New CDC advisers will skip some expected topics and explore a target of antivaccine activists

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By MIKE STOBBE and LAURAN NEERGAARD, Associated Press

U.S. Health Secretary Robert F. Kennedy Jr.’s new vaccine advisers meet next week, but their agenda suggests they’ll skip some expected topics — including a vote on COVID-19 shots — while taking up a longtime target of anti-vaccine groups.

The Advisory Committee on Immunization Practices makes recommendations on how to use the nation’s vaccines, setting a schedule for children’s vaccines as well as advice for adult shots. Last week, Kennedy abruptly dismissed the existing 17-member expert panel and handpicked eight replacements, including several anti-vaccine voices.

The agenda for the new committee’s first meeting, posted Wednesday, shows it will be shorter than expected. Discussion of COVID-19 shots will open the session, but the agenda lists no vote on that. Instead, the committee will vote on fall flu vaccinations, on RSV vaccinations for pregnant women and children and on the use of a preservative named thimerosal that’s in a subset of flu shots.

It’s not clear who wrote the agenda. No committee chairperson has been named and the U.S. Department of Health and Human Services did not comment.

Committee won’t take up HPV or meningococcal vaccines

Missing from the agenda are some heavily researched vaccine policy proposals the advisers were supposed to consider this month, including shots against HPV and meningococcal bacteria, said Dr. Susan Kressly, president of the American Academy of Pediatrics.

Instead, the committee is talking about subjects “which are settled science,” she said.

“Every American should be asking themselves how and why did we get here, where leaders are promoting their own agenda instead of protecting our people and our communities,” she said. She worried it’s “part of a purposeful agenda to insert dangerous and harmful and unnecessary fear regarding vaccines into the process.”

The committee makes recommendations on how vaccines that have been approved by the Food and Drug Administration should be used. The recommendations traditionally go to the Centers for Disease Control and Prevention director. Historically, nearly all are accepted and then used by insurance companies in deciding what vaccines to cover.

But the CDC has no director and the committee’s recommendations have been going to Kennedy.

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Thimerosal is a longtime target of antivaccine activists

Thimerosal was added to certain vaccines in the early 20th century to make them safer and more accessible by preventing bacterial contamination in multi-dose vials. It’s a tiny amount, but because it’s a form of mercury, it began raising questions in the 1990s.

Kennedy — a leading voice in an antivaccine movement before he became President Donald Trump’s health secretary — has long held there was a tie between thimerosal and autism, and also accused the government of hiding the danger.

Study after study has found no evidence that thimerosal causes autism. But since 2001, all vaccines manufactured for the U.S. market and routinely recommended for children 6 years or younger have contained no thimerosal or only trace amounts, with the exception of inactivated influenza vaccine.

Thimerosal now only appears in multidose flu shot vials, not the single-shot packaging of most of today’s flu shots.

Targeting thimerosal would likely force manufacturers to switch to single-dose vials, which would make the shots “more expensive, less available and more feared,” said Paul Offit, a vaccine expert at Children’s Hospital of Philadelphia.

Doctors’ groups have opposed Kennedy’s vaccine moves

Last week, 30 organizations called on insurers to continue paying for COVID-19 vaccines for pregnant women after Kennedy said the shots would no longer be routinely recommended for that group.

Doctors’ groups also opposed Kennedy’s changes to the vaccine committee. The new members he picked include a scientist who researched mRNA vaccine technology and became a conservative darling for his criticisms of COVID-19 vaccines, a top critic of pandemic-era lockdowns and a leader of a group that has been widely considered to be a source of vaccine misinformation.

The American Academy of Pediatrics has long put out its own immunization recommendations. In recent decades it has matched what the government recommended. But asked if they might soon diverge, depending on potential changes in the government’s vaccination recommendations, Kressly said; “Nothing’s off the table.”

“We will do whatever is necessary to make sure that every child in every community gets the vaccines that they deserve to stay healthy and safe,” she said.

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.

Honda recalls more than 259,000 cars across the US due to brake pedal issue

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NEW YORK (AP) — Honda is recalling more than 259,000 of its cars across the U.S. due to a problem that can cause the brake pedal to shift out of position, potentially interfering with a driver’s ability to stop or slow down.

According to documents published by the National Highway Traffic Safety Administration, the recall covers certain Honda Pilots between model years 2023 and 2025 — as well cars under the auto maker’s luxury Acura brand: 2021-2025 Acura TLX and 2023-2025 Acura MDX vehicles.

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The NHTSA’s recall report notes that the brake pedal pivot pin in some of these vehicles was not secured properly during production. That can lead the pedal to shift out of place and “may lead to unintended application,” the report notes, increasing crash risks.

“The issue could also cause an abnormal brake pedal feeling during operation, illuminate the brake malfunction light in the instrument cluster, or cause the vehicle’s brake lights to remain lit even when the brake pedal is not applied,” America Honda said in a statement Wednesday.

As a remedy, Honda says authorized dealers will inspect the vehicles covered by this recall and replace the brake pedal assembly if necessary, free of charge. Per the NHTSA’s report, the company estimates 1% of these vehicles have this issue.

Dealer notifications began on June 13. And mailed owner notification letters are set to follow on July 28. In the meantime, drivers can also confirm if their specific vehicle is included in this recall and find more information using the NHTSA site or Honda’s recall lookup.

Between February 2024 and June 5, the NHSTA notes, Honda received three warranty claims related to this issue — but no reports of injuries.

Honda began investigating the faulty brake pedal in April 2024, after receiving a report of a vehicle experiencing this issue. The company later determined that improper assembly of the brake pedal pivot pin occurred at a supplier’s U.S. plant, which has since been closed. Production was transferred to a plant in Mexico — where the supplier now uses a camera sensor “to verify whether the pivot pin is staked,” the recall report notes.

Senate Republicans hold hearing on Biden’s mental fitness as Democrats boycott

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By JOEY CAPPELLETTI, Associated Press

WASHINGTON (AP) — Nearly six months after Joe Biden left the White House, Senate Republicans are still scrutinizing his presidency, kicking off the first in what’s expected to be a series of congressional hearings this year on his mental fitness in office.

Republicans on the Senate Judiciary Committee brought in three witnesses Wednesday — none of whom served in Biden’s administration — to scrutinize his time in office, arguing that Biden, his staff and the media must be held accountable. Democrats boycotted the hearing and criticized Republicans for “arm chair diagnosing” Biden when the committee could be looking into serious matters.

Sen. John Cornyn of Texas, who co-chaired the hearing, said that they will aim to “shine a light on exactly what went on in the White House during Biden’s presidency.”

“We simply cannot ignore what transpired because President Biden is no longer in office,” Cornyn said.

A spokesperson for Biden declined to comment on the hearing.

Sen. Katie Britt, R-Ala., questions the witnesses during a Senate Committee on the Judiciary hearing oon Capitol Hill, Wednesday, June 18, 2025, in Washington. (AP Photo/Rod Lamkey, Jr.)

It was the first in what could be several hearings about Biden in the coming months. Over in the House, the Oversight Committee has subpoenaed several of Biden’s former staff members, along with his White House doctor, ordering him to testify at a June 27 hearing “as part of the investigation into the cover-up of President Joe Biden’s cognitive decline.”

Questions about Biden’s age and fitness erupted last summer after his disastrous performance in a debate against Donald Trump, which ultimately led to his withdrawal from the race.

Even after Trump won back the presidency in November, Republicans have continued to hammer on Biden’s age, citing in part new reporting about Biden that was published this year.

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Trump now alleges that Biden administration officials may have forged the former president’s signature and taken sweeping actions without his knowledge, though he provided no evidence of that happening. But Trump has ordered lawyers at the White House and the Justice Department to investigate.

Republicans played clips during the hearing Wednesday of Democrats defending Biden. In the montage, the Democrats talk about how Biden was mentally sharp when he was in office.

“Most Democrats on this committee have chosen to all but boycott the hearing and have failed to call a single witness,” said Sen. Eric Schmitt, R-Mo. “They have chosen to ignore this issue, like they ignored President Biden’s decline.”

Sen. Dick Durbin, the committee’s top Democrat, criticized Republicans for holding a hearing on the last president at a time when “numerous critical challenges facing the nation that are under our jurisdiction.”

“Apparently arm chair diagnosing former President Biden is more important than the issues of grave concern,” said Durbin of Illinois.

After his opening remarks, Durbin played a video montage of his own — but with clips of Trump speaking that he said reflected the “cognitive ability” of the current president. Durbin left the hearing after his opening remarks.

Three witnesses testified: former White House Press Secretary Sean Spicer, former White House official Theodore Wold and University of Virginia law professor John Harrison. Spicer and Wold both served under Trump.

Sean Spicer, former White House press secretary, host of The Sean Spicer Show, arrives to testify at a Senate Committee on the Judiciary hearing oon Capitol Hill, Wednesday, June 18, 2025, in Washington. (AP Photo/Rod Lamkey, Jr.)

Much of the focus was on Biden’s alleged use of an autopen. Trump has repeated long-standing allegations that the Biden White House relied on an autopen to sign presidential pardons, executive orders and other key documents, claiming that its use cast doubt on their validity.

GOP Sen. Katie Britt also questioned Spicer on “what mechanisms should we put in place” to hold the media accountable “for not actually following what is clearly in front of them.”

FDA approves the world’s only twice-a-year shot to prevent HIV

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By LAURAN NEERGAARD, Associated Press

WASHINGTON (AP) — The U.S. has approved the world’s only twice-a-year shot to prevent HIV, maker Gilead Sciences announced Wednesday. It’s the first step in an anticipated global rollout that could protect millions – although it’s unclear how many in the U.S. and abroad will get access to the powerful new option.

While a vaccine to prevent HIV still is needed, some experts say the shot — a drug called lenacapvir — could be the next best thing. It nearly eliminated new infections in two groundbreaking studies of people at high risk, better than daily preventive pills they can forget to take.

“This really has the possibility of ending HIV transmission,” said Greg Millett, public policy director at amfAR, The Foundation for AIDS Research.

Condoms help guard against HIV infection if used properly but what’s called PrEP — regularly using preventive medicines such as the daily pills or a different shot given every two months — is increasingly important. Lenacapavir’s six-month protection makes it the longest-lasting type, an option that could attract people wary of more frequent doctor visits or stigma from daily pills.

But upheaval in U.S. healthcare — including cuts to public health agencies and Medicaid — and slashing of American foreign aid to fight HIV are clouding the prospects.

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Millett said “gaping holes in the system” in the U.S. and globally “are going to make it difficult for us to make sure we not only get lenacapavir into people’s bodies but make sure they come back” even as little as twice a year.

Gilead’s drug already is sold to treat HIV under the brand name Sunlenca. The prevention dose will be sold under a different name, Yeztugo. It’s given as two injections under the skin of the abdomen, leaving a small “depot” of medication to slowly absorb into the body.

Gilead didn’t immediately announce its price. The drug only prevents HIV transmission – it doesn’t block other sexually transmitted diseases.

Global efforts at ending the HIV pandemic by 2030 have stalled. There still are more than 30,000 new infections in the U.S. each year and about 1.3 million worldwide.

Only about 400,000 Americans already use some form of PrEP, a fraction of those estimated to benefit. A recent study found states with high use of PrEP saw a decrease in HIV infections, while rates continued rising elsewhere.

About half of new infections are in women, who often need protection they can use without a partner’s knowledge or consent. One rigorous study in South Africa and Uganda compared more than 5,300 sexually active young women and teen girls given twice-yearly lenacapavir or the daily pills. There were no HIV infections in those receiving the shot while about 2% in the comparison group caught HIV from infected sex partners.

A second study found the twice-yearly shot nearly as effective in gay men and gender-nonconforming people in the U.S. and in several other countries hard-hit by HIV.

Ian Haddock of Houston had tried PrEP off and on since 2015 but he jumped at the chance to participate in the lenacapavir study and continues with the twice-yearly shots as part of the research follow-up.

“Now I forget that I’m on PrEP because I don’t have to carry around a pill bottle,” said Haddock, who leads the Normal Anomaly Initiative, a nonprofit serving Black LGBTQ+ communities.

“Men, women, gay, straight – it really just kinds of expands the opportunity for prevention,” he added. Just remembering a clinic visit every six months “is a powerful tool versus constantly having to talk about, like, condoms, constantly making sure you’re taking your pill every day.”

“Everyone in every country who’s at risk of HIV needs access to PrEP,” added Dr. Gordon Crofoot of Houston, who helped lead the study in men. “We need to get easier access to PrEP that’s highly effective like this is.”

The Associated Press Health and Science Department receives support from the Howard Hughes Medical Institute’s Department of Science Education and the Robert Wood Johnson Foundation. The AP is solely responsible for all content.