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在英国 SIREN 医护人员队列中,疫苗加强针和既往感染对轻度/无症状和中度 COVID-19 感染的保护作用:2023 年 10 月至 2024 年 3 月。

Protection of vaccine boosters and prior infection against mild/asymptomatic and moderate COVID-19 infection in the UK SIREN healthcare worker cohort: October 2023 to March 2024.

机构信息

MRC Biostatistics Unit, University of Cambridge, UK.

UK Health Security Agency, London, UK.

出版信息

J Infect. 2024 Nov;89(5):106293. doi: 10.1016/j.jinf.2024.106293. Epub 2024 Sep 27.

Abstract

OBJECTIVES

Bivalent original/BA.4-5 and monovalent XBB.1.5 mRNA boosters were offered to UK healthcare workers (HCWs) in the autumn of 2023. We aimed to estimate booster vaccine effectiveness (VE) and post-infection immunity among the SIREN HCW cohort over the subsequent 6-month period of XBB.1.5 and JN.1 variant circulation.

METHODS

Between October 2023 to March 2024, 2867 SIREN study participants tested fortnightly for SARS-CoV-2 and completed symptoms questionnaires. We used multi-state models, adjusted for vaccination, prior infection, and demographic covariates, to estimate protection against mild/asymptomatic and moderate SARS-CoV-2 infection.

RESULTS

Half of the participants (1422) received a booster during October 2023 (280 bivalent, 1142 monovalent), and 536 (19%) had a PCR-confirmed infection over the study period. Bivalent booster VE was 15.1% (-55.4 to 53.6%) at 0-2 months and 4.2% (-46.4 to 37.3%) at 2-4 months post-vaccination. Monovalent booster VE was 44.2% (95% CI 21.7 to 60.3%) at 0-2 months, and 24.1% (-0.7 to 42.9%) at 2-4 months. VE was greater against moderate infection than against mild/asymptomatic infection, but neither booster showed evidence of protection after 4 months. Controlling for vaccination, compared to an infection >2 years prior, infection within the past 6 months was associated with 58.6% (30.3 to 75.4%) increased protection against moderate infection and 38.5% (5.8 to 59.8%) increased protection against mild/asymptomatic infection.

CONCLUSIONS

Monovalent XBB.1.5 boosters provided short-term protection against SARS-CoV-2 infection, particularly against moderate symptoms. Vaccine formulations that target the circulating variant may be suitable for inclusion in seasonal vaccination campaigns among HCWs.

摘要

目的

2023 年秋季,向英国医护人员(HCWs)提供二价原始/BA.4-5 和单价 XBB.1.5 mRNA 加强针。我们旨在估计 SIREN HCW 队列在随后的 6 个月 XBB.1.5 和 JN.1 变体循环期间,加强针疫苗的有效性(VE)和感染后免疫力。

方法

在 2023 年 10 月至 2024 年 3 月期间,2867 名 SIREN 研究参与者每两周进行一次 SARS-CoV-2 检测,并完成症状问卷。我们使用多状态模型,调整了疫苗接种、既往感染和人口统计学协变量,以估计对轻度/无症状和中度 SARS-CoV-2 感染的保护作用。

结果

一半的参与者(1422 人)在 2023 年 10 月接受了加强针接种(280 人接种二价疫苗,1142 人接种单价疫苗),在研究期间有 536 人(19%)经 PCR 确诊感染。二价加强针在接种后 0-2 个月的 VE 为 15.1%(-55.4 至 53.6%),在 2-4 个月的 VE 为 4.2%(-46.4 至 37.3%)。单价加强针在接种后 0-2 个月的 VE 为 44.2%(95%CI 21.7 至 60.3%),在 2-4 个月的 VE 为 24.1%(-0.7 至 42.9%)。加强针对中度感染的效果优于对轻度/无症状感染的效果,但两种加强针在接种后 4 个月均未显示出保护作用。与疫苗接种相比,与感染时间超过 2 年相比,过去 6 个月内的感染与中度感染的保护作用增加 58.6%(30.3 至 75.4%)和轻度/无症状感染的保护作用增加 38.5%(5.8 至 59.8%)相关。

结论

单价 XBB.1.5 加强针提供了针对 SARS-CoV-2 感染的短期保护,特别是针对中度症状。针对流行变异株的疫苗制剂可能适合纳入 HCWs 的季节性疫苗接种活动。

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