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中国北京门诊环境中季末流感疫苗对实验室确诊流感的有效性:一项检测阴性设计

End-of-Season Influenza Vaccine Effectiveness Against Laboratory-Confirmed Influenza in Outpatient Settings, Beijing, China: A Test-Negative Design.

作者信息

Zhang Jiaojiao, Feng Zhaomin, Shen Ying, Shi Weixian, Sun Ying, Zhao Jiachen, Wu Dan, Li Jia, Ma Chunna, Duan Wei, Ma Jiaxin, Wang Yingying, Zhang Lu, Hu Xiaodi, Wang Quanyi, Zhang Daitao, Yang Peng

机构信息

Beijing Key Laboratory of Surveillance, Early Warning and Pathogen Research on Emerging Infectious Diseases, Beijing Center for Disease Prevention and Control, Beijing 100013, China.

Beijing Research Center for Respiratory Infectious Diseases, Beijing 100013, China.

出版信息

Vaccines (Basel). 2025 Jul 30;13(8):809. doi: 10.3390/vaccines13080809.

Abstract

This study aimed to estimate the end-of-season influenza vaccine effectiveness (VE) for the 2024/25 season in Beijing, China. We used a test-negative design (TND) to assess influenza VE among outpatients with influenza-like illness (ILI) enrolled through the influenza virological surveillance in sentinel hospitals in Beijing from week 44, 2024 to week 14, 2025. Cases were ILI patients who tested positive for influenza; controls were those who tested negative. Among 18,405 ILI patients tested, 3690 (20.0%) were positive for influenza, with A(H1N1)pdm09 as the predominant strain (98.9%). The overall influenza vaccination coverage was 12.4%. Adjusted VE was 48.3% (95%CI: 40.4%-55.3%) against any influenza and 48.2% (95%CI: 40.3%-55.1%) against A(H1N1)pdm09, with the highest VE observed in adults aged 18-59 years (79.0%). The adjusted VE was similar for those vaccinated in 2023/24 only (53.1%) or both 2023/24 and 2024/25 seasons (50.8%), but lower for those vaccinated only in the 2024/25 season (48.5%). The adjusted VE was higher during the epidemic period (52.5%) than in the pre-epidemic (48.1%) and post-epidemic (35.3%) periods. Our findings indicate moderate VE against laboratory-confirmed influenza, especially A(H1N1)pdm09, during the end of the 2024/25 season in Beijing, China. Influenza vaccination provided protective effects across different epidemic periods. These timely estimates support ongoing public health communication and immunization strategies.

摘要

本研究旨在评估2024/25赛季中国北京地区流感疫苗的季末有效性(VE)。我们采用检测阴性设计(TND),对2024年第44周(44周)至2025年第14周在北京哨点医院通过流感病毒学监测招募的流感样疾病(ILI)门诊患者的流感VE进行评估。病例为流感检测呈阳性的ILI患者;对照为检测呈阴性的患者。在18405例接受检测的ILI患者中,3690例(20.0%)流感检测呈阳性,其中A(H1N1)pdm09为主要毒株(98.9%)。总体流感疫苗接种率为12.4%。针对任何流感的调整后VE为48.3%(95%CI:40.4%-55.3%),针对A(H1N1)pdm09的调整后VE为48.2%(95%CI:40.3%-55.1%),在18-59岁成年人中观察到的VE最高(79.0%)。仅在2023/24赛季接种疫苗的人群(53.1%)或在2023/24和2024/25两个赛季均接种疫苗的人群(50.8%)的调整后VE相似,但仅在2024/25赛季接种疫苗的人群的调整后VE较低(48.5%)。流行期的调整后VE(52.5%)高于流行前期(48.1%)和流行后期(35.3%)。我们的研究结果表明,在中国北京地区,2024/25赛季末针对实验室确诊流感,尤其是A(H1N1)pdm09的VE为中等水平。流感疫苗接种在不同流行期均提供了保护作用。这些及时的评估结果为正在进行的公共卫生宣传和免疫策略提供了支持。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1810/12390381/f37946b31c3f/vaccines-13-00809-g001.jpg

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