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Evolution of antibody immunity following Omicron BA.1 breakthrough infection
Understanding the evolution of antibody immunity following heterologous SAR-CoV-2 breakthrough infection will inform the development of next-generation vaccines. Here, we tracked SARS-CoV-2 receptor binding domain (RBD)-specific antibody responses up to six months following Omicron BA.1 breakthrough...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516849/ https://www.ncbi.nlm.nih.gov/pubmed/36172124 http://dx.doi.org/10.1101/2022.09.21.508922 |
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author | Kaku, Chengzi I. Starr, Tyler N. Zhou, Panpan Dugan, Haley L. Khalifé, Paul Song, Ge Champney, Elizabeth R. Mielcarz, Daniel W. Geoghegan, James C. Burton, Dennis R. Raiees, Andrabi Bloom, Jesse D. Walker, Laura M. |
author_facet | Kaku, Chengzi I. Starr, Tyler N. Zhou, Panpan Dugan, Haley L. Khalifé, Paul Song, Ge Champney, Elizabeth R. Mielcarz, Daniel W. Geoghegan, James C. Burton, Dennis R. Raiees, Andrabi Bloom, Jesse D. Walker, Laura M. |
author_sort | Kaku, Chengzi I. |
collection | PubMed |
description | Understanding the evolution of antibody immunity following heterologous SAR-CoV-2 breakthrough infection will inform the development of next-generation vaccines. Here, we tracked SARS-CoV-2 receptor binding domain (RBD)-specific antibody responses up to six months following Omicron BA.1 breakthrough infection in mRNA-vaccinated individuals. Cross-reactive serum neutralizing antibody and memory B cell (MBC) responses declined by two- to four-fold through the study period. Breakthrough infection elicited minimal de novo Omicron-specific B cell responses but drove affinity maturation of pre-existing cross-reactive MBCs toward BA.1. Public clones dominated the neutralizing antibody response at both early and late time points, and their escape mutation profiles predicted newly emergent Omicron sublineages. The results demonstrate that heterologous SARS-CoV-2 variant exposure drives the evolution of B cell memory and suggest that convergent neutralizing antibody responses continue to shape viral evolution. |
format | Online Article Text |
id | pubmed-9516849 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-95168492022-09-29 Evolution of antibody immunity following Omicron BA.1 breakthrough infection Kaku, Chengzi I. Starr, Tyler N. Zhou, Panpan Dugan, Haley L. Khalifé, Paul Song, Ge Champney, Elizabeth R. Mielcarz, Daniel W. Geoghegan, James C. Burton, Dennis R. Raiees, Andrabi Bloom, Jesse D. Walker, Laura M. bioRxiv Article Understanding the evolution of antibody immunity following heterologous SAR-CoV-2 breakthrough infection will inform the development of next-generation vaccines. Here, we tracked SARS-CoV-2 receptor binding domain (RBD)-specific antibody responses up to six months following Omicron BA.1 breakthrough infection in mRNA-vaccinated individuals. Cross-reactive serum neutralizing antibody and memory B cell (MBC) responses declined by two- to four-fold through the study period. Breakthrough infection elicited minimal de novo Omicron-specific B cell responses but drove affinity maturation of pre-existing cross-reactive MBCs toward BA.1. Public clones dominated the neutralizing antibody response at both early and late time points, and their escape mutation profiles predicted newly emergent Omicron sublineages. The results demonstrate that heterologous SARS-CoV-2 variant exposure drives the evolution of B cell memory and suggest that convergent neutralizing antibody responses continue to shape viral evolution. Cold Spring Harbor Laboratory 2022-09-22 /pmc/articles/PMC9516849/ /pubmed/36172124 http://dx.doi.org/10.1101/2022.09.21.508922 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Kaku, Chengzi I. Starr, Tyler N. Zhou, Panpan Dugan, Haley L. Khalifé, Paul Song, Ge Champney, Elizabeth R. Mielcarz, Daniel W. Geoghegan, James C. Burton, Dennis R. Raiees, Andrabi Bloom, Jesse D. Walker, Laura M. Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title | Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title_full | Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title_fullStr | Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title_full_unstemmed | Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title_short | Evolution of antibody immunity following Omicron BA.1 breakthrough infection |
title_sort | evolution of antibody immunity following omicron ba.1 breakthrough infection |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9516849/ https://www.ncbi.nlm.nih.gov/pubmed/36172124 http://dx.doi.org/10.1101/2022.09.21.508922 |
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