Figure 6
Figure 6. IL-21 partially reverses Treg-mediated inhibition of CD8 T-cell proliferation. (A) Sorted Tregs (5 × 104/well) were cultured with IL-2 (12.5 U/mL), IL-7 (10 ng/mL), IL-15 (30 ng/mL), or IL-21 (30 ng/mL) in the presence or absence of anti-CD3 and autologous dendritic cells. (B) Sorted CD8+CD25− effector T cells (5 × 104/well) were cultured with Tregs at ratio of 1:1 (CD8+/Tregs) in the presence of anti-CD3 and autologous dendritic cells. IL-21 (30 ng/mL) was added as indicated. Proliferation was measured by [3H]thymidine incorporation pulsed on day 3 and harvested 16 to 20 hours later. The results of CPM were calculated from triplicate wells with standard error of the mean. The P value was obtained by applying paired sample t test to evaluate the influence of Tregs on the CD8 proliferation with and without IL-21. Error bars represent plus or minus standard error calculated from triplicate results for each data point.

IL-21 partially reverses Treg-mediated inhibition of CD8 T-cell proliferation. (A) Sorted Tregs (5 × 104/well) were cultured with IL-2 (12.5 U/mL), IL-7 (10 ng/mL), IL-15 (30 ng/mL), or IL-21 (30 ng/mL) in the presence or absence of anti-CD3 and autologous dendritic cells. (B) Sorted CD8+CD25 effector T cells (5 × 104/well) were cultured with Tregs at ratio of 1:1 (CD8+/Tregs) in the presence of anti-CD3 and autologous dendritic cells. IL-21 (30 ng/mL) was added as indicated. Proliferation was measured by [3H]thymidine incorporation pulsed on day 3 and harvested 16 to 20 hours later. The results of CPM were calculated from triplicate wells with standard error of the mean. The P value was obtained by applying paired sample t test to evaluate the influence of Tregs on the CD8 proliferation with and without IL-21. Error bars represent plus or minus standard error calculated from triplicate results for each data point.

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