Literature DB >> 34214046

Chimeric spike mRNA vaccines protect against Sarbecovirus challenge in mice.

David R Martinez1, Alexandra Schäfer2, Sarah R Leist2, Gabriela De la Cruz3, Ande West2, Elena N Atochina-Vasserman4, Lisa C Lindesmith2, Norbert Pardi4, Robert Parks5, Maggie Barr5, Dapeng Li5, Boyd Yount2, Kevin O Saunders5, Drew Weissman4, Barton F Haynes5, Stephanie A Montgomery6, Ralph S Baric1.   

Abstract

The emergence of severe acute respiratory syndrome coronavirus (SARS-CoV) in 2003 and SARS-CoV-2 in 2019 highlights the need to develop universal vaccination strategies against the broader Sarbecovirus subgenus. Using chimeric spike designs, we demonstrate protection against challenge from SARS-CoV, SARS-CoV-2, SARS-CoV-2 B.1.351, bat CoV (Bt-CoV) RsSHC014, and a heterologous Bt-CoV WIV-1 in vulnerable aged mice. Chimeric spike messenger RNAs (mRNAs) induced high levels of broadly protective neutralizing antibodies against high-risk Sarbecoviruses. By contrast, SARS-CoV-2 mRNA vaccination not only showed a marked reduction in neutralizing titers against heterologous Sarbecoviruses, but SARS-CoV and WIV-1 challenge in mice resulted in breakthrough infections. Chimeric spike mRNA vaccines efficiently neutralized D614G, mink cluster five, and the UK B.1.1.7 and South African B.1.351 variants of concern. Thus, multiplexed-chimeric spikes can prevent SARS-like zoonotic coronavirus infections with pandemic potential.
Copyright © 2021 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works.

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Year:  2021        PMID: 34214046      PMCID: PMC8899822          DOI: 10.1126/science.abi4506

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


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2.  Synthetic recombinant bat SARS-like coronavirus is infectious in cultured cells and in mice.

Authors:  Michelle M Becker; Rachel L Graham; Eric F Donaldson; Barry Rockx; Amy C Sims; Timothy Sheahan; Raymond J Pickles; Davide Corti; Robert E Johnston; Ralph S Baric; Mark R Denison
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3.  Structural basis for broad coronavirus neutralization.

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Journal:  Nat Struct Mol Biol       Date:  2021-05-12       Impact factor: 15.369

4.  Memory CD8 T cells mediate severe immunopathology following respiratory syncytial virus infection.

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Journal:  PLoS Pathog       Date:  2018-01-02       Impact factor: 6.823

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10.  Safety and Immunogenicity of Two RNA-Based Covid-19 Vaccine Candidates.

Authors:  Edward E Walsh; Robert W Frenck; Ann R Falsey; Nicholas Kitchin; Judith Absalon; Alejandra Gurtman; Stephen Lockhart; Kathleen Neuzil; Mark J Mulligan; Ruth Bailey; Kena A Swanson; Ping Li; Kenneth Koury; Warren Kalina; David Cooper; Camila Fontes-Garfias; Pei-Yong Shi; Özlem Türeci; Kristin R Tompkins; Kirsten E Lyke; Vanessa Raabe; Philip R Dormitzer; Kathrin U Jansen; Uğur Şahin; William C Gruber
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  50 in total

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