Treg cells are important regulators of immune responses. In Cell, Mathis and colleagues show that phenotypically and functionally distinct Treg cells accumulate in injured skeletal muscle and contribute to repair processes. Treg cells in injured muscle have a 'regulatory T cell' profile but distinctly express amphiregulin, which functions as a muscle-repair factor by enhancing the differentiation of precursors of muscle cells and dampens the expression of proteins associated with fibrosis. Treg cells in muscle tissue undergo clonal expansion and have a T cell receptor repertoire distinct from that of splenic Treg cells or conventional T cells. Intramuscular depletion of Treg cells results in enhanced inflammatory responses in the injured muscle with impaired regeneration of muscle fibers. Along with data describing a role for Treg cells in visceral fat, these observations support the idea that Treg cells have homeostatic functions beyond the immune system.

Cell 155, 1282–1295 (2013)