Figure 3
Figure 3. Effects of inhibiting endosomal acidification on ISCOMATRIX facilitated HLA-A2-restricted cross-presentation of NY-ESO-1 or Melan-A by MoDCs. Immature MoDCs (1 × 105) were either untreated or treated with 5 or 10nM Con-B for 45 minutes before and throughout the 18-hour pulse with 10 μg/mL NY-ESO-1/ISCOMATRIX vaccine or 10 μg/mL NY-ESO-1 (A) or Melan-A protein (B) together with 10 μg/mL ISCOMATRIX adjuvant in 96-well, round-bottom plates. In parallel, untreated or inhibitor-treated MoDCs were pulsed with cognate peptide for 30 minutes and then washed thoroughly before the 4-hour coculture with CTL lines to control for nonspecific effects of the inhibitor. A standard ICS was then performed, and IFN-γ levels were assessed by flow cytometry. Data are mean ± SD of 3 separate donors. *P < .01 vs no Con-B treatment.

Effects of inhibiting endosomal acidification on ISCOMATRIX facilitated HLA-A2-restricted cross-presentation of NY-ESO-1 or Melan-A by MoDCs. Immature MoDCs (1 × 105) were either untreated or treated with 5 or 10nM Con-B for 45 minutes before and throughout the 18-hour pulse with 10 μg/mL NY-ESO-1/ISCOMATRIX vaccine or 10 μg/mL NY-ESO-1 (A) or Melan-A protein (B) together with 10 μg/mL ISCOMATRIX adjuvant in 96-well, round-bottom plates. In parallel, untreated or inhibitor-treated MoDCs were pulsed with cognate peptide for 30 minutes and then washed thoroughly before the 4-hour coculture with CTL lines to control for nonspecific effects of the inhibitor. A standard ICS was then performed, and IFN-γ levels were assessed by flow cytometry. Data are mean ± SD of 3 separate donors. *P < .01 vs no Con-B treatment.

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