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一项在中国广州市进行的关于吸入用腺病毒载体新冠病毒疫苗作为第二剂加强针的有效性的观察性前瞻性队列研究:预防严重急性呼吸综合征冠状病毒 2 感染的效果。

An Observational Prospective Cohort Study of Vaccine Effectiveness Against Severe Acute Respiratory Syndrome Coronavirus 2 Infection of an Aerosolized, Inhaled Adenovirus Type 5-Vectored Coronavirus Disease 2019 Vaccine Given as a Second Booster Dose in Guangzhou City, China.

机构信息

National Immunization Program, Chinese Center for Disease Control and Prevention, Beijing, China.

Department of Immunization Program Planning, Guangzhou Center for Disease Control and Prevention, Guangzhou, China.

出版信息

J Infect Dis. 2024 Jan 12;229(1):117-121. doi: 10.1093/infdis/jiad338.

DOI:10.1093/infdis/jiad338
PMID:37565805
Abstract

Using a prospective, observational cohort study during the post-"dynamic COVID-zero" wave in China, we estimated short-term relative effectiveness against Omicron BA.5 infection of inhaled aerosolized adenovirus type 5-vectored ancestral strain coronavirus disease 2019 (COVID-19) vaccine as a second booster dose approximately 1 year after homologous boosted primary series of inactivated COVID-19 vaccine compared with no second booster. Participants reported nucleic acid or antigen test results weekly until they tested positive or completed predesignated follow-up. After excluding participants infected <14 days after study entry, relative effectiveness among the 6576 participants was 61% in 18- to 59-year-olds and 38% in ≥60-year-olds and was sustained for 12 weeks.

摘要

采用在中国“动态清零”后阶段的前瞻性、观察性队列研究,我们估计,与无第二剂加强针相比,在同源加强免疫接种灭活 COVID-19 疫苗后约 1 年,吸入雾化腺病毒 5 型载体新冠病毒病 2019(COVID-19)疫苗作为第二剂加强针,对奥密克戎 BA.5 感染的短期相对有效性。参与者每周报告核酸或抗原检测结果,直到他们检测呈阳性或完成预定的随访。在排除研究入组后 <14 天感染的参与者后,在 18 至 59 岁的 6576 名参与者中,相对有效性为 61%,在 ≥60 岁的参与者中为 38%,并持续 12 周。

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