Th17: An effector CD4 T cell lineage with regulatory T cell ties

被引:1092
作者
Weaver, Casey T. [1 ]
Harrington, Laurie E.
Mangan, Paul R.
Gavrieli, Maya
Murphy, Kenneth M.
机构
[1] Univ Alabama Birmingham, Dept Pathol, Birmingham, AL 35294 USA
[2] Univ Alabama Birmingham, Dept Microbiol, Birmingham, AL 35294 USA
[3] Washington Univ, Sch Med, Dept Pathol, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Ctr Immunol, St Louis, MO 63110 USA
[5] Washington Univ, Sch Med, Howard Hughes Med Inst, St Louis, MO 63110 USA
关键词
D O I
10.1016/j.immuni.2006.06.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The naive CD4 T cell is a multipotential precursor with defined antigen recognition specificity but substantial plasticity for development down distinct effector or regulatory lineages, contingent upon signals from cells of the innate immune system. The range of identified effector CD4 T cell lineages has recently expanded with description of an IL-17-producing subset, called Th17, which develops; via cytokine signals distinct from, and antagonized by, products of the Th1 and Th2 lineages. Remarkably, Th17 development depends on the pleiotropic cytokine TGF-beta, which is also linked to regulatory T cell development and function, providing a unique mechanism for matching CD4 T cell effector and regulatory lineage specification. Here, we review Th17 lineage development, emphasizing similarities and differences with established effector and regulatory T cell developmental programs that have important implications for immune regulation, immune pathogenesis, and host defense.
引用
收藏
页码:677 / 688
页数:12
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