Regulation of cutaneous malignancy by γδ T cells

Abstract

The localization of γδ T cells within epithelia suggests that these cells may contribute to the down-regulation of epithelial malignancies. We report that mice lacking 7S cells are highly susceptible to multiple regimens of cutaneous carcinogenesis. After exposure to carcinogens, skin cells expressed Rae-1 and H60, major histocompatibility complex-related molecules structurally resembling human MICA. Each of these is a ligand for NKG2d, a receptor expressed by cytolytic T cells and natural killer (NK) cells. In vitro, skin-associated NKC2d+ γδ cells killed skin carcinoma cells by a mechanism that was sensitive to blocking NKC2d engagement. Thus, local T cells may use evolutionary conserved proteins to negatively regulate malignancy.