双特异性和多特异性抗体的可开发性考虑因素。

IF 5.6 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL mAbs Pub Date : 2024-01-01 Epub Date: 2024-08-27 DOI:10.1080/19420862.2024.2394229
Alaa Amash, Gesa Volkers, Patrick Farber, Daniel Griffin, K Shawn Davison, Allison Goodman, Raffi Tonikian, Aaron Yamniuk, Bryan Barnhart, Tim Jacobs
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引用次数: 0

摘要

双特异性抗体(bsAb)和多特异性抗体(msAb)包含多种多样的形式,可同时结合多个表位,为解决以往难以治疗或无法治愈的疾病提供了新的机制。通过对候选抗体的可开发性进行早期评估,可以将潜力较低的抗体降级,将最有前途的候选抗体提升到进一步开发的水平。基于蛋白质的疗法要想具有竞争力(如高浓度制剂和长半衰期),对可开发性有一系列严格的要求,对它们的评估需要一套强大的方法工具包,而其中很少有经过验证可用于检测 bsAbs/msAbs 的方法。在评估 bsAbs/msAbs 的可开发性时,重要的考虑因素包括其分子形式、免疫原性的可能性、特异性、稳定性和大批量生产的潜力。在此,我们总结了可开发性评估的关键方面,并就如何针对特定 bsAb/msAb 制定全面计划提供指导。
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Developability considerations for bispecific and multispecific antibodies.

Bispecific antibodies (bsAb) and multispecific antibodies (msAb) encompass a diverse variety of formats that can concurrently bind multiple epitopes, unlocking mechanisms to address previously difficult-to-treat or incurable diseases. Early assessment of candidate developability enables demotion of antibodies with low potential and promotion of the most promising candidates for further development. Protein-based therapies have a stringent set of developability requirements in order to be competitive (e.g. high-concentration formulation, and long half-life) and their assessment requires a robust toolkit of methods, few of which are validated for interrogating bsAbs/msAbs. Important considerations when assessing the developability of bsAbs/msAbs include their molecular format, likelihood for immunogenicity, specificity, stability, and potential for high-volume production. Here, we summarize the critical aspects of developability assessment, and provide guidance on how to develop a comprehensive plan tailored to a given bsAb/msAb.

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来源期刊
mAbs
mAbs 工程技术-仪器仪表
CiteScore
10.70
自引率
11.30%
发文量
77
审稿时长
6-12 weeks
期刊介绍: mAbs is a multi-disciplinary journal dedicated to the art and science of antibody research and development. The journal has a strong scientific and medical focus, but also strives to serve a broader readership. The articles are thus of interest to scientists, clinical researchers, and physicians, as well as the wider mAb community, including our readers involved in technology transfer, legal issues, investment, strategic planning and the regulation of therapeutics.
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