Myeloid-derived suppressor cells reveal radioprotective properties through arginase-induced l-arginine depletion.

Background and purpose High arginase-1 (Arg) expression by myeloid-derived suppressor cells (MDSC) is known to inhibit antitumor T-cell responses through depletion of l -arginine. We have previously shown that nitric oxide (NO), an immune mediator produced from l -arginine, is a potent radiosensitizer of hypoxic tumor cells. This study therefore examines whether Arg + overexpressing MDSC may confer radioresistance through depleting the substrate for NO synthesis. Material and methods MDSC and Arg expression were studied in preclinical mouse CT26 and 4T1 tumor models and further validated in rectal cancer patients in comparison with healthy donors. The radioprotective effect of MDSC was analyzed in hypoxic tumor cells with regard to l -arginine depletion. Results In both mouse tumors and cancer patients, MDSC expansion was associated with Arg activation causing accelerated l -arginine consumption. l -Arginine depletion in turn profoundly suppressed the capacity of classically activated macrophages to synthesize NO resulting in impaired tumor cell radiosensitivity. In advanced cT3-4 rectal cancer, circulating neutrophils revealed Arg overexpression approaching that in MDSC, therefore mounting a protumor compartment wherein Arg + neutrophils increased from 17% to over 90%. Conclusions Protumor Arg + MDSC reveal a unique ability to radioprotect tumor cells through l -arginine depletion, a common mechanism behind both T-cell and macrophage inhibition. [ABSTRACT FROM AUTHOR]