Development of PLZF-expressing innate T cells

被引:78
作者
Alonzo, Eric S. [1 ,2 ]
Sant'Angelot, Derek B. [1 ,2 ,3 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Sloan Kettering Inst, Program Immunol, New York, NY 10065 USA
[2] Mem Sloan Kettering Canc Ctr, Louis V Gerstner Jr Grad Sch Biomed Sci, New York, NY 10065 USA
[3] Cornell Univ, Weill Grad Sch Med Sci, New York, NY 10065 USA
关键词
THYMOCYTE-THYMOCYTE INTERACTION; GERMINAL CENTER FORMATION; ZINC-FINGER; LINEAGE FATE; NKT CELLS; CORTICAL THYMOCYTES; NEGATIVE SELECTION; POSITIVE SELECTION; IGE PRODUCTION; DELTA LINEAGE;
D O I
10.1016/j.coi.2010.12.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent studies have shown that the transcriptional regulator promyelocytic leukemia zinc finger (PLZF) controls the development of essentially all of the innate-like features of invariant Natural Killer T (NKT) cells. For example, PLZF-deficient NKT cells do not acquire an 'activated' phenotype nor do they acquire the capacity to secrete multiple cytokines upon primary stimulation. The function of a subset of gamma delta T cells has now also been shown to be dependent upon expression of PLZF. Furthermore, IL-4 produced by PLZF-expressing cells causes some CD8 T cells to acquire innate-like features. Therefore, it is becoming clear that PLZF has a broad impact on the immune response. Here we discuss the current understanding of how expression of PLZF, the innate T cell determinant, is initiated during T cell development.
引用
收藏
页码:220 / 227
页数:8
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