Abstract
Introduction: Interleukin 2 (IL-2) induces an essential signal for T regulatory (Treg) cells. Without a functional IL-2R, only immature CD4 + Foxp3low CD25neg T cells develop, and these cells fail to suppress autoreactive T cells in the periphery. Discussion: IL-2 functions during Treg cell development by upregulating Foxp3 and CD25 and by increasing the number of thymic Treg cells. Upon exiting the thymus during neonatal life, IL-2 is responsible for rapid amplification of the number of Treg cells in peripheral lymph nodes to insure suppression of autoreactive T cells that escape negative selection, thereby maintaining tolerance. The homeostasis of Treg cells in mature immunocompetent mice also depends on IL-2. However, there is an alternative mechanism for Treg cells homeostasis that may represent a minor IL-2-independent pathway or the consequence of weak and very transient IL-2R signaling. Conclusion: Thus, IL-2 provides importance signals for Treg cell development and for their homeostasis in peripheral immune tissues.
Original language | English (US) |
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Pages (from-to) | 635-639 |
Number of pages | 5 |
Journal | Journal of Clinical Immunology |
Volume | 28 |
Issue number | 6 |
DOIs | |
State | Published - Nov 1 2008 |
Keywords
- Foxp3
- IL-2R
- IL-7R
- Survival
- Thymic development
ASJC Scopus subject areas
- Immunology and Allergy
- Immunology