Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England.
Effectiveness of COVID-19 booster vaccines against COVID-19-related symptoms, hospitalization and death in England.
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DOI:
10.1038/s41591-022-01699-1
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发表时间:
2022-04
期刊:
影响因子:
82.9
通讯作者:
Bernal, Jamie Lopez
中科院分区:
文献类型:
--
作者:
Andrews, Nick;Stowe, Julia;Kirsebom, Freja;Toffa, Samuel;Sachdeva, Ruchira;Gower, Charlotte;Ramsay, Mary;Bernal, Jamie Lopez
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. A test-negative case–control analysis of data from the National Immunisation Management System in England demonstrates significant levels of increased protection against hospitalization or death from COVID with mRNA booster vaccines following a primary two-dose course of either ChAdOx1-S or BNT162b2 vaccines.
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DOI:
10.1016/s0140-6736(21)00677-2
发表时间:
2021-05-01
期刊:
Lancet (London, England)
影响因子:
--
作者:
Vasileiou E;Simpson CR;Shi T;Kerr S;Agrawal U;Akbari A;Bedston S;Beggs J;Bradley D;Chuter A;de Lusignan S;Docherty AB;Ford D;Hobbs FR;Joy M;Katikireddi SV;Marple J;McCowan C;McGagh D;McMenamin J;Moore E;Murray JL;Pan J;Ritchie L;Shah SA;Stock S;Torabi F;Tsang RS;Wood R;Woolhouse M;Robertson C;Sheikh A
通讯作者:
Sheikh A
DOI:
10.1016/s1473-3099(21)00330-3
发表时间:
2021-11
期刊:
The Lancet. Infectious diseases
影响因子:
--
作者:
Hyams C;Marlow R;Maseko Z;King J;Ward L;Fox K;Heath R;Tuner A;Friedrich Z;Morrison L;Ruffino G;Antico R;Adegbite D;Szasz-Benczur Z;Garcia Gonzalez M;Oliver J;Danon L;Finn A
通讯作者:
Finn A
DOI:
10.1056/nejmoa2114255
发表时间:
2021-10-07
期刊:
The New England journal of medicine
影响因子:
--
作者:
Bar-On YM;Goldberg Y;Mandel M;Bodenheimer O;Freedman L;Kalkstein N;Mizrahi B;Alroy-Preis S;Ash N;Milo R;Huppert A
通讯作者:
Huppert A
DOI:
10.1056/nejmoa2108891
发表时间:
2021-08-12
期刊:
The New England journal of medicine
影响因子:
--
作者:
Lopez Bernal J;Andrews N;Gower C;Gallagher E;Simmons R;Thelwall S;Stowe J;Tessier E;Groves N;Dabrera G;Myers R;Campbell CNJ;Amirthalingam G;Edmunds M;Zambon M;Brown KE;Hopkins S;Chand M;Ramsay M
通讯作者:
Ramsay M
影响因子:
16.6
作者:
Amirthalingam G;Bernal JL;Andrews NJ;Whitaker H;Gower C;Stowe J;Tessier E;Subbarao S;Ireland G;Baawuah F;Linley E;Warrener L;O'Brien M;Whillock C;Moss P;Ladhani SN;Brown KE;Ramsay ME
通讯作者:
Ramsay ME