3A and B). The polyfunctional CD4+ T-cell response peaked 28 days after vaccination in most adolescents, and 84 days after vaccination in most children. However, in some children this response peaked 7 days after vaccination (Fig. 3A and B and Supporting Information Fig. 4). The polyfunctional CD4+ T-cell population was long-lived in both age groups as frequencies detected at 168 days after vaccination still exceeded pre-vaccination levels (Fig. 3A and B and Supporting Information Fig. 4). A novel population of polyfunctional CD4+ T cells that co-expressed all four of IFN-γ, IL-2, TNF-α and IL-17, which we have termed Th1/Th17 cells, was induced by MVA85A vaccination in adolescents

(Fig. 3A and D). In contrast, the find more Autophagy signaling pathway inhibitors frequency of this population in children was much smaller (Fig. 3C and F). In children, we also assessed expression of GM-CSF; the majority of Ag85A-specific IFN-γ-, IL-2- and TNF-α-expressing cells co-expressed this cytokine (Fig. 3B and E and Supporting Information Fig. 3). Overall, >50% of Ag85A-specific CD4+ T cells were polyfunctional (i.e. the cells expressed ≥3 cytokines) at all time points following vaccination,

both in adolescents and in children (Fig. 3D–H). In children, the proportion of cytokine-producing T cells that were polyfunctional increased over time; by 168 days post-vaccination >60% of Ag85A-specific cells expressed ≥3 cytokines (Fig. 3E, F and H). Interestingly, in contrast to the Ag85A-specific response, the BCG-specific response was markedly less polyfunctional throughout the follow-up period;

more than 75% of BCG-specific CD4+ T cells expressed one or two cytokines only (Fig. 3G and H). We also compared the magnitude of the Ag85A-specific T-cell response between adolescents and children 7 days after vaccination (Supporting Information Table 2). The frequencies selleck chemicals llc of IFN-γ-expressing T cells, whether measured by ELISpot or flow cytometry, did not differ between the two groups. IL-2-expressing CD4+ T-cell frequencies were also not different. However, when total cytokine+ CD4+ T-cell frequencies, TNF-α-expressing, or IFN-γ, IL-2 and TNF-α co-expressing polyfunctional CD4+ T-cell frequencies were compared, lower frequencies were observed in children. Because lymphocyte and CD4 counts are highest in infants and decrease with age 26, 27, we hypothesized that adjustment for cell counts would negate these differences. However, absolute lymphocyte and CD4 counts for the vaccinees were not available. We therefore classified the subjects into different age categories, and adjusted the corresponding lymphocyte or CD4 counts for median cell counts reported in Ugandan children 26. Adjustment of these T-cell response data for age-specific CD4 counts did not negate the differences observed for total cytokine+ and TNF-α levels (Supporting Information Table 2).