Cadherin 6 (CDH6)靶向嵌合抗原受体修饰T细胞的构建与表征

Li Pang, Fang Ren, Xiaoxuan Xu, Lingyang Fu, Tifang Wang, Zhiqiang Guo
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引用次数: 1

摘要

在本研究中,我们构建了cadherin 6 (CDH6)靶向CAR修饰的T细胞(CAR-T细胞),并通过体外方法研究了其靶向特异性识别和肿瘤特异性杀细胞作用。利用在线生物信息学工具分析不同类型肿瘤中CDH6转录水平的表达及其与临床病理参数的相关性。采用传统的分子克隆方法构建编码cdh6特异性CAR的慢病毒载体,采用3质粒瞬时共转染法制备慢病毒。采用离心感染法制备靶向cdh6的CAR-T细胞,并通过体外共培养实验研究CAR-T细胞靶细胞的特异性识别和细胞杀伤作用。在转录水平上,CDH6在卵巢癌组织中显著过表达(P < 0.05)。虽然与肿瘤分期和患者预后无关,但CDH6的过表达与谱系特异性转录因子PAX8的表达呈正相关。在本研究中,我们成功建立了靶向cdh6的CAR-T细胞,该细胞与cdh6阳性卵巢癌细胞体外共培养后,可分泌效应细胞因子并产生特异性杀细胞作用。因此,CDH6作为卵巢组织的谱系特异性因子,可能是CAR-T细胞治疗卵巢癌的理想靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction and Characterization of Cadherin 6 (CDH6)-Targeting Chimeric Antigen Receptor (CAR) Modified T Cells.
In this study, we constructed cadherin 6 (CDH6)-targeting chimeric antigen receptor (CAR) modified T cells (CAR-T cells) and investigated their target-specific recognition and tumor-specific cytocidal effect through in vitro approach. CDH6 expression at the transcriptional level and its correlation with clinicopathological parameters in various tumor types were analyzed using online bioinformatics tool. Conventional molecular cloning method was used to construct the lentiviral vector encoding CDH6-specific CAR and the lentivirus was prepared using 3-plasmid transient cotransfection method. CDH6-targeting CAR-T cells were prepared using centrifugal infection method, and the specific recognition and cytocidal effects of CAR-T cell targets were investigated through in vitro co-culture experiments. At the transcription level, CDH6 was significantly overexpressed in ovarian cancer tissues (P < 0.05). Although it was not correlated with tumor stage and patient's prognosis, the overexpression of CDH6 was positively associated with the expression of paired-box 8 (PAX8), a lineage-specific transcription factor. In the present study, we successfully established CDH6-targeting CAR-T cells that can secrete effector cytokines and produce specific cytocidal effects after being co-cultured with CDH6-positive ovarian cancer cells in vitro. Thus, CDH6, as a lineage-specific factor of ovarian tissue, may be an ideal target for CAR-T cell therapy of ovarian cancer.
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