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Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network

BACKGROUND: We estimated combined protection conferred by prior SARS‐CoV‐2 infection and COVID‐19 vaccination against COVID‐19‐associated acute respiratory illness (ARI). METHODS: During SARS‐CoV‐2 Delta (B.1.617.2) and Omicron (B.1.1.529) variant circulation between October 2021 and April 2022, pro...

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Autores principales: Tartof, Sara Y., Xie, Fagen, Yadav, Ruchi, Wernli, Karen J., Martin, Emily T., Belongia, Edward A., Gaglani, Manjusha, Zimmerman, Richard K., Talbot, H. Keipp, Thornburg, Natalie, Flannery, Brendan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209645/
https://www.ncbi.nlm.nih.gov/pubmed/37246146
http://dx.doi.org/10.1111/irv.13143
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author Tartof, Sara Y.
Xie, Fagen
Yadav, Ruchi
Wernli, Karen J.
Martin, Emily T.
Belongia, Edward A.
Gaglani, Manjusha
Zimmerman, Richard K.
Talbot, H. Keipp
Thornburg, Natalie
Flannery, Brendan
author_facet Tartof, Sara Y.
Xie, Fagen
Yadav, Ruchi
Wernli, Karen J.
Martin, Emily T.
Belongia, Edward A.
Gaglani, Manjusha
Zimmerman, Richard K.
Talbot, H. Keipp
Thornburg, Natalie
Flannery, Brendan
author_sort Tartof, Sara Y.
collection PubMed
description BACKGROUND: We estimated combined protection conferred by prior SARS‐CoV‐2 infection and COVID‐19 vaccination against COVID‐19‐associated acute respiratory illness (ARI). METHODS: During SARS‐CoV‐2 Delta (B.1.617.2) and Omicron (B.1.1.529) variant circulation between October 2021 and April 2022, prospectively enrolled adult patients with outpatient ARI had respiratory and filter paper blood specimens collected for SARS‐CoV‐2 molecular testing and serology. Dried blood spots were tested for immunoglobulin‐G antibodies against SARS‐CoV‐2 nucleocapsid (NP) and spike protein receptor binding domain antigen using a validated multiplex bead assay. Evidence of prior SARS‐CoV‐2 infection also included documented or self‐reported laboratory‐confirmed COVID‐19. We used documented COVID‐19 vaccination status to estimate vaccine effectiveness (VE) by multivariable logistic regression by prior infection status. RESULTS: Four hundred fifty‐five (29%) of 1577 participants tested positive for SARS‐CoV‐2 infection at enrollment; 209 (46%) case‐patients and 637 (57%) test‐negative patients were NP seropositive, had documented previous laboratory‐confirmed COVID‐19, or self‐reported prior infection. Among previously uninfected patients, three‐dose VE was 97% (95% confidence interval [CI], 60%–99%) against Delta, but not statistically significant against Omicron. Among previously infected patients, three‐dose VE was 57% (CI, 20%–76%) against Omicron; VE against Delta could not be estimated. CONCLUSIONS: Three mRNA COVID‐19 vaccine doses provided additional protection against SARS‐CoV‐2 Omicron variant‐associated illness among previously infected participants.
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spelling pubmed-102096452023-05-26 Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network Tartof, Sara Y. Xie, Fagen Yadav, Ruchi Wernli, Karen J. Martin, Emily T. Belongia, Edward A. Gaglani, Manjusha Zimmerman, Richard K. Talbot, H. Keipp Thornburg, Natalie Flannery, Brendan Influenza Other Respir Viruses Original Articles BACKGROUND: We estimated combined protection conferred by prior SARS‐CoV‐2 infection and COVID‐19 vaccination against COVID‐19‐associated acute respiratory illness (ARI). METHODS: During SARS‐CoV‐2 Delta (B.1.617.2) and Omicron (B.1.1.529) variant circulation between October 2021 and April 2022, prospectively enrolled adult patients with outpatient ARI had respiratory and filter paper blood specimens collected for SARS‐CoV‐2 molecular testing and serology. Dried blood spots were tested for immunoglobulin‐G antibodies against SARS‐CoV‐2 nucleocapsid (NP) and spike protein receptor binding domain antigen using a validated multiplex bead assay. Evidence of prior SARS‐CoV‐2 infection also included documented or self‐reported laboratory‐confirmed COVID‐19. We used documented COVID‐19 vaccination status to estimate vaccine effectiveness (VE) by multivariable logistic regression by prior infection status. RESULTS: Four hundred fifty‐five (29%) of 1577 participants tested positive for SARS‐CoV‐2 infection at enrollment; 209 (46%) case‐patients and 637 (57%) test‐negative patients were NP seropositive, had documented previous laboratory‐confirmed COVID‐19, or self‐reported prior infection. Among previously uninfected patients, three‐dose VE was 97% (95% confidence interval [CI], 60%–99%) against Delta, but not statistically significant against Omicron. Among previously infected patients, three‐dose VE was 57% (CI, 20%–76%) against Omicron; VE against Delta could not be estimated. CONCLUSIONS: Three mRNA COVID‐19 vaccine doses provided additional protection against SARS‐CoV‐2 Omicron variant‐associated illness among previously infected participants. John Wiley and Sons Inc. 2023-05-25 /pmc/articles/PMC10209645/ /pubmed/37246146 http://dx.doi.org/10.1111/irv.13143 Text en © 2023 The Authors. Influenza and Other Respiratory Viruses published by John Wiley & Sons Ltd. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Tartof, Sara Y.
Xie, Fagen
Yadav, Ruchi
Wernli, Karen J.
Martin, Emily T.
Belongia, Edward A.
Gaglani, Manjusha
Zimmerman, Richard K.
Talbot, H. Keipp
Thornburg, Natalie
Flannery, Brendan
Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title_full Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title_fullStr Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title_full_unstemmed Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title_short Prior SARS‐CoV‐2 infection and COVID‐19 vaccine effectiveness against outpatient illness during widespread circulation of SARS‐CoV‐2 Omicron variant, US Flu VE network
title_sort prior sars‐cov‐2 infection and covid‐19 vaccine effectiveness against outpatient illness during widespread circulation of sars‐cov‐2 omicron variant, us flu ve network
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10209645/
https://www.ncbi.nlm.nih.gov/pubmed/37246146
http://dx.doi.org/10.1111/irv.13143
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