on speeding up the production of more robust vaccines “rather than playing card tricks” with current ones, said Dr. Peter J. Hotez, dean of the National School of Tropical Medicine at the Baylor College of Medicine in Houston and the inventor of a coronavirus vaccine.
There are two strategies that might work with the current vaccines, but each is controversial.
The first is being tried in Britain. In December, faced with shortages and an explosive outbreak, the country’s chief medical officers said they would roll out all of the vaccines they had, giving modest protection to as many Britons as possible. Second doses, they said, would be delayed by up to 12 weeks and might be of a different vaccine.
There is some evidence for the idea: Early data from the first 600,000 injections in Israel suggests that even one dose of the Pfizer vaccine cut the risk of infection by about 50 percent.
Nonetheless, some British virologists were outraged, saying single doses could lead to vaccine-resistant strains. The Food and Drug Administration and many American vaccinologists also oppose the idea.
Moncef Slaoui, the chief scientific adviser to Operation Warp Speed, raised a different objection to the British plan. Single doses, he warned, might inadequately “prime” the immune system; then, if those vaccine recipients were later infected, some might do worse than if they had not been vaccinated at all.
He recalled a 1960s incident in which a weak new vaccine against respiratory syncytial virus, a cause of childhood pneumonia, backfired. Some children who received it and later became infected fell sicker than unvaccinated children, and two toddlers died.
“It may be only one in 1,000 who get inadequate priming, but it’s a concern,” Dr. Slaoui said. As an alternative — the second strategy for stretching the vaccines — he proposed using half-doses of the Moderna vaccine.
There is strong evidence for doing that, he said in a telephone interview. During Moderna’s early trials, the 50-microgram vaccine dose produced an immune response virtually identical to the 100-microgram one.
Moderna chose the higher dose as its standard partly to be extra sure it would work; company scientists at the time had no idea that their product would prove 95 percent effective. The higher dose would also have a longer shelf life.
But the vaccine works better than expected, and shelf life is not an issue, so Dr. Slaoui suggested using the lower dose.
“The beauty is, you inject half and get the identical immune response,” he said. “We hope that, in a pandemic situation, the F.D.A. may simply accept it rather than asking for a new trial.”
While the exact order of vaccine recipients may vary by state, most will likely put medical workers and residents of long-term care facilities first. If you want to understand how this decision is getting made, this article will help.
Life will return to normal only when society as a whole gains enough protection against the coronavirus. Once countries authorize a vaccine, they’ll only be able to vaccinate a few percent of their citizens at most in the first couple months. The unvaccinated majority will still remain vulnerable to getting infected. A growing number of coronavirus vaccines are showing robust protection against becoming sick. But it’s also possible for people to spread the virus without even knowing they’re infected because they experience only mild symptoms or none at all. Scientists don’t yet know if the vaccines also block the transmission of the coronavirus. So for the time being, even vaccinated people will need to wear masks, avoid indoor crowds, and so on. Once enough people get vaccinated, it will become very difficult for the coronavirus to find vulnerable people to infect. Depending on how quickly we as a society achieve that goal, life might start approaching something like normal by the fall 2021.
Yes, but not forever. The two vaccines that will potentially get authorized this month clearly protect people from getting sick with Covid-19. But the clinical trials that delivered these results were not designed to determine whether vaccinated people could still spread the coronavirus without developing symptoms. That remains a possibility. We know that people who are naturally infected by the coronavirus can spread it while they’re not experiencing any cough or other symptoms. Researchers will be intensely studying this question as the vaccines roll out. In the meantime, even vaccinated people will need to think of themselves as possible spreaders.
The Pfizer and BioNTech vaccine is delivered as a shot in the arm, like other typical vaccines. The injection won’t be any different from ones you’ve gotten before. Tens of thousands of people have already received the vaccines, and none of them have reported any serious health problems. But some of them have felt short-lived discomfort, including aches and flu-like symptoms that typically last a day. It’s possible that people may need to plan to take a day off work or school after the second shot. While these experiences aren’t pleasant, they are a good sign: they are the result of your own immune system encountering the vaccine and mounting a potent response that will provide long-lasting immunity.
No. The vaccines from Moderna and Pfizer use a genetic molecule to prime the immune system. That molecule, known as mRNA, is eventually destroyed by the body. The mRNA is packaged in an oily bubble that can fuse to a cell, allowing the molecule to slip in. The cell uses the mRNA to make proteins from the coronavirus, which can stimulate the immune system. At any moment, each of our cells may contain hundreds of thousands of mRNA molecules, which they produce in order to make proteins of their own. Once those proteins are made, our cells then shred the mRNA with special enzymes. The mRNA molecules our cells make can only survive a matter of minutes. The mRNA in vaccines is engineered to withstand the cell’s enzymes a bit longer, so that the cells can make extra virus proteins and prompt a stronger immune response. But the mRNA can only last for a few days at most before they are destroyed.
Many experts disagreed with the idea, including Dr. Walter A. Orenstein, associate director of the Emory Vaccine Center in Atlanta. “We need to know more before we can feel comfortable doing that,” he said.
“Let’s stick to the science,” added Dr. Paul A. Offit, director of the Vaccine Education Center at Children’s Hospital of Philadelphia. “There are no efficacy data on a partial dose.”
Although, like Dr. Slaoui, Dr. Offit opposed delaying second doses, he expressed doubt that doing so, as the British have, would raise the risk of worse outcomes in the partially vaccinated.
Trials in which monkeys or other animals were vaccinated and then “challenged” with a deliberate infection did not cause enhanced disease, he noted. Also, the four coronaviruses that cause common colds do not cause worse disease when people get them again. And people who have Covid-19 do not get worse when they receive antibody treatments; generally, they get better.
When less is more
As is often the case, experts disagree about how and what a new vaccine will do. Some point to hard evidence that both fractional doses and delayed doses have worked when doctors have tried them out of desperation.
For example, yellow fever outbreaks in Brazil and the Democratic Republic of Congo have been stymied by campaigns using as little as 20 percent of a dose.
One shot of yellow fever vaccine, invented in the 1930s, gives lifelong protection. But a one-fifth dose can protect for a year or more, said Miriam Alia, a vaccination expert for Doctors Without Borders.
In 2018, almost 25 million Brazilians, including those in Rio de Janeiro and São Paulo, faced a fast-moving outbreak at a time when there were fewer than six million shots in the global supply. The Brazilian government switched to one-fifth doses and sent mobile teams into the slums urging everyone they met to take them, and filling out minimal paperwork. It worked: By 2019, the threat had faded.
The tactic has also been used against polio. Since 2016, there has been a global shortage of the injectable polio vaccine, which many countries use in conjunction with the live oral one. The World Health Organization has overseen trials of different ways to stretch existing supplies.
India first tried half-doses, said Deepak Kapur, chairman of Rotary International’s polio eradication efforts in that country. Later studies showed that it was possible to drop to as low as one-fifth of a dose as long as it was injected just under the skin rather than into the muscle, said Dr. Tunji Funsho, chief of polio eradication for Rotary International’s Nigeria chapter.
“That way, one vial for 10 can reach 50 people,” Dr. Funsho said.
Skin injections work better than muscle ones because the skin contains far more cells that recognize invaders and because sub-skin layers drain into lymph nodes, which are part of the immune system, said Mark R. Prausnitz, a bioengineer at Georgia Tech who specializes in intradermal injection techniques.
“The skin is our interface with the outside world,” Dr. Prausnitz said. “It’s where the body expects to find pathogens.”
Intradermal injection is used for vaccines against rabies and tuberculosis. Ten years ago, Sanofi introduced an intradermal flu vaccine, “but the public didn’t accept it,” Dr. Prausnitz said.
Intradermal injection has disadvantages, however. It takes more training to do correctly. Injectors with needle-angling devices, super-short needles or arrays of multiple needles exist, Dr. Prausnitz said, but are uncommon. Ultimately, he favors micro-needle patches infused with dissolving vaccine.
“It would really be beneficial if we could just mail these to people’s homes and let them do it themselves,” he said.
A bigger disadvantage, Dr. Slaoui, is that intradermal injection produces strong immune reactions. These can be painful, and can bleed a bit and then scab over and leave a scar, as smallpox injections often did before the United States abandoned them in 1972.
The lipid nanoparticles in the Pfizer and Moderna vaccines would be particularly prone to that effect, he said.
“It’s not dangerous,” he added. “But it’s not appealing and not practical.”
Boots on the ground
What the United States can and must do now, health experts said, is train more vaccinators, coordinate everyone delivering shots and get better at logistics.
Thanks to battles against polio, measles and Ebola, some of the world’s poorest countries routinely do better vaccination drives than the United States is now managing to do, said Emily Bancroft, president of Village Reach, a logistics and communications contractor working in Mozambique, Malawi and the Democratic Republic of Congo and also assisting Seattle’s coronavirus vaccine drive.
“You need an army of vaccinators, people who know how to run campaigns, detailed micro-plans and good data tracking,” she said. “Hospitals here don’t even know what they have on their shelves. For routine immunization, getting information once a month is OK. In an epidemic, it’s not OK.”
Training can be done on “injection pads” that resemble human arms. And data collection must be set up so that every team can report on a cellphone and it all flows to a national dashboard, as happens now in the poorest countries.
“The U.S. will get there,” Ms. Bancroft said. “Practice makes perfect. But the rockiness we’re seeing now is the lack of experience.”
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