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CD166 特异性 CAR-T 细胞强效靶向结直肠癌细胞

英文原题:CD166-specific CAR-T cells potently target colorectal cancer cells.

查看英文原题

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

PubMed 2022/10/31(内容时间) Transl Oncol Q2 · IF 4.9(JCR 2025)

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中文摘要

嵌合抗原受体(CAR)T细胞疗法正逐渐成为一种有效的癌症治疗方法,例如用于血液系统恶性肿瘤,但其作为治疗实体瘤(如结直肠癌(CRC))的方法的有效性仍有待进一步开发。一个密集开发的领域是鉴定和表征用于CAR设计和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,并且几种CAR-T 也已在临床前和临床研究中探索用于治疗CRC,具有良好的安全性和有效性发现。

在此,我们基于CD6的胞外域构建了一种CAR,并证明其在靶标阳性人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CD166而非CD318。

此外,CD6-CAR-T 细胞以剂量依赖性方式对CD166阳性细胞系显示出强大的细胞毒性,并显著释放细胞因子IFN-。特别是,CD6-CAR-T 细胞显示出靶向CRC癌症干细胞(CSC)的强大细胞毒性,突显了CD6-CAR-T 是治疗CRC的一种有前景的方法。

展开英文摘要原文

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- 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.

论文信息

作者
He S、Li S、Guo J、Zeng X、Liang D、Zhu Y、Li Y、Yang D
第一作者单位
Laboratory of Animal Tumor Models, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China.China
通讯作者单位
Laboratory of Animal Tumor Models, Frontiers Science Center for Disease-related Molecular Network, West China Hospital, Sichuan University, Chengdu, Sichuan 610041, PR China. Electronic address: zhaoxudong@wchscu.cn.China
期刊
Translational oncology2023 Jan
原文标识
PubMed 36327697 · DOI 10.1016/j.tranon.2022.101575