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巴西异源科兴加辉瑞疫苗有效性。

Vaccine effectiveness of heterologous CoronaVac plus BNT162b2 in Brazil.

机构信息

LIB and LEITV Laboratories, Instituto Gonçalo Moniz, Salvador, Brazil.

Universidade Federal de Bahia (UFBA), Salvador, Brazil.

出版信息

Nat Med. 2022 Apr;28(4):838-843. doi: 10.1038/s41591-022-01701-w. Epub 2022 Feb 9.

Abstract

There is considerable interest in the waning of effectiveness of coronavirus disease 2019 (COVID-19) vaccines and vaccine effectiveness (VE) of booster doses. Using linked national Brazilian databases, we undertook a test-negative design study involving almost 14 million people (~16 million tests) to estimate VE of CoronaVac over time and VE of BNT162b2 booster vaccination against RT-PCR-confirmed severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and severe COVID-19 outcomes (hospitalization or death). Compared with unvaccinated individuals, CoronaVac VE at 14-30 d after the second dose was 55.0% (95% confidence interval (CI): 54.3-55.7) against confirmed infection and 82.1% (95% CI: 81.4-82.8) against severe outcomes. VE decreased to 34.7% (95% CI: 33.1-36.2) against infection and 72.5% (95% CI: 70.9-74.0) against severe outcomes over 180 d after the second dose. A BNT162b2 booster, 6 months after the second dose of CoronaVac, improved VE against infection to 92.7% (95% CI: 91.0-94.0) and VE against severe outcomes to 97.3% (95% CI: 96.1-98.1) 14-30 d after the booster. Compared with younger age groups, individuals 80 years of age or older had lower protection after the second dose but similar protection after the booster. Our findings support a BNT162b2 booster vaccine dose after two doses of CoronaVac, particularly for the elderly.

摘要

人们对 2019 年冠状病毒病(COVID-19)疫苗效力下降以及加强针的疫苗效力(VE)非常关注。我们利用巴西国家数据库的关联数据,开展了一项病例对照研究,涉及近 1400 万人(约 1600 万次检测),以评估科兴疫苗随时间推移的 VE,并评估 BNT162b2 加强针接种对 RT-PCR 确诊的严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染和严重 COVID-19 结局(住院或死亡)的 VE。与未接种疫苗的个体相比,第二剂后 14-30 天科兴疫苗对确诊感染的 VE 为 55.0%(95%置信区间[CI]:54.3-55.7),对严重结局的 VE 为 82.1%(95% CI:81.4-82.8)。第二剂后 180 天,感染的 VE 降至 34.7%(95% CI:33.1-36.2),严重结局的 VE 降至 72.5%(95% CI:70.9-74.0)。第二剂科兴疫苗后 6 个月接种一剂 BNT162b2 加强针,提高了对感染的 VE 至 92.7%(95% CI:91.0-94.0),提高了对严重结局的 VE 至 97.3%(95% CI:96.1-98.1),在加强针接种后 14-30 天。与年轻年龄组相比,80 岁及以上个体在接种第二剂后保护力较低,但在接种加强针后保护力相似。我们的研究结果支持接种两剂科兴疫苗后接种一剂 BNT162b2 加强针,尤其是对老年人。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/20df/9018414/e26790d36268/41591_2022_1701_Fig1_HTML.jpg

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