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Image Search Results
Journal: The Journal of Experimental Medicine
Article Title: Phenotype, Localization, and Mechanism of Suppression of CD4 + CD25 + Human Thymocytes
doi: 10.1084/jem.20020110
Figure Lengend Snippet: Cell contact–dependent suppressive activity of CD4 + CD25 + human thymocytes is abrogated by the combined action of anti–CTLA-4 and anti-TGFβ1 mAbs. (A) CD4 + CD25 − thymocytes were stimulated with irradiated T cell–depleted allogeneic PBMNCs in the lower chamber of a transwell plate in the absence or presence of CD4 + CD25 + thymocytes, placed in the same or in the top chamber. On day 5, cells present in the bottom chamber were harvested and their proliferation assessed by measuring 3 [H]TdR uptake. (B) CD4 + CD25 − thymocytes were stimulated with allogeneic irradiated T cell–depleted PBMNCs in the presence of different numbers of autologous purified CD4 + CD25 + thymocytes without (black columns) or with isotype control (IgG1+IgG2a) (gray columns), anti-CTLA-4 (hatched columns), or anti–TGF-β1 mAb (dotted columns), or mixtures of them (white columns). Cell proliferation was measured by assessment of 3 [H]TdR uptake. Mean values (±SD) obtained in four separate experiments are reported.
Article Snippet: The PE-conjugated anti-TNFR2 (22235.311, mouse IgG2a), the purified anti–TGF-β1 (9016.2, mouse IgG1) neutralizing mAb, TGF-βR2 (goat IgG) neutralizing Ab, and biotin-conjugated anti–TGF-β1 (chicken IgY) and
Techniques: Activity Assay, Irradiation, Purification, Control
Journal: The Journal of Experimental Medicine
Article Title: Phenotype, Localization, and Mechanism of Suppression of CD4 + CD25 + Human Thymocytes
doi: 10.1084/jem.20020110
Figure Lengend Snippet: CTLA-4 and TGF-β1–mediated suppression is due to the inhibition of IL-2R α-chain expression and is overcome by IL-15. (A) CFSE-labeled CD4 + CD25 − thymocytes were stimulated with irradiated allogeneic PB non-T cells in absence or presence of autologous CD4 + CD25 + thymocytes with anti–CTLA-4, anti–TGF-β1, anti–CTLA-4 plus anti–TGF-β1 or isotype-matched (IgG1 plus IgG2a) mAbs, and assessed by flow cytometry for proliferation and surface CD25 expression. One representative of three separate experiments is shown. (B) CD25 (left) and CD69 (right) expression by CD4 + CD25 − thymocytes cultured under the experimental conditions mentioned in (A). CD4 + CD25 − thymocytes without mAb added (black columns), or containing isotype control (gray columns), anti–TGF-β1 (dotted columns), anti–CTLA-4 (hatched columns), or anti–CTLA-4 plus anti–TGF-β1 (white columns) mAbs. Columns represent mean values (±SD) found in three separate experiments. (C) Effect of the addition of exogenous IL-2 or IL-15 on the proliferative response of CD4 + CD25 − thymocytes stimulated with irradiated allogeneic non-T cells in absence or presence of CD4 + CD25 + autologous thymocytes. Columns represent mean values (±SD) obtained in three separate experiments.
Article Snippet: The PE-conjugated anti-TNFR2 (22235.311, mouse IgG2a), the purified anti–TGF-β1 (9016.2, mouse IgG1) neutralizing mAb, TGF-βR2 (goat IgG) neutralizing Ab, and biotin-conjugated anti–TGF-β1 (chicken IgY) and
Techniques: Inhibition, Expressing, Labeling, Irradiation, Flow Cytometry, Cell Culture, Control