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Front Immunol ; 12: 671331, 2021.
Artículo en Inglés | MEDLINE | ID: mdl-34566952

RESUMEN

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.


Asunto(s)
Linfocitos T CD4-Positivos/inmunología , Microbioma Gastrointestinal/inmunología , Interleucinas/inmunología , Células Th17/inmunología , Animales , Linfocitos T CD4-Positivos/metabolismo , Interleucinas/biosíntesis , Mucosa Intestinal/microbiología , Ratones , Ratones Endogámicos C57BL , Salmonella typhi , Células Th17/metabolismo , Fiebre Tifoidea/inmunología , Fiebre Tifoidea/microbiología , Interleucina-22
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