Figure 4
Figure 4. Antigen specificity of the in vitro expanded Treg cells. (A) Vβ TCR-usage of the alloantigen-stimulated Treg cells. Fresh CD4+CD25+ T cells (⊡) and CD25+ line (▪) were stained with 15 different FITC-labeled anti–TCR Vβ mAbs and analyzed by flow cytometry. (B) CD25− line (1 × 105; 25−) were cultured for 3 days alone, with 1:1 CD25− line (25−/25−), with decreasing ratios (25−/25+; ratios, 1:1, 1:0.5, 1:0.25) of CD25+ line, in the presence of syngeneic irradiated DCs pulsed with Kb peptide. (C) Freshly isolated CD4+CD25− responder (25−) or CD25+ line cells (1 × 105) were cultured alone or were cocultured 1:1 for 4 days in the presence of soluble anti-CD3 antibody and APCs (□), irradiated mature syngeneic CBA DCs (H2k) (⊡), CBK DCs (H2k+Kb) (▪), or B10.A DCs (H2k+Dd) (). Results are representative of 3 independent experiments. Error bars reflect mean ± SD of triplicate cultures.

Antigen specificity of the in vitro expanded Treg cells. (A) Vβ TCR-usage of the alloantigen-stimulated Treg cells. Fresh CD4+CD25+ T cells (⊡) and CD25+ line (▪) were stained with 15 different FITC-labeled anti–TCR Vβ mAbs and analyzed by flow cytometry. (B) CD25 line (1 × 105; 25) were cultured for 3 days alone, with 1:1 CD25 line (25/25), with decreasing ratios (25/25+; ratios, 1:1, 1:0.5, 1:0.25) of CD25+ line, in the presence of syngeneic irradiated DCs pulsed with Kb peptide. (C) Freshly isolated CD4+CD25 responder (25) or CD25+ line cells (1 × 105) were cultured alone or were cocultured 1:1 for 4 days in the presence of soluble anti-CD3 antibody and APCs (□), irradiated mature syngeneic CBA DCs (H2k) (⊡), CBK DCs (H2k+Kb) (▪), or B10.A DCs (H2k+Dd) (). Results are representative of 3 independent experiments. Error bars reflect mean ± SD of triplicate cultures.

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