Figure 4
Figure 4. Cytokine-induced IFN-γ+ Th cells are controlled by CD25++ Tregs. (A) CD25++ Tregs (II) and CD45RA−IL-18Rα+ memory-effector (III) or CD45RA+IL-18Rα− naive (IV) responder Th cells were sorted from PBMCs (I). (B) CFDA-labeled CD45RA+IL-18Rα− naive responder Th cells were cultured with T-cell stimulation beads in the presence of equal numbers of CFDA−CD45RA+IL-18Rα− control cells or CD25++ Tregs. Proliferation was assessed after 84 hours according to loss of CFDA by FACS. (C) CFDA-labeled CD45RA−IL-18Rα+ responder Th cells were stimulated for 36 hours with IL-12 + IL-18 + IL-15 or with the cytokine cocktail or for 18 hours with T-cell stimulation beads in the presence of equal numbers of CFDA−CD45RA−IL-18Rα+ control cells or CD25++ Tregs. Frequencies of CFDA+IFN-γ+ responder cells were assessed intracellularly by FACS; cocultures with control cells were set to 100%. One representative experiment of 3 (B) or 4 (C), respectively, is shown.

Cytokine-induced IFN-γ+ Th cells are controlled by CD25++ Tregs. (A) CD25++ Tregs (II) and CD45RAIL-18Rα+ memory-effector (III) or CD45RA+IL-18Rα naive (IV) responder Th cells were sorted from PBMCs (I). (B) CFDA-labeled CD45RA+IL-18Rα naive responder Th cells were cultured with T-cell stimulation beads in the presence of equal numbers of CFDACD45RA+IL-18Rα control cells or CD25++ Tregs. Proliferation was assessed after 84 hours according to loss of CFDA by FACS. (C) CFDA-labeled CD45RAIL-18Rα+ responder Th cells were stimulated for 36 hours with IL-12 + IL-18 + IL-15 or with the cytokine cocktail or for 18 hours with T-cell stimulation beads in the presence of equal numbers of CFDACD45RAIL-18Rα+ control cells or CD25++ Tregs. Frequencies of CFDA+IFN-γ+ responder cells were assessed intracellularly by FACS; cocultures with control cells were set to 100%. One representative experiment of 3 (B) or 4 (C), respectively, is shown.

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