دورية أكاديمية

Interleukin 25 regulates type 2 cytokine-dependent immunity and limits chronic inflammation in the gastrointestinal tract.

التفاصيل البيبلوغرافية
العنوان: Interleukin 25 regulates type 2 cytokine-dependent immunity and limits chronic inflammation in the gastrointestinal tract.
المؤلفون: Owyang, Alexander M., Zaph, Colby, Wilson, Emma H., Guild, Katherine J., McClanahan, Terrill, Miller, Hugh R. P., Cua, Daniel J., Goldschmidt, Michael, Hunter, Christopher A., Kastelein, Robert A., Artis, David
المصدر: Journal of Experimental Medicine; 4/17/2006, Vol. 203 Issue 4, p843-849, 7p
مصطلحات موضوعية: INTERLEUKINS, CYTOKINES, CELLULAR immunity, IMMUNOREGULATION, IMMUNITY, INFLAMMATION
مستخلص: The cytokine interleukin (IL) 25 has been implicated in the initiation of type 2 immunity by driving the expression of type 2 cytokines such as IL-5 and IL-13, although its rote in the regulation of immunity and infection-induced inflammation is unknown. Here, we identify a dual function for IL-25: first, in promoting type 2 cytokine-dependent immunity to gastrointestinal helminth infection and, second, in limiting proinflammatory cytokine production and chronic intestinal inflammation. Treatment of genetically susceptible mice with exogenous IL-25 promoted type 2 cytokine responses and immunity to Trichuris. IL-25 was constitutively expressed by CD4+ and CD8+ T cells in the gut of mouse strains that are resistant to Trichuris, and IL-25-deficient mice on a genetically resistant background failed to develop a type 2 immune response or eradicate infection. Furthermore, chronically infected IL-25-/- mice developed severe infection-induced intestinal inflammation associated with heightened expression of interferon-γ and IL-17, identifying a role for IL-25 in limiting pathologic inflammation at mucosal sites. Therefore, IL-25 is not only a critical mediator of type 2 immunity, but is also required for the regulation of inflammation in the gastrointestinal tract. [ABSTRACT FROM AUTHOR]
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قاعدة البيانات: Supplemental Index
الوصف
تدمد:00221007
DOI:10.1084/jem.20051496