Zeijlemaker W P, Roos M T, Schellekens P T, Eijsvoogel V P
Eur J Immunol. 1975 Aug;5(8):579-84. doi: 10.1002/eji.1830050815.
A micro assay system is described for measuring antibody-dependent lymphocytotoxicity with human effector cells. The target cells were mouse mastocytoma cells sensitized with rabbit antibody. The tests were performed in microtiter plates, each well containing 5 x 10(3) 51Cr-labeled target cells, together with varying numbers of effector cells. Whereas highly purified lymphocyte suspensions induced lysis, purified monocyte and granulocyte suspensions had virtually no effect. In parallel experiments it was shown that the latter cell suspensions were very active in lysing sensitized human erythrocytes, which in turn were not lysed by purified lymphocytes. Finally, it was shown that the lytic capacity of lymphocytes was not affected by preservation of the cells at liquid nitrogen temperature. It is concluded that the system described can be used for the clinical analysis of antibody-dependent lymphocytotoxicity in lymphocyte suspensions.
描述了一种用于用人效应细胞测量抗体依赖性淋巴细胞毒性的微量测定系统。靶细胞是用兔抗体致敏的小鼠肥大细胞瘤细胞。试验在微量滴定板中进行,每孔含有5×10³个51Cr标记的靶细胞以及不同数量的效应细胞。高度纯化的淋巴细胞悬液可诱导裂解,而纯化的单核细胞和粒细胞悬液几乎没有作用。在平行实验中表明,后一种细胞悬液在裂解致敏的人红细胞方面非常活跃,而纯化的淋巴细胞则不能裂解人红细胞。最后表明,淋巴细胞的裂解能力不受液氮温度下细胞保存的影响。得出的结论是,所描述的系统可用于淋巴细胞悬液中抗体依赖性淋巴细胞毒性的临床分析。