Regulatory T cells engage in the maintenance of immunological self-tolerance by actively suppressing self-reactive lymphocytes. Little is known, however, about the molecular mechanism of their development. Here we show that Foxp3, which encodes a transcription factor that is genetically defective in an autoimmune and inflammatory syndrome in humans and mice, is specifically expressed in naturally arising CD4+ regulatory T cells. Furthermore, retroviral gene transfer of Foxp3 converts naïve T cells toward a regulatory T cell phenotype similar to that of naturally occurring CD4+ regulatory T cells. Thus, Foxp3 is a key regulatory gene for the development of regulatory T cells.
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Hori et al. (Thu,) studied this question.
www.synapsesocial.com/papers/68f648ee33dca03d982ea4a2 — DOI: https://doi.org/10.1126/science.1079490
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:
Shohei Hori
Takashi Nomura
Shimon Sakaguchi
Science
Kyoto University
RIKEN Center for Integrative Medical Sciences
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