Arafa M S, Abaza S M, El-Shewy K A, Mohareb E W, El-Moamly A A
Department of Parasitology, Faculty of Medicine, Suez Canal University, Ismailia, Egypt.
J Egypt Soc Parasitol. 1999;29(3):911-26.
The objective of the present work is to evaluate Fasciola E/S antigens for diagnosis of early fascioliasis utilizing different diagnostic techniques. Using enzyme-linked immunoelectro-transfer blot (EITB), Fasciola-specific E/ S protein fraction band (49.5 kDa) was determined and electroeluted. The mono-specific antibodies against this specific fraction band were prepared by immunizing pathogen-free rabbit. Assessment of the prepared mono-specific antibodies in diagnosis of human fascioliasis was performed through the detection of E/S copro-antigens by enzyme-linked immunosorbent assay (ELISA) in stool eluates obtained from patients with confirmed fascioliasis, other parasites as well as from other healthy individuals. Serum samples were collected and tested to detect serum antibodies against Fasciola E/S antigen using EITB and counter immunoelectrophoresis (CIEP). Analysis of Fasciola adult worm E/S products by SDS/PAGE revealed a number of bands, the molecular weight (MW) of which ranged from 14-200 kDa; with three major bands (27.5, 32.5 and 55 kDa). Fasciola EIS 49.5 kDa protein fraction proved to be specific to F. gigantica. Cross reaction with S. mansoni was observed at higher MW (110-120 kDa). The sensitivity, specificity and diagnostic accuracy of EITB were 45.2%, 100% and 70.7%, respectively, while those of CIEP were 38.7%, 100% and 67.2%, respectively. ELISA technique using mono-specific anti-49.5 kDa to detect copro-antigens proved to be practical and reliable. It showed higher sensitivity (91.4%) and higher diagnostic accuracy (91.8%), while the specificity was 92.3%. In addition, ELISA had higher negative predictive value (88.9%) and fair positive predictive value (94.1%).
本研究的目的是利用不同的诊断技术评估肝片吸虫排泄分泌(E/S)抗原用于早期肝片吸虫病的诊断。采用酶联免疫电转移印迹法(EITB),确定并电洗脱了肝片吸虫特异性E/S蛋白组分条带(49.5 kDa)。通过免疫无特定病原体的兔子制备了针对该特定条带的单特异性抗体。通过酶联免疫吸附测定(ELISA)检测确诊肝片吸虫病患者、其他寄生虫感染患者以及其他健康个体粪便洗脱液中的E/S粪抗原,对制备的单特异性抗体在人类肝片吸虫病诊断中的应用进行了评估。收集血清样本,采用EITB和对流免疫电泳(CIEP)检测针对肝片吸虫E/S抗原的血清抗体。通过SDS/PAGE分析肝片吸虫成虫E/S产物,发现了多个条带,其分子量(MW)范围为14 - 200 kDa;有三条主要条带(27.5、32.5和55 kDa)。肝片吸虫EIS 49.5 kDa蛋白组分被证明对巨片吸虫具有特异性。在较高分子量(110 - 120 kDa)处观察到与曼氏血吸虫的交叉反应。EITB的敏感性、特异性和诊断准确性分别为45.2%、100%和70.7%,而CIEP的敏感性、特异性和诊断准确性分别为38.7%、100%和67.2%。使用单特异性抗49.5 kDa抗体检测粪抗原的ELISA技术被证明是实用且可靠的。它显示出更高的敏感性(91.4%)和更高的诊断准确性(91.8%),而特异性为92.3%。此外,ELISA具有更高的阴性预测值(88.9%)和较好的阳性预测值(94.1%)。