Pfizer and its collaborator BioNTech have shown that their new COVID-19 booster does what they hoped it would, with the same safety and side effect profile as earlier shots.
In a study released early Friday, the pair found that adults mounted a strong immune response to the new booster, which is targeted to both the original virus and the BA.4 and BA.5 variants.
In a separate report on Friday, results from the first 22 million doses of the Pfizer-BioNTech and Moderna bivalent boosters confirm that adverse reactions are rare and no different than with earlier boosters, according to the Centers for Disease Control and Prevention.
Previous studies of the bivalent booster revealed safety and immune data only in rodents and among people 7 days after the shot.
Now, at 30 days, Pfizer and BioNTech say the fourth shot boosts levels of neutralizing antibodies against the BA.4 and BA.5 variants 13-fold in adults 55 and older and nearly 10-fold in younger adults. People who received a shot targeted solely at the original virus saw a 3-fold increase in neutralizing antibodies against those variants.
Unfortunately, as many had feared, the BA.4 and BA.5 variants are now shrinking in importance. And it’s not clear how well boosters will prevent infection with the newer variants.
BA.5, which has caused the vast majority of COVID-19 infections since early July, now accounts for just under 50% of infections, according to CDC data. BA.4, which is identical to BA.5 in the area targeted by the vaccine, has never accounted for more than about 5% of infections.
One variant that’s now growing exponentially in the U.S., called BQ.1.1, is “very troublesome,” according to Pei-Yong Shi, associate chief research officer and vice president for research innovation at the University of Texas Medical Branch at Galveston.
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“Whether the bivalent vaccine will work against this in terms of protection in the United States — the answer to that is I’m not quite sure,” he said. People who have been boosted with the bivalent shot have some neutralizing antibodies against BQ.1.1, research he posted Wednesday shows, “but it’s pretty low.”
The immune system also has other tools to fight off disease, Shi said, including other antibodies and T cells. It’s not clear yet whether those will be enough in the face of new variants to fully protect people who have been vaccinated or previously infected.
But Shi said, there’s no doubt that the booster can play a role in preventing the spread of COVID-19 this winter.
Some people had been uncomfortable with the bivalent booster because testing had only been completed in rodents, not people before it was authorized and became available.
Federal officials said they were comfortable offering the bivalent booster without human data because the same process is typically followed with the annual flu vaccine, where minor changes are only tested for safety and effectiveness in animals before being offered to people.
Also, trials with bivalent boosters that targeted both the original virus and earlier variants had been shown safe in human testing.
In the new CDC data, of the first 22 million people to receive the bivalent booster, more than 220,000 participated in the government’s v-safe program, which tracks responses to vaccination. Fewer than 1% reported receiving medical care in the week following vaccination and the most commonly reported side effects were fatigue and sore arm.
There were 5,542 reports to the government’s Vaccine Adverse Event Reporting System related to the bivalent booster, but more than 95% were considered “nonserious events,” and others may have occurred close to the vaccine in time, but not caused by the shot, such as a car accident.
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Shi said his data on the bivalent booster’s effectiveness, along with similar results from Emory University, support what…
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