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. Author manuscript; available in PMC: 2010 Mar 17.
Published in final edited form as: J Immunol. 2006 Jan 1;176(1):329–334. doi: 10.4049/jimmunol.176.1.329

FIGURE 2.

FIGURE 2

ABM Tg CD4+CD25+ T cells exhibit powerful, TCR-restricted, suppressive properties in vitro. A, ABM Tg CD4+CD25+ T cells (5 × 104) do not proliferate in response to 3 × 105 irradiated bm12 splenocytes and suppress the proliferation of 5 × 104 CD4+CD25 T cells. B, The proliferation of 5 × 104 ABM Tg CD4+CD25 T cells in response to 3 × 105 irradiated bm12 splenocytes is powerfully suppressed by increasing numbers of ABM Tg, but not polyclonal C57BL/6, TRegs. C, Both 5 × 104 ABM Tg CD4+CD25 and CD4+CD25+ T cells proliferate in response to 104 bm12, but not CB6F1, bone marrow-derived mature dendritic cells. Cell proliferation was estimated in all cases by [3H]TdR incorporation. Data are expressed as the mean cpm of triplicate cultures ± SE. Data portrayed in all panels are representative of at least three independent experiments. D, ABM Tg TRegs (5 × 104) suppress the proliferation of 5 × 104 TEa CD4+CD25 T cells only when bm12 irradiated splenocytes are added to the stimulator CB6F1 cell population.