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BNT162b2 疫苗对完全接种疫苗的个体中 SARS-CoV-2 变体的有效性有轻微影响。

BNT162b2 vaccine effectiveness was marginally affected by the SARS-CoV-2 beta variant in fully vaccinated individuals.

机构信息

Central Virology Laboratory, Israel Ministry of Health, Sheba Medical Center, Tel-Hashomer 5262100, Israel; Department of Epidemiology and Preventive Medicine, School of Public Health, Sackler Faculty of Medicine, Tel-Aviv University, Tel-Aviv 6997801, Israel.

Central Virology Laboratory, Israel Ministry of Health, Sheba Medical Center, Tel-Hashomer 5262100, Israel.

出版信息

J Clin Epidemiol. 2022 Feb;142:38-44. doi: 10.1016/j.jclinepi.2021.10.011. Epub 2021 Oct 29.

Abstract

OBJECTIVE

To evaluate the effectiveness of the Pfizer BNT162b2 vaccine against the SARS-Cov-2 Beta variant.

STUDY DESIGN AND SETTING

Israel's mass vaccination program, using two doses of the Pfizer BNT162b2 vaccine, successfully curtailed the Alpha variant outbreak during winter 2020-2021, However, the virus may mutate and partially evade the immune system. To monitor this, sequencing of selected positive swab samples of interest was initiated. Comparing vaccinated with unvaccinated PCR positive persons, we estimated the odds ratio for a vaccinated case to have the Beta vs. the Alpha variant, using logistic regression, controlling for important confounders.

RESULTS

There were 19 cases of Beta variant (3.2%) among those vaccinated more than 14 days before the positive sample and 79 (3.4%) among the unvaccinated. The estimated odds ratio was 1.26 (95% CI: 0.65-2.46). Assuming the effectiveness against the Alpha variant to be 95%, the estimated effectiveness against the Beta variant was 94% (95% CI: 88%-98%).

CONCLUSION

Despite concerns over the Beta variant, the BNT162b2 vaccine seemed to provide substantial immunity against both the Beta and the Alpha variants. From 14 days following the second vaccine dose, the effectiveness of BNT162b2 vaccine was at most marginally affected by the Beta variant.

摘要

目的

评估辉瑞 BNT162b2 疫苗对 SARS-CoV-2 Beta 变异株的有效性。

研究设计与设置

以色列的大规模疫苗接种计划使用两剂辉瑞 BNT162b2 疫苗,成功遏制了 2020-2021 年冬季的 Alpha 变异株爆发。然而,病毒可能会发生突变并部分逃避免疫系统。为了监测这一点,启动了对选定有意义的阳性拭子样本的测序。通过逻辑回归,控制重要的混杂因素,比较接种疫苗和未接种疫苗的 PCR 阳性者,我们估计接种疫苗的病例与 Alpha 变异株相比发生 Beta 变异株的优势比。

结果

在阳性样本前 14 天以上接种疫苗的人群中,有 19 例 Beta 变异株(3.2%),而未接种疫苗的人群中有 79 例(3.4%)。估计的优势比为 1.26(95%CI:0.65-2.46)。假设对 Alpha 变异株的有效性为 95%,则对 Beta 变异株的估计有效性为 94%(95%CI:88%-98%)。

结论

尽管对 Beta 变异株存在担忧,但 BNT162b2 疫苗似乎对 Beta 和 Alpha 变异株都提供了实质性的免疫力。从第二剂疫苗接种后 14 天起,BNT162b2 疫苗的有效性受 Beta 变异株的影响最多只是略有下降。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/509c/8553421/9ac99077b3cb/gr1_lrg.jpg

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