The vaccine advisory panel for the Centers for Disease Control and Prevention (CDC) on Thursday voted in favor of delaying the administration of the vaccine for measles, mumps, rubella and varicella (chickenpox), commonly called the MMRV. 

The CDC’s Advisory Committee on Immunization Practices (ACIP) is scheduled to vote on three questions during Thursday’s meeting. Five of the members were appointed to the committee just this week. 

First, the panel was asked to consider whether the combined vaccine for measles, mumps, rubella and varicella should not be recommended for children younger than 4. The panel voted 8-3 to approve the change, with one member abstaining.  

This vote would have meant that children who receive their vaccinations through the Vaccines For Children federal program will not be able to receive the MMRV shot until they’re 4 years old. The committee voted, however, in a follow-up motion against aligning the VFC with the recommendation, changing nothing in terms of what the program covers for the time being.

Children can normally get the MMRV vaccine beginning at 12 months of age.

ACIP members Hilary Blackburn, Cody Meissner and Joseph Hibbeln were the three members to vote no on the recommendation.

The panel decided to delay the votes on Hep B vaccine guidance until Friday, when they will also vote on COVID-19 vaccine guidance.

The meeting Thursday was tense, with panel members very aware of the heightened attention on their vote following the firing and resignation of top CDC officials and the growing scrutiny of Health and Human Services Secretary Robert F. Kennedy Jr. on Capitol Hill. 

“We are currently experiencing heated controversies about vaccines. And a key question is, who can you trust? Here’s my advice, when there are different scientific views, only trust scientists who are willing to engage with and publicly debate the scientists with other views,” ACIP Chair Martin Kulldorff said at the start of the meeting. 

The core argument against allowing MMRV vaccinations under the age of 4 appeared to be the slightly increased risk of febrile seizures linked to the injections. Febrile seizures are caused by fevers of all types.

Febrile seizures are common and generally don’t cause any long-lasting effects, though members of the panel noted that they can be traumatic for families to experience. The risk is lower when vaccines are administered when a child is older. 

Kulldorff argued that the risk of seizures could scare parents away from getting the MMRV vaccination. 

Members of the committee who opposed the motion argued that changing the recommendation took away parents’ right to choose when and how to vaccinate their children.

Jason Goldman, president of the American College of Physicians, lambasted the motion as lacking supporting evidence and causing more confusion than benefits.

“When you make this recommendation, you now give license to insurance companies and the Vaccine For Children program not to cover this vaccine. And finally, you are taking away the choice of parents to have informed consent and discussion with their physician on what they want to do for the health and benefit of their children,” Goldman told the committee during public comments.

Others warned that this motion will cause a drop in vaccination rates.

“The disadvantage of giving two doses, or as was suggested, separating the two doses is that we know compliance falls. And the advantage of combination vaccines is that children and adults are more likely to complete the vaccine requirements if it’s given as a single dose,” Meissner said.

According to Andy Pavia, professor and pediatric infectious disease expert at the University of Utah, the immunization practices considered Thursday are “settled science.” 

“This new handpicked ACIP has chosen to address issues that were relatively settled science for which there’s no new information that really suggests a need to do a detailed review,” Pavia said shortly before the vote. “And has already proposed votes that would change things even before hearing the data, and it suggests a great deal of prejudgment of the issues.” 

Former CDC Chief Medical Officer Debra Houry told the Senate Committee on Health, Education, Labor, and Pensions the day before the meeting that the agenda and questions discussed by ACIP were developed almost exclusively by political appointees, with little input from scientific staffers from her agency.  

According to Houry, CDC scientists had no input on the first questions which the committee voted for on Thursday, only being asked for contributions on the COVID-19 vaccine vote scheduled for Friday. 

This story was updated at 6:11 p.m.