Journal article
Human regulatory T cells: a unique, stable thymic subset or a reversible peripheral state of differentiation?
Immunology letters, Vol.114(1), pp.9-15
11/30/2007
DOI: 10.1016/j.imlet.2007.08.012
PMCID: PMC2095117
PMID: 17945352
Abstract
FOXP3 is probably the best marker available currently for identifying natural regulatory T cells (T(reg)s) in mice and humans. Evidence from mouse literature suggests that natural FOXP3(+) T(reg)s are formed in the thymus and expand in the periphery to contribute significantly to peripheral T(reg)s. In this review, we discuss recent reports that show that, in humans, the formation of FOXP3(+) T(reg)s is a natural consequence of T cell activation and that de novo peripheral generation of FOXP3(+) T(reg)s is a much more dominant source of circulating T(reg)s than natural thymically derived T(reg)s. We also suggest that the role of T(reg)s in human diseases must be reviewed in light of these new findings and great caution should be exercised in immunotherapeutic interventions that involve the modulation or generation of putative T(reg)s.
Details
- Title: Subtitle
- Human regulatory T cells: a unique, stable thymic subset or a reversible peripheral state of differentiation?
- Creators
- Vinodh Pillai - Department of Pathology, The University of Texas Southwestern Medical Center, 6000 Harry Hines Blvd., Dallas, TX 75390-9072, USANitin J Karandikar
- Resource Type
- Journal article
- Publication Details
- Immunology letters, Vol.114(1), pp.9-15
- DOI
- 10.1016/j.imlet.2007.08.012
- PMID
- 17945352
- PMCID
- PMC2095117
- NLM abbreviation
- Immunol Lett
- ISSN
- 0165-2478
- eISSN
- 1879-0542
- Publisher
- Netherlands
- Grant note
- R01 AI053439-04 / NIAID NIH HHS R56 AI053439 / NIAID NIH HHS R01 AI053439 / NIAID NIH HHS R56 AI053439-05A1 / NIAID NIH HHS
- Language
- English
- Date published
- 11/30/2007
- Academic Unit
- Pathology
- Record Identifier
- 9984046815402771
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