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Resistance of SARS-CoV-2 variants to neutralization by antibodies induced in convalescent patients with COVID-19

Authors :
Kaho Matsumoto
Yukiko Muramoto
Yoshio Koyanagi
Hiroshi Takahashi
Chihiro Motozono
Takeo Kuwata
Terumasa Ikeda
Kazuya Shimura
Takamasa Ueno
Yoji Nagasaki
Yosuke Maeda
Shuzo Matsushita
Takao Hashiguchi
Tsuneyuki Tatsuke
Takeshi Noda
Hajime Iwagoe
Shashwata Biswas
Kazuhiko Fujii
Tateki Suzuki
Mako Toyoda
Mikiko Shimizu
Hiroto Kishi
Noriko Kuramoto
Jiei Sasaki
Hasan Md Zahid
Chiho Onishi
Rumi Minami
Yu Kaku
Yoko Kawanami
Source :
Cell Reports, Cell Reports, Vol 36, Iss 2, Pp 109385-(2021)
Publication Year :
2021
Publisher :
The Author(s)., 2021.

Abstract

Administration of plasma from convalescent patients or neutralizing monoclonal antibodies (mAbs) is potent therapeutic option for COVID-19 caused by SARS-CoV-2 infection. However, SARS-CoV-2 variants with mutations in the spike protein have emerged in many countries. To evaluate the efficacy of neutralizing antibodies induced in convalescent patients against emerging variants, we isolate anti-Spike mAbs from two convalescent patients with COVID-19 infected with prototypic SARS-CoV-2 by single cell sorting of IgG+ memory B cells. Anti-Spike antibody induction is robust in these patients and five mAbs have potent neutralizing activities. The efficacy of most neutralizing mAbs and convalescent plasma samples is maintained against B.1.1.7 and mink cluster 5 variants but is significantly decreased against variants B.1.351 from South Africa and P.1 from Brazil. However, mAbs with a high affinity to the receptor-binding domain remain effective against these neutralization-resistant variants. Rapid spread of these variants significantly impacts antibody-based therapies and vaccine strategies against SARS-CoV-2.<br />Graphical Abstract<br />Kaku et al. demonstrates that efficacy of neutralizing mAbs and convalescent plasmas is maintained against SARS-CoV-2 variants B.1.1.7 from U.K. and mink cluster 5, but decreases against B.1.351 from South Africa and P.1 from Brazil. Rapid spread of these variants significantly impacts therapies and vaccine strategies against SARS-CoV-2.

Details

Language :
English
ISSN :
22111247
Database :
OpenAIRE
Journal :
Cell Reports
Accession number :
edsair.doi.dedup.....9f93ab503c5ffaf24e74d4dae1a4064d