Perforin and granzymes: function, dysfunction and human pathology

被引:850
作者
Voskoboinik, Ilia [1 ,2 ]
Whisstock, James C. [3 ,4 ]
Trapani, Joseph A. [1 ,2 ]
机构
[1] Peter MacCallum Canc Ctr, Canc Immunol Program, Melbourne, Vic 3002, Australia
[2] Univ Melbourne, Sir Peter MacCallum Dept Oncol, Parkville, Vic 3010, Australia
[3] Monash Univ, Dept Biochem & Mol Biol, Clayton, Vic 3800, Australia
[4] Monash Univ, Australian Res Council, Ctr Excellence Adv Mol Imaging, Clayton, Vic 3800, Australia
基金
澳大利亚研究理事会; 澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
FAMILIAL HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS; CYTOTOXIC T-LYMPHOCYTES; PLASMA-MEMBRANE-REPAIR; PORE-FORMING PROTEIN; GRANULE-MEDIATED APOPTOSIS; NATURAL-KILLER-CELLS; TARGET-CELLS; LYTIC GRANULES; DNA FRAGMENTATION; SERINE PROTEASES;
D O I
10.1038/nri3839
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A defining property of cytotoxic lymphocytes is their expression and regulated secretion of potent toxins, including the pore-forming protein perforin and serine protease granzymes. Until recently, mechanisms of pore formation and granzyme transfer into the target cell were poorly understood, but advances in structural and cellular biology have now begun to unravel how synergy between perforin and granzymes brings about target cell death. These and other advances are demonstrating the surprisingly broad pathophysiological roles of the perforin-granzyme pathway, and this has important implications for understanding immune homeostasis and for developing immunotherapies for cancer and other diseases. In particular, we are beginning to define and understand a range of human diseases that are associated with a failure to deliver active perforin to target cells. In this Review, we discuss the current understanding of the structural, cellular and clinical aspects of perforin and granzyme biology.
引用
收藏
页码:388 / 400
页数:13
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