“…For instance, the ANTICANCER RESEARCH 37: 3461-3471 (2017) 3466 suppressive function of TAMs and MDSCs is partly mediated by the metabolism of L-arginine, which is determined by the expression of high levels of arginase 1 and inducible nitric oxide synthase, both of which inhibit T cell proliferation (16,17,21,22,25). In addition, both TAMs and MDSCs produce Treg-related chemokines to recruit Tregs to the tumor microenvironment (16,17,21,22,(25)(26)(27). Moreover, TAMs and MDSCs express immune checkpoint molecules, such as PD-L1 and B7-1, to suppress the activities of effector memory T cells in the tumor (15,25).…”