双载荷抗体药物共轭物:双管齐下

IF 6 2区 医学 Q1 CHEMISTRY, MEDICINAL European Journal of Medicinal Chemistry Pub Date : 2024-10-23 DOI:10.1016/j.ejmech.2024.116995
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引用次数: 0

摘要

抗体药物共轭物(ADC)通过将小分子药物与单克隆抗体(mAbs)共轭,实现了细胞毒性药物的精确输送。近几十年来,ADC 已显示出巨大的临床疗效。然而,传统的 ADC 常常遇到各种临床难题,包括疗效不佳、不良反应严重以及耐药性的产生,从而限制了其更广泛的临床应用。令人鼓舞的是,新一代方法--双负载 ADC--已成为应对这些挑战的开创性策略。双载荷 ADC 的特点是将两种不同的治疗载荷整合到同一个抗体上,通过促进协同效应和降低耐药性风险来提高疗效。然而,由于抗体上存在多个功能基团,双载荷 ADC 的合成非常复杂。在本综述中,我们全面总结了从 ADC 成分设计到正交化学的双负载 ADC 构建策略。随后的章节探讨了当前面临的挑战并提出了前瞻性策略,重点介绍了双负载 ADC 研究的最新进展,从而为下一代 ADC 的开发奠定基础。
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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Dual-payload antibody–drug conjugates: Taking a dual shot
Antibody-drug conjugates (ADCs) enable the precise delivery of cytotoxic agents by conjugating small-molecule drugs with monoclonal antibodies (mAbs). Over recent decades, ADCs have demonstrated substantial clinical efficacy. However, conventional ADCs often encounter various clinical challenges, including suboptimal efficacy, significant adverse effects, and the development of drug resistance, limiting their broader clinical application. Encouragingly, a next-generation approach—dual-payload ADCs—has emerged as a pioneering strategy to address these challenges. Dual-payload ADCs are characterized by the incorporation of two distinct therapeutic payloads on the same antibody, enhancing treatment efficacy by promoting synergistic effects and reducing the risk of drug resistance. However, the synthesis of dual-payload ADCs is complex due to the presence of multiple functional groups on antibodies. In this review, we comprehensively summarize the construction strategies for dual-payload ADCs, ranging from the design of ADC components to orthogonal chemistry. The subsequent sections explore current challenges and propose prospective strategies, highlighting recent advancements in dual-payload ADC research, thereby laying the foundation for the development of next-generation ADCs.
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来源期刊
CiteScore
11.70
自引率
9.00%
发文量
863
审稿时长
29 days
期刊介绍: The European Journal of Medicinal Chemistry is a global journal that publishes studies on all aspects of medicinal chemistry. It provides a medium for publication of original papers and also welcomes critical review papers. A typical paper would report on the organic synthesis, characterization and pharmacological evaluation of compounds. Other topics of interest are drug design, QSAR, molecular modeling, drug-receptor interactions, molecular aspects of drug metabolism, prodrug synthesis and drug targeting. The journal expects manuscripts to present the rational for a study, provide insight into the design of compounds or understanding of mechanism, or clarify the targets.
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