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Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England

Booster vaccination with messenger RNA (mRNA) vaccines has been offered to adults in England starting on 14 September 2021. We used a test-negative case–control design to estimate the relative effectiveness of a booster dose of BNT162b2 (Pfizer-BioNTech) compared to only a two-dose primary course (a...

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Autores principales: Andrews, Nick, Stowe, Julia, Kirsebom, Freja, Toffa, Samuel, Sachdeva, Ruchira, Gower, Charlotte, Ramsay, Mary, Lopez Bernal, Jamie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018410/
https://www.ncbi.nlm.nih.gov/pubmed/35045566
http://dx.doi.org/10.1038/s41591-022-01699-1
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author Andrews, Nick
Stowe, Julia
Kirsebom, Freja
Toffa, Samuel
Sachdeva, Ruchira
Gower, Charlotte
Ramsay, Mary
Lopez Bernal, Jamie
author_facet Andrews, Nick
Stowe, Julia
Kirsebom, Freja
Toffa, Samuel
Sachdeva, Ruchira
Gower, Charlotte
Ramsay, Mary
Lopez Bernal, Jamie
author_sort Andrews, Nick
collection PubMed
description Booster vaccination with messenger RNA (mRNA) vaccines has been offered to adults in England starting on 14 September 2021. We used a test-negative case–control design to estimate the relative effectiveness of a booster dose of BNT162b2 (Pfizer-BioNTech) compared to only a two-dose primary course (at least 175 days after the second dose) or unvaccinated individuals from 13 September 2021 to 5 December 2021, when Delta variant was dominant in circulation. Outcomes were symptomatic coronavirus disease 2019 (COVID-19) and hospitalization. The relative effectiveness against symptomatic disease 14–34 days after a BNT162b2 or mRNA-1273 (Moderna) booster after a ChAdOx1-S (AstraZeneca) and BNT162b2 as a primary course ranged from around 85% to 95%. Absolute vaccine effectiveness ranged from 94% to 97% and was similar in all age groups. Limited waning was seen 10 or more weeks after the booster. Against hospitalization or death, absolute effectiveness of a BNT162b2 booster ranged from around 97% to 99% in all age groups irrespective of the primary course, with no evidence of waning up to 10 weeks. This study provides real-world evidence of substantially increased protection from the booster vaccine dose against mild and severe disease irrespective of the primary course.
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spelling pubmed-90184102022-04-29 Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England Andrews, Nick Stowe, Julia Kirsebom, Freja Toffa, Samuel Sachdeva, Ruchira Gower, Charlotte Ramsay, Mary Lopez Bernal, Jamie Nat Med Article Booster vaccination with messenger RNA (mRNA) vaccines has been offered to adults in England starting on 14 September 2021. We used a test-negative case–control design to estimate the relative effectiveness of a booster dose of BNT162b2 (Pfizer-BioNTech) compared to only a two-dose primary course (at least 175 days after the second dose) or unvaccinated individuals from 13 September 2021 to 5 December 2021, when Delta variant was dominant in circulation. Outcomes were symptomatic coronavirus disease 2019 (COVID-19) and hospitalization. The relative effectiveness against symptomatic disease 14–34 days after a BNT162b2 or mRNA-1273 (Moderna) booster after a ChAdOx1-S (AstraZeneca) and BNT162b2 as a primary course ranged from around 85% to 95%. Absolute vaccine effectiveness ranged from 94% to 97% and was similar in all age groups. Limited waning was seen 10 or more weeks after the booster. Against hospitalization or death, absolute effectiveness of a BNT162b2 booster ranged from around 97% to 99% in all age groups irrespective of the primary course, with no evidence of waning up to 10 weeks. This study provides real-world evidence of substantially increased protection from the booster vaccine dose against mild and severe disease irrespective of the primary course. Nature Publishing Group US 2022-01-14 2022 /pmc/articles/PMC9018410/ /pubmed/35045566 http://dx.doi.org/10.1038/s41591-022-01699-1 Text en © Crown 2022 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
Andrews, Nick
Stowe, Julia
Kirsebom, Freja
Toffa, Samuel
Sachdeva, Ruchira
Gower, Charlotte
Ramsay, Mary
Lopez Bernal, Jamie
Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title_full Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title_fullStr Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title_full_unstemmed Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title_short Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England
title_sort effectiveness of covid-19 booster vaccines against covid-19-related symptoms, hospitalization and death in england
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9018410/
https://www.ncbi.nlm.nih.gov/pubmed/35045566
http://dx.doi.org/10.1038/s41591-022-01699-1
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