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SARS-CoV-2 variants, spike mutations and immune escape.

Published version
Peer-reviewed

Type

Article

Change log

Authors

Carabelli, Alessandro M  ORCID logo  https://orcid.org/0000-0003-3625-4021
Gupta, Ravindra K 

Abstract

Although most mutations in the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) genome are expected to be either deleterious and swiftly purged or relatively neutral, a small proportion will affect functional properties and may alter infectivity, disease severity or interactions with host immunity. The emergence of SARS-CoV-2 in late 2019 was followed by a period of relative evolutionary stasis lasting about 11 months. Since late 2020, however, SARS-CoV-2 evolution has been characterized by the emergence of sets of mutations, in the context of 'variants of concern', that impact virus characteristics, including transmissibility and antigenicity, probably in response to the changing immune profile of the human population. There is emerging evidence of reduced neutralization of some SARS-CoV-2 variants by postvaccination serum; however, a greater understanding of correlates of protection is required to evaluate how this may impact vaccine effectiveness. Nonetheless, manufacturers are preparing platforms for a possible update of vaccine sequences, and it is crucial that surveillance of genetic and antigenic changes in the global virus population is done alongside experiments to elucidate the phenotypic impacts of mutations. In this Review, we summarize the literature on mutations of the SARS-CoV-2 spike protein, the primary antigen, focusing on their impacts on antigenicity and contextualizing them in the protein structure, and discuss them in the context of observed mutation frequencies in global sequence datasets.

Description

Keywords

Humans, Amino Acids, Epitopes, Antigenic Variation, Protein Conformation, Mutation, Immune Evasion, Spike Glycoprotein, Coronavirus, COVID-19, SARS-CoV-2, COVID-19 Vaccines

Journal Title

Nature reviews. Microbiology

Conference Name

Journal ISSN

1740-1526

Volume Title

19

Publisher

Sponsorship
Wellcome Trust (220977/Z/20/Z, 206298/Z/17/Z)
Biotechnology and Biological Sciences Research Council (BB/R012679/1)
European Research Council (725422)