In ATC, this high macrophage infiltration in ATC tumor samples results in an altered-immunosuppressed immune microenvironment in 50% of cases and a hot immune environment in 34%, with a high expression of several inhibitory immune checkpoint mediators such as anti-cytotoxic T-lymphocyte-associated protein 4 (CTLA-4), programmed death-ligand 1–2 (PD-L1/PD-L2), TIGIT, etc., known to inhibit cytotoxic CD8+ T-cell functions [50]. This evidence concerns the gene CD274 and neoplasm.