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Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant

The SARS-CoV-2 Omicron variant can escape neutralization by vaccine-elicited and convalescent antibodies. Memory B cells (MBCs) represent another layer of protection against SARS-CoV-2, as they persist after infection and vaccination and improve their affinity. Whether MBCs elicited by mRNA vaccines...

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Autores principales: Sokal, Aurélien, Broketa, Matteo, Barba-Spaeth, Giovanna, Meola, Annalisa, Fernández, Ignacio, Fourati, Slim, Azzaoui, Imane, de La Selle, Andrea, Vandenberghe, Alexis, Roeser, Anais, Bouvier-Alias, Magali, Crickx, Etienne, Languille, Laetitia, Michel, Marc, Godeau, Bertrand, Gallien, Sébastien, Melica, Giovanna, Nguyen, Yann, Zarrouk, Virginie, Canoui-Poitrine, Florence, Noizat-Pirenne, France, Megret, Jérôme, Pawlotsky, Jean-Michel, Fillatreau, Simon, Simon-Lorière, Etienne, Weill, Jean-Claude, Reynaud, Claude-Agnès, Rey, Félix A., Bruhns, Pierre, Chappert, Pascal, Mahévas, Matthieu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Published by Elsevier Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986479/
https://www.ncbi.nlm.nih.gov/pubmed/35483354
http://dx.doi.org/10.1016/j.immuni.2022.04.002
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author Sokal, Aurélien
Broketa, Matteo
Barba-Spaeth, Giovanna
Meola, Annalisa
Fernández, Ignacio
Fourati, Slim
Azzaoui, Imane
de La Selle, Andrea
Vandenberghe, Alexis
Roeser, Anais
Bouvier-Alias, Magali
Crickx, Etienne
Languille, Laetitia
Michel, Marc
Godeau, Bertrand
Gallien, Sébastien
Melica, Giovanna
Nguyen, Yann
Zarrouk, Virginie
Canoui-Poitrine, Florence
Noizat-Pirenne, France
Megret, Jérôme
Pawlotsky, Jean-Michel
Fillatreau, Simon
Simon-Lorière, Etienne
Weill, Jean-Claude
Reynaud, Claude-Agnès
Rey, Félix A.
Bruhns, Pierre
Chappert, Pascal
Mahévas, Matthieu
author_facet Sokal, Aurélien
Broketa, Matteo
Barba-Spaeth, Giovanna
Meola, Annalisa
Fernández, Ignacio
Fourati, Slim
Azzaoui, Imane
de La Selle, Andrea
Vandenberghe, Alexis
Roeser, Anais
Bouvier-Alias, Magali
Crickx, Etienne
Languille, Laetitia
Michel, Marc
Godeau, Bertrand
Gallien, Sébastien
Melica, Giovanna
Nguyen, Yann
Zarrouk, Virginie
Canoui-Poitrine, Florence
Noizat-Pirenne, France
Megret, Jérôme
Pawlotsky, Jean-Michel
Fillatreau, Simon
Simon-Lorière, Etienne
Weill, Jean-Claude
Reynaud, Claude-Agnès
Rey, Félix A.
Bruhns, Pierre
Chappert, Pascal
Mahévas, Matthieu
author_sort Sokal, Aurélien
collection PubMed
description The SARS-CoV-2 Omicron variant can escape neutralization by vaccine-elicited and convalescent antibodies. Memory B cells (MBCs) represent another layer of protection against SARS-CoV-2, as they persist after infection and vaccination and improve their affinity. Whether MBCs elicited by mRNA vaccines can recognize the Omicron variant remains unclear. We assessed the affinity and neutralization potency against the Omicron variant of several hundred naturally expressed MBC-derived monoclonal IgG antibodies from vaccinated COVID-19-recovered and -naive individuals. Compared with other variants of concern, Omicron evaded recognition by a larger proportion of MBC-derived antibodies, with only 30% retaining high affinity against the Omicron RBD, and the reduction in neutralization potency was even more pronounced. Nonetheless, neutralizing MBC clones could be found in all the analyzed individuals. Therefore, despite the strong immune escape potential of the Omicron variant, these results suggest that the MBC repertoire generated by mRNA vaccines still provides some protection against the Omicron variant in vaccinated individuals.
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spelling pubmed-89864792022-04-07 Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant Sokal, Aurélien Broketa, Matteo Barba-Spaeth, Giovanna Meola, Annalisa Fernández, Ignacio Fourati, Slim Azzaoui, Imane de La Selle, Andrea Vandenberghe, Alexis Roeser, Anais Bouvier-Alias, Magali Crickx, Etienne Languille, Laetitia Michel, Marc Godeau, Bertrand Gallien, Sébastien Melica, Giovanna Nguyen, Yann Zarrouk, Virginie Canoui-Poitrine, Florence Noizat-Pirenne, France Megret, Jérôme Pawlotsky, Jean-Michel Fillatreau, Simon Simon-Lorière, Etienne Weill, Jean-Claude Reynaud, Claude-Agnès Rey, Félix A. Bruhns, Pierre Chappert, Pascal Mahévas, Matthieu Immunity Article The SARS-CoV-2 Omicron variant can escape neutralization by vaccine-elicited and convalescent antibodies. Memory B cells (MBCs) represent another layer of protection against SARS-CoV-2, as they persist after infection and vaccination and improve their affinity. Whether MBCs elicited by mRNA vaccines can recognize the Omicron variant remains unclear. We assessed the affinity and neutralization potency against the Omicron variant of several hundred naturally expressed MBC-derived monoclonal IgG antibodies from vaccinated COVID-19-recovered and -naive individuals. Compared with other variants of concern, Omicron evaded recognition by a larger proportion of MBC-derived antibodies, with only 30% retaining high affinity against the Omicron RBD, and the reduction in neutralization potency was even more pronounced. Nonetheless, neutralizing MBC clones could be found in all the analyzed individuals. Therefore, despite the strong immune escape potential of the Omicron variant, these results suggest that the MBC repertoire generated by mRNA vaccines still provides some protection against the Omicron variant in vaccinated individuals. Published by Elsevier Inc. 2022-06-14 2022-04-07 /pmc/articles/PMC8986479/ /pubmed/35483354 http://dx.doi.org/10.1016/j.immuni.2022.04.002 Text en © 2022 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Sokal, Aurélien
Broketa, Matteo
Barba-Spaeth, Giovanna
Meola, Annalisa
Fernández, Ignacio
Fourati, Slim
Azzaoui, Imane
de La Selle, Andrea
Vandenberghe, Alexis
Roeser, Anais
Bouvier-Alias, Magali
Crickx, Etienne
Languille, Laetitia
Michel, Marc
Godeau, Bertrand
Gallien, Sébastien
Melica, Giovanna
Nguyen, Yann
Zarrouk, Virginie
Canoui-Poitrine, Florence
Noizat-Pirenne, France
Megret, Jérôme
Pawlotsky, Jean-Michel
Fillatreau, Simon
Simon-Lorière, Etienne
Weill, Jean-Claude
Reynaud, Claude-Agnès
Rey, Félix A.
Bruhns, Pierre
Chappert, Pascal
Mahévas, Matthieu
Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title_full Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title_fullStr Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title_full_unstemmed Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title_short Analysis of mRNA vaccination-elicited RBD-specific memory B cells reveals strong but incomplete immune escape of the SARS-CoV-2 Omicron variant
title_sort analysis of mrna vaccination-elicited rbd-specific memory b cells reveals strong but incomplete immune escape of the sars-cov-2 omicron variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8986479/
https://www.ncbi.nlm.nih.gov/pubmed/35483354
http://dx.doi.org/10.1016/j.immuni.2022.04.002
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