T-bet, a Th1 transcription factor regulates the expression of Tim-3

被引:90
作者
Anderson, Ana C. [1 ]
Lord, Graham M. [2 ,3 ]
Dardalhon, Valerie [1 ]
Lee, David H. [1 ]
Sabatos-Peyton, Catherine A. [1 ]
Glimcher, Laurie H. [2 ,3 ]
Kuchroo, Vijay K. [1 ]
机构
[1] Brigham & Womens Hosp, Ctr Neurol Dis, Dept Neurol, Boston, MA 02215 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA USA
[3] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
基金
美国国家卫生研究院;
关键词
Autoimmunity; T cells; Transcription factors; LINEAGE COMMITMENT; HELPER TYPE-1; TISSUE INFLAMMATION; MULTIPLE-SCLEROSIS; DENDRITIC CELLS; IFN-GAMMA; AUTOIMMUNE; RESPONSES; CD4(+); DISTINCT;
D O I
10.1002/eji.200939842
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
T-cell immunoglobulin, mucin domain-3 (Tim-3) is a membrane protein expressed at late stages of IFN-gamma secreting CD4(+) Th1 cell differentiation and constitutively on DC. Ligation of Tim-3 on Th1 cells terminates Th1 immune responses. In addition, Tim-3 plays a role in tolerance induction, although the mechanism by which this is accomplished has yet to be elucidated. While it is clear that Tim-3 plays an important role in the immune system, little is known regarding the molecular pathways that regulate Tim-3 expression. In the current study, we examine the role of Th1-associated transcription factors in regulating Tim-3 expression. Our experiments reveal that Tim-3 expression is regulated by the Th1-specific transcription factor T-bet. This introduces a novel paradigm into the generation of a Th1 response, whereby a transcription factor responsible for effector Th1 cell differentiation also increases the expression of a specific counter-regulatory molecule to ensure appropriate termination of pro-inflammatory Th1 immune responses.
引用
收藏
页码:859 / 866
页数:8
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