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

Authors :
Nadine Rouphael
Allison Beck
Amy E Kirby
Pengbo Liu
Muktha S Natrajan
Lilin Lai
Varun Phadke
Juton Winston
Vanessa Raabe
Matthew H Collins
Tigisty Girmay
Alicarmen Alvarez
Nour Beydoun
Vinit Karmali
Joanne Altieri-Rivera
Lisa C Lindesmith
Evan J Anderson
Yuke Wang
Jill El-Khorazaty
Carey Petrie
Ralph S Baric
Shahida Baqar
Christine L Moe
Mark J Mulligan
Source :
J Infect Dis
Publication Year :
2021

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.

Details

ISSN :
15376613 and 02473224
Volume :
226
Issue :
10
Database :
OpenAIRE
Journal :
The Journal of infectious diseases
Accession number :
edsair.doi.dedup.....741cbf30fbcc3eb48e5588650421a7d9