抗原
抗体-药物偶联物
细胞毒性T细胞
癌症
医学
癌症研究
抗药性
药品
抗体
药理学
单克隆抗体
免疫学
靶向治疗
体外
生物
内科学
微生物学
生物化学
作者
Hadi Nasiri,Zahra Valedkarimi,Leili Aghebati‐Maleki,Jafar Majidi
摘要
Over the recent decades, the use of antibody–drug conjugates (ADCs) has led to a paradigm shift in cancer chemotherapy. Antibody–based treatment of various human tumors has presented dramatic efficacy and is now one of the most promising strategies used for targeted therapy of patients with a variety of malignancies, including hematological cancers and solid tumors. Monoclonal antibodies (mAbs) are able to selectively deliver cytotoxic drugs to tumor cells, which express specific antigens on their surface, and has been suggested as a novel category of agents for use in the development of anticancer targeted therapies. In contrast to conventional treatments that cause damage to healthy tissues, ADCs use mAbs to specifically attach to antigens on the surface of target cells and deliver their cytotoxic payloads. The therapeutic success of future ADCs depends on closely choosing the target antigen, increasing the potency of the cytotoxic cargo, improving the properties of the linker, and reducing drug resistance. If appropriate solutions are presented to address these issues, ADCs will play a more important role in the development of targeted therapeutics against cancer in the next years. We review the design of ADCs, and focus on how ADCs can be exploited to overcome multiple drug resistance (MDR).
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