Santiago N, Hillyer G V
Department of Pathology, University of Puerto Rico School of Medicine, San Juan 00936-5067.
J Parasitol. 1988 Oct;74(5):810-8.
In evaluating potential mechanisms of immunity in fascioliasis we compared the time-course analysis of the antibody responses between a resistant (cattle) and a susceptible model (sheep). Sera from sheep and cows experimentally infected with F. hepatica were reacted with both somatic (FhWWE) and excretory-secretory (ES) antigens in order to evaluate the antibody repertoires in the 2 different hosts. Analysis of these sera by ELISA showed a significant increase in antibody levels by 2 wk in most infected cattle using both somatic and ES antigens, whereas with most infected sheep antibodies are not clearly detected until week 4. By EITB, both infected sheep and cows recognize major somatic polypeptides in a molecular weight range of 30-38 kDa by 8 wk. Cattle recognized 3 additional major antigens of 56, 64, and 69 kDa as early as 6 wk. Various polypeptides of 20-25 kDa are prominently detected by most sheep and very faintly, if at all, by the cow sera. The sera from both sheep and cows also identify ES polypeptides of 20-28 kDa. The patterns of polypeptides recognized by sheep infected with S. mansoni and challenged with F. hepatica in EITB are almost identical to those with a simple F. hepatica primary infection. No significant differences were detected in the antibody kinetics in ELISA between these 2 groups. Differences and similarities between these models could eventually help determine which antibodies may be predictive of resistance or susceptibility in fascioliasis.
在评估肝片吸虫病免疫的潜在机制时,我们比较了抗性模型(牛)和易感模型(羊)之间抗体反应的时间进程分析。将实验感染肝片吸虫的绵羊和奶牛的血清与体细胞抗原(FhWWE)和排泄分泌(ES)抗原反应,以评估两种不同宿主中的抗体库。通过ELISA分析这些血清显示,在大多数感染的牛中,使用体细胞抗原和ES抗原时,抗体水平在2周时显著增加,而在大多数感染的绵羊中,直到第4周才清楚地检测到抗体。通过免疫印迹法(EITB),到8周时,感染的绵羊和奶牛都识别分子量在30 - 38 kDa范围内的主要体细胞多肽。牛早在6周时就识别出另外3种分子量分别为56、64和69 kDa的主要抗原。大多数绵羊能明显检测到20 - 25 kDa的各种多肽,而奶牛血清中几乎检测不到(即使检测到也非常微弱)。绵羊和奶牛的血清还能识别20 - 28 kDa的ES多肽。在EITB中,感染曼氏血吸虫并受到肝片吸虫攻击的绵羊所识别的多肽模式与单纯肝片吸虫初次感染的模式几乎相同。ELISA检测这两组之间的抗体动力学没有显著差异。这些模型之间的差异和相似性最终可能有助于确定哪些抗体可预测肝片吸虫病的抗性或易感性。