CD4+/CD8+ double-positive T cells: more than just a developmental stage?

被引:225
作者
Overgaard, Nana H. [1 ,2 ]
Jung, Ji-Won [1 ]
Steptoe, Raymond J. [1 ]
Wells, James W. [1 ]
机构
[1] Univ Queensland, Translat Res Inst, Diamantina Inst, Brisbane, Qld, Australia
[2] Copenhagen Univ Hosp, Dept Hematol, Ctr Canc Immune Therapy, Herlev, Denmark
基金
澳大利亚研究理事会;
关键词
immune regulation; cytotoxic potential; T cell plasticity; CD4(+)CD8(+) LYMPHOCYTES; PHENOTYPIC ANALYSIS; CYNOMOLGUS MONKEYS; GENE-EXPRESSION; NKT CELLS; IN-VIVO; CD4; BLOOD; POPULATION; COEXPRESSION;
D O I
10.1189/jlb.1RU0814-382
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
CD4(+)/CD8(+) DP thymocytes are a well-described T cell developmental stage within the thymus. However, once differentiated, the CD4(+) lineage or the CD8(+) lineage is generally considered to be fixed. Nevertheless, mature CD4(+)/CD8(+) DP T cells have been described in the blood and peripheral lymphoid tissues of numerous species, as well as in numerous disease settings, including cancer. The expression of CD4 and CD8 is regulated by a very strict transcriptional program involving the transcription factors Runx3 and ThPOK. Initially thought to be mutually exclusive within CD4(+) and CD8(+) T cells, CD4(+)/CD8(+) T cell populations, outside of the thymus, have recently been described to express concurrently ThPOK and Runx3. Considerable heterogeneity exists within the CD4(+)/CD8(+) DP T cell pool, and the function of CD4(+)/CD8(+) T cell populations remains controversial, with conflicting reports describing cytotoxic or suppressive roles for these cells. In this review, we describe how transcriptional regulation, lineage of origin, heterogeneity of CD4 and CD8 expression, age, species, and specific disease settings influence the functionality of this rarely studied T cell population.
引用
收藏
页码:31 / 38
页数:8
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