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Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome

Expansion of the SARS-CoV-2 BA.4 and BA.5 Omicron subvariants in populations with prevalent immunity from prior infection and vaccination, and associated burden of severe COVID-19, has raised concerns about epidemiologic characteristics of these lineages including their association with immune escap...

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Autores principales: Lewnard, Joseph A., Hong, Vennis, Kim, Jeniffer S., Shaw, Sally F., Lewin, Bruno, Takhar, Harpreet, Tartof, Sara Y.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012300/
https://www.ncbi.nlm.nih.gov/pubmed/36918548
http://dx.doi.org/10.1038/s41467-023-37051-5
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author Lewnard, Joseph A.
Hong, Vennis
Kim, Jeniffer S.
Shaw, Sally F.
Lewin, Bruno
Takhar, Harpreet
Tartof, Sara Y.
author_facet Lewnard, Joseph A.
Hong, Vennis
Kim, Jeniffer S.
Shaw, Sally F.
Lewin, Bruno
Takhar, Harpreet
Tartof, Sara Y.
author_sort Lewnard, Joseph A.
collection PubMed
description Expansion of the SARS-CoV-2 BA.4 and BA.5 Omicron subvariants in populations with prevalent immunity from prior infection and vaccination, and associated burden of severe COVID-19, has raised concerns about epidemiologic characteristics of these lineages including their association with immune escape or severe clinical outcomes. Here we show that BA.4/BA.5 cases in a large US healthcare system had at least 55% (95% confidence interval: 43–69%) higher adjusted odds of prior documented infection than time-matched BA.2 cases, as well as 15% (9–21%) and 38% (27–49%) higher adjusted odds of having received 3 and ≥4 COVID-19 vaccine doses, respectively. However, after adjusting for differences in epidemiologic characteristics among cases with each lineage, BA.4/BA.5 infection was not associated with differential risk of emergency department presentation, hospital admission, or intensive care unit admission following an initial outpatient diagnosis. This finding held in sensitivity analyses correcting for potential exposure misclassification resulting from unascertained prior infections. Our results demonstrate that the reduced severity associated with prior (BA.1 and BA.2) Omicron lineages, relative to the Delta variant, has persisted with BA.4/BA.5, despite the association of BA.4/BA.5 with increased risk of breakthrough infection among previously vaccinated or infected individuals.
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spelling pubmed-100123002023-03-14 Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome Lewnard, Joseph A. Hong, Vennis Kim, Jeniffer S. Shaw, Sally F. Lewin, Bruno Takhar, Harpreet Tartof, Sara Y. Nat Commun Article Expansion of the SARS-CoV-2 BA.4 and BA.5 Omicron subvariants in populations with prevalent immunity from prior infection and vaccination, and associated burden of severe COVID-19, has raised concerns about epidemiologic characteristics of these lineages including their association with immune escape or severe clinical outcomes. Here we show that BA.4/BA.5 cases in a large US healthcare system had at least 55% (95% confidence interval: 43–69%) higher adjusted odds of prior documented infection than time-matched BA.2 cases, as well as 15% (9–21%) and 38% (27–49%) higher adjusted odds of having received 3 and ≥4 COVID-19 vaccine doses, respectively. However, after adjusting for differences in epidemiologic characteristics among cases with each lineage, BA.4/BA.5 infection was not associated with differential risk of emergency department presentation, hospital admission, or intensive care unit admission following an initial outpatient diagnosis. This finding held in sensitivity analyses correcting for potential exposure misclassification resulting from unascertained prior infections. Our results demonstrate that the reduced severity associated with prior (BA.1 and BA.2) Omicron lineages, relative to the Delta variant, has persisted with BA.4/BA.5, despite the association of BA.4/BA.5 with increased risk of breakthrough infection among previously vaccinated or infected individuals. Nature Publishing Group UK 2023-03-14 /pmc/articles/PMC10012300/ /pubmed/36918548 http://dx.doi.org/10.1038/s41467-023-37051-5 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
Lewnard, Joseph A.
Hong, Vennis
Kim, Jeniffer S.
Shaw, Sally F.
Lewin, Bruno
Takhar, Harpreet
Tartof, Sara Y.
Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title_full Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title_fullStr Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title_full_unstemmed Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title_short Association of SARS-CoV-2 BA.4/BA.5 Omicron lineages with immune escape and clinical outcome
title_sort association of sars-cov-2 ba.4/ba.5 omicron lineages with immune escape and clinical outcome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10012300/
https://www.ncbi.nlm.nih.gov/pubmed/36918548
http://dx.doi.org/10.1038/s41467-023-37051-5
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