Figure 4
Figure 4. Induction of CD4+ T-cell responses. (Top panel) Polarization of naive CD4+CD45RA+ T cells. CD4+CD45RA+ naive T cells were isolated via magnetic bead-based techniques and restimulated once after 5 days with allogeneic DC (1:10) that were matured as indicated. After 10 days, cells were harvested and stimulated with PMA and ionomycin. For detection of IFN-γ and IL-2, cells were stimulated for 6 hours. For detection of IL-4 cells were stimulated for 16 hours. Brefeldin A was added during the last 2 hours of incubation. For detection of intracellular cytokines, cells were permeabilized with 0.1% saponin, stained with the indicated antibodies and analyzed by FACS. (Bottom panel) Allogeneic mixed lymphocyte reactions. T cells (105/well) that had been isolated using magnetic bead-mediated negative selection were cocultured at the indicated stimulator to responder ratios with allogeneic DCs that had been matured with CC or CD40L in the presence or absence of LTC4 or PGE2 for 24 hours. After 5 days, cell proliferation was determined using the WST-1 reagent according to the manual provided by the manufacturer. The data are shown as the mean ± SEM of triplicate cultures and represent 1 of 2 experiments that yielded similar results.

Induction of CD4+ T-cell responses. (Top panel) Polarization of naive CD4+CD45RA+ T cells. CD4+CD45RA+ naive T cells were isolated via magnetic bead-based techniques and restimulated once after 5 days with allogeneic DC (1:10) that were matured as indicated. After 10 days, cells were harvested and stimulated with PMA and ionomycin. For detection of IFN-γ and IL-2, cells were stimulated for 6 hours. For detection of IL-4 cells were stimulated for 16 hours. Brefeldin A was added during the last 2 hours of incubation. For detection of intracellular cytokines, cells were permeabilized with 0.1% saponin, stained with the indicated antibodies and analyzed by FACS. (Bottom panel) Allogeneic mixed lymphocyte reactions. T cells (105/well) that had been isolated using magnetic bead-mediated negative selection were cocultured at the indicated stimulator to responder ratios with allogeneic DCs that had been matured with CC or CD40L in the presence or absence of LTC4 or PGE2 for 24 hours. After 5 days, cell proliferation was determined using the WST-1 reagent according to the manual provided by the manufacturer. The data are shown as the mean ± SEM of triplicate cultures and represent 1 of 2 experiments that yielded similar results.

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