T-bet expression by Th cells promotes type 1 inflammation but is dispensable for colitis

• DOI: 10.1038/mi.2016.5
• Publication Date: 2016-02-17T13:21:18Z
• Authors: J. Zimmermann; A.A. Kühl; M. Weber; J.R. Grün; J. Löffler; C. Haftmann; R. Riedel; P. Maschmeyer; K. Lehmann; K. Westendorf; M-F Mashreghi; M. Löhning; M. Mack; A. Radbruch; H.D. Chang
• Keywords: Inflammation; Mice, Knockout; 0301 basic medicine; Macrophages; Interleukin-17; Gene Expression; Cell Differentiation; T-Lymphocytes, Helper-Inducer; Th1 Cells; Colitis; Monocytes; 3. Good health; Disease Models, Animal; Interferon-gamma; Mice; 03 medical and health sciences; Animals; Th17 Cells; Lymphocyte Count; T-Box Domain Proteins

The transcription factor T-bet is highly expressed by Th cells isolated from the inflamed intestine of Crohn's disease patients, and has been regarded a critical driver of murine T cell-induced colitis. However, we show here that T-bet expression by Th cells is not required for the manifestation of T-cell-induced colitis in the presence of segmented filamentous bacteria and Helicobacter hepaticus. T-bet expression by Th cells controls their survival and localization, their repertoire of chemokine and chemokine receptor expression, the accumulation of monocytes and macrophages in the inflamed colon, and their differentiation to the M1 type, i.e., type 1 inflammation. Nevertheless, T-bet-deficient Th cells efficiently induce colitis, as reflected by weight loss, diarrhea, and colon histopathology. T-bet-deficient Th cells differentiate into Th1/17 cells, able to express IFN-γ and IL-17A upon restimulation. While neutralization of IL-17A exacerbated colitis induced by wild-type or T-bet-deficient Th cells, neutralization of IFN-γ completely abolished colitis.