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CD166特异性嵌合抗原受体T细胞能有效靶向结直肠癌细胞。

CD166-specific CAR-T cells potently target colorectal cancer cells.

作者信息

He Shuai, Li Shirong, Guo Jing, Zeng Xiaozhu, Liang Dandan, Zhu Yongjie, Li Yi, Yang Dong, Zhao Xudong

机构信息

Laboratory of Animal Tumor Models, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China.

Core Facilities, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China.

出版信息

Transl Oncol. 2023 Jan;27:101575. doi: 10.1016/j.tranon.2022.101575. Epub 2022 Oct 31.

Abstract

Chimeric antigen receptor (CAR) T-cell therapy is emerging as an effective cancer treatment, such as for hematological malignancies, however its effectiveness as an approach to treat solid tumors, such as in colorectal cancer (CRC), remains to be better developed. One area of intense development has been in the identification and characterization of novel cancer-related ligand receptors for CAR design and evaluation. It is known that the CD6 receptors CD166 and CD318 are highly expressed in CRC, and several CAR-Ts have also been explored in preclinical and clinical studies for the treatment of CRC, with promising safety and efficacy findings. Here, we constructed a CAR based on the extracellular domain of CD6 and demonstrate its cytotoxic effect in target positive human CRC cell lines. Unexpectedly, we found that CD6-CAR-T cells targeted CD166 instead of CD318. Furthermore, CD6-CAR-T cells show robust cytotoxicity to CD166-positive cell lines in a dose-dependent manner with cytokine IFN-γ significantly released. Particularly, CD6-CAR-T cells show potent cytotoxicity targeting CRC cancer stem cells (CSCs), highlighting that CD6-CAR-T is a promising approach for the therapy of CRC.

摘要

嵌合抗原受体(CAR)T细胞疗法正在成为一种有效的癌症治疗方法,例如用于治疗血液系统恶性肿瘤,然而,其作为治疗实体瘤(如结直肠癌(CRC))的方法的有效性仍有待进一步完善。一个研究热点领域是鉴定和表征用于CAR设计与评估的新型癌症相关配体受体。已知CD6受体CD166和CD318在CRC中高表达,并且在临床前和临床研究中也探索了几种CAR-T用于治疗CRC,取得了有前景的安全性和有效性结果。在此,我们构建了一种基于CD6胞外域的CAR,并证明其在靶标阳性的人CRC细胞系中的细胞毒性作用。出乎意料的是,我们发现CD6-CAR-T细胞靶向的是CD166而非CD318。此外,CD6-CAR-T细胞对CD166阳性细胞系表现出强大的剂量依赖性细胞毒性,并显著释放细胞因子IFN-γ。特别地,CD6-CAR-T细胞对CRC癌症干细胞(CSCs)表现出强大的细胞毒性,这突出表明CD6-CAR-T是一种有前景的CRC治疗方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/80fb/9637812/c4a2ae46b386/gr1.jpg

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