NK cells co-cultured with BYL719 supplier autologous SmartDCs were not activated, whereas NK cells co-cultured with SmyleDCs were activated, as modest increased frequencies of IFN-γ (p = 0.161) and TNF-α (p = 0.045) positive NKs were observed ( Fig. S5b and c). We evaluated whether CD8+ T cells obtained from a CMV-seropositive donor could be stimulated in vitro with Conventional DCs or iDCs pulsed with pp65 peptides and result in the expansion of pp65-specific T cells. iDCs produced with donor monocytes and maintained in culture for 7 days were loaded with a pp65 overlapping peptide pool and used to stimulate autologous CD8+ T cells. After 7 days of stimulation, the CD8+ T cell cultures were analyzed for production

of several cytokines ( Fig. 5 and Fig. 6). pp65-antigenic stimulation by

the iDCs was required for high production of IFN-γ (produced by activated CTLs) and, surprisingly, also for high production of IL-13 (a cytokine typically produced by activated Th2 cells). IL-5, a cytokine typically secreted by T effector memory cells, was higher for iDC than for conventional DCs with pp65 antigenic stimulation. Production of TNF-α and IL-8 were also stimulated with antigen, albeit their production by conventional DCs or by iDCs was less dependent on pp65 peptides. Stimulation with conventional DCs or with iDCs loaded with pp65 peptides resulted in a substantial (2- click here to 3-fold) increase in T cell numbers in comparison with the unloaded DCs ( Fig. 5 and Fig. 6). The detection of pp65-reactive CD8+ T cells in the cultures was

performed with tetramers specific to two pp65 epitopes (NLVPMVATV: restricted to HLA-A*0201 and TPRVTGGGAM: restricted to HLA-B*0702) and flow cytometry analyses ( Fig. 5 and Fig. 6). The baseline frequency of CD8+ T cells reactive against these epitopes prior to stimulation was approximately 3%. After stimulation with conventional Etomidate DCs or iDCs pulsed with the peptides, the frequencies increased to 33% (11-fold) for SmyleDC + pp65 and to 20% (6-fold) with SmartDC + pp65. Conventional DCs or iDCs that were not loaded with pp65 antigen did not lead to a noticeable expansion of pp65-reactive T cells. The pp65-reactive T cells that were expanded after the 7 days of stimulation with iDCs pulsed with pp65 antigens were further analyzed for the distribution of T central memory (TCM: CD45RA−/CD62L+) and T effector memory (TEM: CD45RA−/CD62L−) ( Fig. 5 and Fig. 6). Altogether, the data indicated comparable effects of conventional DCs versus iDCs in the stimulation of CTL responses when the antigenic epitopes were provided exogenously as peptides. One particular aspect that seems to favor the stimulation of CTLs by SmyleDCs pulsed with peptides is that these cells did not require maturation with exogenous cytokines to reach the plateau of stimulation and, therefore, seem to be intrinsically more activated than conventional DCs or SmartDCs ( Fig. S6c and d).