McCoy J L, Padarathsingh M, Dean J H, Henriksen O, Natori T, Law L W
J Immunol. 1977 Jul;119(1):306-10.
Macrophage migration inhibition assays, with a direct agarose microdroplet method, were used to monitor TAA activity of preparations of SV-40-induced mKSA cells. These preparations included cell-free crude membranes, papain-solubilized and NP40 detergent-solubilized membrane extracts from mKSA tumor cells. The assay was extremely sensitive and could detect migration inhibition reactivity with all three types of antigenic preparations with concentrations as low at 250 ng protein/ml. The reactivities were quite reproducible from experiment to experiment using the same or different lots of these antigen preparations, and the reactivities were specific in that peritoneal exudate cells from BALB/c mice, immunized with antigenically unrelated but syngeneic plasmacytomas, were not inhibited by these antigens. The results demonstrated the usefulness of this assay in rapidly detecting small concentrations of partially purified TAA preparations by using small number of immune cells.
采用直接琼脂糖微滴法进行巨噬细胞迁移抑制试验,以监测SV - 40诱导的mKSA细胞制剂的肿瘤相关抗原(TAA)活性。这些制剂包括无细胞粗膜、木瓜蛋白酶溶解的和NP40去污剂溶解的mKSA肿瘤细胞膜提取物。该试验极其灵敏,能够检测到浓度低至250 ng蛋白质/毫升的所有三种类型抗原制剂的迁移抑制反应性。使用相同或不同批次的这些抗原制剂,实验之间的反应性相当可重复,并且这些反应性具有特异性,因为用抗原无关但同基因的浆细胞瘤免疫的BALB/c小鼠的腹腔渗出细胞不受这些抗原的抑制。结果表明,该试验通过使用少量免疫细胞,在快速检测低浓度的部分纯化TAA制剂方面很有用。