Horwitz D A, Kight N, Temple A, Allison A C
Immunology. 1979 Feb;36(2):221-8.
A method is described which demonstrates that human adherent mononuclear cells have a strong capacity to kill human nucleated target cells. Cytotoxicity was measured by the release of 51chromium from two established cell lines. Freshly prepared monolayers killed both non-sensitized and anti-body coated K562 and CLA-4 target cells. These spontaneous events decreased after short term culture. A second peak of cytotoxic activity was induced by activating the effector cells with endotoxin-treated serum or phytohaemagglutinin. Cytotoxicity was inhibited by silica particles. Studies with alpha-naphthyl esterase showed that 95% of freshly prepared cells and 99% of monolayers cultured for 68 h were monocytes. These studies suggest that adherent monocytes are the predominant cytotoxic effector cell although a contributing effect by the small numbers of contaminating lymphocytes can not be excluded. Evaluation of monocyte cytotoxicity should have a useful role in clinical investigation.
本文描述了一种方法,该方法证明人类贴壁单核细胞具有强大的杀伤人类有核靶细胞的能力。通过从两种既定细胞系中释放⁵¹铬来测量细胞毒性。新鲜制备的单层细胞可杀死未致敏和抗体包被的K562和CLA - 4靶细胞。这些自发事件在短期培养后减少。用内毒素处理的血清或植物血凝素激活效应细胞可诱导细胞毒性活性的第二个峰值。细胞毒性被二氧化硅颗粒抑制。用α - 萘酯酶进行的研究表明,新鲜制备的细胞中有95%以及培养68小时的单层细胞中有99%是单核细胞。这些研究表明,贴壁单核细胞是主要的细胞毒性效应细胞,尽管不能排除少量污染淋巴细胞的辅助作用。评估单核细胞细胞毒性在临床研究中应具有有益作用。