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Induced regulatory T cells (iTreg cells) differ from nTreg cells in that they develop upon antigen recognition in secondary lymphoid tissues, and not the thymus. T hey develop when naive T cells are activated in the presence of the cytokine transforming growth factor-ß (TGF-ß) and in the absence of IL-6 and other pro-inflammatory cytokines. Thus, it is the presence or absence of IL-6 that determines whether TGF-ß co-signaling leads to the development of immunosuppressive Treg cells or of TH17 cells, which promote inflammation and the generation of immunity (Fig. 9.33). The generation of IL-6 by innate immune cells is regulated by the presence or absence of pathogens, with pathogen products tending to stimulate its production. In the absence of pathogens, IL-6 production is low, favoring differentiation of the immunosuppressive Treg cells and so preventing unwanted immune responses. Like nTreg cells, iTreg cells are distinguished by expression of the transcription factor FoxP3 and cell-surface CD25, and appear to be functionally equivalent to nTreg cells. Both iTreg and nTreg cells themselves can produce TGF-ß, as well as IL-10, which act in an inhibitory manner to suppress immune responses and inflammation, and may act to support further iTreg differentiation. #studytips #immunology #studywithme #biology #examtips #foryou
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