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Differential neutralization and inhibition of SARS-CoV-2 variants by antibodies elicited by COVID-19 mRNA vaccines.

Authors :
Wang L
Kainulainen MH
Jiang N
Di H
Bonenfant G
Mills L
Currier M
Shrivastava-Ranjan P
Calderon BM
Sheth M
Mann BR
Hossain J
Lin X
Lester S
Pusch EA
Jones J
Cui D
Chatterjee P
Jenks MH
Morantz EK
Larson GP
Hatta M
Harcourt JL
Tamin A
Li Y
Tao Y
Zhao K
Lacek K
Burroughs A
Wang W
Wilson M
Wong T
Park SH
Tong S
Barnes JR
Tenforde MW
Self WH
Shapiro NI
Exline MC
Files DC
Gibbs KW
Hager DN
Patel M
Halpin AL
McMullan LK
Lee JS
Xia H
Xie X
Shi PY
Davis CT
Spiropoulou CF
Thornburg NJ
Oberste MS
Dugan VG
Wentworth DE
Zhou B
Source :
Nature communications [Nat Commun] 2022 Jul 27; Vol. 13 (1), pp. 4350. Date of Electronic Publication: 2022 Jul 27.
Publication Year :
2022

Abstract

The evolution of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in the emergence of new variant lineages that have exacerbated the COVID-19 pandemic. Some of those variants were designated as variants of concern/interest (VOC/VOI) by national or international authorities based on many factors including their potential impact on vaccine-mediated protection from disease. To ascertain and rank the risk of VOCs and VOIs, we analyze the ability of 14 variants (614G, Alpha, Beta, Gamma, Delta, Epsilon, Zeta, Eta, Theta, Iota, Kappa, Lambda, Mu, and Omicron) to escape from mRNA vaccine-induced antibodies. The variants show differential reductions in neutralization and replication by post-vaccination sera. Although the Omicron variant (BA.1, BA.1.1, and BA.2) shows the most escape from neutralization, sera collected after a third dose of vaccine (booster sera) retain moderate neutralizing activity against that variant. Therefore, vaccination remains an effective strategy during the COVID-19 pandemic.<br /> (© 2022. This is a U.S. Government work and not under copyright protection in the US; foreign copyright protection may apply.)

Details

Language :
English
ISSN :
2041-1723
Volume :
13
Issue :
1
Database :
MEDLINE
Journal :
Nature communications
Publication Type :
Academic Journal
Accession number :
35896523
Full Text :
https://doi.org/10.1038/s41467-022-31929-6