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多聚体抗 DR5 IgM 激动型抗体 IGM-8444 是一种有效的诱导癌细胞凋亡的药物,与化疗药物和 BCL-2 抑制剂 ABT-199 具有协同作用。

Multimeric Anti-DR5 IgM Agonist Antibody IGM-8444 Is a Potent Inducer of Cancer Cell Apoptosis and Synergizes with Chemotherapy and BCL-2 Inhibitor ABT-199.

机构信息

IGM Biosciences Inc., Mountain View, California.

出版信息

Mol Cancer Ther. 2021 Dec;20(12):2483-2494. doi: 10.1158/1535-7163.MCT-20-1132. Epub 2021 Oct 28.

Abstract

Death receptor 5 (DR5) is an attractive target for cancer therapy due to its broad upregulated expression in multiple cancers and ability to directly induce apoptosis. Though anti-DR5 IgG antibodies have been evaluated in clinical trials, limited efficacy has been attributed to insufficient receptor crosslinking. IGM-8444 is an engineered, multivalent agonistic IgM antibody with 10 binding sites to DR5 that induces cancer cell apoptosis through efficient DR5 multimerization. IGM-8444 bound to DR5 with high avidity and was substantially more potent than an IgG with the same binding domains. IGM-8444 induced cytotoxicity in a broad panel of solid and hematologic cancer cell lines but did not kill primary human hepatocytes , a potential toxicity of DR5 agonists. In multiple xenograft tumor models, IGM-8444 monotherapy inhibited tumor growth, with strong and sustained tumor regression observed in a gastric PDX model. When combined with chemotherapy or the BCL-2 inhibitor ABT-199, IGM-8444 exhibited synergistic tumor cytotoxicity and enhanced efficacy, without augmenting hepatotoxicity. These results support the clinical development of IGM-8444 in solid and hematologic malignancies as a monotherapy and in combination with chemotherapy or BCL-2 inhibition.

摘要

死亡受体 5(DR5)在多种癌症中广泛上调表达,能够直接诱导细胞凋亡,因此成为癌症治疗的一个有吸引力的靶点。尽管抗 DR5 IgG 抗体已在临床试验中进行了评估,但由于受体交联不足,其疗效有限。IGM-8444 是一种经过工程改造的、多价激动性 IgM 抗体,具有 10 个与 DR5 结合的位点,通过有效的 DR5 多聚化诱导癌细胞凋亡。IGM-8444 与 DR5 具有高亲和力结合,并且比具有相同结合结构域的 IgG 更有效。IGM-8444 在广泛的实体瘤和血液系统癌细胞系中诱导细胞毒性,但不会杀死原代人肝细胞,这是 DR5 激动剂的潜在毒性。在多个异种移植肿瘤模型中,IGM-8444 单药治疗抑制肿瘤生长,在胃 PDX 模型中观察到强烈和持续的肿瘤消退。当与化疗或 BCL-2 抑制剂 ABT-199 联合使用时,IGM-8444 表现出协同的肿瘤细胞毒性和增强的疗效,而不会增加肝毒性。这些结果支持 IGM-8444 在实体瘤和血液系统恶性肿瘤中的临床开发,无论是单药治疗还是与化疗或 BCL-2 抑制联合治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7187/9398157/5f486c44c7da/2483fig1.jpg

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