Takamoto M, Wang Z X, Watanabe N, Sugane K
Department of Immunology and Infectious Disease, Shinshu University Graduate School of Medicine, Matsumoto, Japan.
Parasitol Res. 2001 Nov;87(11):919-23. doi: 10.1007/s004360100467.
We studied and evaluated an ELISA system, using a sandwich method with a monoclonal antibody against the Fc domain of IgE molecules and biotinylated antigens, to detect parasite antigen-specific IgE quantitatively. The specific IgE ELISA titre increases linearly in a dose-dependent manner when the concentration of total IgE in samples is less than 2,000 ng/ml. Sera from IgE-deficient SJA/9 mice infected with Trichinella spiralis failed to give any measurable IgE, suggesting that other classes of immunoglobulins have no effect on this assay. The titre showed a good correlation with PCA titre. A high concentration of the serum from Toxocara canis-infected mice reduced the T. spiralis-specific IgE ELISA titre, suggesting that the ELISA system is influenced by a huge amount of IgE against epitopes different from those of target antigens. This ELISA system can also be applied for detecting other classes or subclasses of antigen-specific immunoglobulins.
我们研究并评估了一种酶联免疫吸附测定(ELISA)系统,该系统采用夹心方法,使用针对IgE分子Fc结构域的单克隆抗体和生物素化抗原,以定量检测寄生虫抗原特异性IgE。当样品中总IgE浓度低于2000 ng/ml时,特异性IgE ELISA滴度以剂量依赖方式呈线性增加。感染旋毛虫的IgE缺陷型SJA/9小鼠的血清未能产生任何可测量的IgE,这表明其他类别的免疫球蛋白对该检测无影响。该滴度与被动皮肤过敏反应(PCA)滴度显示出良好的相关性。来自感染犬弓首蛔虫小鼠的高浓度血清降低了旋毛虫特异性IgE ELISA滴度,这表明ELISA系统受到大量针对与靶抗原不同表位的IgE的影响。该ELISA系统也可用于检测其他类别或亚类的抗原特异性免疫球蛋白。