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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
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.
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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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