KIR3DL1 and myelodysplastic syndrome: Recent studies suggest that NK cell dysfunction in MDS may be attributed to the presence of NK cells with immature phenotypes characterized by an increase in the proportion of CD56bright NK cells, higher “early” KIR expression (KIR2DL2/3), and lower “late” KIR expression (KIR2DL1 and KIR3DL) in MDS patients [22,24,29].