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重塑实体瘤治疗:小型化抗体药物偶联物的新潜力

Reforming solid tumor treatment: the emerging potential of smaller format antibody-drug conjugate.

作者信息

Ma Xiaojie, Wang Mingkai, Ying Tianlei, Wu Yanling

机构信息

MOE/NHC/CAMS Key Laboratory of Medical Molecular Virology, Shanghai Frontiers Science Center of Pathogenic Microorganisms and Infection, Shanghai Institute of Infectious Disease and Biosecurity, School of Basic Medical Sciences, Shanghai Medical College, Fudan University, Shanghai 200032, China.

Shanghai Engineering Research Center for Synthetic Immunology, Fudan University, Shanghai 200032, China.

出版信息

Antib Ther. 2024 Feb 16;7(2):114-122. doi: 10.1093/abt/tbae005. eCollection 2024 Apr.

Abstract

In recent years, substantial therapeutic efficacy of antibody-drug conjugates (ADCs) has been validated through approvals of 16 ADCs for the treatment of malignant tumors. However, realization of the maximum clinical use of ADCs requires surmounting extant challenges, mainly the limitations in tumor penetration capabilities when targeting solid tumors. To resolve the hurdle of suboptimal tumor penetration, miniaturized antibody fragments with engineered formats have been harnessed for ADC assembly. By virtue of their reduced molecular sizes, antibody fragment-drug conjugates hold considerable promise for efficacious delivery of cytotoxic agents, thus conferring superior therapeutic outcomes. This review will focus on current advancements in novel ADC development utilizing smaller antibody formats from ~6 to 80 kDa, with particular emphasis on single-domain antibodies, which have been widely applied in novel ADC design. Additionally, strategies to optimize clinical translation are discussed, including half-life extension, acceleration of internalization, and reduction of immunogenic potential.

摘要

近年来,通过16种抗体药物偶联物(ADC)获批用于治疗恶性肿瘤,其显著的治疗效果得到了验证。然而,要实现ADC的最大临床应用,需要克服现存的挑战,主要是靶向实体瘤时肿瘤穿透能力的限制。为了解决肿瘤穿透欠佳的障碍,具有工程化形式的小型化抗体片段已被用于ADC组装。凭借其减小的分子尺寸,抗体片段-药物偶联物在有效递送细胞毒性药物方面具有很大潜力,从而带来更好的治疗效果。本综述将聚焦于利用约6至80 kDa的较小抗体形式进行新型ADC开发的当前进展,尤其着重于已广泛应用于新型ADC设计的单域抗体。此外,还讨论了优化临床转化的策略,包括延长半衰期、加速内化以及降低免疫原性潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/39b4/10983081/8e552d133860/tbae005f1.jpg

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