%0 Journal Article %T Genetic models reveal origin, persistence and non-redundant functions of IL-17¨Cproducing ¦Ã¦Ä T cells %J JEM | The Journal of Experimental Medicine %D 2018 %R 10.1084/jem.20181439 %X ¦Ã¦Ä T cells are highly conserved in jawed vertebrates, suggesting an essential role in the immune system. However, ¦Ã¦Ä T cell¨Cdeficient Tcrd£¿/£¿ mice display surprisingly mild phenotypes. We hypothesized that the lack of ¦Ã¦Ä T cells in constitutive Tcrd£¿/£¿ mice is functionally compensated by other lymphocytes taking over genuine ¦Ã¦Ä T cell functions. To test this, we generated a knock-in model for diphtheria toxin¨Cmediated conditional ¦Ã¦Ä T cell depletion. In contrast to IFN-¦Ã¨Cproducing ¦Ã¦Ä T cells, IL-17¨Cproducing ¦Ã¦Ä T cells (T¦Ã¦Ä17 cells) recovered inefficiently after depletion, and their niches were filled by expanding Th17 cells and ILC3s. Complementary genetic fate mapping further demonstrated that T¦Ã¦Ä17 cells are long-lived and persisting lymphocytes. Investigating the function of ¦Ã¦Ä T cells, conditional depletion but not constitutive deficiency protected from imiquimod-induced psoriasis. Together, we clarify that fetal thymus-derived T¦Ã¦Ä17 cells are nonredundant local effector cells in IL-17¨Cdriven skin pathology. %U http://jem.rupress.org/content/215/12/3006