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用于靶向疾病治疗的多特异性抗体的机制驱动设计

Mechanism-Driven Design of Multispecific Antibodies for Targeted Disease Treatment.

作者信息

Fine Justyn, Meksiriporn Bunyarit, Tan Jiacheng, Spangler Jamie B

机构信息

Program in Molecular Biophysics, Johns Hopkins University, Baltimore, Maryland 21208, USA.

Translational Tissue Engineering Center, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA; email:

出版信息

Annu Rev Chem Biomol Eng. 2024 Jan 26. doi: 10.1146/annurev-chembioeng-100522-102155.

Abstract

Antibody-based therapeutics constitute a rapidly growing class of pharmaceutical compounds. However, monoclonal antibodies, which specifically engage only one target, often lack the mechanistic intricacy to treat complex diseases. To expand the utility of antibody therapies, significant efforts have been invested in designing multispecific antibodies, which engage multiple targets using a single molecule. These efforts have culminated in remarkable translational progress, including nine US Food and Drug Administration-approved multispecific antibodies, with countless others in various stages of preclinical or clinical development. In this review, we discuss several categories of multispecific antibodies that have achieved clinical approval or shown promise in earlier stages of development. We focus on the molecular mechanisms used by multispecific antibodies and how these mechanisms inform their customized design and formulation. In particular, we discuss multispecific antibodies that target multiple disease markers, multiparatopic antibodies, and immune-interfacing antibodies. Overall, these innovative multispecific antibody designs are fueling exciting advances across the immunotherapeutic landscape. Expected final online publication date for the , Volume 15 is June 2024. Please see http://www.annualreviews.org/page/journal/pubdates for revised estimates.

摘要

基于抗体的治疗药物是一类迅速发展的药物化合物。然而,仅特异性结合一个靶点的单克隆抗体往往缺乏治疗复杂疾病所需的机制复杂性。为了扩大抗体疗法的应用范围,人们在设计多特异性抗体方面投入了大量精力,多特异性抗体能够利用单个分子结合多个靶点。这些努力已经取得了显著的转化进展,包括九种获得美国食品药品监督管理局批准的多特异性抗体,还有无数其他抗体正处于临床前或临床开发的各个阶段。在这篇综述中,我们讨论了几类已获得临床批准或在早期开发阶段显示出前景的多特异性抗体。我们重点关注多特异性抗体所使用的分子机制,以及这些机制如何为其定制设计和配方提供依据。特别是,我们讨论了靶向多种疾病标志物的多特异性抗体、多位点抗体和免疫衔接抗体。总体而言,这些创新的多特异性抗体设计正在推动免疫治疗领域取得令人兴奋的进展。第15卷的预计最终在线出版日期为2024年6月。请访问http://www.annualreviews.org/page/journal/pubdates查看修订后的估计日期。

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