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Front Immunol ; 12: 671331, 2021.
Article in English | MEDLINE | ID: mdl-34566952

ABSTRACT

The intestinal microbiota modulates IL-22 production in the intestine, including the induction of IL-22-producing CD4+ T helper cells. Which specific bacteria are responsible for the induction of these cells is less well understood. Here, we demonstrate through the use of novel gnotobiotic knock-in reporter mice that segmented filamentous bacteria (SFB), which are known for their ability to induce Th17 cells, also induce distinct IL-17A negative CD4+ T cell populations in the intestine. A subset of these cells instead produces IL-22 upon restimulation ex vivo and also during enteric infections. Furthermore, they produce a distinct set of cytokines compared to Th17 cells including the differential expression of IL-17F and IFN-γ. Importantly, genetic models demonstrate that these cells, presumably Th22 cells, develop independently of intestinal Th17 cells. Together, our data identifies that besides Th17, SFB also induces CD4+ T cell populations, which serve as immediate source of IL-22 during intestinal inflammation.


Subject(s)
CD4-Positive T-Lymphocytes/immunology , Gastrointestinal Microbiome/immunology , Interleukins/immunology , Th17 Cells/immunology , Animals , CD4-Positive T-Lymphocytes/metabolism , Interleukins/biosynthesis , Intestinal Mucosa/microbiology , Mice , Mice, Inbred C57BL , Salmonella typhi , Th17 Cells/metabolism , Typhoid Fever/immunology , Typhoid Fever/microbiology , Interleukin-22
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