Next generation of multispecific antibody engineering

Q2 Medicine Antibody Therapeutics Pub Date : 2023-12-08 DOI:10.1093/abt/tbad027
Daniel Keri, Matt Walker, Isha Singh, Kyle Nishikawa, Fernando Garces
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Abstract

Multispecific antibodies recognize two or more epitopes located on the same or distinct targets. This added capability through protein design allows these man-made molecules to address unmet medical needs that are no longer possible with single targeting such as with monoclonal antibodies or cytokines alone. However, the approach to the development of these multispecific molecules has been met with numerous road bumps, which suggests that a new workflow for multispecific molecules is required. The investigation of the molecular basis that mediates the successful assembly of the building blocks into non-native quaternary structures will lead to the writing of a playbook for multispecifics. This is a must do if we are to design workflows that we can control and in turn predict success. Here, we reflect on the current state-of-the-art of therapeutic biologics and look at the building blocks, in terms of proteins, and tools that can be used to build the foundations of such a next-generation workflow.
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新一代多特异性抗体工程
多特异性抗体识别位于相同或不同靶标上的两个或多个表位。这种通过蛋白质设计增加的能力使这些人造分子能够解决单靶向(如单克隆抗体或细胞因子)无法满足的医疗需求。然而,这些多特异性分子的开发方法遇到了许多障碍,这表明需要一种新的多特异性分子工作流程。对介导构建块成功组装成非原生第四纪结构的分子基础的研究将导致编写多特异性的剧本。这是必须做的,如果我们要设计工作流程,我们可以控制,并反过来预测成功。在这里,我们反思了目前最先进的治疗生物制剂,并从蛋白质和工具的角度来看待构建模块,这些模块可用于构建下一代工作流程的基础。
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来源期刊
Antibody Therapeutics
Antibody Therapeutics Medicine-Immunology and Allergy
CiteScore
8.70
自引率
0.00%
发文量
30
审稿时长
8 weeks
期刊最新文献
AI-based antibody discovery platform identifies novel, diverse, and pharmacologically active therapeutic antibodies against multiple SARS-CoV-2 strains. FcRider: a recombinant Fc nanoparticle with endogenous adjuvant activities for hybrid immunization. A pan-allelic human SIRPα-blocking antibody, ES004-B5, promotes tumor killing by enhancing macrophage phagocytosis and subsequently inducing an effective T-cell response. Correction to: A case study of a bispecific antibody manufacturability assessment and optimization during discovery stage and its implications. The process using a synthetic library that generates multiple diverse human single domain antibodies.
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