Figure 2
T cells from allogeneic CD8α+ DC–vaccinated mice. Reduced expansion and proinflammatory cytokine secretion were shown in vitro in BALB/c mice that were immunized with diluent control or allogeneic B6 BM-derived CD8α+ DCs or CD8α− DCs as described in “Methods.” BALB/c CD90+ T cells (2 × 105/well) were then harvested from them and cultured for 96 hours with either syngeneic or irradiated (3000 cGy) allogeneic B6 BM DCs (1 × 104/well). During the final 16 hours of a 96-hour culture, cells were pulsed with [3H] thymidine and assayed for (A) proliferation. Supernatants were collected at 80 hours and assayed by for (B) IL-2, (C) IFN-γ, and (D) IL-10. Error bars represent SE. *P < .05 between diluent control and allogeneic CD8α+ DC–vaccinated groups. Data are from one of 3 similar experiments. *P < .05 between diluent control and allogeneic CD8α+ DC–vaccinated groups.

T cells from allogeneic CD8α+ DC–vaccinated mice. Reduced expansion and proinflammatory cytokine secretion were shown in vitro in BALB/c mice that were immunized with diluent control or allogeneic B6 BM-derived CD8α+ DCs or CD8α DCs as described in “Methods.” BALB/c CD90+ T cells (2 × 105/well) were then harvested from them and cultured for 96 hours with either syngeneic or irradiated (3000 cGy) allogeneic B6 BM DCs (1 × 104/well). During the final 16 hours of a 96-hour culture, cells were pulsed with [3H] thymidine and assayed for (A) proliferation. Supernatants were collected at 80 hours and assayed by for (B) IL-2, (C) IFN-γ, and (D) IL-10. Error bars represent SE. *P < .05 between diluent control and allogeneic CD8α+ DC–vaccinated groups. Data are from one of 3 similar experiments. *P < .05 between diluent control and allogeneic CD8α+ DC–vaccinated groups.

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