Greene W K, Carnegie R L, Shaw S E, Thompson R C, Penhale W J
Institute for Molecular Genetics and Animal Disease, School of Veterinary Studies, Murdoch University, Western Australia.
Parasite Immunol. 1993 Feb;15(2):69-74. doi: 10.1111/j.1365-3024.1993.tb00586.x.
Flea allergens, fractionated by polyacrylamide gel electrophoresis and transferred to nitrocellulose, were identified using 20 flea-allergic dog sera in an enhanced chemiluminescent assay for canine IgE antibodies. At least 15 different flea components in the molecular weight range of 14-150 K bound IgE and every serum demonstrated a different pattern of binding. Three of the components with apparent molecular weights of 25, 40 and 58 K were each bound by at least 40% of the sera. No reactivity was seen when normal dog sera were used. These results demonstrate a greater number of flea allergens and a far greater diversity of the IgE antibody response to flea allergens than has previously been described, and suggest that immediate hypersensitivity may be an important mechanism in the pathogenesis of canine flea allergy.
通过聚丙烯酰胺凝胶电泳分离并转移至硝酸纤维素膜上的跳蚤变应原,在用于检测犬IgE抗体的增强化学发光分析中,使用20份对跳蚤过敏的犬血清进行鉴定。分子量在14 - 150K范围内至少有15种不同的跳蚤成分与IgE结合,且每份血清显示出不同的结合模式。三种表观分子量为25K、40K和58K的成分每种至少被40%的血清所结合。使用正常犬血清时未观察到反应性。这些结果表明,与先前描述的相比,跳蚤变应原的数量更多,对跳蚤变应原的IgE抗体反应的多样性也大得多,这表明速发型超敏反应可能是犬跳蚤过敏发病机制中的一个重要机制。