Abstract

Several mechanisms control discrimination between self and non-self, including the thymic deletion of autoreactive T cells and the induction of anergy in the periphery. In addition to these passive mechanisms, evidence has accumulated for the active suppression of autoreactivity by a population of regulatory or suppressor T cells that co-express CD4 and CD25 (the interleukin-2 receptor alpha-chain). CD4+ CD25+ T cells are powerful inhibitors of T-cell activation both in vivo and in vitro. The enhancement of suppressor-cell function might prove useful for the treatment of immune-mediated diseases, whereas the downregulation of these cells might be beneficial for the enhancement of the immunogenicity of vaccines that are specific for tumour antigens.

Keywords

IL-2 receptorSuppressorImmunogenicityImmunologyImmune systemDownregulation and upregulationBiologyCell biologyImmune tolerancePopulationAntigenT cellInterleukin 10MedicineGeneGenetics

MeSH Terms

AbataceptAnimalsAntigen-Presenting CellsAntigensCDAntigensDifferentiationCD4 AntigensCTLA-4 AntigenCytokinesHomeostasisHumansImmune ToleranceImmunoconjugatesIn Vitro TechniquesLymphocyte ActivationMiceModelsImmunologicalRatsReceptorsInterleukin-2T-LymphocytesRegulatoryThymus GlandTransforming Growth Factor beta

Affiliated Institutions

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Publication Info

Year
2002
Type
review
Volume
2
Issue
6
Pages
389-400
Citations
2102
Access
Closed

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Cite This

Ethan M. Shevach (2002). CD4+CD25+ suppressor T cells: more questions than answers. Nature reviews. Immunology , 2 (6) , 389-400. https://doi.org/10.1038/nri821

Identifiers

DOI
10.1038/nri821
PMID
12093005

Data Quality

Data completeness: 81%