药品
化学
结合
抗体-药物偶联物
治疗窗口
抗体
食品药品监督管理局
药代动力学
药理学
计算生物学
纳米技术
单克隆抗体
医学
免疫学
生物
数学分析
材料科学
数学
作者
Vijay Chudasama,Antoine Maruani,Stephen Caddick
出处
期刊:Nature Chemistry
[Nature Portfolio]
日期:2016-01-04
卷期号:8 (2): 114-119
被引量:323
摘要
Antibody-drug conjugates (ADCs) comprise antibodies covalently attached to highly potent drugs using a variety of conjugation technologies. As therapeutics, they combine the exquisite specificity of antibodies, enabling discrimination between healthy and diseased tissue, with the cell-killing ability of cytotoxic drugs. This powerful and exciting class of targeted therapy has shown considerable promise in the treatment of various cancers with two US Food and Drug Administration approved ADCs currently on the market (Adcetris and Kadcyla) and approximately 40 currently undergoing clinical evaluation. However, most of these ADCs exist as heterogeneous mixtures, which can result in a narrow therapeutic window and have major pharmacokinetic implications. In order for ADCs to deliver their full potential, sophisticated site-specific conjugation technologies to connect the drug to the antibody are vital. This Perspective discusses the strategies currently used for the site-specific construction of ADCs and appraises their merits and disadvantages.
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