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靶向 DLK1 的 CAR-T 细胞疗法治疗肝细胞癌

英文原题:DLK1-directed chimeric antigen receptor T-cell therapy for hepatocellular carcinoma.

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DLK1-directed chimeric antigen receptor T-cell therapy for hepatocellular carcinoma.

PubMed 2022/09/06(内容时间) Liver Int Q1 · IF 6.2(JCR 2025)

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研究概要

DLK1 靶向的 CAR-T 细胞在体外和体内特异性抑制 DLK1 阳性肝细胞癌细胞。

中文摘要

Delta样同源物1(DLK1)是一种跨膜蛋白,在肝细胞癌(HCC)中高表达。本研究探讨靶向DLK1的嵌合抗原受体(CAR)T细胞能否特异性清除DLK1阳性肝癌细胞,并成为肝癌免疫治疗策略。

研究人员首先对自制的人抗DLK1单克隆抗体进行鉴定,测定其单链可变片段(scFv)序列,并将其整合至第二代CAR慢病毒载体中,进而制备靶向DLK1的CAR-T 细胞。随后在体外和体内评估这些细胞对不同肝癌细胞的细胞毒活性。

经基因修饰表达靶向DLK1 CAR的人T细胞能够杀伤DLK1阳性肝癌细胞。此外,CAR以DLK1依赖的方式增强了T细胞增殖和活化。值得注意的是,靶向DLK1的CAR-T 细胞显著抑制了由人肝癌细胞系HepG2或Huh-7建立的皮下及腹膜异种移植瘤。

靶向DLK1的CAR-T 细胞可在体内外特异性抑制DLK1阳性肝癌细胞。本研究提示,新的跨膜抗原DLK1可作为CAR-T 治疗的潜在靶点,并有望进一步发展为肝细胞癌免疫治疗的临床策略。

展开英文摘要原文

Delta-like homologue 1 (DLK1), a transmembrane protein, is highly expressed in hepatocellular carcinoma (HCC). We explored whether DLK1-directed chimeric antigen receptor (CAR) T cells can specifically eliminate DLK1-positive HCC cells and serve as a therapeutic strategy for HCC immunotherapy.

We first characterized a homemade anti-human DLK1 monoclonal antibody, sequenced the single-chain Fragment variable (scFv) and integrated it into the second-generation CAR lentiviral vector, and then developed the DLK1-directed CAR-T cells. The cytotoxic activities of DLK1-directed CAR-T cells against different HCC cells were evaluated in vitro and in vivo.

The genetically modified human T cells with the DLK1-directed CARs produced cytotoxic activity against DLK1-positive HCC cells. Additionally, the DLK1-directed CARs enhanced T cell proliferation and activation in a DLK1-dependent manner. Interestingly, the DLK1-targeted CAR-T cells significantly inhibited both subcutaneous and peritoneal xenograft tumours derived from human liver cancer cell lines HepG2 or Huh-7.

DLK1-directed CAR-T cells specifically suppresses DLK1-positive HCC cells in vitro and in vivo. This study provides a novel transmembrane antigen DLK1 as a potential therapeutic target appropriate for CAR-T cell therapy, which may be further developed as a clinical therapeutic strategy for HCC immunotherapy.

论文信息

作者
Zhai Y、He K、Huang L、Shang X、Wang G、Yuan G、Han ZG
单位
Key Laboratory of Systems Biomedicine (Ministry of Education), Shanghai Center for Systems Biomedicine, Shanghai Jiao Tong University, Shanghai, China.China
文献类型
非美国政府资助研究
期刊
Liver international : official journal of the International Association for the Study of the Liver2022 Nov
原文标识
PubMed 36002393 · DOI 10.1111/liv.15411