Mimura Wataru, Ishiguro Chieko, Terada-Hirashima Junko, Matsunaga Nobuaki, Maeda Megumi, Murata Fumiko, Fukuda Haruhisa
Section of Clinical Epidemiology, Department of Data Science, Center for Clinical Sciences, National Center for Global Health and Medicine, Tokyo, Japan.
Department of Respiratory Medicine, Center Hospital of the National Center for Global Health and Medicine, Tokyo, Japan.
Open Forum Infect Dis. 2023 Oct 17;10(10):ofad475. doi: 10.1093/ofid/ofad475. eCollection 2023 Oct.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) Omicron BA.5 became prevalent in July 2022 in Japan. Bivalent messenger RNA (mRNA) vaccines were approved as booster doses for individuals who received the primary series or booster dose by monovalent vaccines. We aimed to assess the effectiveness of bivalent vaccines in Japanese adults aged ≥65 years.
We conducted a population-based cohort study using data collected from January 2019 to February 2023 in Japan. We included individuals aged ≥65 years in a municipality who received the first or second booster dose of monovalent mRNA vaccines. We estimated the effectiveness of the second or third booster dose of bivalent mRNA vaccines during the Omicron BA.5-predominant period (July-December 2022), compared with ≥90 days after the booster dose of monovalent vaccines. We used a Cox proportional hazard regression model with vaccination status as a time-dependent covariate.
A total of 81 977 individuals aged ≥65 years (mean [standard deviation] age, 78.3 [7.4] years; 33 487 male [40.8%]) were included in the study cohort. Among them, 57 396 were vaccinated with the second or third dose of bivalent vaccines (BA.1 or BA.4/5). The effectiveness against coronavirus disease 2019 (COVID-19) was estimated to be 57.9% (95% confidence interval, 52.7%-62.5%) for ≥14 days after the second or third bivalent booster dose, compared with 90 days after the first or second monovalent booster dose.
The study showed that the bivalent mRNA vaccines as the second and third doses would provide protection against COVID-19 among adults ≥65 years in Japan.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)奥密克戎BA.5于2022年7月在日本开始流行。二价信使核糖核酸(mRNA)疫苗被批准作为接受单价疫苗基础免疫系列或加强剂量接种者的加强针。我们旨在评估二价疫苗对65岁及以上日本成年人的有效性。
我们利用2019年1月至2023年2月在日本收集的数据进行了一项基于人群的队列研究。我们纳入了某自治市中接受了单价mRNA疫苗第一剂或第二剂加强针的65岁及以上个体。我们估计了在奥密克戎BA.5为主的时期(2022年7月至12月),与单价疫苗加强针接种后≥90天相比,二价mRNA疫苗第二剂或第三剂的有效性。我们使用了以疫苗接种状态作为时间依存协变量的Cox比例风险回归模型。
研究队列共纳入了81977名65岁及以上个体(平均[标准差]年龄为78.3[7.4]岁;男性33487名[40.8%])。其中,57396人接种了二价疫苗(BA.1或BA.4/5)的第二剂或第三剂。与单价疫苗第一剂或第二剂加强针接种后90天相比,二价疫苗加强针第二剂或第三剂接种后≥14天预防2019冠状病毒病(COVID-19)的有效性估计为57.9%(95%置信区间,52.7%-62.5%)。
该研究表明,二价mRNA疫苗作为第二剂和第三剂可为日本65岁及以上成年人提供针对COVID-19的保护。