Sarkari B, Hatam G R, Mikaeili F, Sadeghi H, Ebrahimi S
Department of Parasitology and Mycology, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.
Trop Biomed. 2008 Aug;25(2):96-9.
An antigen-based ELISA system was evaluated for diagnosis of visceral leishmaniasis (VL). Urine samples from confirmed VL cases were tested by the system in comparison with urine samples from patients with non-VL infectious disease and patients with non-infectious diseases. Antigen was detected in urine of 21 out of 35 (60%) of VL cases. No cross reaction was found with samples from healthy individuals except in 3 samples from non-VL infectious diseases. Two samples from cutaneous leishmaniasis patient and one from patient with toxoplasmosis. The results obtained with the antigen-based ELISA were compared to those obtained with direct agglutination test (DAT), an antibody-based ELISA and indirect immunofluorescent antibody (IFA) revealed that the antigen-based ELISA is comparable in terms of specificity (91.2%; 95% CI=75.2-97.7%) but with a lower sensitivity (60%; 95% CI=42.2-75.6%). These results suggest that the antigen detection in urine by the noninvasive antigen-based ELISA system might offer a useful method for diagnosis of VL.
评估了一种基于抗原的酶联免疫吸附测定(ELISA)系统用于内脏利什曼病(VL)的诊断。用该系统检测确诊VL病例的尿液样本,并与非VL传染病患者和非传染病患者的尿液样本进行比较。35例VL病例中有21例(60%)尿液中检测到抗原。除了3份来自非VL传染病患者的样本外,未发现与健康个体样本有交叉反应。2份样本来自皮肤利什曼病患者,1份来自弓形虫病患者。将基于抗原的ELISA所获得的结果与直接凝集试验(DAT)、基于抗体的ELISA和间接免疫荧光抗体(IFA)所获得的结果进行比较,结果显示基于抗原的ELISA在特异性方面相当(91.2%;95%可信区间=75.2-97.7%),但敏感性较低(60%;95%可信区间=42.2-75.6%)。这些结果表明,基于非侵入性抗原的ELISA系统检测尿液中的抗原可能为VL的诊断提供一种有用的方法。