Reovirus infection triggers inflammatory responses to dietary antigens and development of celiac disease
Author(s) -
Romain Bouziat,
Reinhard Hinterleitner,
Judy J. Brown,
Jennifer Stencel-Baerenwald,
Mine R. Ikizler,
Toufic Mayassi,
Marlies Meisel,
Sangman M. Kim,
Valentina Discepolo,
Andrea J. Pruijssers,
Jordan D. Ernest,
Jason A. Iskarpatyoti,
L M M Costes,
Ian Lawrence,
Brad A. Palanski,
Mukund Varma,
Matthew A. Zurenski,
Solomiia Khomandiak,
Nicole McAllister,
Pavithra Aravamudhan,
Karl W. Boehme,
Fengling Hu,
Janneke N. Samsom,
Hans-Christian Reinecker,
Sonia S. Kupfer,
Stefano Guandalini,
Carol E. Semrad,
Valérie Abadie,
Chaitan Khosla,
Luis B. Barreiro,
Ramnik J. Xavier,
Aylwin Ng,
Terence S. Dermody,
Bana Jabrì
Publication year - 2017
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.aah5298
Subject(s) - disease , immunology , immunity , antigen , inflammatory bowel disease , virus , immune system , biology , medicine , virology
Viral infections have been proposed to elicit pathological processes leading to the initiation of T helper 1 (T H 1) immunity against dietary gluten and celiac disease (CeD). To test this hypothesis and gain insights into mechanisms underlying virus-induced loss of tolerance to dietary antigens, we developed a viral infection model that makes use of two reovirus strains that infect the intestine but differ in their immunopathological outcomes. Reovirus is an avirulent pathogen that elicits protective immunity, but we discovered that it can nonetheless disrupt intestinal immune homeostasis at inductive and effector sites of oral tolerance by suppressing peripheral regulatory T cell (pT reg ) conversion and promoting T H 1 immunity to dietary antigen. Initiation of T H 1 immunity to dietary antigen was dependent on interferon regulatory factor 1 and dissociated from suppression of pT reg conversion, which was mediated by type-1 interferon. Last, our study in humans supports a role for infection with reovirus, a seemingly innocuous virus, in triggering the development of CeD.
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