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SARS-CoV-2 neutralizing antibodies: Longevity, breadth, and evasion by emerging viral variants.

Authors :
Fiona Tea
Alberto Ospina Stella
Anupriya Aggarwal
David Ross Darley
Deepti Pilli
Daniele Vitale
Vera Merheb
Fiona X Z Lee
Philip Cunningham
Gregory J Walker
Christina Fichter
David A Brown
William D Rawlinson
Sonia R Isaacs
Vennila Mathivanan
Markus Hoffmann
Stefan Pöhlman
Ohan Mazigi
Daniel Christ
Dominic E Dwyer
Rebecca J Rockett
Vitali Sintchenko
Veronica C Hoad
David O Irving
Gregory J Dore
Iain B Gosbell
Anthony D Kelleher
Gail V Matthews
Fabienne Brilot
Stuart G Turville
Source :
PLoS Medicine, Vol 18, Iss 7, p e1003656 (2021)
Publication Year :
2021
Publisher :
Public Library of Science (PLoS), 2021.

Abstract

The Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) antibody neutralization response and its evasion by emerging viral variants and variant of concern (VOC) are unknown, but critical to understand reinfection risk and breakthrough infection following vaccination. Antibody immunoreactivity against SARS-CoV-2 antigens and Spike variants, inhibition of Spike-driven virus-cell fusion, and infectious SARS-CoV-2 neutralization were characterized in 807 serial samples from 233 reverse transcription polymerase chain reaction (RT-PCR)-confirmed Coronavirus Disease 2019 (COVID-19) individuals with detailed demographics and followed up to 7 months. A broad and sustained polyantigenic immunoreactivity against SARS-CoV-2 Spike, Membrane, and Nucleocapsid proteins, along with high viral neutralization, was associated with COVID-19 severity. A subgroup of "high responders" maintained high neutralizing responses over time, representing ideal convalescent plasma donors. Antibodies generated against SARS-CoV-2 during the first COVID-19 wave had reduced immunoreactivity and neutralization potency to emerging Spike variants and VOC. Accurate monitoring of SARS-CoV-2 antibody responses would be essential for selection of optimal responders and vaccine monitoring and design.

Subjects

Subjects :
Medicine

Details

Language :
English
ISSN :
15491277 and 15491676
Volume :
18
Issue :
7
Database :
Directory of Open Access Journals
Journal :
PLoS Medicine
Publication Type :
Academic Journal
Accession number :
edsdoj.9d1dac9be74d4ec29e5d0a3a9bd84bf7
Document Type :
article
Full Text :
https://doi.org/10.1371/journal.pmed.1003656