Dual targeting strategies with bispecific antibodies

被引:342
作者
Kontermann, Roland E. [1 ]
机构
[1] Univ Stuttgart, Inst Zellbiol & Immunol, Stuttgart, Germany
关键词
bispecific antibodies; dual targeting; dual retargeting; cancer therapy; inflammatory diseases; allergic diseases; GROWTH-FACTOR RECEPTOR; MOUSE XENOGRAFT MODEL; FACTOR-I RECEPTOR; LIGAND-DIRECTED TOXIN; VARIABLE-DOMAIN IMMUNOGLOBULIN; CELL-ENGAGING ANTIBODY; B-CELL; CANCER-THERAPY; ANTIGEN-BINDING; RECOMBINANT IMMUNOTOXIN;
D O I
10.4161/mabs.4.2.19000
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Monoclonal antibodies are widely used for the treatment of cancer, inflammatory and infectious diseases and other disorders. Most of the marketed antibodies are monospecific and therefore capable of interacting and interfering with a single target. However, complex diseases are often multifactorial in nature, and involve redundant or synergistic action of disease mediators or upregulation of different receptors, including crosstalk between their signaling networks. Consequently, blockade of multiple, different pathological factors and pathways may result in improved therapeutic efficacy. This result can be achieved by combining different drugs, or use of the dual targeting strategies applying bispecific antibodies that have emerged as an alternative to combination therapy. This review discusses the various dual targeting strategies for which bispecific antibodies have been developed and provides an overview of the established bispecific antibody formats.
引用
收藏
页码:182 / 197
页数:16
相关论文
共 151 条
[1]   Ligand-based targeting of apoptosis in cancer: The potential of recombinant human apoptosis ligand 2/tumor necrosis factor-related apoptosis-inducing ligand (rhApo2L/TRAIL) [J].
Ashkenazi, Avi ;
Holland, Pamela ;
Eckhardt, S. Gail .
JOURNAL OF CLINICAL ONCOLOGY, 2008, 26 (21) :3621-3630
[2]   Tumor regression in cancer patients by very low doses of a T cell-engaging antibody [J].
Bargou, Ralf ;
Leo, Eugen ;
Zugmaier, Gerhard ;
Klinger, Matthias ;
Goebeler, Mariele ;
Knop, Stefan ;
Noppeney, Richard ;
Viardot, Andreas ;
Hess, Georg ;
Schuler, Martin ;
Einsele, Hermann ;
Brandl, Christian ;
Wolf, Andreas ;
Kirchinger, Petra ;
Klappers, Petra ;
Schmidt, Margit ;
Riethmueller, Gert ;
Reinhardt, Carsten ;
Baeuerle, Patrick A. ;
Kufer, Peter .
SCIENCE, 2008, 321 (5891) :974-977
[3]   Platelet-derived growth factor receptor (PDGFR): A target for anticancer therapeutics [J].
Board, R ;
Jayson, GC .
DRUG RESISTANCE UPDATES, 2005, 8 (1-2) :75-83
[4]   Variants of the Antibody Herceptin That Interact with HER2 and VEGF at the Antigen Binding Site [J].
Bostrom, Jenny ;
Yu, Shang-Fan ;
Kan, David ;
Appleton, Brent A. ;
Lee, Chingwei V. ;
Billeci, Karen ;
Man, Wenyan ;
Peale, Franklin ;
Ross, Sarajane ;
Wiesmann, Christian ;
Fuh, Germaine .
SCIENCE, 2009, 323 (5921) :1610-1614
[5]  
Brüsselbach S, 1999, TUMOR TARGET, V4, P115
[6]   Angiogenesis in cancer and other diseases [J].
Carmeliet, P ;
Jain, RK .
NATURE, 2000, 407 (6801) :249-257
[7]   Passive antibody therapy for infectious diseases [J].
Casadevall, A ;
Dadachova, E ;
Pirofski, L .
NATURE REVIEWS MICROBIOLOGY, 2004, 2 (09) :695-703
[8]   Therapeutic antibodies for autoimmunity and inflammation [J].
Chan, Andrew C. ;
Carter, Paul J. .
NATURE REVIEWS IMMUNOLOGY, 2010, 10 (05) :301-316
[9]   Therapeutic nanoparticles for drug delivery in cancer [J].
Cho, Kwangjae ;
Wang, Xu ;
Nie, Shuming ;
Chen, Zhuo ;
Shin, Dong M. .
CLINICAL CANCER RESEARCH, 2008, 14 (05) :1310-1316
[10]   Therapeutic potential of anticancer immunotoxins [J].
Choudhary, Swati ;
Mathew, Mrudula ;
Verma, Rama S. .
DRUG DISCOVERY TODAY, 2011, 16 (11-12) :495-503