Unraveling natural Killer T-Cells Development

被引:42
|
作者
Bennstein, Sabrina Bianca [1 ]
机构
[1] Univ Oxford, John Radcliffe Hosp, Nuffield Dept Surg Sci, Oxford, England
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 8卷
关键词
invariant NKT cells; natural killer T cells; natural killer T type II cells; natural killer T development; natural killer T lineage; natural killer T subsets; INVARIANT NKT CELLS; TRANSCRIPTION FACTOR PLZF; INKT CELLS; LINEAGE DIFFERENTIATION; EFFECTOR FUNCTION; MAMMALIAN TARGET; CUTTING EDGE; ZINC-FINGER; EXPRESSION; SUBSETS;
D O I
10.3389/fimmu.2017.01950
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Natural killer T-cells are a subset of innate-like T-cells with the ability to bridge innate and adaptive immunity. There is great interest in harnessing these cells to improve tumor therapy; however, greater understanding of invariant NKT ( iNKT) cell biology is needed. The first step is to learn more about NKT development within the thymus. Recent studies suggest lineage separation of murine iNKT cells into iNKT1, iNKT2, and iNKT17 cells instead of shared developmental stages. This review will focus on these new studies and will discuss the evidence for lineage separation in contrast to shared developmental stages. The author will also highlight the classifications of murine iNKT cells according to identified transcription factors and cytokine production, and will discuss transcriptional and posttranscriptional regulations, and the role of mammalian target of rapamycin. Finally, the importance of these findings for human cancer therapy will be briefly discussed.
引用
收藏
页数:7
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