The Impact of Evolving SARS-CoV-2 Mutations and Variants on COVID-19 Vaccines.


Journal

mBio
ISSN: 2150-7511
Titre abrégé: mBio
Pays: United States
ID NLM: 101519231

Informations de publication

Date de publication:
26 04 2022
Historique:
pubmed: 31 3 2022
medline: 29 4 2022
entrez: 30 3 2022
Statut: ppublish

Résumé

The emergence of several new variants of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in recent months has raised concerns around the potential impact on ongoing vaccination programs. Data from clinical trials and real-world evidence suggest that current vaccines remain highly effective against the alpha variant (B.1.1.7), while some vaccines have reduced efficacy and effectiveness against symptomatic disease caused by the beta variant (B.1.351) and the delta variant (B.1.617.2); however, effectiveness against severe disease and hospitalization caused by delta remains high. Although data on the effectiveness of the primary regimen against omicron (B.1.1.529) are limited, booster programs using mRNA vaccines have been shown to restore protection against infection and symptomatic disease (regardless of the vaccine used for the primary regimen) and maintain high effectiveness against hospitalization. However, effectiveness against infection and symptomatic disease wanes with time after the booster dose. Studies have demonstrated reductions of varying magnitude in neutralizing activity of vaccine-elicited antibodies against a range of SARS-CoV-2 variants, with the omicron variant in particular exhibiting partial immune escape. However, evidence suggests that T-cell responses are preserved across vaccine platforms, regardless of variant of concern. Nevertheless, various mitigation strategies are under investigation to address the potential for reduced efficacy or effectiveness against current and future SARS-CoV-2 variants, including modification of vaccines for certain variants (including omicron), multivalent vaccine formulations, and different delivery mechanisms.

Identifiants

pubmed: 35352979
doi: 10.1128/mbio.02979-21
pmc: PMC9040821
doi:

Substances chimiques

Antibodies, Viral 0
COVID-19 Vaccines 0
Viral Vaccines 0

Types de publication

Journal Article Review Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0297921

Subventions

Organisme : NIGMS NIH HHS
ID : P20 GM121307
Pays : United States
Organisme : BioNtech
ID : N/A

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Auteurs

Gary McLean (G)

School of Human Sciences, London Metropolitan Universitygrid.23231.31 and National Heart and Lung Institute, Imperial College London, London, United Kingdom.

Jeremy Kamil (J)

Louisiana State University Health, Shreveport, Louisiana, USA.

Benhur Lee (B)

Icahn School of Medicine at Mount Sinai, New York, New York, USA.

Penny Moore (P)

Centre for HIV and STIs, National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
MRC Antibody Immunity Research Unit, School of Pathology, The University of the Witwatersrand, Johannesburg, South Africa.

Thomas F Schulz (TF)

Institute of Virology, Hannover Medical Schoolgrid.10423.34, Hannover, Germany.
Cluster of Excellence 2155 RESIST, Hannover, Germany.
German Centre for Infection Research, Hannover-Braunschweig Site, Germany.

Özlem Türeci (Ö)

BioNTech, Mainz, Germany.

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