Cutting edge: Granzymes A and B are not essential for perforin-mediated tumor rejection

被引:74
作者
Smyth, MJ [1 ]
Street, SEA [1 ]
Trapani, AA [1 ]
机构
[1] Peter MacCallum Canc Inst, Canc Immunol Program, Melbourne, Vic 8006, Australia
关键词
D O I
10.4049/jimmunol.171.2.515
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Controversy still exists regarding the biological function of granzyme serine proteases released with perforin from the cytotoxic granules of NK cells and CTLs. In particular, it is not clear whether the major granzymes, A and A play an essential role in tumor rejection mediated by the perforin pathway. We have now examined the relative importance of perforin and granzyme A and B clusters in five different tumor models that stringently distinguish their importance. We conclude that granzyme A and B clusters are not essential for CTL- and NK cell-mediated rejection of spontaneous and experimental tumors, raising the likelihood that either perforin alone or in combination with an additional granzyme or granule component(s) mediates cytotoxicity of tumor cells in vivo.
引用
收藏
页码:515 / 518
页数:4
相关论文
共 38 条
[21]   CYTOTOXICITY WITH TARGET DNA BREAKDOWN BY RAT BASOPHILIC LEUKEMIA-CELLS EXPRESSING BOTH CYTOLYSIN AND GRANZYME-A [J].
SHIVER, JW ;
SU, LS ;
HENKART, PA .
CELL, 1992, 71 (02) :315-322
[22]   Granzyme A initiates an alternative pathway for granule-mediated apoptosis [J].
Shresta, S ;
Graubert, TA ;
Thomas, DA ;
Raptis, SZ ;
Ley, TJ .
IMMUNITY, 1999, 10 (05) :595-605
[23]   GRANZYME-B PLAYS A CRITICAL ROLE IN CYTOTOXIC LYMPHOCYTE-INDUCED APOPTOSIS [J].
SHRESTA, S ;
HEUSEL, JW ;
MACIVOR, DM ;
WESSELSCHMIDT, RL ;
RUSSELL, JH ;
LEY, TJ .
IMMUNOLOGICAL REVIEWS, 1995, 146 :211-221
[24]  
SIMON MM, 1994, METHOD ENZYMOL, V244, P68
[25]   In vitro- and ex vivo-derived cytolytic leukocytes from granzyme A x B double knockout mice are defective in granule-mediated apoptosis but not lysis of target cells [J].
Simon, MM ;
Hausmann, M ;
Tran, T ;
Ebnet, K ;
Tschopp, J ;
ThaHla, R ;
Mullbacher, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1997, 186 (10) :1781-1786
[26]   The anti-tumor activity of IL-12: Mechanisms of innate immunity that are model and dose dependent [J].
Smyth, MJ ;
Taniguchi, M ;
Street, SEA .
JOURNAL OF IMMUNOLOGY, 2000, 165 (05) :2665-2670
[27]   New aspects of natural-killer-cell surveillance and therapy of cancer [J].
Smyth, MJ ;
Hayakawa, Y ;
Takeda, K ;
Yagita, H .
NATURE REVIEWS CANCER, 2002, 2 (11) :850-861
[28]  
Smyth MJ, 1999, J IMMUNOL, V162, P6658
[29]   Sequential production of interferon-γ by NK1.1+ T cells and natural killer cells is essential for the antimetastatic effect of α-galactosylceramide [J].
Smyth, MJ ;
Crowe, NY ;
Pellicci, DG ;
Kyparissoudis, K ;
Kelly, JM ;
Takeda, K ;
Yagita, H ;
Godfrey, DI .
BLOOD, 2002, 99 (04) :1259-1266
[30]   Perforin-dependent cytolytic responses in β2-microglobulin-deficient mice [J].
Smyth, MJ ;
Snook, MB .
CELLULAR IMMUNOLOGY, 1999, 196 (01) :51-59