A SARS-CoV-2 ferritin nanoparticle vaccine elicits protective immune responses in nonhuman primates

Michael Joyce(Henry M. Jackson Foundation), Hannah A. D. King(Henry M. Jackson Foundation), Inès Lakhal-Naouar(Henry M. Jackson Foundation), Aslaa Ahmed(Naval Medical Research Command), Kristina K. Peachman(Chemring Countermeasures (United Kingdom)), Camila Macedo Cincotta(Henry M. Jackson Foundation), Caroline Subra(Henry M. Jackson Foundation), Rita E. Chen(Washington University in St. Louis), Paul V. Thomas(Henry M. Jackson Foundation), Wei‐Hung Chen(Henry M. Jackson Foundation), Rajeshwer S. Sankhala(Henry M. Jackson Foundation), Agnes Hajduczki(Henry M. Jackson Foundation), Elizabeth J. Martinez(Henry M. Jackson Foundation), Caroline E. Peterson(Henry M. Jackson Foundation), William C. Chang(Henry M. Jackson Foundation), Misook Choe(Henry M. Jackson Foundation), Clayton Smith(National Institutes of Health), Parker J. Lee(Henry M. Jackson Foundation), Jarrett A. Headley(Henry M. Jackson Foundation), Mekdi G. Taddese(Henry M. Jackson Foundation), Hanne Andersen Elyard(Bioqual), Anthony Cook(Bioqual), Alexander Anderson(Oak Ridge Associated Universities), Kathryn McGuckin Wuertz(Military University), Ming Dong(Henry M. Jackson Foundation), Isabella Swafford(Henry M. Jackson Foundation), James Brett Case(Washington University in St. Louis), Jeffrey R. Currier(Naval Medical Research Command), Kerri G. Lal(Henry M. Jackson Foundation), Sebastian Molnar(Henry M. Jackson Foundation), Manoj S. Nair(Aaron Diamond AIDS Research Center), Vincent Dussupt(Henry M. Jackson Foundation), Sharon P. Daye(Infrared Fiber Systems (United States)), Xiankun Zeng(United States Army Medical Research Institute of Infectious Diseases), Erica K. Barkei(Infrared Fiber Systems (United States)), Hilary Staples(Texas Biomedical Research Institute), Kendra J. Alfson(Texas Biomedical Research Institute), Ricardo Carrion(Texas Biomedical Research Institute), Shelly J. Krebs(Henry M. Jackson Foundation), Dominic Paquin‐Proulx(Henry M. Jackson Foundation), Nicos Karasavva(Henry M. Jackson Foundation), Victoria R. Polonis(Military University), Linda L. Jagodzinski(Chemring Countermeasures (United Kingdom)), Mihret F. Amare(Henry M. Jackson Foundation), Sandhya Vasan(Henry M. Jackson Foundation), Paul T. Scott(Walter Reed Army Institute of Research), Yaoxing Huang(Aaron Diamond AIDS Research Center), David D. Ho(Aaron Diamond AIDS Research Center), Natalia de Val(National Institutes of Health), Michael Diamond(Washington University in St. Louis), Mark G. Lewis(Bioqual), Mangala Rao(Military University), Gary R. Matyas(Military University), Gregory D. Gromowski(Naval Medical Research Command), Sheila A. Peel(Chemring Countermeasures (United Kingdom)), Nelson L. Michael(Infrared Fiber Systems (United States)), Diane L. Bolton(Henry M. Jackson Foundation), Kayvon Modjarrad(Walter Reed Army Institute of Research)
Science Translational Medicine
February 16, 2022
Cited by 142Open Access
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Abstract

The emergence of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) variants stresses the continued need for next-generation vaccines that confer broad protection against coronavirus disease 2019 (COVID-19). We developed and evaluated an adjuvanted SARS-CoV-2 spike ferritin nanoparticle (SpFN) vaccine in nonhuman primates. High-dose (50 μg) SpFN vaccine, given twice 28 days apart, induced a Th1-biased CD4 T cell helper response and elicited neutralizing antibodies against SARS-CoV-2 wild-type and variants of concern, as well as against SARS-CoV-1. These potent humoral and cell-mediated immune responses translated into rapid elimination of replicating virus in the upper and lower airways and lung parenchyma of nonhuman primates following high-dose SARS-CoV-2 respiratory challenge. The immune response elicited by SpFN vaccination and resulting efficacy in nonhuman primates supports the utility of SpFN as a vaccine candidate for SARS-causing betacoronaviruses.


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