In human melanoma samples infiltrated by T cells and GARP-expressing Tregs, we found evidence of TGF-β signaling within the T cell compartment, suggesting that blockade of Treg-derived TGF-β1 activity with anti-GARP:TGF-β1 mAbs may be sufficient to increase CD8+ T-cell-mediated anti-tumor immunity, while avoiding potential toxicity associated with a more global inhibition of TGF-β signaling. Here, CD8A is linked to neoplasm.