A Novel Transcription Factor, T-bet, Directs Th1 Lineage Commitment

被引:0
|
作者
Szabo, Susanne J. [1 ]
Kim, Sean T. [1 ]
Costa, Gina L. [3 ]
Zhang, Xiankui [4 ]
Fathman, C. Garrison [3 ]
Glimcher, Laurie H. [1 ,2 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Publ Hlth, Dept Med, Boston, MA 02115 USA
[3] Stanford Univ, Sch Med, Div Rheumatol & Immunol, Stanford, CA 94305 USA
[4] Med Univ S Carolina, Dept Med, Div Rheumatol & Immunol, Charleston, SC 29425 USA
来源
JOURNAL OF IMMUNOLOGY | 2015年 / 194卷 / 07期
基金
美国国家卫生研究院;
关键词
INTERFERON-GAMMA PROMOTER; CYTOKINE GENE-EXPRESSION; HELPER-CELL SUBSETS; REGULATORY FACTOR-I; NATURAL-KILLER; IFN-GAMMA; DNA-BINDING; SIGNAL TRANSDUCER; IMMUNE-RESPONSES; TRANSGENIC MICE;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Naive Thelper cells differentiate into wo subsets, Th1 and Th2, each with distinct functions and cytokine profiles. Here, we report the isolation of T-bet, a Th1-specific T box transcription factor that controls the expression correlates with IFN gamma expression in Th1 and NK cells. Ectopic expression of T-bet both transactivates the IFN gamma gene and induces endogenous IFN gamma production. Remarkably, retroviral gene tranduction of T-bet into polarized Th2 and Tc2 primary T cells redirects them into Th1 and Tc1 cells, respectively, as evidenced by the simultaneous induction of IFN gamma and repression of IL-4 and IL-5. Thus, T-bet initiates Th1 lineage development from naive Thp cells both by activating Th1 genetic programs and by repressing the opposing Th2 programs.
引用
收藏
页码:2961 / 2975
页数:15
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