Statistical analysis was performed using graphpad prism statistical software (GraphPad Software, San Diego, CA). Non-parametric Mann–Whitney U-tests were used to determine differences between groups of subjects, and a two-tailed Spearman correlation at the 95% confidence interval was

used to assess the relationship between two groups of variables. We examined the number of NK cells and CD4+ and CD8+ T cells in a Brazilian cohort of HIV-1-seropositive subjects. The https://www.selleckchem.com/products/PD-98059.html cohort included 31 HIV-1-infected patients, of whom 16 patients were seropositive for HSV-2. A description of the cohort may be found in Table 1. These subjects were subdivided into individuals who were seropositive (n = 15) or seronegative (n = 16) for HSV-2 (HSV-2-negative subjects are hereafter referred to as ‘HIV-1 mono-infected’). Although there was no difference in the mean HIV-1 plasma viral load between these two groups, subjects co-infected with HSV-2 showed a pan-lymphocytosis, with elevated numbers of NK cells, CD4+ T cells, and CD8+ T cells relative to HIV-1 mono-infected subjects,

but this difference was Y27632 not significant except for CD4+ T cells (Fig. 1b). The numbers of both NK cells and CD4+ T cells were not significantly different for HIV-1-seronegative controls. Similar to our previous study,20 we observed a significantly elevated number of CD4+ T cells in subjects co-infected with HSV-2 relative to HIV-1 mono-infected subjects (mean = 859 cells/μl versus 474 cells/μl for HIV-1 mono-infected patients; P = 0·002). Furthermore,

the number of CD8+ T cells was higher than for seronegative controls for both HIV-1 mono-infected subjects (558 cells/μl versus 866 cells/μl; P = 0·017) and HSV-2 co-infected subjects (1215 cells/μl; P = 0·006). As a result, NK cell and T-cell levels in HSV-2 co-infected subjects were increased beyond the elevated levels seen in HIV-1 mono-infected subjects. We next evaluated the subset distribution of NK cells with respect to the level of CD56 expression. NK cells were separated into CD56bright CD16neg; CD56dim CD16pos; or CD56neg CD16pos subsets. The last group has been described as both increased in number Ceramide glucosyltransferase and dysfunctional in HIV-1-infected subjects.23 The frequency of these populations was examined as a percentage of total NK cells, and no significant difference was detected in the mean subset frequencies between subject groups (data not shown). We then used this percentage to calculate the absolute number of NK cells present in these subsets. The results of this calculation demonstrate that the elevated number of total NK cells is primarily attributable to an increase in the number of CD56dim NK cells (Fig. 1c). HIV-1 mono-infected subjects had a decreased mean number of CD56dim NK cells (227 cells/μl) relative to uninfected controls (354 cells/μl; P = 0·009), and HSV-2 co-infected subjects (331 cells/μl; P = 0·026).