Fig. 5.
Fig. 5. Flu-specific CTL activation by DCs transduced with the lentiviral vector HFIG. / DCs were infected with HIG or HFIG or left uninfected. The ability of HFIG-transduced DCs to activate Flu-specific CTLs (DC.HFIG) was compared with untransduced or HIG-transduced DCs either nonpulsed (DC−, DC.HIG−) or pulsed (DC+, DC.HIG+) with the Flu peptide. CTL assays were performed after incubation of the DCs with autologous T cells for 8 to 10 days. T2 cells pulsed with the Flu peptide (T2+) or with the irrelevant MART-1 peptide (T2−) were used as targets. Data are shown for 1 of 3 independent experiments.

Flu-specific CTL activation by DCs transduced with the lentiviral vector HFIG.

DCs were infected with HIG or HFIG or left uninfected. The ability of HFIG-transduced DCs to activate Flu-specific CTLs (DC.HFIG) was compared with untransduced or HIG-transduced DCs either nonpulsed (DC, DC.HIG) or pulsed (DC+, DC.HIG+) with the Flu peptide. CTL assays were performed after incubation of the DCs with autologous T cells for 8 to 10 days. T2 cells pulsed with the Flu peptide (T2+) or with the irrelevant MART-1 peptide (T2) were used as targets. Data are shown for 1 of 3 independent experiments.

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