Type 1 Diabetes (T1D) results from insulin-producing beta cells destruction by diabetogenic T lymphocytes in humans and nonobese diabetic (NOD) mice. The breakdown of tolerance has been associated with a defect in the number and the function of naturally occurring regulatory T cells (nTreg) that are the master player in peripheral tolerance. Gene knockout experiments in mouse models have shown a nonredundant activity of IL-2 related to its critical role in inducing nTreg and controlling peripheral T cell tolerance. Whereas strong evidence has suggested that IL-2 is critically required for nTreg-mediated T1D control, several fundamental questions remain to be addressed. In this paper, we highlight the recent findings and controversies regarding the tolerogenic properties of IL-2 mediated through nTreg. We further discuss a potential link between the immunomodulatory role of interleukin-2 and the pathogenesis of type 1 diabetes. Copyright © 2011 Aziz Alami Chentoufi et al.
CITATION STYLE
Chentoufi, A. A., Gaudreau, S., Nguyen, A., Sabha, M., Amrani, A., & Elghazali, G. (2011). Type i diabetes-associated tolerogenic properties of interleukin-2. Clinical and Developmental Immunology. https://doi.org/10.1155/2011/289343
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