Encephalitogenic T cells that stably express both T-bet and RORγt consistently produce IFNγ but have a spectrum of IL-17 profiles

被引:47
作者
Abromson-Leeman, Sara [1 ]
Bronson, Roderick T. [1 ]
Dorf, Martin E. [1 ]
机构
[1] Harvard Univ, Sch Med, Dept Pathol, Boston, MA 02115 USA
关键词
Th1/Th17; cells; Inflammation; Cytokines; Transcription factors; EAE/MS; TH17; CELLS; AUTOIMMUNE INFLAMMATION; LINEAGE; DIFFERENTIATION; PHENOTYPE; INTERLEUKIN-17; LYMPHOCYTES; SPECIFICITY; PLASTICITY; DIRECTS;
D O I
10.1016/j.jneuroim.2009.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Th1/Thl7 cells, secreting both IFN gamma and IL-17, are often associated with inflammatory pathology. We cloned and studied the cytokine phenotypes of MBP-specific, TCR-identical encephalitogenic CD4+ cells in relationship to Th1- and Th17-associated transcription factors T-bet and ROR gamma t. IFN gamma-producing cells could be sub-divided into those that are T-bet(+)/ROR gamma t(-) and those that are T-bet(+)/ROR gamma t(+). The latter comprises a spectrum of phenotypes, as defined by IL-17 production, and can be induced to up-regulate IL-23R with IL-12 or IL-23. The former, bona fide Th1 cells, lack IL-23R expression under all conditions. In vivo, T-bet(+)/ROR gamma t(-) and T-bet(+)/ROR gamma t(+) clones induce EAE equally well. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:10 / 24
页数:15
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