Parish C R, Müllbacher A
J Immunol Methods. 1983 Mar 11;58(1-2):225-37. doi: 10.1016/0022-1759(83)90277-6.
A colorimetric method has been developed for detecting the lysis of target cells by cytotoxic T lymphocytes (Tc). The method entails incubating Tc cells with thioglycollate-induced macrophage targets and estimating macrophage survival at the end of the assay by staining viable macrophages with the dye neutral red. The method is substantially more sensitive than the 51Cr release assay and can be used to detect alloreactive Tc cells and H-2-restricted Tc cells against viruses, haptens and minor-H antigens. Furthermore, the assay is applicable to limit dilution analysis of Tc cell precursors. The method is cheap, avoids radioactive materials and by measuring optical densities with automated spectrophotometers developed for microELISA systems, results can be obtained 50-100 times faster than with the radioactive procedure.
已开发出一种比色法,用于检测细胞毒性T淋巴细胞(Tc)对靶细胞的裂解作用。该方法包括将Tc细胞与巯基乙酸诱导的巨噬细胞靶标一起孵育,并在测定结束时通过用染料中性红对存活的巨噬细胞进行染色来评估巨噬细胞的存活率。该方法比51Cr释放测定法灵敏得多,可用于检测同种反应性Tc细胞以及针对病毒、半抗原和次要组织相容性抗原的H-2限制性Tc细胞。此外,该测定法适用于Tc细胞前体的有限稀释分析。该方法成本低廉,避免使用放射性材料,并且通过使用为微量酶联免疫吸附测定系统开发的自动分光光度计测量光密度,获得结果的速度比放射性方法快50至100倍。