López A F, Vadas M A
Proc Natl Acad Sci U S A. 1984 Mar;81(6):1818-21. doi: 10.1073/pnas.81.6.1818.
From a panel of monoclonal antibodies (MAb) produced against purified human neutrophils, MAb WEM-G1 was selected for its ability to stimulate granulocyte function as assessed by the capacity to kill antibody-coated tumor target cells. MAb WEM-G1 bound to neutrophils and eosinophils and not to monocytes, lymphocytes, or erythrocytes, and thus identified a granulocyte differentiation antigen. It enhanced killing by both neutrophils and eosinophils in a dose-dependent fashion, with a range of effector-to-target ratios and dilutions of anti-target cell antibody. The effect of MAb WEM-G1 was additive with that of colony-stimulating factor (CSF-alpha). Similarly, the ability of neutrophils to exhibit enhanced cytotoxicity in the presence of WEM-G1 was increased by preincubation of neutrophils with CSF-alpha. Immunoprecipitation analysis showed that WEM-G1 identified a cell-surface protein on human neutrophils of approximate molecular weight 110,000. It is suggested that this structure is involved in regulation of the function of human granulocytes.
从一组针对纯化人中性粒细胞产生的单克隆抗体(MAb)中,选择了MAb WEM-G1,因为根据其杀死抗体包被肿瘤靶细胞的能力评估,它具有刺激粒细胞功能的能力。MAb WEM-G1与中性粒细胞和嗜酸性粒细胞结合,而不与单核细胞、淋巴细胞或红细胞结合,因此识别出一种粒细胞分化抗原。它以剂量依赖的方式增强中性粒细胞和嗜酸性粒细胞的杀伤作用,适用于一系列效应细胞与靶细胞比例以及抗靶细胞抗体的稀释度。MAb WEM-G1的作用与集落刺激因子(CSF-α)的作用相加。同样,通过用CSF-α预孵育中性粒细胞,在存在WEM-G1的情况下中性粒细胞表现出增强的细胞毒性的能力也增加了。免疫沉淀分析表明,WEM-G1识别出一种人中性粒细胞上分子量约为110,000的细胞表面蛋白。有人认为这种结构参与了人类粒细胞功能的调节。