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Control of Regulatory T Cell Development by the Transcription Factor <i>Foxp3</i>

Science · 2003 · Vol. 299(5609) · pp. 1057–1061
Shohei HoriTakashi NomuraShimon Sakaguchi

Abstract

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.

Immune Cell Function and InteractionT-cell and B-cell ImmunologyCAR-T cell therapy researchTranscription factorCell biologyControl (management)BiologyChemistryGeneticsComputer scienceGene

MeSH terms

AnimalsAutoimmune DiseasesDNA-Binding ProteinsGastritisImmune ToleranceLymphocyte ActivationMice, Inbred BALB CMice, TransgenicMutationReceptors, Antigen, T-CellRecombinant Fusion ProteinsT-LymphocytesThymus GlandTransduction, GeneticInflammatory Bowel Diseases
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