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一种新型全人源激动型单链片段可变抗体,靶向死亡受体 5,具有体外和体内强大的抗肿瘤活性。

A Novel Fully Human Agonistic Single Chain Fragment Variable Antibody Targeting Death Receptor 5 with Potent Antitumor Activity In Vitro and In Vivo.

机构信息

State Key Laboratory of Natural Medicines, School of Life Science and Technology, China Pharmaceutical University, Nanjing 210009, China.

出版信息

Int J Mol Sci. 2017 Sep 27;18(10):2064. doi: 10.3390/ijms18102064.

DOI:10.3390/ijms18102064
PMID:28953230
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5666746/
Abstract

Agonistic antibodies, which bind specifically to death receptor 5 (DR5), can trigger apoptosis in tumor cells through the extrinsic pathway. In this present study, we describe the use of a phage display to isolate a novel fully human agonistic single chain fragment variable (scFv) antibody, which targets DR5. After five rounds of panning a large (1.2 × 10⁸ clones) phage display library on DR5, a total of over 4000 scFv clones were screened by the phage ELISA. After screening for agonism in a cell-viability assay in vitro, a novel DR5-specific scFv antibody TR2-3 was isolated, which inhibited COLO205 and MDA-MB-231 tumor cell growth without any cross-linking agents. The activity of TR2-3 in inducing apoptosis in cancer cells was evaluated by using an Annexin V-PE apoptosis detection kit in combination with flow cytometry and the Hoechst 33342 and propidium iodide double staining analysis. In addition, the activation of caspase-dependent apoptosis was evaluated by Western blot assays. The results indicated that TR2-3 induced robust apoptosis of the COLO205 and MDA-MB-231 cells in a dose-dependent and time-dependent manner, while it remarkably upregulated the cleavage of caspase-3 and caspase-8. Furthermore, TR2-3 suppressed the tumor growth significantly in the xenograft model. Taken together, these data suggest that TR2-3 exhibited potent antitumor activity both in vitro and in vivo. This work provides a novel human antibody, which might be a promising candidate for cancer therapy by targeting DR5.

摘要

激动性抗体特异性结合死亡受体 5(DR5),可通过外在途径触发肿瘤细胞凋亡。在本研究中,我们描述了利用噬菌体展示技术分离一种新型的、针对 DR5 的完全人源激动性单链片段可变区(scFv)抗体。经过五轮针对 DR5 的噬菌体展示文库淘选,用噬菌体 ELISA 筛选了总共超过 4000 个 scFv 克隆。在体外细胞活力测定中筛选出激动性后,分离到一种新型的 DR5 特异性 scFv 抗体 TR2-3,它在没有任何交联剂的情况下抑制 COLO205 和 MDA-MB-231 肿瘤细胞生长。用 Annexin V-PE 凋亡检测试剂盒结合流式细胞术和 Hoechst 33342 和碘化丙啶双重染色分析评估 TR2-3 在诱导癌细胞凋亡中的活性。此外,通过 Western blot 分析评估 caspase 依赖性凋亡的激活。结果表明,TR2-3 以剂量和时间依赖性方式诱导 COLO205 和 MDA-MB-231 细胞的强烈凋亡,同时显著上调 caspase-3 和 caspase-8 的切割。此外,TR2-3 在异种移植模型中显著抑制肿瘤生长。总之,这些数据表明 TR2-3 在体内外均具有强大的抗肿瘤活性。这项工作提供了一种新型的人源抗体,它可能是一种有前途的通过靶向 DR5 进行癌症治疗的候选药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/a73ab726a4a4/ijms-18-02064-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/387a7ccca3af/ijms-18-02064-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/b79b10d47a81/ijms-18-02064-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/0ad2639fb5a7/ijms-18-02064-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/c3b6d79c8d67/ijms-18-02064-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/170168bfcd9d/ijms-18-02064-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/a73ab726a4a4/ijms-18-02064-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/387a7ccca3af/ijms-18-02064-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/a9b2d562ca39/ijms-18-02064-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/ef1f012fdb82/ijms-18-02064-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/b79b10d47a81/ijms-18-02064-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/0ad2639fb5a7/ijms-18-02064-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/c3b6d79c8d67/ijms-18-02064-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e6af/5666746/170168bfcd9d/ijms-18-02064-g008.jpg
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