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Biochemist Peter Kim receives $18 million grant to develop broadly effective antiviral vaccine
Peter Kim

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Awards & Honors October 06, 2025

Biochemist Peter Kim receives $18 million grant to develop broadly effective antiviral vaccine

By Bruce Goldman

The goal is to develop vaccines against the deadly Ebola, Marburg and related viruses, including those that have yet to emerge.

The Coalition for Epidemic Preparedness Innovations has awarded a team led by Peter Kim, PhD, the Virginia and D.K. Ludwig Professor in Biochemistry, a four-year, $18 million grant to develop vaccines that could offer broad protection from filoviruses, a family of viruses that includes the highly fatal Ebola and Marburg.

CEPI, based in Oslo, Norway, is an international organization with the goal of accelerating the development of vaccines and other biologic countermeasures against epidemic or pandemic threats.

Kim and his fellow researchers will use the award to design and test new vaccine candidates that could provide all-in-one protection against currently known filoviruses as well as those that are limited to nonhuman hosts but could jump from animals to humans.

“We aim to create a single, broad-spectrum vaccine that will protect against three viruses causing frequent outbreaks in Africa — Zaire Ebola virus, Sudan Ebola virus and Marburg virus — which, collectively, have an average fatality rate of around 50%,” said Kim, the project’s principal investigator.

The researchers will use artificial intelligence to design immunogens — the substances in a vaccine that provoke an immune response — that, they hope, will protect against more than one filovirus. These immunogens will be presented on a ferritin-based protein-nanoparticle framework to create a range of candidates that will be tested in laboratory and animal studies. The researchers will rapidly advance the most promising vaccine candidate to the point where it is ready to quickly enter clinical trials should an unknown filovirus outbreak emerge.

The ferritin nanoparticle-based vaccine is favorable for use in low- and middle-income countries as it does not require frozen storage, which can limit access in low-resource settings. It has already been tested in Phase I clinical trials for influenza and COVID-19 vaccines, which were shown to be safe.

“Our goal is to make the vaccine stable enough that it will maintain stability without requiring freezer storage and that it will be inexpensive to manufacture,” Kim said.

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Senior science writer

Bruce Goldman

Bruce Goldman, MS, is a senior science writer in the Office of Communications. He covers immunology, infectious disease, transplantation, neurosciences, neurosurgery, bioengineering, molecular and cellular physiology, and biochemistry. A recovering philosophy major from the University of Wisconsin, he’s done his best to cover his tracks by obtaining yet another bachelor’s degree, this time in engineering physics from the University of Colorado, and attending finishing school, in cell biology, at Harvard University, where he received an award for his teaching of an undergraduate biology course. Articles he has written while at Stanford Medicine have won well over a dozen awards from the Association of American Medical Colleges and the Council for Advancement and Support of Education. He is a member of the National Association of Science Writers and the co-author of two books about the future: 2020 Visions: Long View of a Changing World (Portable Stanford) and Fast Forward (Harper). Once upon a time, he drove a car to Afghanistan. He can play guitar with his toes, but only while fast asleep and dreaming.