The development of immunoconjugates for targeted cancer therapy

被引:75
|
作者
Smaglo, Brandon G. [1 ]
Aldeghaither, Dalal [1 ]
Weiner, Louis M. [1 ]
机构
[1] Georgetown Univ, Med Ctr, Lombardi Comprehens Canc Ctr, Washington, DC 20057 USA
关键词
SINGLE-CHAIN FV; PHASE-I TRIAL; METASTATIC COLORECTAL-CANCER; RECOMBINANT IMMUNOTOXIN; BREAST-CANCER; TRASTUZUMAB EMTANSINE; ANTIBODY FRAGMENTS; PRETARGETED RADIOIMMUNOTHERAPY; GEMTUZUMAB OZOGAMICIN; BRENTUXIMAB VEDOTIN;
D O I
10.1038/nrclinonc.2014.159
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Immunoconjugates are specific, highly effective, minimally toxic anticancer therapies that are beginning to show promise in the clinic. Immunoconjugates consist of three separate components: an antibody that binds to a cancer cell antigen with high specificity, an effector molecule that has a high capacity to kill the cancer cell, and a linker that will ensure the effector does not separate from the antibody during transit and will reliably release the effector to the cancer cell or tumour stroma. The high affinity antibody-antigen interaction allows specific and selective delivery of a range of effectors, including pharmacologic agents, radioisotopes, and toxins, to cancer cells. Some anticancer molecules are not well tolerated when administered systemically owing to unacceptable toxicity to the host. However, this limitation can be overcome through the linking of such cytotoxins to specific antibodies, which mask the toxic effects of the drug until it reaches its target. Conversely, many unconjugated antibodies are highly specific for a cancer target, but have low therapeutic potential and can be repurposed as delivery vehicles for highly potent effectors. In this Review, we summarize the successes and shortcomings of immunoconjugates, and discuss the future potential for the development of these therapies.
引用
收藏
页码:637 / 648
页数:12
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