Anti-CD40 monoclonal antibody

被引:23
作者
Geldart, T
Illidge, T
机构
[1] CRUK Paterson Inst Canc Res & Christie NHS Trust, Manchester M20 4BX, Lancs, England
[2] Southampton Gen Hosp, Sch Med, Canc Sci Div, Canc Res UK Oncol Unit, Southampton SO16 6YD, Hants, England
关键词
anti-CD40; monoclonal antibody; therapy; novel treatment; immunotherapy;
D O I
10.1080/10428190500085255
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Normal, bi-directional interactions between CD40 and its natural ligand CD154 (CD40 ligand) are central to the generation of both T cell-dependent, humoral immune responses and cytotoxic T-cell responses. CD40 is expressed on a broad range of hematological and epithelial malignancies. The development of monoclonal antibodies directed against CD40 allows effective targeting of malignant cells through multiple mechanisms that include the recruitment of immune effector mechanisms such as complement-dependent cytotoxicity and antibody-dependent cellular cytotoxicity, direct anti-proliferative effects on neoplastic cells and, importantly, by the activation of tumor-targeted cellular cytotoxicity. This review provides the background to the early clinical trial data that are now beginning to emerge for this potentially exciting new treatment approach.
引用
收藏
页码:1105 / 1113
页数:9
相关论文
共 96 条
[1]  
AGATHANGGELOU A, 1995, AM J PATHOL, V147, P1152
[2]   Role for CD40-CD40 ligand interactions in the immune response to solid tumours [J].
Alexandroff, AB ;
Jackson, AM ;
Paterson, T ;
Haley, JL ;
Ross, JA ;
Longo, DL ;
Murphy, WJ ;
James, K ;
Taub, DD .
MOLECULAR IMMUNOLOGY, 2000, 37 (09) :515-526
[3]   Tumor necrosis factor receptor-associated factors (TRAFs) - a family of adaptor proteins that regulates life and death [J].
Arch, RH ;
Gedrich, RW ;
Thompson, CB .
GENES & DEVELOPMENT, 1998, 12 (18) :2821-2830
[4]   IDENTIFICATION OF A SOURCE OF BIOLOGICALLY-ACTIVE CD40 LIGAND [J].
ARMITAGE, RJ ;
SATO, TA ;
MACDUFF, BM ;
CLIFFORD, KN ;
ALPERT, AR ;
SMITH, CA ;
FANSLOW, WC .
EUROPEAN JOURNAL OF IMMUNOLOGY, 1992, 22 (08) :2071-2076
[5]  
Aruffo A, 1994, Curr Opin Hematol, V1, P12
[6]   THE CD40 LIGAND, GP39, IS DEFECTIVE IN ACTIVATED T-CELLS FROM PATIENTS WITH X-LINKED HYPER-IGM SYNDROME [J].
ARUFFO, A ;
FARRINGTON, M ;
HOLLENBAUGH, D ;
LI, X ;
MILATOVICH, A ;
NONOYAMA, S ;
BAJORATH, J ;
GROSMAIRE, LS ;
STENKAMP, R ;
NEUBAUER, M ;
ROBERTS, RL ;
NOELLE, RJ ;
LEDBETTER, JA ;
FRANCKE, U ;
OCHS, HD .
CELL, 1993, 72 (02) :291-300
[7]  
Balasa B, 1997, J IMMUNOL, V159, P4620
[8]   Help for cytotoxic-T-cell responses is mediated by CD40 signalling [J].
Bennett, SRM ;
Carbone, FR ;
Karamalis, F ;
Flavell, RA ;
Miller, JFAP ;
Heath, WR .
NATURE, 1998, 393 (6684) :478-480
[9]  
Biancone L, 1999, INT J MOL MED, V3, P343
[10]  
Bugajska U, 2002, J NATL CANCER I, V94, P1381