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Isolation of a panel of ultra-potent human antibodies neutralizing SARS-CoV-2 and viral variants of concern

Authors :
Andrey A. Gorchakov
Sergey V. Kulemzin
Sergey V. Guselnikov
Konstantin O. Baranov
Tatyana N. Belovezhets
Ludmila V. Mechetina
Olga Yu. Volkova
Alexander M. Najakshin
Nikolai A. Chikaev
Anton N. Chikaev
Pavel P. Solodkov
Victor F. Larichev
Marina A. Gulyaeva
Alexander G. Markhaev
Yulia V. Kononova
Alexander Yu. Alekseyev
Alexander M. Shestopalov
Gaukhar M. Yusubalieva
Tatiana V. Klypa
Alexander V. Ivanov
Vladimir T. Valuev-Elliston
Vladimir P. Baklaushev
Alexander V. Taranin
Source :
Cell Discovery, Vol 7, Iss 1, Pp 1-15 (2021)
Publication Year :
2021
Publisher :
Nature Publishing Group, 2021.

Abstract

Abstract In the absence of virus-targeting small-molecule drugs approved for the treatment and prevention of COVID-19, broadening the repertoire of potent SARS-CoV-2-neutralizing antibodies represents an important area of research in response to the ongoing pandemic. Systematic analysis of such antibodies and their combinations can be particularly instrumental for identification of candidates that may prove resistant to the emerging viral escape variants. Here, we isolated a panel of 23 RBD-specific human monoclonal antibodies from the B cells of convalescent patients. A surprisingly large proportion of such antibodies displayed potent virus-neutralizing activity both in vitro and in vivo. Four of the isolated nAbs can be categorized as ultrapotent with an apparent IC100 below 16 ng/mL. We show that individual nAbs as well as dual combinations thereof retain activity against currently circulating SARS-CoV-2 variants of concern (such as B.1.1.7, B.1.351, B.1.617, and C.37), as well as against other viral variants. When used as a prophylactics or therapeutics, these nAbs could potently suppress viral replication and prevent lung pathology in SARS-CoV-2-infected hamsters. Our data contribute to the rational development of oligoclonal therapeutic nAb cocktails mitigating the risk of SARS-CoV-2 escape.

Subjects

Subjects :
Cytology
QH573-671

Details

Language :
English
ISSN :
20565968 and 93438737
Volume :
7
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Cell Discovery
Publication Type :
Academic Journal
Accession number :
edsdoj.934387379f904a258f5fe50970741e70
Document Type :
article
Full Text :
https://doi.org/10.1038/s41421-021-00340-8