Hirashima M, Hirotsu Y, Hayashi H
Immunology. 1983 Jan;48(1):69-77.
An eosinophil chemotactic factor (ECF) was produced in the cell-free culture supernatants (CFS) of peritoneal exudate cells (PEC) from guinea-pigs immunized with dinitrophenyl derivatives of ascaris extract (DNP-As), when stimulated by the antigen in vitro without activation by immune complexes. A 2 or 6 hr pulse of the antigen was sufficient for ECF production, whereas long time incubation (48 hr) was required for the production of a sufficient amount of the factor. Treatment of PEC by cycloheximide resulted in the reduction of ECF production, suggesting that protein synthesis is essential. Its generation appeared carrier-specific and the source of the factor is presumed to be lymphocytes, probably T lymphocyte. The factor with a molecular weight of 70,000 shared a common antigenicity with delayed eosinophil chemotactic factor-a (delayed ECF-a), which was isolated from the skin lesions showing delayed tissue eosinophilia in vivo.
用蛔虫提取物的二硝基苯基衍生物(DNP-As)免疫的豚鼠腹腔渗出细胞(PEC)的无细胞培养上清液(CFS)中,在无免疫复合物激活的情况下经体外抗原刺激可产生嗜酸性粒细胞趋化因子(ECF)。抗原刺激2或6小时足以产生ECF,而产生足够量的该因子则需要长时间孵育(48小时)。用放线菌酮处理PEC会导致ECF产生减少,表明蛋白质合成至关重要。其产生似乎具有载体特异性,该因子的来源推测为淋巴细胞,可能是T淋巴细胞。分子量为70,000的该因子与从体内显示迟发性组织嗜酸性粒细胞增多的皮肤病变中分离出的迟发性嗜酸性粒细胞趋化因子-a(迟发性ECF-a)具有共同抗原性。