Building better monoclonal antibody-based therapeutics

被引:504
|
作者
Weiner, George J. [1 ]
机构
[1] Univ Iowa Hosp & Clin, Holden Comprehens Canc Ctr, Iowa City, IA 52242 USA
基金
美国国家卫生研究院;
关键词
B-CELL LYMPHOMA; CONJUGATE GLEMBATUMUMAB VEDOTIN; LYMPHOCYTIC-LEUKEMIA CELLS; METASTATIC BREAST-CANCER; ANTI-CD20; ANTIBODY; DEPENDENT CYTOTOXICITY; BRENTUXIMAB VEDOTIN; OBINUTUZUMAB GA101; CD20; FC-RECEPTORS;
D O I
10.1038/nrc3930
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
For 20 years, monoclonal antibodies (mAbs) have been a standard component of cancer therapy, but there is still much room for improvement. Efforts continue to build better cancer therapeutics based on mAbs. Anticancer mAbs function through various mechanisms, including directly targeting the malignant cells, modifying the host response, delivering cytotoxic moieties and retargeting cellular immunity towards the malignant cells. Characteristics of mAbs that affect their efficacy include antigen specificity, overall structure, affinity for the target antigen and how a mAb component is incorporated into a construct that can trigger target cell death. This Review discusses the various approaches to using mAb-based therapeutics to treat cancer and the strategies used to take advantage of the unique potential of each approach, and provides examples of current mAb-based treatments.
引用
收藏
页码:361 / 370
页数:10
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