Recombinant antibody constructs in cancer therapy

被引:183
作者
Hudson, PJ [1 ]
机构
[1] Commonwealth Sci & Ind Res Org, Mol Sci Unit, Cooperat Res Ctr Diagnost Technol, Parkville, Vic 3052, Australia
关键词
D O I
10.1016/S0952-7915(99)00013-8
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 [免疫学];
摘要
Recombinant antibodies and their fragments now represent over 30% of all biological proteins undergoing clinical trials for diagnosis and therapy. The focus on antibodies as the ideal cancer-targeting reagents recently culminated in approval by the Food and Drugs Administration for the first engineered therapeutic antibodies. In the past year, important advances have been made in the design, selection and production of new types of engineered antibodies. Innovative selection methods have enabled the isolation of high-affinity cancer-targeting and antiviral antibodies, the latter capable of redirecting viruses for gene therapy applications. In other strategies for cancer diagnosis and therapy, recombinant antibody fragments have been fused to radioisotopes, drugs, toxins, enzymes and biosensor surfaces. Bispecific antibodies and related fusion proteins have been produced for cancer immunotherapy, effectively enhancing the human immune response in anticancer vaccines and T cell recruitment strategies.
引用
收藏
页码:548 / 557
页数:10
相关论文
共 88 条
[1]
Adams GP, 1998, CANCER RES, V58, P485
[2]
Prolonged in vivo tumour retention of a human diabody targeting the extracellular domain of human HER2/neu [J].
Adams, GP ;
Schier, R ;
McCall, AM ;
Crawford, RS ;
Wolf, EJ ;
Weiner, LM ;
Marks, JD .
BRITISH JOURNAL OF CANCER, 1998, 77 (09) :1405-1412
[3]
Almog O, 1998, PROTEINS, V31, P128, DOI 10.1002/(SICI)1097-0134(19980501)31:2<128::AID-PROT3>3.3.CO
[4]
2-D
[5]
Arano Y, 1999, CANCER RES, V59, P128
[6]
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
[7]
Targeted adeno-associated virus vector transduction of nonpermissive cells mediated by a bispecific F(ab′γ)2 antibody [J].
Bartlett, JS ;
Kleinschmidt, J ;
Boucher, RC ;
Samulski, RJ .
NATURE BIOTECHNOLOGY, 1999, 17 (02) :181-186
[8]
Bauer S, 1999, CANCER RES, V59, P1961
[9]
Beresford GW, 1999, INT J CANCER, V81, P911, DOI 10.1002/(SICI)1097-0215(19990611)81:6<911::AID-IJC12>3.0.CO
[10]
2-O