Fig. 2.
Fig. 2. CD4+CD25+ cells are hyporesponsive to polyclonal T-cell stimuli. / (A-D) The proliferative responses of CD4+CD25+(■) and CD4+CD25− (▪) cells to various stimuli are shown. In each experiment, 1 × 104 to 2 × 104 responder cells were cultured with PHA (2 μg/mL) plus 1 × 104 irradiated autologous ACs with or without IL-2 (10 U/mL, A); irradiated allogeneic PBMCs (B); soluble anti-CD3 with ACs (C); and soluble anti-CD3 with IL-2 (10 U/mL) in the presence of ACs (D). Conc indicates concentration. (E-F) Production of IL-2 (E) and IFN-γ (F) in the supernatants from the culture of CD4+CD25+ or CD4+CD25−(2 × 104) cells stimulated with PHA for 3 days in the presence of autologous ACs.

CD4+CD25+ cells are hyporesponsive to polyclonal T-cell stimuli.

(A-D) The proliferative responses of CD4+CD25+(■) and CD4+CD25 (▪) cells to various stimuli are shown. In each experiment, 1 × 104 to 2 × 104 responder cells were cultured with PHA (2 μg/mL) plus 1 × 104 irradiated autologous ACs with or without IL-2 (10 U/mL, A); irradiated allogeneic PBMCs (B); soluble anti-CD3 with ACs (C); and soluble anti-CD3 with IL-2 (10 U/mL) in the presence of ACs (D). Conc indicates concentration. (E-F) Production of IL-2 (E) and IFN-γ (F) in the supernatants from the culture of CD4+CD25+ or CD4+CD25(2 × 104) cells stimulated with PHA for 3 days in the presence of autologous ACs.

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