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SARS-COV-2 Variants: Differences and Potential of Immune Evasion.

Authors :
Hirabara SM
Serdan TDA
Gorjao R
Masi LN
Pithon-Curi TC
Covas DT
Curi R
Durigon EL
Source :
Frontiers in cellular and infection microbiology [Front Cell Infect Microbiol] 2022 Jan 18; Vol. 11, pp. 781429. Date of Electronic Publication: 2022 Jan 18 (Print Publication: 2021).
Publication Year :
2022

Abstract

The structural spike (S) glycoprotein of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) plays an essential role in infection and is an important target for neutralizing antibody recognition. Mutations in the S gene can generate variants of concern (VOCs), which improve "viral fitness" through selective or survival advantages, such as increased ACE-2 receptor affinity, infectivity, viral replication, higher transmissibility, resistance to neutralizing antibodies and immune escape, increasing disease severity and reinfection risk. Five VOCs have been recognized and include B.1.1.7 (U.K.), B.1.351 (South Africa), P.1 (Brazil), B.1.617.2 (India), and B.1.1.529 (multiple countries). In this review, we addressed the following critical points concerning VOCs: a) characteristics of the SARS-CoV-2 VOCs with mutations in the S gene; b) possible evasion of variants from neutralizing antibodies generated through vaccination, previous infection, or immune therapies; c) potential risk of new pandemic waves induced by the variants worldwide; and d) perspectives for further studies and actions aimed at preventing or reducing the impact of new variants during the current COVID-19 pandemic.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2022 Hirabara, Serdan, Gorjao, Masi, Pithon-Curi, Covas, Curi and Durigon.)

Details

Language :
English
ISSN :
2235-2988
Volume :
11
Database :
MEDLINE
Journal :
Frontiers in cellular and infection microbiology
Publication Type :
Academic Journal
Accession number :
35118007
Full Text :
https://doi.org/10.3389/fcimb.2021.781429