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抗体药物偶联物的演进:实现精确的药物抗体比和多特异性。

The Evolution of Antibody-Drug Conjugates: Toward Accurate DAR and Multi-specificity.

机构信息

State Key Laboratory of Elemento-Organic Chemistry and Frontiers Science Center for New Organic Matter, College of Chemistry, Nankai University, Tianjin, 300071, China.

出版信息

ChemMedChem. 2024 Sep 2;19(17):e202400109. doi: 10.1002/cmdc.202400109. Epub 2024 Jul 2.

Abstract

Antibody-drug conjugates (ADCs) consist of antibodies, linkers and payloads. They offer targeted delivery of potent cytotoxic drugs to tumor cells, minimizing off-target effects. However, the therapeutic efficacy of ADCs is compromised by heterogeneity in the drug-to-antibody ratio (DAR), which impacts both cytotoxicity and pharmacokinetics (PK). Additionally, the emergence of drug resistance poses significant challenges to the clinical advancement of ADCs. To overcome these limitations, a variety of strategies have been developed, including the design of multi-specific drugs with accurate DAR. This review critically summarizes the current challenges faced by ADCs, categorizing key issues and evaluating various innovative solutions. We provide an in-depth analysis of the latest methodologies for achieving homogeneous DAR and explore design strategies for multi-specific drugs aimed at combating drug resistance. Our discussion offers a current perspective on the advancements made in refining ADC technologies, with an emphasis on enhancing therapeutic outcomes.

摘要

抗体药物偶联物(ADCs)由抗体、连接子和有效载荷组成。它们将有效的细胞毒性药物靶向递送至肿瘤细胞,最大限度地减少脱靶效应。然而,药物抗体比(DAR)的异质性会影响细胞毒性和药代动力学(PK),从而影响 ADC 的治疗效果。此外,耐药性的出现对 ADC 的临床进展构成了重大挑战。为了克服这些限制,已经开发了多种策略,包括设计具有准确 DAR 的多特异性药物。本综述批判性地总结了 ADC 目前面临的挑战,对关键问题进行分类,并评估了各种创新解决方案。我们深入分析了实现均匀 DAR 的最新方法,并探讨了旨在克服耐药性的多特异性药物的设计策略。我们的讨论提供了对改进 ADC 技术所取得进展的当前观点,重点是提高治疗效果。

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