Distinct effects of T-bet in TH1 lineage commitment and IFN-γ production in CD4 and CD8 T cells

被引:974
作者
Szabo, SJ
Sullivan, BM
Stemmann, C
Satoskar, AR
Sleckman, BP
Glimcher, LH [1 ]
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Immunol & Infect Dis, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[3] Ohio State Univ, Dept Microbiol, Columbus, OH 43210 USA
[4] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO 63110 USA
关键词
D O I
10.1126/science.1065543
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
T-bet is a member of the T-box family of transcription factors that appears to regulate lineage commitment in CD4 T helper (T-H) lymphocytes in part by activating the hallmark T(H)1 cytokine, interferon-gamma (IFN-gamma), IFN-gamma is aLso produced by natural killer (NK) cells and most prominently by CD8 cytotoxic T cells, and is vital. for the control of microbial pathogens. Although T-bet is expressed in all these cell types, it is required for control of IFN-gamma production in CD4 and NK cells, but not in CD8 cells. This difference is aLso apparent in the function of these cell subsets. Thus, the regulation of a single cytokine, IFN-gamma, is controlled by distinct transcriptional mechanisms within the T cell lineage.
引用
收藏
页码:338 / 342
页数:5
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