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首页> 外文期刊>Journal of Physics, D. Applied Physics: A Europhysics Journal >Label-free purification of viable human T-lymphocyte cells from a mixture of viable and non-viable cells after transfection by electroporation
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Label-free purification of viable human T-lymphocyte cells from a mixture of viable and non-viable cells after transfection by electroporation

机译:通过电穿孔转染后,从可行和非活细胞的混合物中无标记纯化活性人T淋巴细胞细胞

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摘要

Recent developments in chimeric antigen receptor (CAR) T-cell therapy for cancer have shown promising results. CAR T-cells are engineered mainly by AC or DC electroporation to express CAR molecules on their surfaces. Electroporation has detrimental effects on the majority of T-cells and causes cell death via apoptosis or necrosis. These non-viable cells have potentially harmful effects on other healthy T-cells. Because there are no unique biomarkers that pinpoint the apoptosis and necrosis of T-cells, currently available cell separation methods are incapable of purifying healthy T-cells after electroporation. To address this critical issue, we have used dielectrophoretic cell isolation in a simple microfluidics chip. Our results indicate that it is possible to purify cell samples after electroporation and achieve similar to 100% purity and >90% target cell recovery. Therefore, this work presents a viable solution to a critical need in CAR T-cell manufacturing.
机译:嵌入抗原受体(CAR)T细胞治疗的最新发展已显示出现有前途的结果。 汽车T细胞主要通过AC或DC电穿孔工程,以表达其表面上的汽车分子。 电穿孔对大多数T细胞具有不利影响,并通过细胞凋亡或坏死导致细胞死亡。 这些不活体细胞对其他健康T细胞具有潜在的有害影响。 因为没有针对T细胞的细胞凋亡和坏死没有独特的生物标志物,所以目前可用的细胞分离方法不能在电穿孔后净化健康的T细胞。 为了解决这一关键问题,我们在简单的微流体芯片中使用了介电泳细胞分离。 我们的结果表明,在电穿孔后可以纯化细胞样品,并达到类似于100%纯度和> 90%的靶细胞回收。 因此,这项工作呈现了汽车T细胞制造中的关键需求的可行解决方案。

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