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本文引用的文献

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Asymptomatic transmission and high community burden of seasonal influenza in an urban and a rural community in South Africa, 2017-18 (PHIRST): a population cohort study.2017-18 年南非城乡季节性流感的无症状传播和高社区负担(PHIRST):一项人群队列研究。
Lancet Glob Health. 2021 Jun;9(6):e863-e874. doi: 10.1016/S2214-109X(21)00141-8.
2
The Future of Flu: A Review of the Human Challenge Model and Systems Biology for Advancement of Influenza Vaccinology.流感的未来:人类挑战模型和系统生物学在流感疫苗学中的应用综述。
Front Cell Infect Microbiol. 2019 Apr 17;9:107. doi: 10.3389/fcimb.2019.00107. eCollection 2019.
3
A Dose-finding Study of a Wild-type Influenza A(H3N2) Virus in a Healthy Volunteer Human Challenge Model.健康志愿者人体挑战模型中野生型甲型 H3N2 流感病毒的剂量探索研究。
Clin Infect Dis. 2019 Nov 27;69(12):2082-2090. doi: 10.1093/cid/ciz141.
4
Using the Influenza Patient-reported Outcome (FLU-PRO) diary to evaluate symptoms of influenza viral infection in a healthy human challenge model.使用流感患者报告结局(FLU-PRO)日记评估健康人体挑战模型中流感病毒感染的症状。
BMC Infect Dis. 2018 Jul 28;18(1):353. doi: 10.1186/s12879-018-3220-8.
5
The human viral challenge model: accelerating the evaluation of respiratory antivirals, vaccines and novel diagnostics.人类病毒挑战模型:加速呼吸道抗病毒药物、疫苗和新型诊断方法的评估。
Respir Res. 2018 Jun 22;19(1):123. doi: 10.1186/s12931-018-0784-1.
6
A Universal Influenza Vaccine: The Strategic Plan for the National Institute of Allergy and Infectious Diseases.通用流感疫苗:美国国立过敏和传染病研究所的战略计划。
J Infect Dis. 2018 Jul 2;218(3):347-354. doi: 10.1093/infdis/jiy103.
7
Reliability, Validity, and Responsiveness of InFLUenza Patient-Reported Outcome (FLU-PRO©) Scores in Influenza-Positive Patients.流感阳性患者中流感患者报告结局(FLU-PRO©)评分的可靠性、有效性和反应性
Value Health. 2018 Feb;21(2):210-218. doi: 10.1016/j.jval.2017.04.014. Epub 2017 Jun 7.
8
Viral Shedding and Transmission Potential of Asymptomatic and Paucisymptomatic Influenza Virus Infections in the Community.社区中无症状和轻症流感病毒感染的病毒脱落及传播潜力
Clin Infect Dis. 2017 Mar 15;64(6):736-742. doi: 10.1093/cid/ciw841.
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Single-dose Live Oral Cholera Vaccine CVD 103-HgR Protects Against Human Experimental Infection With Vibrio cholerae O1 El Tor.单剂量口服霍乱活疫苗CVD 103-HgR可预防霍乱弧菌O1 El Tor引起的人体实验性感染。
Clin Infect Dis. 2016 Jun 1;62(11):1329-1335. doi: 10.1093/cid/ciw145. Epub 2016 Mar 21.
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Development of the Flu-PRO: a patient-reported outcome (PRO) instrument to evaluate symptoms of influenza.流感患者报告结局量表(Flu-PRO)的开发:一种用于评估流感症状的患者报告结局(PRO)工具。
BMC Infect Dis. 2016 Jan 5;16:1. doi: 10.1186/s12879-015-1330-0.

一项多中心、对照的健康成年人感染甲型 H1N1pdm09 流感病毒的人体感染研究。

A Multicenter, Controlled Human Infection Study of Influenza A(H1N1)pdm09 in Healthy Adults.

机构信息

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.

出版信息

J Infect Dis. 2023 Aug 11;228(3):287-298. doi: 10.1093/infdis/jiad021.

DOI:10.1093/infdis/jiad021
PMID:36702771
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10420403/
Abstract

BACKGROUND

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.

METHODS

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.

RESULTS

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.

CONCLUSIONS

We achieved a 71.1% attack rate of MMID. High baseline HAI and MN were associated with protection from illness. Clinical Trials Registration. NCT04044352.

摘要

背景

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。

方法

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。

结果

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。

结论

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。