Mosaic nanoparticles elicit cross-reactive immune responses to zoonotic coronaviruses in mice

Author:

Cohen Alexander A.1ORCID,Gnanapragasam Priyanthi N. P.1,Lee Yu E.1ORCID,Hoffman Pauline R.1ORCID,Ou Susan1ORCID,Kakutani Leesa M.1ORCID,Keeffe Jennifer R.1ORCID,Wu Hung-Jen2ORCID,Howarth Mark2ORCID,West Anthony P.1ORCID,Barnes Christopher O.1,Nussenzweig Michel C.3ORCID,Bjorkman Pamela J.1ORCID

Affiliation:

1. Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

2. Department of Biochemistry, University of Oxford, Oxford OX1 3QU, UK.

3. Laboratory of Molecular Immunology, The Rockefeller University, New York, NY 10065, USA.

Abstract

Fighting zoonotic coronaviruses In the past 20 years, three betacoronaviruses thought to have originated in bats have caused devastating disease in humans. The global pandemic caused by the latest such virus, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), highlights the need to protect against other strains that could present a threat to humans. Cohen et al. constructed nanoparticles displaying the protein domain that binds the host cell receptor (receptor-binding domain or RBD), either a homotypic SARS-CoV-2 particle or mosaic particles displaying RBDs from four or eight different betacoronaviruses. In mice, antibodies to the SARS-CoV-2 RBD were elicited just as well by mosaic particles as by homotypic nanoparticles. The mosaic nanoparticles elicited antibodies that, beyond recognizing the strains displayed, also recognized mismatched strains. Science , this issue p. 735

Funder

National Institutes of Health

Caltech Merkin Institute for Translational Research

George Mason University Fast Grant

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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