CD56-negative NK cells with impaired effector function expand in CMV and EBV co-infected healthy donors with age.

Natural killer cells lacking expression of CD56 (CD56(neg) NK cells) have been described in chronic HIV and hepatitis C virus infection. Features and functions of CD56(neg) NK cells in the context of latent infection with CMV and/or EBV with age are not known. In a cohort of healthy donors >60 years of age, we found that co-infection with CMV and EBV drives expansion of CD56(neg) NK cells. Functionally, CD56(neg) NK cells displayed reduced cytotoxic capacity and IFN-gamma production, a feature that was enhanced with CMV/EBV co-infection. Further, the frequency of CD56(neg) NK cells correlated with accumulation of end-stage-differentiated T cells and a reduced CD4/CD8 T cell ratio, reflecting an immune risk profile. CD56(neg) NK cells had a mature phenotype characterized by low CD57 and KIR expression and lacked characteristics of cell senescence. No changes in their activating NK cell receptor expression, and no upregulation of the negative co-stimulation receptors PD-1 or TIM-3 were observed. In all, our data identify expansion of dysfunctional CD56(neg) NK cells in CMV+EBV+ elderly individuals suggesting that these cells may function as shape-shifters of cellular immunity and argue for a previously unrecognized role of EBV in mediating immune risk in the elderly.