CAR-T(CAR-T)细胞疗法在非肿瘤性疾病中的应用
Chimeric antigen receptor T (CAR-T) cell therapy in non-oncological diseases.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Patient-Derived Three-Dimensional Tumor Organoid Model for In Vitro Chimeric Antigen Receptor T Cell Screening.
Patient-Derived Three-Dimensional Tumor Organoid Model for In Vitro Chimeric Antigen Receptor T Cell Screening.
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CAR-T(CAR-T)细胞疗法已在血液系统恶性肿瘤中取得令人振奋的临床疗效,但实体瘤CAR-T 治疗仍需进一步发展。患者来源肿瘤类器官是保留患者异质性的体外疾病模型,已用于检测化疗药物和靶向药物的疗效与安全性。本文介绍一种将肿瘤类器官与CAR-T 细胞共培养的体外疗效测试模型。研究者将患者结直肠癌样本在基底膜基质中构建为三维(3D)结构肿瘤类器官。类器官可稳定生长并连续传代。成熟类器官经清洗和离心从基质中分离后,加入不同效靶(E:T)比的CAR-T 细胞,建立免疫细胞—类器官共培养体系。共培养6至24小时后,通过明场成像观察类器官形态和细胞间结构。实验还在共培养体系中进行死细胞染色,以反映类器官活力并评估CAR-T 细胞对肿瘤类器官的细胞毒作用。该实验可有效观察CAR-T 细胞与3D肿瘤类器官之间的相互作用,结果可用于评估CAR-T 细胞的肿瘤杀伤活性。
Chimeric antigen receptor T (CAR-T) cell therapy has achieved exciting clinical efficacy in hematological malignancies, but CAR-T cell therapy for solid tumors still requires further development. Patient-derived tumor organoids are in vitro disease models that retain patient heterogeneity and have been used to test the efficacy and safety of chemotherapy and targeted drugs. This method describes an in vitro efficacy testing model of co-culturing tumor organoids with CAR-T cells. Colorectal cancer samples from patients are constructed into tumor organoids with a three-dimensional (3D) structure in a basement membrane matrix. The tumor organoids can grow stably and be passaged continuously.
Mature tumor organoids are separated from the matrix by washing and centrifugation, and CAR-T cells are added at different effector-to-target (E:T) ratios to form an immune-organoid co-culture system. After 6-24 h, the morphology and intercellular structures of the organoids are observed by bright-field imaging.
This experiment further performs dead cell staining in the co-culture system, which can reflect the viability of the organoids and evaluate the cytotoxic effect of CAR-T cells on tumor organoids. This experiment can effectively observe the interaction between CAR-T cells and 3D tumor organoids, and the results can be used to assess the tumor-killing activity of CAR-T cells.
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