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Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population

The SARS-CoV-2 Omicron variant has demonstrated enhanced transmissibility and escape of vaccine-derived immunity. Although first-generation vaccines remain effective against severe disease and death, robust evidence on vaccine effectiveness (VE) against all Omicron infections, irrespective of sympto...

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Autores principales: Lau, Jonathan J., Cheng, Samuel M. S., Leung, Kathy, Lee, Cheuk Kwong, Hachim, Asmaa, Tsang, Leo C. H., Yam, Kenny W. H., Chaothai, Sara, Kwan, Kelvin K. H., Chai, Zacary Y. H., Lo, Tiffany H. K., Mori, Masashi, Wu, Chao, Valkenburg, Sophie A., Amarasinghe, Gaya K., Lau, Eric H. Y., Hui, David S. C., Leung, Gabriel M., Peiris, Malik, Wu, Joseph T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941049/
https://www.ncbi.nlm.nih.gov/pubmed/36652990
http://dx.doi.org/10.1038/s41591-023-02219-5
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author Lau, Jonathan J.
Cheng, Samuel M. S.
Leung, Kathy
Lee, Cheuk Kwong
Hachim, Asmaa
Tsang, Leo C. H.
Yam, Kenny W. H.
Chaothai, Sara
Kwan, Kelvin K. H.
Chai, Zacary Y. H.
Lo, Tiffany H. K.
Mori, Masashi
Wu, Chao
Valkenburg, Sophie A.
Amarasinghe, Gaya K.
Lau, Eric H. Y.
Hui, David S. C.
Leung, Gabriel M.
Peiris, Malik
Wu, Joseph T.
author_facet Lau, Jonathan J.
Cheng, Samuel M. S.
Leung, Kathy
Lee, Cheuk Kwong
Hachim, Asmaa
Tsang, Leo C. H.
Yam, Kenny W. H.
Chaothai, Sara
Kwan, Kelvin K. H.
Chai, Zacary Y. H.
Lo, Tiffany H. K.
Mori, Masashi
Wu, Chao
Valkenburg, Sophie A.
Amarasinghe, Gaya K.
Lau, Eric H. Y.
Hui, David S. C.
Leung, Gabriel M.
Peiris, Malik
Wu, Joseph T.
author_sort Lau, Jonathan J.
collection PubMed
description The SARS-CoV-2 Omicron variant has demonstrated enhanced transmissibility and escape of vaccine-derived immunity. Although first-generation vaccines remain effective against severe disease and death, robust evidence on vaccine effectiveness (VE) against all Omicron infections, irrespective of symptoms, remains sparse. We used a community-wide serosurvey with 5,310 subjects to estimate how vaccination histories modulated risk of infection in infection-naive Hong Kong during a large wave of Omicron BA.2 epidemic in January–July 2022. We estimated that Omicron infected 45% (41–48%) of the local population. Three and four doses of BNT162b2 or CoronaVac were effective against Omicron infection 7 days after vaccination (VE of 48% (95% credible interval 34–64%) and 69% (46–98%) for three and four doses of BNT162b2, respectively; VE of 30% (1–66%) and 56% (6–97%) for three and four doses of CoronaVac, respectively). At 100 days after immunization, VE waned to 26% (7–41%) and 35% (10–71%) for three and four doses of BNT162b2, and to 6% (0–29%) and 11% (0–54%) for three and four doses of CoronaVac. The rapid waning of VE against infection conferred by first-generation vaccines and an increasingly complex viral evolutionary landscape highlight the necessity for rapidly deploying updated vaccines followed by vigilant monitoring of VE.
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spelling pubmed-99410492023-02-22 Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population Lau, Jonathan J. Cheng, Samuel M. S. Leung, Kathy Lee, Cheuk Kwong Hachim, Asmaa Tsang, Leo C. H. Yam, Kenny W. H. Chaothai, Sara Kwan, Kelvin K. H. Chai, Zacary Y. H. Lo, Tiffany H. K. Mori, Masashi Wu, Chao Valkenburg, Sophie A. Amarasinghe, Gaya K. Lau, Eric H. Y. Hui, David S. C. Leung, Gabriel M. Peiris, Malik Wu, Joseph T. Nat Med Article The SARS-CoV-2 Omicron variant has demonstrated enhanced transmissibility and escape of vaccine-derived immunity. Although first-generation vaccines remain effective against severe disease and death, robust evidence on vaccine effectiveness (VE) against all Omicron infections, irrespective of symptoms, remains sparse. We used a community-wide serosurvey with 5,310 subjects to estimate how vaccination histories modulated risk of infection in infection-naive Hong Kong during a large wave of Omicron BA.2 epidemic in January–July 2022. We estimated that Omicron infected 45% (41–48%) of the local population. Three and four doses of BNT162b2 or CoronaVac were effective against Omicron infection 7 days after vaccination (VE of 48% (95% credible interval 34–64%) and 69% (46–98%) for three and four doses of BNT162b2, respectively; VE of 30% (1–66%) and 56% (6–97%) for three and four doses of CoronaVac, respectively). At 100 days after immunization, VE waned to 26% (7–41%) and 35% (10–71%) for three and four doses of BNT162b2, and to 6% (0–29%) and 11% (0–54%) for three and four doses of CoronaVac. The rapid waning of VE against infection conferred by first-generation vaccines and an increasingly complex viral evolutionary landscape highlight the necessity for rapidly deploying updated vaccines followed by vigilant monitoring of VE. Nature Publishing Group US 2023-01-18 2023 /pmc/articles/PMC9941049/ /pubmed/36652990 http://dx.doi.org/10.1038/s41591-023-02219-5 Text en © The Author(s) 2023, corrected publication 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
Lau, Jonathan J.
Cheng, Samuel M. S.
Leung, Kathy
Lee, Cheuk Kwong
Hachim, Asmaa
Tsang, Leo C. H.
Yam, Kenny W. H.
Chaothai, Sara
Kwan, Kelvin K. H.
Chai, Zacary Y. H.
Lo, Tiffany H. K.
Mori, Masashi
Wu, Chao
Valkenburg, Sophie A.
Amarasinghe, Gaya K.
Lau, Eric H. Y.
Hui, David S. C.
Leung, Gabriel M.
Peiris, Malik
Wu, Joseph T.
Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title_full Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title_fullStr Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title_full_unstemmed Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title_short Real-world COVID-19 vaccine effectiveness against the Omicron BA.2 variant in a SARS-CoV-2 infection-naive population
title_sort real-world covid-19 vaccine effectiveness against the omicron ba.2 variant in a sars-cov-2 infection-naive population
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9941049/
https://www.ncbi.nlm.nih.gov/pubmed/36652990
http://dx.doi.org/10.1038/s41591-023-02219-5
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