| Literature DB >> 30392830 |
Romain Bouziat1, Scott B Biering2, Elaine Kouame1, Kishan A Sangani1, Soowon Kang3, Jordan D Ernest1, Mukund Varma4, Judy J Brown5, Kelly Urbanek6, Terence S Dermody7, Aylwin Ng4, Reinhard Hinterleitner1, Seungmin Hwang8, Bana Jabri9.
Abstract
Intestinal reovirus infection can trigger T helper 1 (TH1) immunity to dietary antigen, raising the question of whether other viruses can have a similar impact. Here we show that the acute CW3 strain of murine norovirus, but not the persistent CR6 strain, induces TH1 immunity to dietary antigen. This property of CW3 is dependent on its major capsid protein, a virulence determinant. Transcriptional profiling of mesenteric lymph nodes following infection reveals an immunopathological signature that does not segregate with protective immunity but with loss of oral tolerance, in which interferon regulatory factor 1 is critical. These data show that viral capacity to trigger specific inflammatory pathways at sites where T cell responses to dietary antigens take place interferes with the development of tolerance to an oral antigen. Collectively, these data provide a foundation for the development of therapeutic strategies to prevent TH1-mediated complex immune disorders triggered by viral infections.Entities:
Keywords: IRF1; T helper 1; T(H)1; celiac disease; inflammation; interferon regulatory factor 1; major capsid protein; norovirus; oral tolerance; reovirus
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Year: 2018 PMID: 30392830 PMCID: PMC6326098 DOI: 10.1016/j.chom.2018.10.004
Source DB: PubMed Journal: Cell Host Microbe ISSN: 1931-3128 Impact factor: 21.023