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Homeostatic Regulation of Salmonella-Induced Mucosal Inflammation and Injury by IL-23
Author(s) -
Muyiwa Awoniyi,
Samuel I. Miller,
Christopher Wilson,
Adeline M. Hajjar,
Kelly D. Smith
Publication year - 2012
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0037311
Subject(s) - inflammation , immunology , immunity , salmonella , innate immune system , acquired immune system , biology , intestinal mucosa , homeostasis , immune system , salmonella infection , interleukin 23 , interleukin 10 , microbiology and biotechnology , interleukin 17 , bacteria , medicine , genetics
IL-12 and IL-23 regulate innate and adaptive immunity to microbial pathogens through influencing the expression of IFN-γ, IL-17, and IL-22. Herein we define the roles of IL-12 and IL-23 in regulating host resistance and intestinal inflammation during acute Salmonella infection. We find that IL-23 alone is dispensable for protection against systemic spread of bacteria, but synergizes with IL-12 for optimal protection. IL-12 promotes the production of IFN-γ by NK cells, which is required for resistance against Salmonella and also for induction of intestinal inflammation and epithelial injury. In contrast, IL-23 controls the severity of inflammation by inhibiting IL-12A expression, reducing IFN-γ and preventing excessive mucosal injury. Our studies demonstrate that IL-23 is a homeostatic regulator of IL-12-dependent, IFN-γ-mediated intestinal inflammation.

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