Center for Vaccine Development and Global Health, University of Maryland School of Medicine, Baltimore.
Cincinnati Children's Hospital Medical Center, University of Cincinnati, Ohio; Departments of.
J Infect Dis. 2023 Aug 11;228(3):287-298. doi: 10.1093/infdis/jiad021.
We evaluated the associations between baseline influenza virus-specific hemagglutination inhibition (HAI) and microneutralization (MN) titers and subsequent symptomatic influenza virus infection in a controlled human infection study.
We inoculated unvaccinated healthy adults aged 18-49 years with an influenza A/California/04/2009/H1N1pdm-like virus (NCT04044352). We collected serial safety labs, serum for HAI and MN, and nasopharyngeal swabs for reverse-transcription polymerase chain reaction (RT-PCR) testing. Analyses used the putative seroprotective titer of ≥40 for HAI and MN. The primary clinical outcome was mild-to-moderate influenza disease (MMID), defined as ≥1 postchallenge positive qualitative RT-PCR test with a qualifying symptom/clinical finding.
Of 76 participants given influenza virus challenge, 54 (71.1%) experienced MMID. Clinical illness was generally very mild. MMID attack rates among participants with baseline titers ≥40 by HAI and MN were 64.9% and 67.9%, respectively, while MMID attack rates among participants with baseline titers <40 by HAI and MN were 76.9% and 78.3%, respectively. The estimated odds of developing MMID decreased by 19% (odds ratio, 0.81 [95% confidence interval, .62-1.06]; P = .126) for every 2-fold increase in baseline HAI. There were no significant adverse events.
We achieved a 71.1% attack rate of MMID. High baseline HAI and MN were associated with protection from illness. Clinical Trials Registration. NCT04044352.
我们在一项对照人体感染研究中评估了基线流感病毒特异性血凝抑制(HAI)和微量中和(MN)滴度与随后出现的有症状流感病毒感染之间的关联。
我们用流感 A/加利福尼亚/04/2009/H1N1pdm 样病毒(NCT04044352)对未接种疫苗的 18-49 岁健康成年人进行了接种。我们采集了一系列的安全性实验室样本、血清进行 HAI 和 MN 检测以及鼻咽拭子进行逆转录聚合酶链反应(RT-PCR)检测。分析采用 HAI 和 MN 的假定血清保护滴度≥40。主要临床结局是轻度至中度流感疾病(MMID),定义为≥1 次接种后定性 RT-PCR 检测呈阳性,伴有符合条件的症状/临床发现。
在 76 名接受流感病毒挑战的参与者中,54 名(71.1%)发生了 MMID。临床疾病通常非常轻微。基线 HAI 和 MN 滴度≥40 的参与者中 MMID 的发病率分别为 64.9%和 67.9%,而基线 HAI 和 MN 滴度<40 的参与者中 MMID 的发病率分别为 76.9%和 78.3%。HAI 基线每增加 2 倍,发生 MMID 的估计几率降低 19%(比值比,0.81 [95%置信区间,0.62-1.06];P=0.126)。没有发生显著的不良事件。
我们实现了 71.1%的 MMID 发病率。高基线 HAI 和 MN 与免于患病相关。临床试验注册。NCT04044352。