Division of Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
Department of Clinical Pharmacology, Netherlands Cancer Institute - Antoni van Leeuwenhoek (NKI-AVL), Amsterdam, The Netherlands.
Cytometry A. 2019 Oct;95(10):1053-1065. doi: 10.1002/cyto.a.23873. Epub 2019 Aug 12.
We report the development and validation of a 12 parameter immunofluorescence flow cytometry method for the sensitive determination of cell concentrations, their expression of PD-1, and PD-1 receptor occupancy. Cell subsets include CD4 and CD8 -T-cells, B-cells, natural killer cells, classical-, intermediate- and non-classical monocytes, and myeloid- and plasmacytoid dendritic cells. Cells were isolated from peripheral blood by density gradient centrifugation. The validation parameters included specificity, linearity, limit of quantification, precision, biological within- and between subject variations. The lower limit of quantification was 5.0% of PD-1 cells. Samples were stable for at least 153 days of storage at -80°C. The clinical applicability of the method was demonstrated in 11 advanced cancer patients by the successful determination of immune cell concentrations, relative number of PD-1 immune cells, and number of PD-1 molecules per immune cell. Shortly after infusion of nivolumab, receptor occupancy on CD8 -T-cells was 98%. Similar values were found predose cycle 2, suggesting receptor occupancy remained high throughout the entire cycle. © 2019 International Society for Advancement of Cytometry.
我们报告了一种 12 参数免疫荧光流式细胞术方法的开发和验证,该方法可用于灵敏地测定细胞浓度、其 PD-1 表达和 PD-1 受体占有率。细胞亚群包括 CD4 和 CD8-T 细胞、B 细胞、自然杀伤细胞、经典型、中间型和非经典型单核细胞、髓系和浆细胞样树突状细胞。细胞通过密度梯度离心从外周血中分离出来。验证参数包括特异性、线性、定量下限、精密度、生物学内和个体间变异性。PD-1 细胞的定量下限为 5.0%。样本在 -80°C 下储存至少 153 天是稳定的。该方法的临床适用性通过成功测定 11 名晚期癌症患者的免疫细胞浓度、PD-1 免疫细胞的相对数量以及每个免疫细胞的 PD-1 分子数量得到了证明。在输注纳武利尤单抗后不久,CD8-T 细胞上的受体占有率为 98%。在第 2 周期的预剂量时也发现了类似的值,这表明在整个周期中受体占有率一直保持较高水平。 © 2019 国际细胞分析学会。