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Journal article

Vaccination with SARS-CoV-2 variants of concern protects mice from challenge with wild-type virus

Abstract:
Funder: open philanthropy projectFunder: jpb foundationVaccines against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) have been highly efficient in protecting against Coronavirus Disease 2019 (COVID-19). However, the emergence of viral variants that are more transmissible and, in some cases, escape from neutralizing antibody responses has raised concerns. Here, we evaluated recombinant protein spike antigens derived from wild-type SARS-CoV-2 and from variants B.1.1.7, B.1.351, and P.1 for their immunogenicity and protective effect in vivo against challenge with wild-type SARS-CoV-2 in the mouse model. All proteins induced high neutralizing antibodies against the respective viruses but also induced high cross-neutralizing antibody responses. The decline in neutralizing titers between variants was moderate, with B.1.1.7-vaccinated animals having a maximum fold reduction of 4.8 against B.1.351 virus. P.1 induced the most cross-reactive antibody responses but was also the least immunogenic in terms of homologous neutralization titers. However, all antigens protected from challenge with wild-type SARS-CoV-2 in a mouse model
Publication status:
Published
Peer review status:
Peer reviewed

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Role:
Author
ORCID:
0000-0002-8029-8227
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Role:
Author
ORCID:
0000-0002-6754-7209
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Role:
Author
ORCID:
0000-0002-5314-8530


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Funder identifier:
10.13039/100000060
Grant:
HHSN272201400008C
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Funder identifier:
10.13039/100007457
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Funder identifier:
10.13039/100014895


Publisher:
Public Library of Science
Journal:
PLoS Biology More from this journal
Volume:
19
Issue:
12
Pages:
e3001384-e3001384
Publication date:
2021-12-16
DOI:
EISSN:
1545-7885
ISSN:
1544-9173


Language:
English
Keywords:
Pubs id:
1230965
Local pid:
pubs:1230965
Source identifiers:
W4200572066
Deposit date:
2026-04-08
ARK identifier:
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