Journal
NATURE REVIEWS IMMUNOLOGY
Volume 10, Issue 7, Pages 490-500Publisher
NATURE PUBLISHING GROUP
DOI: 10.1038/nri2785
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Funding
- Fondation pour la Recherche Medicale
- Japan Society for the Promotion of Science
- Ministry of Education, Sports and Culture of Japan
- US NIH [UO1DK6192601, RO1NS2424710, PO1AI39671, PO1NS38037]
- National Multiple Sclerosis Society [RG2172C9, RG3308A10]
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Forkhead box P3 (FOXP3)(+) regulatory T (T-Reg) cells are potent mediators of dominant self tolerance in the periphery. But confusion as to the identity, stability and suppressive function of human T-Reg cells has, to date, impeded the general therapeutic use of these cells. Recent studies have suggested that human T-Reg cells are functionally and phenotypically diverse. Here we discuss recent findings regarding human T-Reg cells, including the ontogeny and development of T-Reg cell subsets that have naive or memory phenotypes, the unique mechanisms of suppression mediated by T-Reg cell subsets and factors that regulate T-Reg cell lineage commitment. We discuss future studies that are needed for the successful therapeutic use of human T-Reg cells.
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