Serine Protease Inhibitor 6 Protects iNKT Cells from Self-Inflicted Damage

被引:21
|
作者
Ansari, A. Wahid [1 ]
Temblay, Jeff N. [1 ]
Alyahya, Syarifah H. [1 ]
Ashton-Rickardt, Philip G. [1 ]
机构
[1] Univ London Imperial Coll Sci Technol & Med, Immunobiol Sect, Dept Med, Div Immunol & Inflammat, London W12 0NN, England
来源
JOURNAL OF IMMUNOLOGY | 2010年 / 185卷 / 02期
基金
美国国家卫生研究院;
关键词
KILLER T-CELLS; NKT CELLS; GRANZYME-B; CYTOTOXIC LYMPHOCYTES; CYTOKINE PRODUCTION; IMMUNE-RESPONSE; ACTIVATION; DEATH; EXPANSION; RECEPTOR;
D O I
10.4049/jimmunol.1000651
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 role played by apoptosis in the homeostasis of effector cells of the innate immune system is unclear. Serine protease inhibitor 6 (Spi6) is an inhibitor of granzyme B (GrB) that protects cytotoxic T lymphocytes of the adaptive immune system from apoptosis. To determine whether Spi6 also protects cells of the innate immune system from self-inflicted damage we have examined invariant NKT (iNKT) cells. Spi6-deficient iNKT cells harbored increased levels of GrB after TCR stimulation with the PBS-57 glycolipid Ag and were susceptible to apoptosis. The increased apoptosis of Spi6 knock-out (KO) iNKT cells lead to a complete loss in the production of IL-4 and IFN-gamma by Spi6 KO iNKT cells after PBS-57 challenge. The increased activation-induced apoptosis resulted in impaired survival and a decreased clonal burst size of Spi6 KO iNKT cells, which could be corrected by GrB deficiency. However, the clonal burst of Spi6 KO iNKT cells after TCR-independent activation with lymphocytic choriomeningitis virus was not affected. Our findings demonstrate that Spi6 protects cytotoxic cells of the innate immune system from GrB-mediated self-inflicted triggered by the recognition of Ag. The Journal of Immunology, 2010, 185: 877-883.
引用
收藏
页码:877 / 883
页数:7
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