CTLA-4 MODULATES THE DIFFERENTIATION OF INDUCIBLE FOXP3+ TREG CELLS BUT IL-10 MEDIATES THEIR FUNCTION IN EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS.

Ctla-4 modulates the differentiation of inducible Foxp3+ Treg cells but IL-10 mediates their function in experimental autoimmune encephalomyelitis.

Ctla-4 modulates the differentiation of inducible Foxp3+ Treg cells but IL-10 mediates their function in experimental autoimmune encephalomyelitis.

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In vitro induced Foxp3+ T regulatory (iTreg) cells form a novel and promising target for therapeutic tolerance induction.However, the potential of these cells as a target for the treatment Long Term Care Bed Accessories of various immune diseases, as well as the factors involved in their development and function, remain debated.Here, we demonstrate in a myelin basic protein (MBP)-specific murine model of CNS autoimmune disease that adoptive transfer of antigen-specific iTreg cells ameliorates disease progression.Moreover, we show that the co-stimulatory molecule CTLA-4 mediates in vitro differentiation Inline - Wheels Street of iTreg cells.

Finally, we demonstrate that the secreted, immunosuppressive cytokine IL-10 controls the ability of antigen-specific iTreg cells to suppress autoimmune disease.Overall, we conclude that antigen-specific iTreg cells, which depend on various immune regulatory molecules for their differentiation and function, represent a major target for effective immunotherapy of autoimmune disease.

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