Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2038690 | Cell | 2006 | 4 Pages |
Abstract
Regulatory T cells suppress autoimmune responses to self-antigens. Recent studies, including one in this issue of Cell ( Wu et al., 2006), suggest that the ability of T cells to choose between launching a productive immune response, functional inactivation, or developing into regulatory T cells depends upon the interplay of the key transcriptional regulators FOXP3 and NFAT.
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Authors
Alexander Y. Rudensky, Marc Gavin, Ye Zheng,