CDC panel votes to recommend Pfizer-BioNTech booster for 65 and older, high-risk

CDC panel votes to recommend Pfizer-BioNTech booster for 65 and older, high-risk

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A key Centers for Disease Control (CDC) advisory panel voted unanimously to back a third booster dose of the Pfizer-BioNTech’s COVID-19 vaccine for Americans 65 years of age and older and those living in long term care facilities.


What You Need To Know

  • A CDC advisory panel voted unanimously to back a third booster dose of the Pfizer-BioNTech’s COVID-19 vaccine for Americans 65 years of age and older and those living in long term care facilities
  • They also separately voted in favor of boosters for Americans 18 to 64 with underlying medical conditions that may put them at higher risk of severe disease
  • Once CDC Director Dr. Rochelle Walensky approves, booster shots could be made available within a matter of days
  • The COVID-19 vaccines used in the U.S. still offer strong protection against severe illness, hospitalization and death, but immunity against milder infection appears to be waning months after people’s initial vaccination

They also separately voted in favor of boosters for Americans 18 to 64 with underlying medical conditions that may put them at higher risk of severe disease. 

The additional dose for approved groups would be administered at least six months after a person’s last shot of the Pfizer-BioNTech vaccine.

The news came one day after the Food and Drug Administration (FDA) authorized the booster doses, bringing them one step closer to being administered nationwide.

The CDC panel’s recommendation must now be signed off on by the CDC director, Dr. Rochelle Walensky, who spoke to the panelists at the beginning of Thursday’s meeting.

“Now, you have an opportunity to again lead our public health response with recommendations on how we can best utilize the tools we have to protect those at greatest risk,” she said.

Once Dr. Walensky approves, booster shots could be made available within a matter of days, since the Biden administration had already been preparing for their rollout as early as Monday.

CDC panelists did not, however, vote to recommend the extra dose for people in high-risk professions, such as health care workers or teachers, a group that the FDA panel did approve boosters for. The final decision could be up to Walensky.

The approval of Pfizer’s booster shot, however, is sure to create confusion for Americans who got the Moderna or Johnson & Johnson vaccines early on, an issue some advisers brought up in the Advisory Committee on Immunization Practices meeting Thursday.

The government still hasn’t considered boosters for those brands and has no data on whether it’s safe or effective to mix-and-match and give those people a Pfizer shot.

“I just don’t understand how later this afternoon we can say to people 65 and older you’re at risk for severe illness and death but only half of you can protect yourselves right now,” said Dr. Sarah Long of Drexel University.

But for most people, if you’re not in a group recommended for a booster, “it’s really because we think you’re well-protected,” said Dr. Matthew Daley of Kaiser Permanente Colorado. “This isn’t about who deserves a booster, but who needs a booster.”

The COVID-19 vaccines used in the U.S. still offer strong protection against severe illness, hospitalization and death, but immunity against milder infection appears to be waning months after people’s initial vaccination.

The widespread dispensing of the boosters would represent an important new phase in the nation’s vaccination drive. Britain and Israel are already rolling out a third round of shots over strong objections from the World Health Organization that poor countries don’t have enough for their initial doses.

The priority still is vaccinating the unvaccinated “here in America and around the world,” CDC Director Dr. Rochelle Walensky told the meeting.

She acknowledged that the data on boosters “are not perfect.” “Yet collectively they form a picture for us,” she said, “and they are what we have in this moment to make a decision about the next stage in this pandemic.”

The FDA rejected a sweeping Biden administration plan announced a month ago to offer boosters to the general population, instead embracing a more targeted approach for now. Acting FDA Commissioner Dr. Janet Woodcock cautioned that booster decisions could very well change as real-world data come in.

“As we learn more about the safety and effectiveness of COVID-19 vaccines, including the use of a booster dose, we will continue to evaluate the rapidly changing science and keep the public informed,” Woodcock said.

The CDC panel on Thursday also wrestled with how to tell when a booster is needed. While an extra dose revs up numbers of virus-fighting antibodies, those naturally wane over time and no one knows how long the antibody boost from a third Pfizer dose will last — or how much protection it really adds since the immune system also forms additional defenses after vaccination.

The U.S. has already authorized third doses of the Pfizer and Moderna vaccines for certain people with weakened immune systems, such as cancer patients and transplant recipients. Other Americans, healthy or not, have managed to get boosters, in some cases simply by asking.

The Associated Press contributed to this report.

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