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Mucosal Immunol ; 6(6): 1157-67, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23515135

ABSTRACT

Thymic stromal lymphopoietin (TSLP) is constitutively expressed in the intestine and is known to regulate inflammation in models of colitis. We show that steady-state TSLP expression requires intestinal bacteria and has an important role in limiting the expansion of colonic T helper type 17 (Th17) cells. Inappropriate expansion of the colonic Th17 cells occurred in response to an entirely benign intestinal microbiota, as determined following the colonization of germ-free C57BL/6 or TSLPR(-/-) mice with the altered Schaedler flora (ASF). TSLP-TSLPR (TSLP receptor) interactions also promoted the expansion of colonic Helios(-)Foxp3(+) regulatory T cells, necessary for the control of inappropriate Th17 responses following ASF bacterial colonization. In summary, these data reveal an important role for TSLP-TSLPR signaling in promoting steady-state mutualistic T-cell responses following intestinal bacterial colonization.


Subject(s)
Bacteria/immunology , Colitis/immunology , Cytokines/metabolism , Intestines/immunology , T-Lymphocytes, Regulatory/immunology , Th17 Cells/immunology , Animals , Cell Communication , Cell Proliferation , Cells, Cultured , Cytokines/genetics , Cytokines/immunology , Forkhead Transcription Factors/metabolism , Humans , Immunity, Cellular , Immunoglobulins/metabolism , Immunomodulation , Intestines/microbiology , Mice , Mice, Inbred C57BL , Mice, Knockout , Microbiota/immunology , Receptors, Cytokine/metabolism , Thymic Stromal Lymphopoietin
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