mRNA vaccination boosts cross-variant neutralizing antibodies elicited by SARS-CoV-2 infection

Author:

Stamatatos Leonidas12ORCID,Czartoski Julie1ORCID,Wan Yu-Hsin1ORCID,Homad Leah J.1ORCID,Rubin Vanessa1ORCID,Glantz Hayley1ORCID,Neradilek Moni1ORCID,Seydoux Emilie1ORCID,Jennewein Madeleine F.1ORCID,MacCamy Anna J.1ORCID,Feng Junli1,Mize Gregory1ORCID,De Rosa Stephen C.13ORCID,Finzi Andrés456ORCID,Lemos Maria P.1ORCID,Cohen Kristen W.1ORCID,Moodie Zoe1ORCID,McElrath M. Juliana127ORCID,McGuire Andrew T.123ORCID

Affiliation:

1. Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

2. Department of Global Health, University of Washington, Seattle, WA, USA.

3. Department of Laboratory Medicine and Pathology, University of Washington, Seattle, WA, USA.

4. Centre de Recherche du CHUM, Montréal, QC, Canada.

5. Département de Microbiologie, Infectiologie et Immunologie, Université de Montréal, Montreal, QC, Canada.

6. Department of Microbiology and Immunology, McGill University, Montreal, QC, Canada.

7. Department of Medicine, University of Washington, Seattle, WA, USA.

Abstract

Boosterism could save lives Postinfection immune protection against severe acute respiratory syndrome coronavirus 2 reinfection is not fully understood. It will be devastating if waves of new variants emerge that undermine natural immune protection. Stamatatos et al. investigated immune responsiveness 4 to 8 months after previously infected individuals were given a messenger RNA–based vaccine developed for the original Wuhan variant (see the Perspective by Crotty). Before vaccination, postinfection serum antibody neutralization responses to virus variants were variable and weak. Vaccination elevated postinfection serum-neutralizing capacity approximately 1000-fold against Wuhan-Hu-1 and other strains, and serum neutralization against the variant B.1.351 was enhanced. Although responses were relatively muted against the variant, they still showed characteristic memory responses. Vaccination with the Wuhan-Hu-1 variant may thus offer a valuable boost to protective responses against subsequent infection with variant viruses. Science , abg9175, this issue p. 1413 ; see also abj2258, p. 1392

Funder

National Institute of Allergy and Infectious Diseases

Paul G. Allen Family Foundation

Fred Hutchinson Cancer Research Center

Joel D. Meyers Endowed Chair

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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