Fink P C, Klaproth C, Peter H H
Infection. 1984 Sep-Oct;12(5):322-7. doi: 10.1007/BF01651145.
The effect of lipopolysaccharides (LPS), lipid A and interferon on cell-mediated cytotoxicity was investigated using 51Cr-labeled K-562 tumor cells as targets. As effectors, peripheral blood mononuclear cells from healthy blood donors were obtained by Ficoll gradient centrifugation: mononuclear phagocytes were eliminated by iron phagocytosis and plastic adherence. A T cell-enriched population was obtained by passing mononuclear phagocyte-depleted mononuclear cells through nylon wool columns. LPS and lipid A augmented cell-mediated cytotoxicity provided mononuclear phagocytes were present. Supernatants from LPS-treated mononuclear phagocytes and T cells enhanced mononuclear phagocyte-mediated cytotoxicity to a higher degree than LPS and lipid A alone. This finding suggests the participation of a lymphokine. In contrast, the interferon preparation increased the cell-mediated cytotoxicity both of mononuclear phagocyte-containing and of mononuclear phagocyte-depleted effectors. Here, the participation of natural killer cells as effectors is suggested.
以51Cr标记的K-562肿瘤细胞为靶细胞,研究了脂多糖(LPS)、脂质A和干扰素对细胞介导细胞毒性的影响。作为效应细胞,通过Ficoll梯度离心从健康献血者的外周血中获得单个核细胞:通过铁吞噬作用和塑料黏附去除单核吞噬细胞。将去除单核吞噬细胞的单个核细胞通过尼龙毛柱,获得富含T细胞的群体。如果存在单核吞噬细胞,LPS和脂质A会增强细胞介导的细胞毒性。LPS处理的单核吞噬细胞和T细胞的上清液比单独的LPS和脂质A更能增强单核吞噬细胞介导的细胞毒性。这一发现提示有淋巴因子参与。相反,干扰素制剂增加了含单核吞噬细胞的效应细胞和去除单核吞噬细胞的效应细胞的细胞介导细胞毒性。在此,提示自然杀伤细胞作为效应细胞参与其中。