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Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination
SARS-CoV-2 Omicron infections are common among individuals who are vaccinated or have recovered from prior variant infection, but few reports have immunologically assessed serial Omicron infections. We characterized SARS-CoV-2 humoral responses in an individual who acquired laboratory-confirmed Omic...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485663/ https://www.ncbi.nlm.nih.gov/pubmed/36148225 http://dx.doi.org/10.3389/fimmu.2022.947021 |
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author | Lapointe, Hope R. Mwimanzi, Francis Cheung, Peter K. Sang, Yurou Yaseen, Fatima Kalikawe, Rebecca Datwani, Sneha Waterworth, Rachel Umviligihozo, Gisele Ennis, Siobhan Young, Landon Dong, Winnie Kirkby, Don Burns, Laura Leung, Victor Holmes, Daniel T. DeMarco, Mari L. Simons, Janet Matic, Nancy Montaner, Julio S.G. Brumme, Chanson J. Prystajecky, Natalie Niikura, Masahiro Lowe, Christopher F. Romney, Marc G. Brockman, Mark A. Brumme, Zabrina L. |
author_facet | Lapointe, Hope R. Mwimanzi, Francis Cheung, Peter K. Sang, Yurou Yaseen, Fatima Kalikawe, Rebecca Datwani, Sneha Waterworth, Rachel Umviligihozo, Gisele Ennis, Siobhan Young, Landon Dong, Winnie Kirkby, Don Burns, Laura Leung, Victor Holmes, Daniel T. DeMarco, Mari L. Simons, Janet Matic, Nancy Montaner, Julio S.G. Brumme, Chanson J. Prystajecky, Natalie Niikura, Masahiro Lowe, Christopher F. Romney, Marc G. Brockman, Mark A. Brumme, Zabrina L. |
author_sort | Lapointe, Hope R. |
collection | PubMed |
description | SARS-CoV-2 Omicron infections are common among individuals who are vaccinated or have recovered from prior variant infection, but few reports have immunologically assessed serial Omicron infections. We characterized SARS-CoV-2 humoral responses in an individual who acquired laboratory-confirmed Omicron BA.1.15 ten weeks after a third dose of BNT162b2, and BA.2 thirteen weeks later. Responses were compared to 124 COVID-19-naive vaccinees. One month post-second and -third vaccine doses, the participant’s wild-type and BA.1-specific IgG, ACE2-displacement and virus neutralization activities were average for a COVID-19-naive triple-vaccinated individual. BA.1 infection boosted the participant’s responses to the cohort ≥95th percentile, but even this strong “hybrid” immunity failed to protect against BA.2. Reinfection increased BA.1 and BA.2-specific responses only modestly. Though vaccines clearly protect against severe disease, results highlight the continued importance of maintaining additional protective measures to counteract the immune-evasive Omicron variant, particularly as vaccine-induced immune responses naturally decline over time. |
format | Online Article Text |
id | pubmed-9485663 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94856632022-09-21 Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination Lapointe, Hope R. Mwimanzi, Francis Cheung, Peter K. Sang, Yurou Yaseen, Fatima Kalikawe, Rebecca Datwani, Sneha Waterworth, Rachel Umviligihozo, Gisele Ennis, Siobhan Young, Landon Dong, Winnie Kirkby, Don Burns, Laura Leung, Victor Holmes, Daniel T. DeMarco, Mari L. Simons, Janet Matic, Nancy Montaner, Julio S.G. Brumme, Chanson J. Prystajecky, Natalie Niikura, Masahiro Lowe, Christopher F. Romney, Marc G. Brockman, Mark A. Brumme, Zabrina L. Front Immunol Immunology SARS-CoV-2 Omicron infections are common among individuals who are vaccinated or have recovered from prior variant infection, but few reports have immunologically assessed serial Omicron infections. We characterized SARS-CoV-2 humoral responses in an individual who acquired laboratory-confirmed Omicron BA.1.15 ten weeks after a third dose of BNT162b2, and BA.2 thirteen weeks later. Responses were compared to 124 COVID-19-naive vaccinees. One month post-second and -third vaccine doses, the participant’s wild-type and BA.1-specific IgG, ACE2-displacement and virus neutralization activities were average for a COVID-19-naive triple-vaccinated individual. BA.1 infection boosted the participant’s responses to the cohort ≥95th percentile, but even this strong “hybrid” immunity failed to protect against BA.2. Reinfection increased BA.1 and BA.2-specific responses only modestly. Though vaccines clearly protect against severe disease, results highlight the continued importance of maintaining additional protective measures to counteract the immune-evasive Omicron variant, particularly as vaccine-induced immune responses naturally decline over time. Frontiers Media S.A. 2022-09-06 /pmc/articles/PMC9485663/ /pubmed/36148225 http://dx.doi.org/10.3389/fimmu.2022.947021 Text en Copyright © 2022 Lapointe, Mwimanzi, Cheung, Sang, Yaseen, Kalikawe, Datwani, Waterworth, Umviligihozo, Ennis, Young, Dong, Kirkby, Burns, Leung, Holmes, DeMarco, Simons, Matic, Montaner, Brumme, Prystajecky, Niikura, Lowe, Romney, Brockman and Brumme https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Lapointe, Hope R. Mwimanzi, Francis Cheung, Peter K. Sang, Yurou Yaseen, Fatima Kalikawe, Rebecca Datwani, Sneha Waterworth, Rachel Umviligihozo, Gisele Ennis, Siobhan Young, Landon Dong, Winnie Kirkby, Don Burns, Laura Leung, Victor Holmes, Daniel T. DeMarco, Mari L. Simons, Janet Matic, Nancy Montaner, Julio S.G. Brumme, Chanson J. Prystajecky, Natalie Niikura, Masahiro Lowe, Christopher F. Romney, Marc G. Brockman, Mark A. Brumme, Zabrina L. Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title | Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title_full | Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title_fullStr | Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title_full_unstemmed | Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title_short | Serial infection with SARS-CoV-2 Omicron BA.1 and BA.2 following three-dose COVID-19 vaccination |
title_sort | serial infection with sars-cov-2 omicron ba.1 and ba.2 following three-dose covid-19 vaccination |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9485663/ https://www.ncbi.nlm.nih.gov/pubmed/36148225 http://dx.doi.org/10.3389/fimmu.2022.947021 |
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