Lei Hao, Niu Beidi, Sun Zhou, Wang Yaojing, Che Xinren, Du Shengqiang, Liu Yan, Zhang Ke, Zhao Shi, Yang Shigui, Wang Zhe, Zhao Gang
School of Public Health, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, Zhejiang, P.R. China.
Hangzhou Disease Prevention and Control Center, Hangzhou, P.R. China.
Hum Vaccin Immunother. 2025 Dec;21(1):2435156. doi: 10.1080/21645515.2024.2435156. Epub 2024 Dec 20.
From 2020, influenza viruses circulation was largely affected by the global coronavirus disease (COVID-19) pandemic, notably leading to the extinction of the B/Yamagata lineage and raising questions about the relevance of the quadrivalent influenza vaccine, which includes this lineage. Evaluating vaccine effectiveness (VE) against influenza infections is important to inform future vaccine programs. A test-negative case-control study was conducted in five tertiary hospitals in Hangzhou, the capital city of Zhejiang province, China, enrolling medically-attended patients aged >6 months who presented with influenza-like illness (ILI) from October 1, 2023, to March 31, 2024. The VE was estimated using multivariate logistic regression models adjusted for sex, age, influenza detection methods, and influenza testing timing. Of the 157,291 medically-attended ILI participants enrolled 56,704 (36%) tested positive for influenza. Adjusted overall VE against any medically-attended influenza infection was 48% (95% Confidence interval [CI]: 46%-51%). The overall VE of the trivalent inactivated influenza vaccine (IIV3) was 59% (95% CI: 50%-66%), followed by the trivalent live attenuated vaccine (LAIV3) (VE = 53%, 95% CI: 42%-62%) and quadrivalent inactivated influenza vaccine (IIV4) (VE = 47%, 95% CI: 45%-50%). IIV3 provided even better protection against medically-attended influenza B infection than IIV4 (VE = 87%, 95% CI: 81%-92% for IIV3 versus VE = 53%, 95% CI: 50%-57% for IIV4). In the 2023/24 season in Hangzhou, China, the influenza vaccine offered moderate protection during a major epidemic. The results supported the World Health Organization recommendation to exclude the B/Yamagata lineage antigen in quadrivalent influenza vaccines in 2023.
自2020年以来,流感病毒的传播在很大程度上受到全球冠状病毒病(COVID-19)大流行的影响,尤其导致了B/山形谱系的灭绝,并引发了关于包含该谱系的四价流感疫苗相关性的问题。评估流感疫苗针对流感感染的有效性(VE)对于为未来的疫苗计划提供信息很重要。在中国浙江省省会杭州的五家三级医院进行了一项检测阴性病例对照研究,纳入了2023年10月1日至2024年3月31日期间因流感样疾病(ILI)就诊的6个月以上的患者。使用针对性别、年龄、流感检测方法和流感检测时间进行调整的多变量逻辑回归模型来估计VE。在纳入的157,291名因ILI就诊的参与者中,56,704人(36%)流感检测呈阳性。针对任何因流感就诊感染的调整后总体VE为48%(95%置信区间[CI]:46%-51%)。三价灭活流感疫苗(IIV3)的总体VE为59%(95%CI:50%-66%),其次是三价减毒活疫苗(LAIV3)(VE = 53%,95%CI:42%-62%)和四价灭活流感疫苗(IIV4)(VE = 47%,95%CI:45%-50%)。IIV3对因流感就诊的B型流感感染提供的保护甚至优于IIV4(IIV3的VE = 87%,95%CI:81%-92%,而IIV4 的VE = 53%,95%CI:50%-57%)。在2023/24赛季的中国杭州,流感疫苗在一次重大疫情期间提供了适度的保护。这些结果支持了世界卫生组织在2023年将B/山形谱系抗原排除在四价流感疫苗之外的建议。