Abundant c-Fas-associated death domain-like interleukin-1-converting enzyme inhibitory protein expression determines resistance of T helper 17 cells to activation-induced cell death

被引:31
作者
Yu, Yu [1 ,2 ]
Iclozan, Cristina [1 ,2 ]
Yamazaki, Tomohide [3 ]
Yang, Xuexian [3 ]
Anasetti, Claudio [1 ,2 ,4 ]
Dong, Chen [3 ]
Yu, Xue-Zhong [1 ,2 ,4 ]
机构
[1] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Immunol, Tampa, FL 33612 USA
[2] Univ S Florida, Coll Med, H Lee Moffitt Canc Ctr & Res Inst, Dept Blood & Marrow Transplantat, Tampa, FL 33612 USA
[3] Univ Texas MD Anderson Canc Ctr, Dept Immunol, Houston, TX 77030 USA
[4] Univ S Florida, Dept Oncol Sci, Tampa, FL USA
基金
美国国家卫生研究院;
关键词
SIGNALING COMPLEX; APOPTOSIS; DIFFERENTIATION; INFLAMMATION; DISTINCT; LINEAGE; FLIP; TH17; TH2;
D O I
10.1182/blood-2009-03-210153
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Activation-induced cell death (AICD) plays an important role in peripheral T-cell tolerance. AICD in CD4 T helper (Th) cells, including Th1 and Th2 effectors, has been extensively studied. Recently, interleukin-17-producing CD4(+) T cells (Th17 cells) have been identified as a unique Th subset, but their susceptibility to AICD and the underlying molecular mechanisms have not been defined. In this study, we found that Th17 cells were significantly less susceptible to AICD than Th1 cells, and Th17 cell resistance to AICD is due to the high levels of c-Fas-associated death domain-like interleukin-1-converting enzyme inhibitory protein preventing Fas-mediated apoptosis. The resistance of Th17 cells to AICD reveals a novel mechanism to explain the high pathogenicity of Th17 cells in autoimmune diseases, and may also provide a rationale to generate tumor-specific Th17 cells for adoptive immunotherapy. (Blood. 2009; 114: 1026-1028)
引用
收藏
页码:1026 / 1028
页数:3
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