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2021 年比利时接触者追踪研究:疫苗对关注变异株 SARS-CoV2 感染的传播有效性及接种后时间。

Vaccine effectiveness against onward transmission of SARS-CoV2-infection by variant of concern and time since vaccination, Belgian contact tracing, 2021.

机构信息

Department of Epidemiology and Public Health, Sciensano, Juliette Wytsmansstraat 14, 1000 Brussel, Belgium.

Department of Epidemiology and Public Health, Sciensano, Juliette Wytsmansstraat 14, 1000 Brussel, Belgium.

出版信息

Vaccine. 2022 May 11;40(22):3027-3037. doi: 10.1016/j.vaccine.2022.04.025. Epub 2022 Apr 12.

Abstract

BACKGROUND

During the first half of 2021, we observed high vaccine effectiveness (VE) against SARS-CoV2-infection. The replacement of the alpha-'variant of concern' (VOC) by the delta-VOC and uncertainty about the time course of immunity called for a re-assessment.

METHODS

We estimated VE against transmission of infection (VET) from Belgian contact tracing data for high-risk exposure contacts between 26/01/2021 and 14/12/2021 by susceptibility (VEs) and infectiousness of breakthrough cases (VEi) for a complete schedule of Ad26.COV2.S, ChAdOx1, BNT162b2, mRNA-1273 as well as infection-acquired and hybrid immunity. We used a multilevel Bayesian model and adjusted for personal characteristics (age, sex, household), background exposure, calendar week, VOC and time since immunity conferring-event.

FINDINGS

VET-estimates were higher for mRNA-vaccines, over 90%, compared to viral vector vaccines: 66% and 80% for Ad26COV2.S and ChAdOx1 respectively (Alpha, 0-50 days after vaccination). Delta was associated with a 40% increase in odds of transmission and a decrease of VEs (72-64%) and especially of VEi (71-46% for BNT162b2). Infection-acquired and hybrid immunity were less affected by Delta. Waning further reduced VET-estimates: from 81% to 63% for BNT162b2 (Delta, 150-200 days after vaccination). We observed lower initial VEi in the age group 65-84 years (32% vs 46% in the age group 45-64 years for BNT162b2) and faster waning. Hybrid immunity waned slower than vaccine-induced immunity.

INTERPRETATION

VEi and VEs-estimates, while remaining significant, were reduced by Delta and waned over time. We observed faster waning in the oldest age group. We should seek to improve vaccine-induced protection in older persons and those vaccinated with viral-vector vaccines.

摘要

背景

在 2021 年上半年,我们观察到针对 SARS-CoV2 感染的高疫苗有效性(VE)。阿尔法“关注变体”(VOC)被德尔塔 VOC 取代,以及对免疫持续时间的不确定性,这都需要重新评估。

方法

我们通过比利时高危接触者追踪数据,估算了 2021 年 1 月 26 日至 12 月 14 日期间,针对突破性感染的传播疫苗有效性(VET),以及针对腺病毒载体疫苗(Ad26.COV2.S、ChAdOx1)、信使 RNA 疫苗(BNT162b2、mRNA-1273)的完全接种方案,感染获得性和混合免疫的易感性(VE)和传染性(VEi)。我们使用多层次贝叶斯模型,并根据个人特征(年龄、性别、家庭)、背景暴露、日历周、VOC 和免疫事件发生后的时间进行调整。

结果

与病毒载体疫苗相比,mRNA 疫苗的 VET 估计值更高,超过 90%:Ad26.COV2.S 和 ChAdOx1 分别为 66%和 80%(阿尔法,接种后 0-50 天)。德尔塔与传播几率增加 40%以及 VE 降低(BNT162b2 为 72-64%,特别是 VEi 降低 71-46%)有关。感染获得性和混合免疫受德尔塔的影响较小。进一步衰减降低了 VET 估计值:从 BNT162b2 的 81%降至 63%(德尔塔,接种后 150-200 天)。我们观察到 65-84 岁年龄组初始 VEi 较低(BNT162b2 为 32%,45-64 岁年龄组为 46%),衰减速度较快。混合免疫衰减速度比疫苗诱导的免疫慢。

解释

尽管 VEi 和 VE 估计值仍然显著,但它们被德尔塔削弱,并随着时间的推移而衰减。我们观察到最年长的年龄组衰减速度较快。我们应该寻求提高老年人和接种病毒载体疫苗人群的疫苗诱导保护。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/93a3/9001203/eedbad04e11a/gr1_lrg.jpg

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