Interestingly, its function changes according to the disease phase: in low-risk MDS, anti-leukemia cytotoxic (CD8+), helper (Th17) T cells and NK cells are expanded, in the presence of low counts of pro-leukemia T-regulatory lymphocytes (Treg); in high-risk MDS and AML, instead, Treg prevails over CD8+, Th17 and NK cells, suggesting that tumor clones acquire immune tolerance during disease progression (19, 20). This evidence concerns the gene CD8A and acute myeloid leukemia.