双特异性抗体
计算机科学
免疫原性
娴熟的
计算生物学
抗体
生物
免疫学
单克隆抗体
药理学
前药
作者
Alaa Amash,Gesa Volkers,Patrick Farber,Daniel O. Griffin,Katy Davison,Allison Goodman,Raffi Tonikian,Aaron P. Yamniuk,Bryan C. Barnhart,Timothy M. Jacobs
出处
期刊:mAbs
[Informa]
日期:2024-08-27
卷期号:16 (1)
标识
DOI:10.1080/19420862.2024.2394229
摘要
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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