Discovery of a novel highly specific, fully human PSCA antibody and its application as an antibody-drug conjugate in prostate cancer.

IF 5.6 2区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
mAbs Pub Date : 2024-01-01 Epub Date: 2024-08-08 DOI:10.1080/19420862.2024.2387240
Xiaojie Chu, Seungmin Shin, Du-San Baek, Liyong Zhang, Alex Conard, Megan Shi, Ye-Jin Kim, Cynthia Adams, Maggie Hines, Xianglei Liu, Chuan Chen, Zehua Sun, Dontcho V Jelev, John W Mellors, Dimiter S Dimitrov, Wei Li
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引用次数: 0

Abstract

Prostate stem cell antigen (PSCA) is expressed in all stages of prostate cancer, including in advanced androgen-independent tumors and bone metastasis. PSCA may associate with prostate carcinogenesis and lineage plasticity in prostate cancer. PSCA is also a promising theranostic marker for a variety of other solid tumors, including pancreatic adenocarcinoma and renal cell carcinoma. Here, we identified a novel fully human PSCA antibody using phage display methodology. The structure-based affinity maturation yielded a high-affinity binder, F12, which is highly specific and does not bind to 6,000 human membrane proteins based on a membrane proteome array assay. F12 targets PSCA amino acids 63-69 as tested by the peptide scanning microarray, and it cross-reacts with the murine PSCA. IgG1 F12 efficiently internalizes into PSCA-expressing tumor cells. The antimitotic reagent monomethyl auristatin E (MMAE)-conjugated IgG1 F12 (ADC, F12-MMAE) exhibits dose-dependent efficacy and specificity in a human prostate cancer PC-3-PSCA xenograft NSG mouse model. This is a first reported ADC based on a fully human PSCA antibody and MMAE that is characterized in a xenograft murine model, which warrants further optimizations and investigations in additional preclinical tumor models, including prostate and other solid tumors.

发现一种新型高特异性全人源 PSCA 抗体,并将其作为抗体-药物共轭物应用于前列腺癌治疗。
前列腺干细胞抗原(PSCA)在前列腺癌的各个阶段都有表达,包括晚期雄激素依赖性肿瘤和骨转移。前列腺干细胞抗原可能与前列腺癌的癌变和细胞系可塑性有关。PSCA 还是胰腺腺癌和肾细胞癌等其他多种实体瘤很有希望的治疗标记物。在这里,我们利用噬菌体展示方法鉴定了一种新型全人源 PSCA 抗体。根据膜蛋白质组阵列检测,该抗体具有高度特异性,不会与 6000 种人类膜蛋白结合。肽扫描微阵列检测表明,F12 的靶标是 PSCA 的 63-69 氨基酸,它与鼠 PSCA 有交叉反应。IgG1 F12 能有效内化表达 PSCA 的肿瘤细胞。在人类前列腺癌 PC-3-PSCA 异种移植 NSG 小鼠模型中,单甲基乌司他丁 E(MMAE)共轭 IgG1 F12(ADC,F12-MMAE)抗沉淀试剂表现出剂量依赖性疗效和特异性。这是首次报道基于全人 PSCA 抗体和 MMAE 的 ADC 在异种移植小鼠模型中的特性,值得在其他临床前肿瘤模型(包括前列腺和其他实体瘤)中进一步优化和研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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