Influenza Division, National Center for Immunization and Respiratory Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia, USA.
Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee, USA.
Clin Infect Dis. 2023 Apr 17;76(8):1358-1363. doi: 10.1093/cid/ciac941.
In the United States, influenza activity during the 2021-2022 season was modest and sufficient enough to estimate influenza vaccine effectiveness (VE) for the first time since the beginning of the coronavirus disease 2019 pandemic. We estimated influenza VE against laboratory-confirmed outpatient acute illness caused by predominant A(H3N2) viruses.
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 severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination, participants who tested positive for SARS-CoV-2 were excluded from VE estimations. Estimates were adjusted for site, age, month of illness, race/ethnicity, and general health status.
Among 6260 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 1948 SARS-CoV-2-positive patients, 4312 patients were included in analyses of influenza VE; 2463 (57%) were vaccinated against influenza. Effectiveness against A(H3N2) for all ages was 36% (95% confidence interval, 20%-49%) overall.
Influenza vaccination in 2021-2022 provided protection against influenza A(H3N2)-related outpatient visits among young persons.
在美国,2021-2022 年流感季节的活动适度,足以自 2019 年冠状病毒病大流行开始以来首次估计流感疫苗的有效性 (VE)。我们估计了针对主要 A(H3N2)病毒引起的门诊急性疾病的流感 VE。
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、因急性呼吸道疾病伴有咳嗽而寻求门诊治疗的患者。使用阴性检测设计,我们评估了针对 A(H3N2)的 VE。由于流感和严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)疫苗接种之间存在很强的相关性,因此排除了 SARS-CoV-2 检测呈阳性的参与者进行 VE 估计。估计结果针对地点、年龄、发病月份、种族/民族和一般健康状况进行了调整。
在 6260 名参与者中,468 人(7%)仅检测出流感呈阳性,其中 440 人(94%)为 A(H3N2)。所有 206 种测序的 A(H3N2)病毒均被鉴定为属于遗传组 3C.2a1b 亚组 2a.2,与属于 3C.2a1b 亚组 2a.1 的 2021-2022 年 A(H3N2)疫苗成分具有抗原差异。排除 1948 例 SARS-CoV-2 阳性患者后,4312 例患者纳入流感 VE 分析;2463 例(57%)接种了流感疫苗。所有年龄段针对 A(H3N2)的有效性总体为 36%(95%置信区间,20%-49%)。
2021-2022 年的流感疫苗接种为年轻人提供了针对 A(H3N2)相关门诊就诊的保护。