Activation of Axl or Mertk on cancer cell results in suppression of antigen processing and presentation to T cells, while Mertk on tumor macrophages results in phagocytosis of dying cells to the exclusion of dendritic cell uptake. Cell uptake drives suppressive differentiation of macrophages, which can, in turn, suppress T cells in the tumor environment. Where TAM family members are absent, antigen is more available for uptake by dendritic cells that can expand naive T cells that can traffic to the tumor. Tumor-infiltrating T cells find decreased macrophage suppression and increased antigen presentation, permitting increased control of tumors.