Heilman D H, Bast R C
J Bacteriol. 1967 Jan;93(1):15-20. doi: 10.1128/jb.93.1.15-20.1967.
A quantitative in vitro technique was used to compare the ability of different endotoxins to inhibit the migration of macrophages from explants of rabbit spleen cultured in a coagulated plasma medium. The order of potency was different from that observed in chick embryo assays, and in assays with mice, of the same endotoxins. In general, however, the sensitivity of the macrophage inhibition test was comparable to that of other bioassay methods. A highly purified endotoxin from Salmonella enteritidis (Ribi) in a concentration of 0.004 mug/ml regularly inhibited macrophage migration. The in vitro method was used to detect a progressive loss of biological activity in fractions obtained during acid hydrolysis of the purified endotoxin. The selective toxicity of very low concentrations of endotoxin for mammalian macrophages was important in estimating the degree of specificity of the reaction. The pattern of cellular response in explant cultures made it possible to differentiate endotoxic damage from the specific cytotoxic action of antigen associated with delayed hypersensitivity.
采用一种定量体外技术,比较不同内毒素抑制巨噬细胞从兔脾脏外植体在凝固血浆培养基中迁移的能力。其效力顺序与在鸡胚试验以及用相同内毒素对小鼠进行的试验中观察到的顺序不同。然而,总体而言,巨噬细胞抑制试验的灵敏度与其他生物测定方法相当。肠炎沙门氏菌(里比)的一种高度纯化内毒素,浓度为0.004微克/毫升时可规律性地抑制巨噬细胞迁移。该体外方法用于检测纯化内毒素酸水解过程中获得的各组分生物活性的逐渐丧失。极低浓度内毒素对哺乳动物巨噬细胞的选择性毒性在评估反应的特异性程度方面很重要。外植体培养中的细胞反应模式使得区分内毒素损伤与与迟发型超敏反应相关的抗原的特异性细胞毒性作用成为可能。