| Literature DB >> 34214046 |
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.Entities:
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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