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BNT162b2、mRNA-1273和ChAdOx1-S疫苗在全国大规模疫苗接种环境中预防严重新冠病毒疾病结局的有效性:队列研究

Effectiveness of BNT162b2, mRNA-1273, and ChAdOx1-S vaccines against severe covid-19 outcomes in a nationwide mass vaccination setting: cohort study.

作者信息

Bouillon Kim, Baricault Bérangère, Botton Jérémie, Jabagi Marie-Joëlle, Bertrand Marion, Semenzato Laura, Le Vu Stéphane, Drouin Jérôme, Dray-Spira Rosemary, Weill Alain, Zureik Mahmoud

机构信息

EPI-PHARE Scientific Interest Group in Epidemiology of Health Products, Saint-Denis, France.

Faculty of Pharmacy, Paris-Saclay University, Châtenay-Malabry, France.

出版信息

BMJ Med. 2022 Jun 13;1(1):e000104. doi: 10.1136/bmjmed-2021-000104. eCollection 2022.

Abstract

OBJECTIVE

To estimate the effectiveness of the three covid-19 vaccines by Pfizer-BioNTech (BNT162b2), Moderna (mRNA-1273), and Oxford-AstraZeneca (ChAdOx1-S) in people after receiving two doses.

DESIGN

Cohort study.

SETTING

Nationwide, population based data in France, from the French National Health Data System (Système National des Données de Santé), between 27 December 2020 and 30 April 2021.

PARTICIPANTS

Adults aged ≥50 years receiving a first dose of BNT162b2, mRNA-1273, or ChAdOx1-S were randomly selected (1:1) and matched on the date of vaccination with one unvaccinated control. Individuals were matched on year of birth, sex, region of residence, and residence in a nursing home (for individuals aged ≥75 years). All individuals were followed up until 20 August 2021.

MAIN OUTCOME MEASURES

Primary outcome measure was vaccine effectiveness estimated at least 14 days after the second dose against covid-19 related hospital admission using Cox proportional hazards models adjusted for baseline characteristics and comorbidities. Vaccine effectiveness against covid-19 related death in hospital was also investigated.

RESULTS

11 256 832 vaccinated individuals were included in the study (63.6% (n=7 161 658) with the BNT162b2 vaccine, 7.6% (n=856 599) with the mRNA-1273 vaccine, and 28.8% (n=3 238 575) with the ChAdOx1-S vaccine), along with 11 256 832 matched unvaccinated controls. During follow-up (up to 20 August 2021), 43 158 covid-19 related hospital admissions and 7957 covid-19 related deaths in hospital were registered. Compared with unvaccinated controls, vaccine effectiveness of two doses against covid-19 related hospital admission was 91% (95% confidence interval 91% to 92%), 95% (93% to 96%), and 91% (89% to 94%) for the BNT162b2, mRNA-1273, and ChAdOx1-S vaccines, respectively. Similar results were observed for vaccine effectiveness of two doses against covid-19 related deaths in hospital (BNT162b2, 91% (90% to 93%); mRNA-1273, 96% (92% to 98%); and ChAdOx1 nCoV-19, 88% (68% to 95%)). At 5-6 months after receiving the second dose of vaccine, effectiveness remained high at 94% (92% to 95%) for the BNT162b2 vaccine and 98% (93% to 100%) for the mRNA-1273 vaccine. Vaccine effectiveness of ChAdOx1-S estimated at 3-4 months was 90% (63% to 97%). All three vaccines remained effective at the time of circulation of the delta variant of SARS-CoV-2 between 1 July and 20 August 2021 (effectiveness between 89% and 95%).

CONCLUSIONS

These findings provide evidence indicating that two doses of ChAdOx1-S is as effective as two doses of mRNA vaccines in France against the alpha and delta variants of SARS-CoV-2. The effectiveness of ChAdOx1-S should be further examined with a longer follow-up and in the light of the circulation of new SARS-CoV-2 variants of concern.

摘要

目的

评估辉瑞 - 生物科技公司(BNT162b2)、莫德纳公司(mRNA - 1273)和牛津 - 阿斯利康公司(ChAdOx1 - S)的三种新冠疫苗在接种两剂后对人群的有效性。

设计

队列研究。

背景

基于法国全国人口数据,来自法国国家卫生数据系统(Système National des Données de Santé),时间为2020年12月27日至2021年4月30日。

参与者

随机选取(1:1)年龄≥50岁且接种第一剂BNT162b2、mRNA - 1273或ChAdOx1 - S的成年人,并在接种日期与一名未接种疫苗的对照进行匹配。个体在出生年份、性别、居住地区以及养老院居住情况(对于年龄≥75岁的个体)方面进行匹配。所有个体随访至2021年8月20日。

主要结局指标

主要结局指标是使用针对基线特征和合并症进行调整的Cox比例风险模型,在第二剂接种至少14天后评估疫苗对新冠相关住院治疗的有效性。还调查了疫苗对医院内新冠相关死亡的有效性。

结果

11256832名接种疫苗的个体纳入研究(63.6%(n = 7161658)接种BNT162b2疫苗,7.6%(n = 856599)接种mRNA - 1273疫苗,28.8%(n = 3238575)接种ChAdOx1 - S疫苗),以及11256832名匹配的未接种疫苗对照。在随访期间(至2021年8月20日),记录了43158例新冠相关住院治疗和7957例医院内新冠相关死亡。与未接种疫苗的对照相比,两剂疫苗对新冠相关住院治疗的有效性,BNT162b2疫苗为91%(95%置信区间91%至92%),mRNA - 1273疫苗为95%(93%至96%),ChAdOx1 - S疫苗为91%(89%至9)。两剂疫苗对医院内新冠相关死亡的有效性观察到类似结果(BNT162b2,91%(90%至93%);mRNA - 1273,96%(92%至98%);ChAdOx1 nCoV - 19,88%(68%至95%))。在接种第二剂疫苗5 - 6个月后,BNT162b2疫苗有效性仍高达94%(92%至95%),mRNA - 1273疫苗为98%(93%至100%)。ChAdOx1 - S疫苗在3 - 4个月时评估的有效性为90%(63%至97%)。在2021年7月1日至8月20日期间SARS-CoV-2德尔塔变异株传播时,所有三种疫苗仍然有效(有效性在89%至95%之间)。

结论

这些发现提供了证据,表明在法国,两剂ChAdOx1 - S疫苗在预防SARS-CoV-2的阿尔法和德尔塔变异株方面与两剂mRNA疫苗同样有效。ChAdOx1 - S疫苗的有效性应通过更长时间的随访并结合新出现的值得关注的SARS-CoV-2变异株的传播情况进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ace6/9978755/2c0b6e43e5f8/bmjmed-2021-000104f01.jpg

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