Laurent G, Kuhlein E, Casellas P, Canat X, Carayon P, Poncelet P, Correll S, Rigal F, Jansen F K
Cancer Res. 1986 May;46(5):2289-94.
In clinical practice, sensitivity of malignant cells to a given immunotoxin remains hypothetical, since standard test systems such as the protein synthesis inhibition assay or the cloning assay are not appropriate. This study evaluated the feasibility of a semi-routine procedure based on dye exclusion assay enumerating the percentage of living cells after fluorescein diacetate-propidium iodide staining. The validity of the method was evaluated using five different subclones derived from the CEM cell line, which expressed a wide range of sensitivity to T101 A-chain immunotoxin. The comparison between dye exclusion assay and standard test systems suggested that this method might allow an easy and reproducible semi-quantitative evaluation of the sensitivity of leukemia cells. In a series of 21 patients suffering from various blood diseases in which the malignant cells expressed the T65 antigen, dye exclusion assay could detect clear T101 immunotoxin cell sensitivity in about 50% of the cases. The mean density of T65 antigen on malignant cells was found to influence dramatically the sensitivity of target cells to T101 immunotoxin.
在临床实践中,恶性细胞对特定免疫毒素的敏感性仍然是假设性的,因为诸如蛋白质合成抑制试验或克隆试验等标准测试系统并不适用。本研究评估了一种基于染料排除试验的半常规程序的可行性,该试验通过荧光素二乙酸酯 - 碘化丙啶染色来计算活细胞的百分比。使用从CEM细胞系衍生的五个不同亚克隆评估该方法的有效性,这些亚克隆对T101 A链免疫毒素表现出广泛的敏感性。染料排除试验与标准测试系统之间的比较表明,该方法可能允许对白血病细胞的敏感性进行简单且可重复的半定量评估。在一系列21例患有各种血液疾病且恶性细胞表达T65抗原的患者中,染料排除试验在约50%的病例中可检测到明显的T101免疫毒素细胞敏感性。发现恶性细胞上T65抗原的平均密度显著影响靶细胞对T101免疫毒素的敏感性。