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.
CAR-T(CAR-T)细胞在血液系统恶性肿瘤中的应用推动了这种免疫治疗形式的显著进展。
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Assessment of CAR-T Cell-Mediated Cytotoxicity in 3D Microfluidic Cancer Co-Culture Models for Combination Therapy.
Assessment of CAR-T Cell-Mediated Cytotoxicity in 3D Microfluidic Cancer Co-Culture Models for Combination Therapy.
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嵌合抗原受体(CAR)T细胞疗法对多种血液系统恶性肿瘤有效,但将这一细胞免疫疗法用于实体瘤仍面临挑战。传统二维体外模型无法再现肿瘤微环境的复杂性,而患者来源异种移植等体内模型成本高且耗费人力。微流控技术可提供小型化方案,在实体瘤复杂的三维临床前模型中评估CAR-T 疗法。本文介绍一种新型微流控免疫分析方法,用于评估CAR-T 细胞对含癌细胞和基质细胞的三维球体的细胞毒性及靶向特异性。通过监测CAR-T 细胞与球体共培养物的相互作用,我们发现CAR-T 细胞会趋向表达靶标的癌细胞,并产生细胞毒效应。在联合治疗测试中,抗PD-L1治疗和卡铂化疗均增强了CAR-T 细胞的细胞毒性。我们提出,这一概念验证微流控免疫分析法可作为节省材料的临床前筛选工具,用于定量评估细胞治疗效果。
Chimeric antigen receptor (CAR)-T cell therapy is efficacious against many haematological malignancies, but challenges remain when using this cellular immunotherapy for treating solid tumours. Classical 2D in vitro models fail to recapitulate the complexity of the tumour microenvironment, whilst in vivo models, such as patient-derived xenografts, are costly and labour intensive. Microfluidic technologies can provide miniaturized solutions to assess CAR-T therapies in 3D complex preclinical models of solid tumours.
Here, we present a novel microfluidic immunoassay for the evaluation of CAR-T cell cytotoxicity and targeting specificity on 3D spheroids containing cancer cells and stromal cells. Monitoring the interaction between CAR-T cells and spheroid co-cultures, we show that CAR-T cells home towards target-expressing cancer cells and elicit a cytotoxic effect. Testing CAR-T cells in combination therapies, we show that CAR-T cell cytotoxicity is enhanced with anti-PD-L1 therapy and carboplatin chemotherapy.
We propose this proof-of-concept microfluidic immunoassay as a material-saving, pre-clinical screening tool for quantification of cell therapy efficacy.
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