Interleukin-2 Receptor Signaling: At the Interface between Tolerance and Immunity

被引:723
作者
Malek, Thomas R. [1 ,2 ]
Castro, Iris [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Microbiol & Immunol, Miami, FL 33101 USA
[2] Univ Miami, Miller Sch Med, Diabet Res Inst, Miami, FL 33101 USA
基金
美国国家卫生研究院;
关键词
REGULATORY T-CELLS; TRANSCRIPTIONAL REPRESSOR BLIMP-1; DE-NOVO INDUCTION; CUTTING EDGE; TGF-BETA; FOXP3; EXPRESSION; IN-VIVO; IL-2; RECEPTOR; AUTOIMMUNE-DISEASE; REG-CELLS;
D O I
10.1016/j.immuni.2010.08.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Interleukin-2 receptor (IL-2R) signaling regulates tolerance and immunity. Here, we review recent work concerning the structure, signaling, and function of the IL-2R, emphasizing the contribution of IL-2 for T cell-dependent activity in vivo. IL-2R signaling influences two discrete aspects of immune responses by CD8(+) T cells, terminal differentiation of effector cells in primary responses, and aspects of memory recall responses. IL-2 also delivers essential signals for thymic development of regulatory T (Treg) cells and later to promote their homeostasis and function. Each of these outcomes on T effector and Treg cells requires distinct amounts of IL-2R signaling, with low IL-2R signaling sufficient for many key aspects of Treg cells. Thus, tolerance is readily maintained and favored with limited IL-2.
引用
收藏
页码:153 / 165
页数:13
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