IL-2: A two-faced master regulator of autoimmunity

被引:50
作者
Sharma, Rahul [1 ]
Fu, Shu Man [1 ,2 ]
Ju, Shyr-Te [1 ,2 ]
机构
[1] Univ Virginia, Dept Med, Ctr Immun Inflammat & Regenerat Med, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
基金
美国国家卫生研究院;
关键词
IL-2; Regulatory T-cells; Th cytokines; Trafficking; Inflammation; Autoimmunity; Scurfy; IMMUNOREGULATORY T-CELLS; SCURFY MICE; THYMIC SELECTION; INTERLEUKIN-2; TOLERANCE; INFLAMMATION; EXPRESSION; TRAFFICKING; RECEPTOR; DISEASE;
D O I
10.1016/j.jaut.2011.01.001
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
CD4(+) T-cell (Th) cytokines provide important regulatory and effector functions of T-cells. Among them, IL-2 plays a unique role. IL-2 is required for the generation and maintenance of regulatory T-cells (Treg) to provide lifelong protection from autoimmune disease. Whether IL-2 is also required for autoimmune disease development is less clear as Il2(-/-) mice themselves spontaneously develop multi-organ inflammation (MOI). In this communication, we discuss evidence that support the thesis that IL-2 is required for the development of autoimmune response, although some aspects of autoimmune response are not regulated by IL-2. Potential IL-2-dependent mechanisms operating at specific stages of the inflammation process are presented. The interplays among Treg, IL-2, autoimmune response and adaptive immunity are discussed. Overall, available information indicates that IL-2 is a two-faced master regulator of autoimmunity: one to prevent autoimmunity while the other promotes autoimmune response. The latter is an unfortunate consequence of IL-2 function that is used to promote the adaptive immune response against foreign antigens and pathogens. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:91 / 97
页数:7
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