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诺如病毒GII.2型受控人体激发模型接种物的剂量反应

Dose-Response of a Norovirus GII.2 Controlled Human Challenge Model Inoculum.

作者信息

Rouphael Nadine, Beck Allison, Kirby Amy E, Liu Pengbo, Natrajan Muktha S, Lai Lilin, Phadke Varun, Winston Juton, Raabe Vanessa, Collins Matthew H, Girmay Tigisty, Alvarez Alicarmen, Beydoun Nour, Karmali Vinit, Altieri-Rivera Joanne, Lindesmith Lisa C, Anderson Evan J, Wang Yuke, El-Khorazaty Jill, Petrie Carey, Baric Ralph S, Baqar Shahida, Moe Christine L, Mulligan Mark J

机构信息

Hope Clinic of the Emory Vaccine Center, Division of Infectious Diseases, Department of Medicine, School of Medicine, Emory University, Atlanta, Georgia, USA.

Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.

出版信息

J Infect Dis. 2022 Nov 11;226(10):1771-1780. doi: 10.1093/infdis/jiac045.

Abstract

BACKGROUND

Genogroup II noroviruses are the most common cause of acute infectious gastroenteritis. We evaluated the use of a new GII.2 inoculum in a human challenge.

METHODS

Forty-four healthy adults (36 secretor-positive and 8 secretor-negative for histo-blood group antigens) were challenged with ascending doses of a new safety-tested Snow Mountain virus (SMV) GII.2 norovirus inoculum (1.2 × 104 to 1.2 × 107 genome equivalent copies [GEC]; n = 38) or placebo (n = 6). Illness was defined as diarrhea and/or vomiting postchallenge in subjects with evidence of infection (defined as GII.2 norovirus RNA detection in stool and/or anti-SMV immunoglobulin G [IgG] seroconversion).

RESULTS

The highest dose was associated with SMV infection in 90%, and illness in 70% of subjects with 10 of 12 secretor-positive (83%) and 4 of 8 secretor-negative (50%) becoming ill. There was no association between prechallenge anti-SMV serum IgG concentration, carbohydrate-binding blockade antibody, or salivary immunoglobulin A and infection. The median infectious dose (ID50) was 5.1 × 105 GEC.

CONCLUSIONS

High rates of infection and illness were observed in both secretor-positive and secretor-negative subjects in this challenge study. However, a high dose will be required to achieve the target of 75% illness to make this an efficient model for evaluating potential norovirus vaccines and therapeutics.

CLINICAL TRIALS REGISTRATION

NCT02473224.

摘要

背景

II 基因组诺如病毒是急性感染性胃肠炎最常见的病因。我们评估了一种新型 GII.2 接种物在人体激发试验中的应用。

方法

44 名健康成年人(36 名组织血型抗原分泌型阳性,8 名分泌型阴性)接受了递增剂量的经安全性测试的雪山病毒(SMV)GII.2 诺如病毒接种物(1.2×10⁴至 1.2×10⁷基因组等效拷贝数[GEC];n = 38)或安慰剂(n = 6)激发。疾病定义为在有感染证据(定义为粪便中检测到 GII.2 诺如病毒 RNA 和/或抗 SMV 免疫球蛋白 G[IgG]血清学转换)的受试者激发后出现腹泻和/或呕吐。

结果

最高剂量与 90%的 SMV 感染相关,在受试者中 70%出现疾病,12 名分泌型阳性者中有 10 名(83%)和 8 名分泌型阴性者中有 4 名(50%)患病。激发前抗 SMV 血清 IgG 浓度、碳水化合物结合阻断抗体或唾液免疫球蛋白 A 与感染之间无关联。半数感染剂量(ID50)为 5.1×10⁵GEC。

结论

在这项激发试验研究中,分泌型阳性和分泌型阴性受试者均观察到高感染率和发病率。然而,需要高剂量才能达到 75%发病的目标,以使该模型成为评估潜在诺如病毒疫苗和治疗方法的有效模型。

临床试验注册

NCT02473224。

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