Rodgers J R, Shawar S M, Guenther M M, Rich R R
Department of Microbiology and Immunology, Baylor College of Medicine, Houston, TX 77030.
J Immunol Methods. 1992 Aug 10;152(2):159-69. doi: 10.1016/0022-1759(92)90137-i.
Some targets of cell-mediated cytolysis do not efficiently release 51Cr but manifestly are killed in direct viability assays. We characterize and validate an alternative and non-radioactive (colorimetric) method for measuring killing of adherent targets by monoclonal CTL. The method obviates concerns about the effects of trypsinization, is technically simple, quantitative and in some cases more sensitive than conventional 51Cr assays. Target loss obeyed first-order kinetics with respect both to [CTL] and time. These results are consistent with an exponential (Poisson) model of killing and support the use of a single kinetic parameter to describe the lytic activity of monoclonal CTL on adherent targets. When monoclonal CTL are used at appropriate effector:target ratios (less than or equal to 1:1), the residuals obtained after least squares linear regression are homoscedastic and normally distributed, justifying the use of commonly available statistical calculators or programs for the analysis of CTL data.
一些细胞介导的细胞溶解作用的靶标不能有效地释放51Cr,但在直接活力测定中明显被杀死。我们描述并验证了一种用于测量单克隆CTL对贴壁靶标的杀伤作用的替代且非放射性(比色法)方法。该方法消除了对胰蛋白酶消化作用影响的担忧,技术上简单、定量,并且在某些情况下比传统的51Cr测定更灵敏。靶标损失在[CTL]和时间方面均遵循一级动力学。这些结果与杀伤的指数(泊松)模型一致,并支持使用单个动力学参数来描述单克隆CTL对贴壁靶标的裂解活性。当以适当的效应细胞:靶标比率(小于或等于1:1)使用单克隆CTL时,最小二乘线性回归后获得的残差是同方差且呈正态分布的,这证明使用常用的统计计算器或程序来分析CTL数据是合理的。