IL-2-and CD25-dependent immunoregulatory mechanisms in the homeostasis of T-cell subsets

被引:197
作者
Letourneau, Sven [1 ]
Krieg, Carsten [1 ]
Pantaleo, Giuseppe [1 ,2 ]
Boyman, Onur [1 ]
机构
[1] Univ Lausanne, CHU Vaudois, Div Immunol & Allergy, CH-1011 Lausanne, Switzerland
[2] Swiss Vaccine Res Inst, Lausanne, Switzerland
关键词
IL-2; CD25; T-cell homeostasis; CD8 T cell; regulatory T cell; T(H)1; T(H)2; T(H)17; cytokine deprivation; RECEPTOR ALPHA-CHAIN; BETA-CHAIN; TH2; DIFFERENTIATION; DENDRITIC CELLS; CUTTING EDGE; IN-VIVO; INTERLEUKIN-2; MEMORY; LYMPHOCYTES; EXPRESSION;
D O I
10.1016/j.jaci.2009.02.011
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
IL-2 plays a pivotal role in regulating the adaptive immune system by controlling the survival and proliferation of regulatory T (Treg) cells, which are required for the maintenance of immune tolerance. Moreover, IL-2 is implicated in the differentiation and homeostasis of effector T-cell subsets, including T(H)1, T(H)2, T(H)17, and memory CD8(+) T cells. The IL-2 receptor is composed of 3 distinct subunits, namely the alpha (CD25), beta (CD122), and gamma (gamma c) chains. Of crucial importance for the delivery of IL-2 signals to Treg cells is the expression of CD25, which, along with CD122 and gamma c, confers high affinity binding to IL-2. Notably, recent findings suggest a novel role for CD25, whereby CD25 molecules on Treg cells and possibly other cells are capable of influencing T-cell homeostasis by means of IL-2 deprivation. This review explores these findings and integrates them into our current understanding of T-cell homeostasis. (J Allergy Clin Immunol 2009;123:758-62.)
引用
收藏
页码:758 / 762
页数:5
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