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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.
Emerging SARS-CoV-2 variants raise concerns on immune evasion. Here, the authors evaluate the neutralization efficiency of COVID-19 mRNA vaccinee sera against representative viruses of 13 WHO-designated SARS-CoV-2 variants of concern/interest.
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1 COVID-19 Emergency Response, Centers for Disease Control and Prevention, Atlanta, USA (GRID:grid.416738.f) (ISNI:0000 0001 2163 0069)
2 Vanderbilt University, Nashville, USA (GRID:grid.152326.1) (ISNI:0000 0001 2264 7217)
3 Harvard University, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
4 Ohio State University, Columbus, USA (GRID:grid.261331.4) (ISNI:0000 0001 2285 7943)
5 Wake Forest Baptist Medical Center, Winston-Salem, USA (GRID:grid.412860.9) (ISNI:0000 0004 0459 1231)
6 Johns Hopkins University, Baltimore, USA (GRID:grid.21107.35) (ISNI:0000 0001 2171 9311)
7 University of Texas Medical Branch, Galveston, USA (GRID:grid.176731.5) (ISNI:0000 0001 1547 9964)