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mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5
Severe acute respiratory syndrome 2 Omicron BA.4 and BA.5 are characterized by high transmissibility and ability to escape natural and vaccine induced immunity. Here we test the neutralizing activity of 482 human monoclonal antibodies isolated from people who received two or three mRNA vaccine doses...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044118/ https://www.ncbi.nlm.nih.gov/pubmed/36977711 http://dx.doi.org/10.1038/s41467-023-37422-y |
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author | Andreano, Emanuele Paciello, Ida Pierleoni, Giulio Maccari, Giuseppe Antonelli, Giada Abbiento, Valentina Pileri, Piero Benincasa, Linda Giglioli, Ginevra Piccini, Giulia De Santi, Concetta Sala, Claudia Medini, Duccio Montomoli, Emanuele Maes, Piet Rappuoli, Rino |
author_facet | Andreano, Emanuele Paciello, Ida Pierleoni, Giulio Maccari, Giuseppe Antonelli, Giada Abbiento, Valentina Pileri, Piero Benincasa, Linda Giglioli, Ginevra Piccini, Giulia De Santi, Concetta Sala, Claudia Medini, Duccio Montomoli, Emanuele Maes, Piet Rappuoli, Rino |
author_sort | Andreano, Emanuele |
collection | PubMed |
description | Severe acute respiratory syndrome 2 Omicron BA.4 and BA.5 are characterized by high transmissibility and ability to escape natural and vaccine induced immunity. Here we test the neutralizing activity of 482 human monoclonal antibodies isolated from people who received two or three mRNA vaccine doses or from people vaccinated after infection. The BA.4 and BA.5 variants are neutralized only by approximately 15% of antibodies. Remarkably, the antibodies isolated after three vaccine doses target mainly the receptor binding domain Class 1/2, while antibodies isolated after infection recognize mostly the receptor binding domain Class 3 epitope region and the N-terminal domain. Different B cell germlines are used by the analyzed cohorts. The observation that mRNA vaccination and hybrid immunity elicit a different immunity against the same antigen is intriguing and its understanding may help to design the next generation of therapeutics and vaccines against coronavirus disease 2019. |
format | Online Article Text |
id | pubmed-10044118 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-100441182023-03-28 mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 Andreano, Emanuele Paciello, Ida Pierleoni, Giulio Maccari, Giuseppe Antonelli, Giada Abbiento, Valentina Pileri, Piero Benincasa, Linda Giglioli, Ginevra Piccini, Giulia De Santi, Concetta Sala, Claudia Medini, Duccio Montomoli, Emanuele Maes, Piet Rappuoli, Rino Nat Commun Article Severe acute respiratory syndrome 2 Omicron BA.4 and BA.5 are characterized by high transmissibility and ability to escape natural and vaccine induced immunity. Here we test the neutralizing activity of 482 human monoclonal antibodies isolated from people who received two or three mRNA vaccine doses or from people vaccinated after infection. The BA.4 and BA.5 variants are neutralized only by approximately 15% of antibodies. Remarkably, the antibodies isolated after three vaccine doses target mainly the receptor binding domain Class 1/2, while antibodies isolated after infection recognize mostly the receptor binding domain Class 3 epitope region and the N-terminal domain. Different B cell germlines are used by the analyzed cohorts. The observation that mRNA vaccination and hybrid immunity elicit a different immunity against the same antigen is intriguing and its understanding may help to design the next generation of therapeutics and vaccines against coronavirus disease 2019. Nature Publishing Group UK 2023-03-28 /pmc/articles/PMC10044118/ /pubmed/36977711 http://dx.doi.org/10.1038/s41467-023-37422-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Andreano, Emanuele Paciello, Ida Pierleoni, Giulio Maccari, Giuseppe Antonelli, Giada Abbiento, Valentina Pileri, Piero Benincasa, Linda Giglioli, Ginevra Piccini, Giulia De Santi, Concetta Sala, Claudia Medini, Duccio Montomoli, Emanuele Maes, Piet Rappuoli, Rino mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title | mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title_full | mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title_fullStr | mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title_full_unstemmed | mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title_short | mRNA vaccines and hybrid immunity use different B cell germlines against Omicron BA.4 and BA.5 |
title_sort | mrna vaccines and hybrid immunity use different b cell germlines against omicron ba.4 and ba.5 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044118/ https://www.ncbi.nlm.nih.gov/pubmed/36977711 http://dx.doi.org/10.1038/s41467-023-37422-y |
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