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BNT162b2 和 CoronaVac 新冠疫苗对奥密克戎 BA.2 亚谱系引起的 SARS-CoV-2 无症状和有症状感染的有效性:一项前瞻性队列研究。

Effectiveness of BNT162b2 and CoronaVac COVID-19 vaccination against asymptomatic and symptomatic infection of SARS-CoV-2 omicron BA.2 in Hong Kong: a prospective cohort study.

机构信息

WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.

WHO Collaborating Centre for Infectious Disease Epidemiology and Control, School of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong Special Administrative Region, China.

出版信息

Lancet Infect Dis. 2023 Apr;23(4):421-434. doi: 10.1016/S1473-3099(22)00732-0. Epub 2022 Dec 12.

Abstract

BACKGROUND

COVID-19 vaccines provide protection against symptomatic infection that might require medical attention and against severe outcomes; however, there is a paucity of evidence regarding the effectiveness of the BNT162b2 and CoronaVac vaccines and their booster regimens against asymptomatic or mild omicron infections in the community. We aimed to measure the effectiveness of BNT162b2 and CoronaVac vaccines against asymptomatic and symptomatic SARS-CoV-2 omicron infections, during a period of omicron BA.2 predominance in Hong Kong.

METHODS

In this prospective cohort study in a population that was generally infection-naive before the large omicron BA.2 wave between January and late May, 2022, we established a public health surveillance platform to monitor the evolving activity of SARS-CoV-2 infections in the community. We recruited a cohort of individuals aged 5 years and older between March 1 and March 7, 2022, from the general population. Individuals were enrolled from all 18 districts of Hong Kong, according to a predefined age-stratified quota, primarily by random digit dialing (generating suitable eight-digit local telephone numbers by randomly picking sets of the first four digits from a sampling frame, and randomly generating the last four digits), and supplemented by our existing cohorts (which included cohorts for studying influenza vaccination from school-based vaccination programmes and cohorts for SARS-CoV-2 seroprevalence from the community), to ensure representativeness of the population in Hong Kong. Participants did weekly rapid antigen testing with a self-collected pooled nasal and throat swab, regardless of symptom and exposure status, from March 1 to April 15, 2022. Individuals reporting a history of SARS-CoV-2 infection confirmed by laboratory PCR testing before enrolment were excluded from the vaccine effectiveness analysis to avoid potential bias due to infection-induced immunity. The primary outcomes of the study were the incidence of SARS-CoV-2 infection, including asymptomatic and symptomatic infections, and the vaccine effectiveness of BNT162b2 and CoronaVac vaccines. The effectiveness of one, two, and three doses of vaccination was estimated with a Cox proportional hazards regression model with time-dependent covariates, allowing for changes in vaccination status over time, after adjustment for demographic factors and pre-existing medical conditions.

FINDINGS

Of the 8636 individuals included in the analysis, 7233 (84%) received at least two doses of vaccine, 3993 (46%) received booster doses, and 903 (10%) reported SARS-CoV-2 infection. Among these infections 589 (65·2%) were symptomatic and 314 (34·8%) were asymptomatic at the time of testing. Statistically significant protection against asymptomatic and symptomatic SARS-CoV-2 omicron infection was found only for those who received a BNT162b2 or CoronaVac booster dose, with a vaccine effectiveness of 41·4% (23·2 to 55·2; p=0·0001) and 32·4% (9·0 to 49·8; p=0·0098), respectively. The vaccine effectiveness of BNT162b2 and CoronaVac boosters was further increased to 50·9% (95% CI 31·0-65·0; p<0·0001) and 41·6% (15·0-59·8; p=0·0049), respectively, for symptomatic omicron infections. A similar pattern of vaccine effectiveness (55·8%, 22·9-74·6; p=0·0040) was also conferred after receipt of a BNT162b2 booster by individuals who received a CoronaVac primary vaccination series.

INTERPRETATION

Two doses of either vaccine did not provide significant protection against COVID-19 infection. However, receipt of a BNT162b2 booster or CoronaVac booster was associated with a significantly lower risk of omicron BA.2 infection and symptomatic infection. Our findings confirm the effectiveness of booster doses to protect against mild and asymptomatic infection.

FUNDING

Henry Fok Foundation and Hong Kong Health Bureau.

摘要

背景

COVID-19 疫苗可预防需要医疗关注的有症状感染和严重后果;然而,关于 BNT162b2 和科兴疫苗及其加强针方案在社区中针对无症状或轻度 omicron 感染的有效性证据有限。我们旨在衡量 BNT162b2 和科兴疫苗在 omicron BA.2 主导的香港社区中对无症状和有症状 SARS-CoV-2 omicron 感染的有效性。

方法

在这项前瞻性队列研究中,我们在 2022 年 1 月至 5 月下旬的 omicron BA.2 大波之前,建立了一个公共卫生监测平台来监测社区中 SARS-CoV-2 感染的演变活动。我们招募了 2022 年 3 月 1 日至 3 月 7 日期间年龄在 5 岁及以上的人群,来自香港的 18 个区,按照预先设定的年龄分层配额进行随机数字拨号(通过从抽样框架中随机选择前四位数字来生成合适的八位本地电话号码,并随机生成后四位数字),并辅以我们现有的队列(包括学校接种计划的流感疫苗接种队列和社区的 SARS-CoV-2 血清流行率队列),以确保香港人群的代表性。参与者从 3 月 1 日至 4 月 15 日每周进行一次快速抗原检测,无论症状和暴露状态如何,都使用自我采集的鼻喉合并拭子。在招募前已通过实验室 PCR 检测确诊为 SARS-CoV-2 感染的个体被排除在疫苗有效性分析之外,以避免因感染诱导的免疫而导致潜在的偏倚。本研究的主要结局是 SARS-CoV-2 感染的发生率,包括无症状和有症状感染,以及 BNT162b2 和科兴疫苗的疫苗有效性。使用 Cox 比例风险回归模型估计了一剂、两剂和三剂疫苗的有效性,该模型具有时间依赖性协变量,允许随着时间的推移改变疫苗接种状态,在调整了人口统计学因素和预先存在的医疗条件后。

结果

在分析的 8636 名个体中,7233 名(84%)至少接种了两剂疫苗,3993 名(46%)接种了加强针,903 名(10%)报告了 SARS-CoV-2 感染。在这些感染中,589 例(65·2%)为有症状感染,314 例(34·8%)为无症状感染。只有接受 BNT162b2 或科兴加强针的个体才能显著预防无症状和有症状的 SARS-CoV-2 omicron 感染,其疫苗有效性分别为 41.4%(23.2-55.2;p=0.0001)和 32.4%(9.0-49.8;p=0.0098)。BNT162b2 和科兴加强针的疫苗有效性进一步提高,分别为 50.9%(95%CI 31.0-65.0;p<0.0001)和 41.6%(15.0-59.8;p=0.0049),用于有症状的 omicron 感染。在接受科兴疫苗基础接种系列的个体中,接受 BNT162b2 加强针也会产生类似的疫苗有效性(55.8%,22.9-74.6;p=0.0040)。

解释

两剂疫苗都不能显著预防 COVID-19 感染。然而,接受 BNT162b2 加强针或科兴加强针接种与 omicron BA.2 感染和有症状感染的风险显著降低相关。我们的发现证实了加强针在预防轻度和无症状感染方面的有效性。

资金

亨利·福基金会和香港卫生署。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8d2c/9744442/b4d00f148295/gr1_lrg.jpg

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