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. Author manuscript; available in PMC: 2009 Nov 15.
Published in final edited form as: J Immunol. 2008 Nov 15;181(10):6955–6963. doi: 10.4049/jimmunol.181.10.6955

Figure 3. Imatinib mesylate hampers Treg suppressive activity and FoxP3 expression.

Figure 3

CD4+CD25+ Treg from lymphoid tissues of BALB/c mice were exposed to increasing but non-toxic concentrations of imatinib mesylate for 48 hrs, recovered and washed 3 times in complete medium to eliminate residual imatinib mesylate. (A) The effect of treated or untreated Treg on the proliferation of responder CD4+CD25 T lymphocytes (CD25) stimulated with mitomycin C-treated allogeneic APC was determined by [3H]-thymidine incorporation assays. *, p<0.02; **, p<0.005. (B) Expression of FoxP3 in CD4+CD25+ Treg treated for 48 hrs with the indicated concentrations of imatinib. Representative results of three independent experiments. (C) TGF-β1 concentration was assessed by ELISA in imatinib mesylate-treated (48 hrs) CD4+CD25+ Treg (CD25+Treg) or CD4+CD25 T cell (CD25) cultures. No significant difference was found between groups. Representative results of two independent experiments.