Antibody Therapeutics in Oncology.

Immunotherapy (Los Angeles, Calif.) Pub Date : 2016-03-01 Epub Date: 2016-02-01
Erik D Wold, Vaughn V Smider, Brunhilde H Felding
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Abstract

One of the newer classes of targeted cancer therapeutics is monoclonal antibodies. Monoclonal antibody therapeutics are a successful and rapidly expanding drug class due to their high specificity, activity, favourable pharmacokinetics, and standardized manufacturing processes. Antibodies are capable of recruiting the immune system to attack cancer cells through complement-dependent cytotoxicity or antibody dependent cellular cytotoxicity. In an ideal scenario the initial tumor cell destruction induced by administration of a therapeutic antibody can result in uptake of tumor associated antigens by antigen-presenting cells, establishing a prolonged memory effect. Mechanisms of direct tumor cell killing by antibodies include antibody recognition of cell surface bound enzymes to neutralize enzyme activity and signaling, or induction of receptor agonist or antagonist activity. Both approaches result in cellular apoptosis. In another and very direct approach, antibodies are used to deliver drugs to target cells and cause cell death. Such antibody drug conjugates (ADCs) direct cytotoxic compounds to tumor cells, after selective binding to cell surface antigens, internalization, and intracellular drug release. Efficacy and safety of ADCs for cancer therapy has recently been greatly advanced based on innovative approaches for site-specific drug conjugation to the antibody structure. This technology enabled rational optimization of function and pharmacokinetics of the resulting conjugates, and is now beginning to yield therapeutics with defined, uniform molecular characteristics, and unprecedented promise to advance cancer treatment.

Abstract Image

肿瘤中的抗体治疗。
一种较新的靶向癌症治疗方法是单克隆抗体。单克隆抗体治疗药物由于其高特异性、活性、良好的药代动力学和标准化的制造工艺,是一种成功且迅速扩大的药物类别。抗体能够通过补体依赖性细胞毒性或抗体依赖性细胞毒性招募免疫系统来攻击癌细胞。在理想情况下,由治疗性抗体的施用诱导的初始肿瘤细胞破坏可导致抗原呈递细胞摄取肿瘤相关抗原,从而建立延长的记忆效应。抗体直接杀伤肿瘤细胞的机制包括抗体识别细胞表面结合酶以中和酶活性和信号,或诱导受体激动剂或拮抗剂活性。这两种方法都会导致细胞凋亡。在另一种非常直接的方法中,抗体被用来将药物输送到目标细胞并导致细胞死亡。这种抗体药物偶联物(adc)通过选择性结合细胞表面抗原、内化和细胞内药物释放,将细胞毒性化合物直接作用于肿瘤细胞。近年来,基于位点特异性药物偶联抗体结构的创新方法,adc治疗癌症的有效性和安全性得到了极大的提高。这项技术能够合理优化所产生的偶联物的功能和药代动力学,现在开始产生具有明确、统一的分子特征的治疗方法,并为推进癌症治疗带来了前所未有的希望。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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