Kotkes P, Pick E
Clin Exp Immunol. 1975 Jan;19(1):105-20.
Mixtures of serum of Freund's complete adjuvant (FCA) immunized guinea-pigs and tuberculin PPD consistently inhibited the in vitro migration of peritoneal exudate cells (PEC) of normal guinea-pigs. It is shown that this inhibitory effect is due to a soluble complex between an IgG2 antibody and PPD. By separation of PPD on Sephadex G-200 two peaks were obtained, corresponding respectively to molecular weights of at least 800,000 and 25,000, separated by a plateau. Material derived from both peaks and from the plateau was able to form inhibitory complexes with anti-PPD IgG2. When a mixture of small molecular weight PPD and anti-PPD IgG2 was fractionated on Sephadex G-200, the inhibitory activity was recovered in the void region only. The detection of both IgG2 and PPD in the latter was taken as evidence for the presence of a high molecular weight antigen-antibody complex. When the mechanism of complex-induced inhibition of migration was examined it was found that: (1) complexes act directly on macrophages present in the peritoneal exudate; (2) removal of the Fc fragment of IgG2 by pepsin abolishes its ability to form migration inhibitory complexes; (3) passive sensitization of macrophages with anti-PPD IgG2, followed by exposure to PPD does not result in inhibition of migration; (4) in order to obtain migration inhibition, the complexes must be present during the entire migration period. A 2-hr pulse with complexes does not induce permanent inhibition; (5) the migration inhibitory activity of antigen--antibody complexes can be abolished by certain concentrations of puromycin and aminophylline.
弗氏完全佐剂(FCA)免疫豚鼠的血清与结核菌素PPD的混合物始终抑制正常豚鼠腹腔渗出细胞(PEC)的体外迁移。结果表明,这种抑制作用是由于IgG2抗体与PPD之间形成了可溶性复合物。通过在Sephadex G - 200上分离PPD,得到了两个峰,分别对应至少800,000和25,000的分子量,中间有一个平台区将它们隔开。来自两个峰以及平台区的物质都能够与抗PPD IgG2形成抑制性复合物。当在Sephadex G - 200上对小分子PPD和抗PPD IgG2的混合物进行分级分离时,抑制活性仅在空体积区域被回收。在后者中检测到IgG2和PPD,这被视为高分子量抗原 - 抗体复合物存在的证据。当研究复合物诱导迁移抑制的机制时发现:(1)复合物直接作用于腹腔渗出液中的巨噬细胞;(2)用胃蛋白酶去除IgG2的Fc片段会消除其形成迁移抑制复合物的能力;(3)用抗PPD IgG2对巨噬细胞进行被动致敏,然后暴露于PPD不会导致迁移抑制;(4)为了获得迁移抑制,复合物必须在整个迁移期间都存在。用复合物进行2小时的脉冲处理不会诱导永久性抑制;(5)抗原 - 抗体复合物的迁移抑制活性可以被一定浓度的嘌呤霉素和氨茶碱消除。