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Heterogeneous susceptibility to rotavirus infection and gastroenteritis in two birth cohort studies: Parameter estimation and epidemiological implications.

Lewnard, JA; Lopman, BA; Parashar, UD; Bennett, A; Bar-Zeev, N; Cunliffe, NA; Samuel, P; Guerrero, ML; Ruiz-Palacios, G; Kang, G; et al. Lewnard, JA; Lopman, BA; Parashar, UD; Bennett, A; Bar-Zeev, N; Cunliffe, NA; Samuel, P; Guerrero, ML; Ruiz-Palacios, G; Kang, G; Pitzer, VE (2019) Heterogeneous susceptibility to rotavirus infection and gastroenteritis in two birth cohort studies: Parameter estimation and epidemiological implications. PLoS Comput Biol, 15 (7). e1007014. ISSN 1553-7358 https://doi.org/10.1371/journal.pcbi.1007014
SGUL Authors: Bennett, Aisleen

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Abstract

Cohort studies, randomized trials, and post-licensure studies have reported reduced natural and vaccine-derived protection against rotavirus gastroenteritis (RVGE) in low- and middle-income countries. While susceptibility of children to rotavirus is known to vary within and between settings, implications for estimation of immune protection are not well understood. We sought to re-estimate naturally-acquired protection against rotavirus infection and RVGE, and to understand how differences in susceptibility among children impacted estimates. We re-analyzed data from studies conducted in Mexico City, Mexico and Vellore, India. Cumulatively, 573 rotavirus-unvaccinated children experienced 1418 rotavirus infections and 371 episodes of RVGE over 17,636 child-months. We developed a model that characterized susceptibility to rotavirus infection and RVGE among children, accounting for aspects of the natural history of rotavirus and differences in transmission rates between settings. We tested whether model-generated susceptibility measurements were associated with demographic and anthropometric factors, and with the severity of RVGE symptoms. We identified greater variation in susceptibility to rotavirus infection and RVGE in Vellore than in Mexico City. In both cohorts, susceptibility to rotavirus infection and RVGE were associated with male sex, lower birth weight, lower maternal education, and having fewer siblings; within Vellore, susceptibility was also associated with lower socioeconomic status. Children who were more susceptible to rotavirus also experienced higher rates of rotavirus-negative diarrhea, and higher risk of moderate-to-severe symptoms when experiencing RVGE. Simulations suggested that discrepant estimates of naturally-acquired immunity against RVGE can be attributed, in part, to between-setting differences in susceptibility of children, but result primarily from the interaction of transmission rates with age-dependent risk for infections to cause RVGE. We found that more children in Vellore than in Mexico City belong to a high-risk group for rotavirus infection and RVGE, and demonstrate that unmeasured individual- and age-dependent susceptibility may influence estimates of naturally-acquired immune protection against RVGE.

Item Type: Article
Additional Information: This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 (https://creativecommons.org/publicdomain/zero/1.0/) public domain dedication.
Keywords: Child, Preschool, Cohort Studies, Disease Susceptibility, Female, Gastroenteritis, Humans, Infant, Infant, Newborn, Male, Mexico, Risk Factors, Rotavirus Infections, Humans, Rotavirus Infections, Gastroenteritis, Disease Susceptibility, Risk Factors, Cohort Studies, Child, Preschool, Infant, Infant, Newborn, Mexico, Female, Male, Bioinformatics, 06 Biological Sciences, 08 Information and Computing Sciences, 01 Mathematical Sciences
SGUL Research Institute / Research Centre: Academic Structure > Infection and Immunity Research Institute (INII)
Journal or Publication Title: PLoS Comput Biol
ISSN: 1553-7358
Language: eng
Dates:
DateEvent
26 July 2019Published
9 April 2019Accepted
Publisher License: Creative Commons: Public Domain Dedication
Projects:
Project IDFunderFunder ID
R01 AI112970NIAID NIH HHSUNSPECIFIED
PubMed ID: 31348775
Go to PubMed abstract
URI: https://openaccess.sgul.ac.uk/id/eprint/112885
Publisher's version: https://doi.org/10.1371/journal.pcbi.1007014

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