Hirashima M, Tashiro K, Hayashi H
Immunology. 1984 Mar;51(3):441-50.
The regulation of tissue eosinophilia induced by dinitrophenyl-ascaris extract (DNP-As) was investigated in guinea-pigs. Biphasic tissue eosinophilia peaking at 6 and 24 hr was observed in the skin lesions in Bordetella pertussis vaccine (Bp)-treated animals. In contrast, only the early phase of tissue eosinophilia was observed in Freund's complete adjuvant (FCA)-treated animals. Although less eosinophil chemotactic activity was detected in 24-hr-old skin extract of FCA-treated animals (FCA-extract), evident activity was recovered in the concanavalin A eluate (Con A-eluate) when FCA-extract was fractionated by Con A Sepharose. The chemotactic factor in Con A-eluate of FCA-extract was confirmed to be the T cell-derived eosinophil chemotactic factor, termed Delayed ECF-a, which has been isolated from allergic skin lesions by immunoadsorption. Another factor from the same skin lesions, Delayed ECF-b (which is a serum-derived one), was not detected in the FCA-extract. When eosinophils were mixed or pretreated with Con A-effluent of FCA-extract, the treated cells failed to be attracted by Delayed ECF-a, while the response to Delayed ECF-b was not affected, indicating that the inhibition was selective for Delayed ECF-a but not for Delayed ECF-b, and the eosinophil chemotactic inhibitory factor (ECIF) acts on eosinophils directly. Major ECIF activity was associated with a mol. wt. of 70,000 and minor with 12,500. Furthermore, the activity was absorbed by eosinophils but not by macrophages suggesting that eosinophils have receptor sites for ECIF. It was thus suggested that the appearance of ECIF, which is selective for the response of eosinophils to Delayed ECF-a, and decreased Delayed ECF-b production resulted in the inhibition of delayed tissue eosinophilia in FCA-treated guinea-pigs.
在豚鼠中研究了二硝基苯基蛔虫提取物(DNP-As)诱导的组织嗜酸性粒细胞增多的调节情况。在百日咳博德特氏菌疫苗(Bp)处理的动物的皮肤病变中观察到双相性组织嗜酸性粒细胞增多,在6小时和24小时达到峰值。相比之下,在弗氏完全佐剂(FCA)处理的动物中仅观察到组织嗜酸性粒细胞增多的早期阶段。虽然在FCA处理的动物的24小时龄皮肤提取物(FCA提取物)中检测到较少的嗜酸性粒细胞趋化活性,但当FCA提取物用伴刀豆球蛋白A琼脂糖凝胶进行分级分离时,在伴刀豆球蛋白A洗脱液(Con A洗脱液)中恢复了明显的活性。FCA提取物的Con A洗脱液中的趋化因子被证实是T细胞衍生的嗜酸性粒细胞趋化因子,称为迟发性嗜酸性粒细胞趋化因子-a(Delayed ECF-a),它已通过免疫吸附从过敏性皮肤病变中分离出来。在FCA提取物中未检测到来自相同皮肤病变的另一种因子,即迟发性嗜酸性粒细胞趋化因子-b(它是血清衍生的)。当嗜酸性粒细胞与FCA提取物的Con A流出物混合或预处理时,处理后的细胞不能被迟发性嗜酸性粒细胞趋化因子-a吸引,而对迟发性嗜酸性粒细胞趋化因子-b的反应不受影响,这表明这种抑制对迟发性嗜酸性粒细胞趋化因子-a具有选择性,而对迟发性嗜酸性粒细胞趋化因子-b没有选择性,并且嗜酸性粒细胞趋化抑制因子(ECIF)直接作用于嗜酸性粒细胞。主要的ECIF活性与分子量70,000相关,次要的与12,500相关。此外,该活性被嗜酸性粒细胞吸收,但未被巨噬细胞吸收,这表明嗜酸性粒细胞具有ECIF的受体位点。因此,有人提出,对嗜酸性粒细胞对迟发性嗜酸性粒细胞趋化因子-a的反应具有选择性的ECIF的出现以及迟发性嗜酸性粒细胞趋化因子-b产生的减少导致了FCA处理的豚鼠中迟发性组织嗜酸性粒细胞增多的抑制。