58 Although kDCs are capable of cytotoxic function, their differentiation into a killer phenotype is largely dependent on the presence of stimulatory factors
such as lipopolysaccharide, IL-15, IFN-α or IFN-γ,59,60 which were not used in any of our cytotoxic functional studies using enriched CD8α− and CD8α+ NK cells (Fig. 5c,e). Given this, we believe that the capacity of CD8α− NK cells to mediate modest (albeit significant) cytotoxic function is in direct correlation Selleck NVP-LDE225 to their activation profile and expression of cytotoxic proteins, and not to the potential acquisition of a killer phenotype by mDCs. Evaluation of PBMCs from SIV-infected macaques for CD8α− NK cells showed that these cells, and their CD16/CD56 subpopulations, are present at frequencies similar to those in naive animals (Fig. 7a,c). On the other hand, we detected a significant decrease in the frequency of CD8α+ CD16+ NK cells, which was accompanied by a significant increase
in the proportion of CD8α+ CD56− CD16− NK cells (Fig. 7b). Interestingly, when comparing CD16/CD56 subpopulations within CD8α− NK cells of naive and SIV-infected macaques, we also observed a decrease in the proportion of CD8α− CD16+ cells MLN0128 supplier and a concomitant rise in the proportion of CD8α− CD56− CD16− NK cells, although these changes did not reach statistical significance (Fig. 7c). This observation suggests that during SIV infection, loss of CD3− CD16+ cells affects both CD8α− and CD8α+ NK cell subsets. Our results are in line with previous descriptions of HIV patients, where CD3− CD8+ CD16+ NK cells are depleted despite an overall increase in CD8+ lymphocytes.61,62 The ability of CD8α− NK cells to mediate ADCC activity during adaptive immune responses when anti-viral antibodies are click here present, could contribute significantly to disease prevention and control.19,21,24 Stratov et al.63 have shown that robust ADCC responses, targeted mainly towards the Env protein, are observed in HIV-infected subjects. Importantly,
the effector cells identified were of the CD3− CD4− CD8− CD14− CD2+ CD56+/− phenotype, which is strikingly similar to the phenotype we describe here for macaque CD8α− NK cells. Despite the significant presence of mDCs in the CD8α− NK cell gate, our results are in line with those reported by Rutjens et al.34 and Reeves et al.,40 and confirm the presence and functional capacity of a CD8α− NK cell population in rhesus macaque PBMCs. Natural killer cells express a wide variety of chemokine receptors and tissue-homing molecules that influence their tissue distribution and migratory potential.29 Chronic SIV infection has been shown to enhance the expression of the gut-homing marker α4/β7 in different subsets of NK cells.47 It will be of interest to analyse the chemokine-receptor and tissue-homing molecule expression profiles of this novel subpopulation of circulatory CD8α− NK cells in naive and SIV-infected macaques.