Induction of FoxP3 and acquisition of T regulatory activity by stimulated human CD4+CD25– T cells

Abstract

CD4(+)CD25(+) regulatory T (T(R)) cells have been described in both humans and mice. In mice, T(R) are thymically derived, and lack of T(R) leads to organ-specific autoimmunity. Recently, the forkhead/winged helix transcription factor, FoxP3, has been shown to be important for the function of T(R) cells in mice. In this study, human T(R) cells were examined and, in results similar to those of studies done in mice, expression of FoxP3 was found exclusively in CD4(+)CD25(+) T cells and correlated with the suppressive activity of these cells. In contrast to the mouse studies, activation of human CD4(+)CD25(–) T cells led to expression of FoxP3. Expression of FoxP3 in activated human CD4(+)CD25(+) cells also correlated with suppression of proliferation by these cells in freshly isolated CD4(+)CD25(–) T cells from the same donor. This suppression was cell-contact dependent and cytokine independent. Thus, in humans, during activation of CD4(+)CD25(–) T cells in an immune response, two populations of cells may arise, effector CD4(+)CD25(+ )and regulatory CD4(+)CD25(+) T cells, with expression of FoxP3 correlated with regulatory activity. These data also raise the possibility that a failure to generate peripheral T(R) cells properly may contribute to autoimmune disease and suggest a possible therapeutic role for FoxP3 in the treatment of such diseases.