Analyses performed on solid-organ transplanted (SOT) recipients with acute HCMV infection clarified the development of this subset in several discrete steps marked by the acquisition on the NK cell surface of a specific set of receptors: (a) increase of NKG2C amount, (b) acquisition of CD57 expression, and (c) increase of CD57 expression, resulting in the terminal full mature subset phenotype CD57+NKG2Cbright HMCV-associated NK cell subset (17). Here, B3GAT1 is linked to cytomegalovirus infection.