News Release 

Ultrapotent COVID-19 vaccine candidate designed via computer

Preclinical data published in Cell show the nanoparticle vaccine spurs extremely high levels of protective antibodies in animal models

University of Washington Health Sciences/UW Medicine

Research News

IMAGE

IMAGE: Artist's depiction of an ultrapotent COVID-19 vaccine candidate in which 60 pieces of a coronavirus protein (red) decorate nanoparticles (blue and white). The vaccine candidate was designed using methods developed... view more 

Credit: Ian Haydon/ UW Medicine Institute for Protein Design

An innovative nanoparticle vaccine candidate for the pandemic coronavirus produces virus-neutralizing antibodies in mice at levels ten-times greater than is seen in people who have recovered from COVID-19 infections. Designed by scientists at the University of Washington School of Medicine in Seattle, the vaccine candidate has been transferred to two companies for clinical development.

Compared to vaccination with the soluble SARS-CoV-2 Spike protein, which is what many leading COVID-19 vaccine candidates are based on, the new nanoparticle vaccine produced ten times more neutralizing antibodies in mice, even at a six-fold lower vaccine dose. The data also show a strong B-cell response after immunization, which can be critical for immune memory and a durable vaccine effect. When administered to a single nonhuman primate, the nanoparticle vaccine produced neutralizing antibodies targeting multiple different sites on the Spike protein. Researchers say this may ensure protection against mutated strains of the virus, should they arise. The Spike protein is part of the coronavirus infectivity machinery.

The findings are published in Cell. The lead authors of this paper are Alexandra Walls, a research scientist in the laboratory of David Veesler, who is an associate professor of biochemistry at the UW School of Medicine; and Brooke Fiala, a research scientist in the laboratory of Neil King, who is an assistant professor of biochemistry at the UW School of Medicine.

The vaccine candidate was developed using structure-based vaccine design techniques invented at UW Medicine. It is a self-assembling protein nanoparticle that displays 60 copies of the SARS-CoV-2 Spike protein's receptor-binding domain in a highly immunogenic array. The molecular structure of the vaccine roughly mimics that of a virus, which may account for its enhanced ability to provoke an immune response.

"We hope that our nanoparticle platform may help fight this pandemic that is causing so much damage to our world," said King, inventor of the computational vaccine design technology at the Institute for Protein Design at UW Medicine. "The potency, stability, and manufacturability of this vaccine candidate differentiate it from many others under investigation."

Hundreds of candidate vaccines for COVID-19 are in development around the world. Many require large doses, complex manufacturing, and cold-chain shipping and storage. An ultrapotent vaccine that is safe, effective at low doses, simple to produce and stable outside of a freezer could enable vaccination against COVID-19 on a global scale.

"I am delighted that our studies of antibody responses to coronaviruses led to the design of this promising vaccine candidate," said Veesler, who spearheaded the concept of a multivalent receptor-binding domain-based vaccine.

###

The lead vaccine candidate from this report is being licensed non-exclusively and royalty-free during the pandemic by the University of Washington. One licensee, Icosavax, Inc., a Seattle biotechnology company co-founded in 2019 by King, is currently advancing studies to support regulatory filings and has initiated the U.S. Food and Drug Administtion's Good Manufacturing Practice.

To accelerate progress by Icosavax to the clinic, Amgen, Inc. has agreed to manufacture a key intermediate for these initial clinical studies. Another licensee, SK bioscience Co., Ltd., based in South Korea, is also advancing its own studies to support clinical and further development.

The research reported in Cell was supported by the National Institute of Allergy and Infectious Diseases (DP1AI158186, HHSN272201700059C, 3U01AI42001-02S1), National Institute of General Medical Sciences (R01GM120553, R01GM099989), Bill & Melinda Gates Foundation (OPP1156262, OPP1126258, OPP1159947), Defense Threat Reduction Agency (HDTRA1-18-1-0001), Pew Biomedical Scholars Award, Investigators in the Pathogenesis of Infectious Disease Award from the Burroughs Wellcome Fund, Fast Grants, Animal Models Contract HHSN272201700036I-75N93020F00001, University of Washington's Proteomics Resource (UWPR95794), North Carolina Coronavirus Relief Fund, and gifts from Jodi Green and Mike Halperin and from The Audacious Project.

News release written by Ian Haydon, UW Medicine Institute for Protein Design.

Disclaimer: AAAS and EurekAlert! are not responsible for the accuracy of news releases posted to EurekAlert! by contributing institutions or for the use of any information through the EurekAlert system.