Gebhard D, Orton S, Edmiston D, Nakagaki K, DeBoer D, Hammerberg B
College of Veterinary Medicine, North Carolina State University, Raleigh, USA.
Immunology. 1995 Jul;85(3):429-34.
Canine popliteal lymph node cells taken at the onset of clinical disease from a rear limb infected with the filarial nematode Brugia pahangi were fused with mouse myeloma cell line P3X63.Ag8.653 cells. Of the several canine immunoglobulin-producing clones from this fusion, one was found to produce canine IgE specific for a filarial nematode antigen. The cell line has undergone limiting dilution cloning six times over the past 3 years and continues to produce monoclonal antibody of the IgE subclass at a rate of greater than 3 mg/l. Sodium dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) of the cell culture supernatant protein that bound to protein A beads, showed bands at molecular weights (MW) of approximately 75,000 and 25,000 that were characteristic of epsilon and kappa or lambda chains, respectively. A mouse monoclonal antibody specific for canine IgE bound the 75,000 MW band, as demonstrated by Western blot. Western blots of aqueous extracts of adult filarial nematodes demonstrated binding of the canine IgE monoclonal antibody to a single 35,000 MW peptide from B. pahangi but not Dirofilaria immitis; immunochemistry using frozen sections of adult worms, microfilariae and fourth stage larvae revealed focal binding of the monoclonal IgE to worm tissue adjacent to dorsal and ventral cords of only Brugia adults.
从感染丝虫线虫彭亨布鲁线虫的后肢在临床疾病发作时采集犬腘淋巴结细胞,将其与小鼠骨髓瘤细胞系P3X63.Ag8.653细胞融合。在此次融合产生的几个产生犬免疫球蛋白的克隆中,发现有一个克隆产生针对丝虫线虫抗原的犬IgE。在过去3年里,该细胞系进行了6次有限稀释克隆,并且继续以大于3mg/l的速率产生IgE亚类的单克隆抗体。与蛋白A珠子结合的细胞培养上清液蛋白的十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)显示,在分子量(MW)约为75,000和25,000处出现条带,分别为ε链和κ链或λ链的特征条带。如蛋白质印迹法所示,一种针对犬IgE的小鼠单克隆抗体与75,000MW的条带结合。成年丝虫线虫水提取物的蛋白质印迹显示,犬IgE单克隆抗体与来自彭亨布鲁线虫的一条单一的35,000MW肽结合,但不与犬恶丝虫结合;使用成年虫体、微丝蚴和第四期幼虫的冰冻切片进行免疫化学分析显示,单克隆IgE仅在彭亨布鲁线虫成虫背索和腹索相邻的虫体组织处有局灶性结合。