Figure 3.
Figure 3. Induction of lymphocyte proliferation in primary and secondary allogeneic cultures. (A) The allostimulatory activity of DCs obtained in the different cytokine combinations was tested in primary cultures, using monocyte-depleted PBMCs. Proliferating lymphocytes were identified in density plots as CD4+/BrdU+ double-positive cells. (B) In primary cultures, IL-16-DCs and TPO-DCs showed higher allostimulatory activity than control SCF-DCs, whereas IL-16/TPO-DCs were unable to stimulate the proliferation of allogeneic T lymphocytes. The mean ± SEM from 9 independent experiments is shown. IL-16-DCs, TPO-DCs, and IL-16/TPO-DCs compared with SCF-DCs with the paired Wilcoxon signed rank test. (C) Tested in a 2-step culture system, IL-16/TPO-DCs induced tolerance of cocultured T cells. Purified naive T cells were cultured alone (left column) or cocultured with either SCF-DCs (center column) or IL-16/TPO-DCs (right column). After 5 days, the T cells were harvested, washed, and rested for 2 days. The rested T cells from primary cultures were subsequently rechallenged with SCF-DCs. Proliferation of T lymphocytes was assessed as BrdU incorporation after 4 days. One representative of 3 independent experiments is shown.

Induction of lymphocyte proliferation in primary and secondary allogeneic cultures. (A) The allostimulatory activity of DCs obtained in the different cytokine combinations was tested in primary cultures, using monocyte-depleted PBMCs. Proliferating lymphocytes were identified in density plots as CD4+/BrdU+ double-positive cells. (B) In primary cultures, IL-16-DCs and TPO-DCs showed higher allostimulatory activity than control SCF-DCs, whereas IL-16/TPO-DCs were unable to stimulate the proliferation of allogeneic T lymphocytes. The mean ± SEM from 9 independent experiments is shown. IL-16-DCs, TPO-DCs, and IL-16/TPO-DCs compared with SCF-DCs with the paired Wilcoxon signed rank test. (C) Tested in a 2-step culture system, IL-16/TPO-DCs induced tolerance of cocultured T cells. Purified naive T cells were cultured alone (left column) or cocultured with either SCF-DCs (center column) or IL-16/TPO-DCs (right column). After 5 days, the T cells were harvested, washed, and rested for 2 days. The rested T cells from primary cultures were subsequently rechallenged with SCF-DCs. Proliferation of T lymphocytes was assessed as BrdU incorporation after 4 days. One representative of 3 independent experiments is shown.

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