2021-2022年美国流感季节流感疫苗对甲型流感(H3N2)相关疾病的有效性

A. Price, B. Flannery, K. Talbot, Carlos G. Grijalva, K. Wernli, H. Phillips, A. Monto, E. Martin, E. Belongia, H. McLean, M. Gaglani, M. Mutnal, K. M. Geffel, M. Nowalk, S. Tartof, A. Florea, C. McLean, S. Kim, M. Patel, J. Chung
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Due to strong correlation between influenza and SARS-CoV-2 vaccination, participants who tested positive for SARS-CoV-2 were excluded from vaccine effectiveness estimations. Estimates were adjusted for site, age, month of illness, race/ethnicity and general health status. Results. Among 6,260 participants, 468 (7%) tested positive for influenza only, including 440 (94%) for A(H3N2). All 206 sequenced A(H3N2) viruses were characterized as belonging to genetic group 3C.2a1b subclade 2a.2, which has antigenic differences from the 2021-2022 season A(H3N2) vaccine component that belongs to clade 3C.2a1b subclade 2a.1. After excluding 1,948 SARS-CoV-2 positive patients, 4,312 patients were included in analyses of influenza VE; 2,463 (57%) were vaccinated against influenza. Effectiveness against A(H3N2) for all ages was 36% (95%CI, 20-49%) overall; 40% (95%CI, 24-53%) for those aged 6 months-49 years; and 10% (95%CI, -60-49%) for those aged [≥]50 years. Conclusion. 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引用次数: 12

摘要

背景。在美国,2021-2022年流感季节的流感活动较为温和,足以自COVID-19大流行开始以来首次估计流感疫苗的有效性。我们估计流感疫苗对实验室确认的门诊急性疾病的有效性,这些疾病是由主要的A(H3N2)病毒引起的。方法。在2021年10月至2022年4月期间,7个地点的研究人员招募了年龄≥6个月的急性呼吸道疾病咳嗽门诊患者。采用试验阴性设计,我们评估了VE对甲型流感(H3N2)的作用。由于流感与SARS-CoV-2疫苗接种之间存在很强的相关性,因此SARS-CoV-2检测呈阳性的参与者被排除在疫苗有效性评估之外。估计数根据地点、年龄、患病月份、种族/族裔和一般健康状况进行了调整。结果。在6260名参与者中,468名(7%)仅流感检测呈阳性,其中440名(94%)为甲型H3N2。所有206个测序的A(H3N2)病毒均属于遗传群3C。2a1b分支2a。2,与属于3C进化支的2021-2022季A(H3N2)疫苗组分存在抗原差异。2a1b亚支系2a1。在排除1948例SARS-CoV-2阳性患者后,将4312例患者纳入流感VE分析;2,463人(57%)接种了流感疫苗。所有年龄段对甲型H3N2的总体有效性为36% (95%CI, 20-49%);6个月至49岁的患者占40% (95%CI, 24-53%);年龄≥50岁者为10% (95%CI, -60-49%)。结论。2021-2022年流感疫苗接种为年轻人提供了预防甲型流感(H3N2)相关门诊就诊的保护,但在老年人中没有可测量的保护。
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Influenza Vaccine Effectiveness Against Influenza A(H3N2)-Related Illness in the United States During the 2021-2022 Influenza Season
Background. In the United States, influenza activity during the 2021-2022 season was modest and sufficient enough to estimate influenza vaccine effectiveness for the first time since the beginning of the COVID-19 pandemic. We estimated influenza vaccine effectiveness against lab-confirmed outpatient acute illness caused by predominant A(H3N2) viruses. Methods. Between October 2021 and April 2022, research staff across 7 sites enrolled patients aged [≥]6 months seeking outpatient care for acute respiratory illness with cough. Using a test-negative design, we assessed VE against influenza A(H3N2). Due to strong correlation between influenza and SARS-CoV-2 vaccination, participants who tested positive for SARS-CoV-2 were excluded from vaccine effectiveness estimations. Estimates were adjusted for site, age, month of illness, race/ethnicity and general health status. Results. Among 6,260 participants, 468 (7%) tested positive for influenza only, including 440 (94%) for A(H3N2). All 206 sequenced A(H3N2) viruses were characterized as belonging to genetic group 3C.2a1b subclade 2a.2, which has antigenic differences from the 2021-2022 season A(H3N2) vaccine component that belongs to clade 3C.2a1b subclade 2a.1. After excluding 1,948 SARS-CoV-2 positive patients, 4,312 patients were included in analyses of influenza VE; 2,463 (57%) were vaccinated against influenza. Effectiveness against A(H3N2) for all ages was 36% (95%CI, 20-49%) overall; 40% (95%CI, 24-53%) for those aged 6 months-49 years; and 10% (95%CI, -60-49%) for those aged [≥]50 years. Conclusion. Influenza vaccination in 2021-2022 provided protection against influenza A(H3N2)-related outpatient visits among young persons, with no measurable protection among older adults.
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