A new anticancer glycolipid monoclonal antibody, SC104, which directly induces tumor cell apoptosis

被引:23
作者
Durrant, Lindy G.
Harding, Stephen J.
Green, Nicola H.
Buckberry, Lorraine D.
Parsons, Tina
机构
[1] Univ Nottingham, Inst Infect Immun & Inflammat, Canc Res UK Dept Clin Oncol, Nottingham NG7 2RD, England
[2] Scancell Ltd, Nottingham, England
关键词
D O I
10.1158/0008-5472.CAN-05-3812
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A novel monoclonal antibody was raised by immunization of mice with colorectal tumor cell lines. The fusion was screened by immunohistochemistry for binding to primary colorectal tumors. Subsequent analysis on primary disaggregated colorectal tumors show that the antibody recognizes a cell surface antigen expressed by the majority of colorectal tumors. Antigen characterization has shown that the antibody recognizes a sialyltetraosyleeramide but does not bind to GM1, GD1a, GT1b, or sialyl Lewis(X) antigens. Binding to a frozen panel of tumor and normal tissue sections revealed that the antigen was also strongly expressed on esophageal, gastric, and endometrial tumors. Its normal tissue distribution was largely restricted to moderate staining of large intestine. Surprisingly, SC104 antibody directly induces tumor cell death without the need for immune effector cells or complement. This may be related in part to its homophilic binding properties that allow cross-linking of antibody and receptors on the cell surface. Caspase activation can be detected following SC104 treatment of colorectal cells, and cotreatment with caspase inhibitors has been shown to inhibit cell death. This suggests that SC104 induces death by a classic apoptotic pathway. Furthermore, SC104 antibody shows additive killing with complement and 5-fluorouracil/leucovorin in vivo, suggesting a new therapeutic approach for this class of antibodies.
引用
收藏
页码:5901 / 5909
页数:9
相关论文
共 22 条
[1]  
CAULFIELD MJ, 1990, J BIOL RESP MODIF, V9, P319
[2]  
Chapman Paul B, 2003, Curr Opin Investig Drugs, V4, P710
[3]  
CHAPMAN PB, 1990, J IMMUNOL, V145, P891
[4]   DEVELOPMENT OF 2ND-GENERATION MONOCLONAL-ANTIBODIES RECOGNIZING LEWIS(Y/B) ANTIGEN BY ANTIIDIOTYPIC IMMUNIZATION [J].
DURRANT, LG ;
SINGHAL, A ;
JACOBS, E ;
PRICE, MR .
HYBRIDOMA, 1993, 12 (06) :647-660
[5]   ANTIGENICITY OF NEWLY ESTABLISHED COLORECTAL-CARCINOMA CELL-LINES [J].
DURRANT, LG ;
ROBINS, RA ;
PIMM, MV ;
PERKINS, AC ;
ARMITAGE, NC ;
HARDCASTLE, JD ;
BALDWIN, RW .
BRITISH JOURNAL OF CANCER, 1986, 53 (01) :37-45
[6]   Complement function in mAb-mediated cancer immunotherapy [J].
Gelderman, KA ;
Tomlinson, S ;
Ross, GD ;
Gorter, A .
TRENDS IN IMMUNOLOGY, 2004, 25 (03) :158-164
[7]   Yttrium 90 ibritumomab tiuxetan radioimmunotherapy for relapsed or refractory low-grade non-Hodgkin's lymphoma [J].
Gordon, LI ;
Witzig, TE ;
Wiseman, GA ;
Flinn, IW ;
Spies, SS ;
Silverman, DH ;
Emmanuolides, C ;
Cripe, L ;
Saleh, M ;
Czuczman, MS ;
Olejnik, T ;
White, CA ;
Grillo-López, AJ .
SEMINARS IN ONCOLOGY, 2002, 29 (01) :87-92
[8]   Immune evasion of tumor cells using membrane-bound complement regulatory proteins [J].
Gorter, A ;
Meri, S .
IMMUNOLOGY TODAY, 1999, 20 (12) :576-582
[9]  
Grant SC, 1999, CLIN CANCER RES, V5, P1319
[10]   Rituximab:: Ongoing and future clinical development [J].
Grillo-López, AJ ;
Hedrick, E ;
Rashford, M ;
Benyunes, M .
SEMINARS IN ONCOLOGY, 2002, 29 (01) :105-112