Monoclonal antibodies and therapy of human cancers

被引:29
作者
Funaro, A
Horenstein, AL
Santoro, P
Cinti, C
Gregorini, A
Malavasi, F
机构
[1] Univ Ancona, Inst Biol & Genet, I-60131 Ancona, Italy
[2] Univ Turin, Dept Genet Biol & Biochem, Turin, Italy
关键词
monoclonal antibody; recombinant antibody; immunotherapy; immunopharmaceutical; pro-drug; immunoconjugate;
D O I
10.1016/S0734-9750(00)00043-4
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
This survey is an overview of the applications of murine, humanized and recombinant monoclonal antibodies for in vivo diagnostic and therapeutic applications. Monoclonal antibodies (mAb) have been applied to the diagnosis and therapy of an array of human diseases. The initial failures of early clinical trials have been overcome through the production of a new generation of mAb which features reduced immunogenicity and improved targeting abilities. The early models of mAb therapy were focused on enhancing the cytolytic mechanisms against the tumor cells. More recently, successful mAb-based therapies were targeted to molecules involved in the regulation of growth of cancer cells. This has highlighted the relevance of understanding receptor-mediated signaling events, and may provide new opportunities for anti-tumor antibody targeting. Despite all the difficulties, clinical data is outlining an increasingly significant role for antibody-mediated cancer therapy as a versatile and powerful instrument in cancer treatment. One reasonable expectation is that treatment at an earlier stage in the disease process or in minimal residual disease may be more advantageous. (C) 2000 Published by Elsevier Science Inc.
引用
收藏
页码:385 / 401
页数:17
相关论文
共 106 条
[1]  
Alpaugh RK, 1998, CLIN CANCER RES, V4, P1903
[2]   Cancer treatment by targeted drug delivery to tumor vasculature in a mouse model [J].
Arap, W ;
Pasqualini, R ;
Ruoslahti, E .
SCIENCE, 1998, 279 (5349) :377-380
[3]  
Arap Wadih, 1998, Current Opinion in Oncology, V10, P560, DOI 10.1097/00001622-199811000-00014
[4]   scFv multimers of the anti-neuraminidase antibody NC10:: length of the linker between VH and VL domains dictates precisely the transition between diabodies and triabodies [J].
Atwell, JL ;
Breheney, KA ;
Lawrence, LJ ;
McCoy, AJ ;
Kortt, AA ;
Hudson, PJ .
PROTEIN ENGINEERING, 1999, 12 (07) :597-604
[5]  
Bagshawe K D, 1999, Expert Opin Investig Drugs, V8, P161, DOI 10.1517/13543784.8.2.161
[6]  
Bagshawe K.D., 1995, TUMOUR TARGETING, V1, P17
[7]   Developments with targeted enzymes in cancer therapy [J].
Bagshawe, KD ;
Sharma, SK ;
Burke, PJ ;
Melton, RG ;
Knox, RJ .
CURRENT OPINION IN IMMUNOLOGY, 1999, 11 (05) :579-583
[8]   Pretargeting with the Affinity Enhancement System for radioimmunotherapy [J].
Barbet, J ;
Kraeber-Bodéré, F ;
Vuillez, JP ;
Gautherot, E ;
Rouvier, R ;
Chatal, JF .
CANCER BIOTHERAPY AND RADIOPHARMACEUTICALS, 1999, 14 (03) :153-166
[9]  
Baselga J, 1998, CANCER RES, V58, P2825
[10]   T cell-mediated eradication of murine metastatic melanoma induced by targeted interleukin 2 therapy [J].
Becker, JC ;
Pancook, JD ;
Gillies, SD ;
Furukawa, K ;
Reisfeld, RA .
JOURNAL OF EXPERIMENTAL MEDICINE, 1996, 183 (05) :2361-2366