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Potent cross-reactive antibodies following Omicron breakthrough in vaccinees.

Authors :
Nutalai R
Zhou D
Tuekprakhon A
Ginn HM
Supasa P
Liu C
Huo J
Mentzer AJ
Duyvesteyn HME
Dijokaite-Guraliuc A
Skelly D
Ritter TG
Amini A
Bibi S
Adele S
Johnson SA
Constantinides B
Webster H
Temperton N
Klenerman P
Barnes E
Dunachie SJ
Crook D
Pollard AJ
Lambe T
Goulder P
Paterson NG
Williams MA
Hall DR
Mongkolsapaya J
Fry EE
Dejnirattisai W
Ren J
Stuart DI
Screaton GR
Source :
Cell [Cell] 2022 Jun 09; Vol. 185 (12), pp. 2116-2131.e18. Date of Electronic Publication: 2022 May 20.
Publication Year :
2022

Abstract

Highly transmissible Omicron variants of SARS-CoV-2 currently dominate globally. Here, we compare neutralization of Omicron BA.1, BA.1.1, and BA.2. BA.2 RBD has slightly higher ACE2 affinity than BA.1 and slightly reduced neutralization by vaccine serum, possibly associated with its increased transmissibility. Neutralization differences between sub-lineages for mAbs (including therapeutics) mostly arise from variation in residues bordering the ACE2 binding site; however, more distant mutations S371F (BA.2) and R346K (BA.1.1) markedly reduce neutralization by therapeutic antibody Vir-S309. In-depth structure-and-function analyses of 27 potent RBD-binding mAbs isolated from vaccinated volunteers following breakthrough Omicron-BA.1 infection reveals that they are focused in two main clusters within the RBD, with potent right-shoulder antibodies showing increased prevalence. Selection and somatic maturation have optimized antibody potency in less-mutated epitopes and recovered potency in highly mutated epitopes. All 27 mAbs potently neutralize early pandemic strains, and many show broad reactivity with variants of concern.<br />Competing Interests: Declaration of interests G.R.S. sits on the GSK Vaccines Scientific Advisory Board and is a founder member of RQ Biotechnology. Oxford University holds intellectual property related to the Oxford-Astra Zeneca vaccine. A.J.P. is Chair of UK DHSC Joint Committee on Vaccination & Immunisation (JCVI) but does not participate in the JCVI COVID-19 committee and is a member of the WHO’s SAGE. The views expressed in this article do not necessarily represent the views of DHSC, JCVI, or WHO. The University of Oxford has entered into a partnership with AstraZeneca on coronavirus vaccine development. T.L. is named as an inventor on a patent application covering this SARS-CoV-2 vaccine and was a consultant to Vaccitech for an unrelated project whilst the study was conducted. The University of Oxford has protected intellectual property disclosed in this publication. S.J.D. is a Scientific Advisor to the Scottish Parliament on COVID-19.<br /> (Copyright © 2022 The Author(s). Published by Elsevier Inc. All rights reserved.)

Details

Language :
English
ISSN :
1097-4172
Volume :
185
Issue :
12
Database :
MEDLINE
Journal :
Cell
Publication Type :
Academic Journal
Accession number :
35662412
Full Text :
https://doi.org/10.1016/j.cell.2022.05.014