Logo image
Human regulatory T cells: a unique, stable thymic subset or a reversible peripheral state of differentiation?
Journal article   Open access   Peer reviewed

Human regulatory T cells: a unique, stable thymic subset or a reversible peripheral state of differentiation?

Vinodh Pillai and Nitin J Karandikar
Immunology letters, Vol.114(1), pp.9-15
11/30/2007
DOI: 10.1016/j.imlet.2007.08.012
PMCID: PMC2095117
PMID: 17945352
url
http://doi.org/10.1016/j.imlet.2007.08.012View
Open Access

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.
Autoimmunity CD4 Antigens - immunology T-Lymphocytes, Regulatory - metabolism Virus Diseases - immunology Lymphocyte Activation Humans Autoimmune Diseases - immunology Thymus Gland - cytology CD8 Antigens - immunology T-Lymphocytes, Regulatory - immunology CD8 Antigens - metabolism Neoplasms - therapy Animals Forkhead Transcription Factors - metabolism Neoplasms - immunology T-Lymphocytes, Regulatory - cytology Autoimmune Diseases - therapy Thymus Gland - immunology Cell Differentiation CD4 Antigens - metabolism

Details

Metrics

Logo image