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

Author:

Rouphael Nadine1ORCID,Beck Allison1,Kirby Amy E2,Liu Pengbo2,Natrajan Muktha S1,Lai Lilin1,Phadke Varun1,Winston Juton1,Raabe Vanessa3ORCID,Collins Matthew H1,Girmay Tigisty1,Alvarez Alicarmen1,Beydoun Nour1ORCID,Karmali Vinit1,Altieri-Rivera Joanne1,Lindesmith Lisa C4,Anderson Evan J5ORCID,Wang Yuke2,El-Khorazaty Jill6,Petrie Carey6,Baric Ralph S4,Baqar Shahida7,Moe Christine L2,Mulligan Mark J3

Affiliation:

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

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

3. New York University Grossman School of Medicine and New York University Vaccine Center , New York, New York , USA

4. Department of Epidemiology, University of North Carolina at Chapel Hill , Chapel Hill, North Carolina , USA

5. Division of Infectious Diseases, Department of Pediatrics, School of Medicine, Emory University , Atlanta, Georgia , USA

6. The Emmes Company, LLC , Rockville, Maryland , USA

7. Division of Microbiology and Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health , Bethesda, Maryland , USA

Abstract

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.

Funder

National Center for Advancing Translational Sciences

NIH

NIAID

Wellcome Trust

Division of Microbiology and Infectious Diseases

Publisher

Oxford University Press (OUP)

Subject

Infectious Diseases,Immunology and Allergy

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