Rapid escape of new SARS-CoV-2 Omicron variants from BA.2-directed antibody responses
Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved..
In November 2021, Omicron BA.1, containing a raft of new spike mutations, emerged and quickly spread globally. Intense selection pressure to escape the antibody response produced by vaccines or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection then led to a rapid succession of Omicron sub-lineages with waves of BA.2 and then BA.4/5 infection. Recently, many variants have emerged such as BQ.1 and XBB, which carry up to 8 additional receptor-binding domain (RBD) amino acid substitutions compared with BA.2. We describe a panel of 25 potent monoclonal antibodies (mAbs) generated from vaccinees suffering BA.2 breakthrough infections. Epitope mapping shows potent mAb binding shifting to 3 clusters, 2 corresponding to early-pandemic binding hotspots. The RBD mutations in recent variants map close to these binding sites and knock out or severely knock down neutralization activity of all but 1 potent mAb. This recent mAb escape corresponds with large falls in neutralization titer of vaccine or BA.1, BA.2, or BA.4/5 immune serum.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2023 |
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Erschienen: |
2023 |
Enthalten in: |
Zur Gesamtaufnahme - volume:42 |
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Enthalten in: |
Cell reports - 42(2023), 4 vom: 25. Apr., Seite 112271 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Dijokaite-Guraliuc, Aiste [VerfasserIn] |
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Links: |
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Anmerkungen: |
Date Completed 04.10.2023 Date Revised 13.03.2024 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.1016/j.celrep.2023.112271 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM355008637 |
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245 | 1 | 0 | |a Rapid escape of new SARS-CoV-2 Omicron variants from BA.2-directed antibody responses |
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500 | |a Date Completed 04.10.2023 | ||
500 | |a Date Revised 13.03.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status MEDLINE | ||
520 | |a Copyright © 2023 The Authors. Published by Elsevier Inc. All rights reserved. | ||
520 | |a In November 2021, Omicron BA.1, containing a raft of new spike mutations, emerged and quickly spread globally. Intense selection pressure to escape the antibody response produced by vaccines or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection then led to a rapid succession of Omicron sub-lineages with waves of BA.2 and then BA.4/5 infection. Recently, many variants have emerged such as BQ.1 and XBB, which carry up to 8 additional receptor-binding domain (RBD) amino acid substitutions compared with BA.2. We describe a panel of 25 potent monoclonal antibodies (mAbs) generated from vaccinees suffering BA.2 breakthrough infections. Epitope mapping shows potent mAb binding shifting to 3 clusters, 2 corresponding to early-pandemic binding hotspots. The RBD mutations in recent variants map close to these binding sites and knock out or severely knock down neutralization activity of all but 1 potent mAb. This recent mAb escape corresponds with large falls in neutralization titer of vaccine or BA.1, BA.2, or BA.4/5 immune serum | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Research Support, N.I.H., Extramural | |
650 | 4 | |a Research Support, Non-U.S. Gov't | |
650 | 4 | |a CP: Immunology | |
650 | 4 | |a CP: Microbiology | |
650 | 4 | |a SARS-CoV-2, BA.2, variant, mutation, RBD, antibodies, binding site, breakthrough, neutralizing, structure, COVID-19 | |
650 | 7 | |a Antibodies, Monoclonal |2 NLM | |
650 | 7 | |a Antibodies, Viral |2 NLM | |
650 | 7 | |a Antibodies, Neutralizing |2 NLM | |
700 | 1 | |a Das, Raksha |e verfasserin |4 aut | |
700 | 1 | |a Zhou, Daming |e verfasserin |4 aut | |
700 | 1 | |a Ginn, Helen M |e verfasserin |4 aut | |
700 | 1 | |a Liu, Chang |e verfasserin |4 aut | |
700 | 1 | |a Duyvesteyn, Helen M E |e verfasserin |4 aut | |
700 | 1 | |a Huo, Jiandong |e verfasserin |4 aut | |
700 | 1 | |a Nutalai, Rungtiwa |e verfasserin |4 aut | |
700 | 1 | |a Supasa, Piyada |e verfasserin |4 aut | |
700 | 1 | |a Selvaraj, Muneeswaran |e verfasserin |4 aut | |
700 | 1 | |a de Silva, Thushan I |e verfasserin |4 aut | |
700 | 1 | |a Plowright, Megan |e verfasserin |4 aut | |
700 | 1 | |a Newman, Thomas A H |e verfasserin |4 aut | |
700 | 1 | |a Hornsby, Hailey |e verfasserin |4 aut | |
700 | 1 | |a Mentzer, Alexander J |e verfasserin |4 aut | |
700 | 1 | |a Skelly, Donal |e verfasserin |4 aut | |
700 | 1 | |a Ritter, Thomas G |e verfasserin |4 aut | |
700 | 1 | |a Temperton, Nigel |e verfasserin |4 aut | |
700 | 1 | |a Klenerman, Paul |e verfasserin |4 aut | |
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700 | 1 | |a Williams, Mark A |e verfasserin |4 aut | |
700 | 1 | |a Hall, David R |e verfasserin |4 aut | |
700 | 1 | |a Fry, Elizabeth E |e verfasserin |4 aut | |
700 | 1 | |a Mongkolsapaya, Juthathip |e verfasserin |4 aut | |
700 | 1 | |a Ren, Jingshan |e verfasserin |4 aut | |
700 | 1 | |a Stuart, David I |e verfasserin |4 aut | |
700 | 1 | |a Screaton, Gavin R |e verfasserin |4 aut | |
700 | 1 | |a Conlon, Christopher |e investigator |4 oth | |
700 | 1 | |a Deeks, Alexandra |e investigator |4 oth | |
700 | 1 | |a Frater, John |e investigator |4 oth | |
700 | 1 | |a Gardiner, Siobhan |e investigator |4 oth | |
700 | 1 | |a Jämsén, Anni |e investigator |4 oth | |
700 | 1 | |a Jeffery, Katie |e investigator |4 oth | |
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