Broadly neutralizing antibodies overcome SARS-CoV-2 Omicron antigenic shift.
Angiotensin-Converting Enzyme 2
/ metabolism
Animals
Antibodies, Monoclonal
/ immunology
Antibodies, Monoclonal, Humanized
/ immunology
Antibodies, Neutralizing
/ immunology
Antibodies, Viral
/ blood
Antigenic Drift and Shift
/ genetics
Broadly Neutralizing Antibodies
/ immunology
COVID-19 Vaccines
/ immunology
Cell Line
Convalescence
Epitopes, B-Lymphocyte
/ immunology
Humans
Immune Evasion
Mice
Neutralization Tests
SARS-CoV-2
/ chemistry
Spike Glycoprotein, Coronavirus
/ chemistry
Vesiculovirus
/ genetics
Journal
Nature
ISSN: 1476-4687
Titre abrégé: Nature
Pays: England
ID NLM: 0410462
Informations de publication
Date de publication:
02 2022
02 2022
Historique:
received:
12
12
2021
accepted:
23
12
2021
pubmed:
12
1
2022
medline:
3
3
2022
entrez:
11
1
2022
Statut:
ppublish
Résumé
The recently emerged SARS-CoV-2 Omicron variant encodes 37 amino acid substitutions in the spike protein, 15 of which are in the receptor-binding domain (RBD), thereby raising concerns about the effectiveness of available vaccines and antibody-based therapeutics. Here we show that the Omicron RBD binds to human ACE2 with enhanced affinity, relative to the Wuhan-Hu-1 RBD, and binds to mouse ACE2. Marked reductions in neutralizing activity were observed against Omicron compared to the ancestral pseudovirus in plasma from convalescent individuals and from individuals who had been vaccinated against SARS-CoV-2, but this loss was less pronounced after a third dose of vaccine. Most monoclonal antibodies that are directed against the receptor-binding motif lost in vitro neutralizing activity against Omicron, with only 3 out of 29 monoclonal antibodies retaining unaltered potency, including the ACE2-mimicking S2K146 antibody
Identifiants
pubmed: 35016195
doi: 10.1038/s41586-021-04386-2
pii: 10.1038/s41586-021-04386-2
pmc: PMC9531318
mid: NIHMS1830838
doi:
Substances chimiques
Antibodies, Monoclonal
0
Antibodies, Monoclonal, Humanized
0
Antibodies, Neutralizing
0
Antibodies, Viral
0
Broadly Neutralizing Antibodies
0
COVID-19 Vaccines
0
Epitopes, B-Lymphocyte
0
S2H97 antibody
0
S2X259
0
Spike Glycoprotein, Coronavirus
0
spike protein, SARS-CoV-2
0
sotrovimab
1MTK0BPN8V
ACE2 protein, human
EC 3.4.17.23
Ace2 protein, mouse
EC 3.4.17.23
Angiotensin-Converting Enzyme 2
EC 3.4.17.23
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
664-670Subventions
Organisme : NIGMS NIH HHS
ID : R01 GM120553
Pays : United States
Organisme : NIAID NIH HHS
ID : DP1 AI158186
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201400008C
Pays : United States
Organisme : Howard Hughes Medical Institute
Pays : United States
Organisme : NIAID NIH HHS
ID : HHSN272201700059C
Pays : United States
Organisme : NIAID NIH HHS
ID : 75N93021C00014
Pays : United States
Organisme : NIAID NIH HHS
ID : U01 AI151698
Pays : United States
Organisme : NIGMS NIH HHS
ID : T32 GM008268
Pays : United States
Commentaires et corrections
Type : UpdateOf
Informations de copyright
© 2021. The Author(s), under exclusive licence to Springer Nature Limited.
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