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Ultra-sensitive detection of tumorigenic cellular impurities in human cell-processed therapeutic products by digital analysis of soft agar colony formation

机译:通过软琼脂菌落形成的数字分析超灵敏地检测人细胞加工的治疗产品中的致瘤细胞杂质

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摘要

Contamination with tumorigenic cellular impurities is one of the most pressing concerns for human cell-processed therapeutic products (hCTPs). The soft agar colony formation (SACF) assay, which is a well-known in vitro assay for the detection of malignant transformed cells, is applicable for the quality assessment of hCTPs. Here we established an image-based screening system for the SACF assay using a high-content cell analyzer termed the digital SACF assay. Dual fluorescence staining of formed colonies and the dissolution of soft agar led to accurate detection of transformed cells with the imaging cytometer. Partitioning a cell sample into multiple wells of culture plates enabled digital readout of the presence of colonies and elevated the sensitivity for their detection. In practice, the digital SACF assay detected impurity levels as low as 0.00001% of the hCTPs, i.e. only one HeLa cell contained in 10,000,000 human mesenchymal stem cells, within 30 days. The digital SACF assay saves time, is more sensitive than in vivo tumorigenicity tests, and would be useful for the quality control of hCTPs in the manufacturing process.
机译:致瘤性细胞杂质的污染是人类细胞加工的治疗产品(hCTP)最为紧迫的问题之一。软琼脂菌落形成(SACF)测定法是用于检测恶性转化细胞的众所周知的体外测定法,可用于hCTP的质量评估。在这里,我们使用称为数字SACF分析的高含量细胞分析仪建立了基于图像的SACF分析筛选系统。形成的菌落的双重荧光染色和软琼脂的溶解导致使用成像细胞仪准确检测转化的细胞。将细胞样品分配到培养板的多个孔中可以数字读出菌落的存在,并提高了检测菌落的敏感性。在实践中,数字SACF分析在30天内检测到hCTP的杂质水平低至0.00001%,即10,000,000人间充质干细胞中仅包含一个HeLa细胞。数字SACF检测可节省时间,比体内致瘤性检测更为灵敏,可用于制造过程中hCTP的质量控制。

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