Thorsteinsson L, Frøland S S, Natvig J B
Scand J Immunol. 1977;6(12):1305-15. doi: 10.1111/j.1365-3083.1977.tb00370.x.
Two different methods for evaluating 'in vitro' cytotoxicity against antibody-coated target cells mediated by mononuclear leukocytes were compared. One was a plaque assay for identification of the cytotoxic cell and the other the classical chromium release assay for antibody-dependent cytotoxicity (ADCC). A marked decrease in plaque-forming cells (PFC) was observed in a cell suspension depleted of peroxidase-positive cells and cells with membrane-bound Ig (B lymphocytes) by fractionation on a nylon fiber column. In contrast, the ADCC activity was considerably increased by these depletions. A similar effect was obtained by removal of phagocytic cells with iron. These results, together with the observations after depletion of E-RFC (T lymphocytes) or EA-RFC (Fc-receptor-bearing cells), suggest that the PFC in the assay system used were of monocytic origin and differnet from the cells responsible for the ADCC.
比较了两种评估单核白细胞介导的针对抗体包被靶细胞的“体外”细胞毒性的不同方法。一种是用于鉴定细胞毒性细胞的蚀斑测定法,另一种是用于抗体依赖性细胞毒性(ADCC)的经典铬释放测定法。通过在尼龙纤维柱上进行分级分离,在过氧化物酶阳性细胞和具有膜结合Ig的细胞(B淋巴细胞)耗尽的细胞悬液中观察到蚀斑形成细胞(PFC)明显减少。相反,这些耗尽使ADCC活性显著增加。用铁去除吞噬细胞也获得了类似的效果。这些结果,连同E-RFC(T淋巴细胞)或EA-RFC(具有Fc受体的细胞)耗尽后的观察结果,表明所用测定系统中的PFC源自单核细胞,且不同于负责ADCC的细胞。