PO.IM01.14 · 免疫学

基于机制的细胞检测方法用于筛选和表征双特异性抗体

Mechanism-driven cell-based assays to screen & characterize bi-specific antibodies

海报缩略图:基于机制的细胞检测方法用于筛选和表征双特异性抗体
编号 5543 展板 15 时间 4/21 02:00–05:00 区域 Section 6 主讲 Venkatesh Chari
分会场 Bi- and Tri-Specific Antibody Therapies
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作者与单位 Authors & Affiliations

Venkatesh Chari, Surekha Bonasu, Luhan Yang, Jennifer Lin-Jones, Jane Lamerdin, Alpana Prasad, Gaurav Agrawal

Eurofins DiscoverX Products LLC., Fremont, CA

摘要 Abstract

中文摘要
近期利用单克隆抗体进行癌症免疫治疗的进展极大地革新了针对晚期恶性肿瘤的治疗策略,激发了对各类治疗性抗体的探索。双特异性抗体(BsAbs)是经工程化设计以靶向两个不同表位或抗原的分子。BsAbs的作用机制可被操控以创造多样化的新功能,包括将免疫细胞与肿瘤细胞连接或阻断信号通路。BsAb类疗法已展现出显著的临床前和临床潜力,如blinatumomab(CD19/CD3)、amivantamab(EGFR/Her3)、ivonescimab(PD-1/VEGF-A)等分子的监管批准所证明。 Eurofins DiscoverX®提供针对肿瘤靶点的强大细胞检测产品组合,并提供三种主要检测形式来表征BsAbs:(1)细胞毒性检测:用于评估BsAbs的反式(in trans)功能活性,特别适用于表征T细胞衔接器(BiTEs)及类似分子;(2)二聚化检测:用于记录靶受体的顺式(in cis)异源二聚化;(3)通路信号检测:用于评估每个BsAb靶点臂的功能活性。 本报告重点介绍了运用这些细胞检测方法监测靶向关键肿瘤抗原(包括CD19、PD-1和VEGF-A)的BsAb主要作用机制(MOA)的案例研究。相关应用将展示对BsAb介导的肿瘤细胞杀伤的评估、抗体候选物的排序,以及对各个BsAb臂的功能和特异性的评估。这些检测方法为新一代BsAb疗法的加速发现和表征提供了必不可少的工具。
查看英文原文 English abstract
Recent advances in cancer immunotherapy using monoclonal antibodies have dramatically revolutionized the therapeutic strategy against advanced malignancies, inspiring the exploration of various types of therapeutic antibodies. Bispecific antibodies (BsAbs) are engineered molecules designed to target two different epitopes or antigens. The mechanism of action of BsAbs can be manipulated to create variable and novel functionalities, including linking immune cells with tumor cells or signaling pathway blockade. BsAb-based therapies have demonstrated significant preclinical and clinical potential, as evidenced by the regulatory approval of molecules like blinatumomab (CD19/CD3), amivantamab (EGFR/Her3), ivonescimab (PD-1/VEGF-A), and others. Eurofins DiscoverX® provides a robust portfolio of cell-based assays for oncology targets and offers three primary assay formats to characterize BsAbs: (1) Cytotoxicity assays: To assess functional activity of BsAbs in trans , specifically for characterizing T-cell engagers (BiTEs) and similar molecules, (2) Dimerization assays: To record hetero dimerization of target receptors in cis , and (3) Pathway signaling assays: To evaluate the functional activity of each individual BsAb target arm This presentation highlights case studies illustrating the use of these cell-based assays to monitor key BsAb MOAs targeting critical tumor antigens, including CD19, PD-1, and VEGF-A. Applications will demonstrate the evaluation of BsAb-mediated tumor cell killing, rank-ordering of antibody candidates, and assessment of the function and specificity of individual BsAb arms. These assays provide essential tools for the accelerated discovery and characterization of next-generation BsAb therapeutics.
利益披露 Disclosure
V. Chari, None.. S. Bonasu, None.. L. Yang, None.. J. Lin-Jones, None.. J. Lamerdin, None.. A. Prasad, None.. G. Agrawal, None.

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