Abstract

Summary: There is accumulating evidence that T‐cell‐mediated dominant control of self‐reactive T‐cells contributes to the maintenance of immunologic self‐tolerance and its alteration can cause autoimmune disease. Efforts to delineate such a regulatory T‐cell population have revealed that CD25 + cells in the CD4 + population in normal naive animals bear the ability to prevent autoimmune disease in vivo and, upon antigenic stimulation, suppress the activation/proliferation of other T cells in vitro . The CD25 + CD4 + regulatory T cells, which are naturally anergic and suppressive, appear to be produced by the normal thymus as a functionally distinct subpopulation of T cells. They play critical roles not only in preventing autoimmunity but also in controlling tumor immunity and transplantation tolerance.

Keywords

IL-2 receptorAutoimmunityImmunologyBiologyTransplantationImmune toleranceImmunityPopulationClonal deletionImmune systemT cellAntigenCell biologyT-cell receptorMedicineInternal medicine

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Year
2001
Type
review
Volume
182
Issue
1
Pages
18-32
Citations
1499
Access
Closed

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Shimon Sakaguchi, Noriko Sakaguchi, Jun Shimizu et al. (2001). Immunologic tolerance maintained by CD25<sup>+</sup> CD4<sup>+</sup> regulatory T cells: their common role in controlling autoimmunity, tumor immunity, and transplantation tolerance. Immunological Reviews , 182 (1) , 18-32. https://doi.org/10.1034/j.1600-065x.2001.1820102.x

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DOI
10.1034/j.1600-065x.2001.1820102.x