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酶联免疫吸附测定法用于阿米巴病血清学诊断的评估

Evaluation of enzyme-linked immunosorbent assay for the serodiagnosis of amebiasis.

作者信息

Yang J, Kennedy M T

出版信息

J Clin Microbiol. 1979 Dec;10(6):778-85. doi: 10.1128/jcm.10.6.778-785.1979.

Abstract

This report describes the development and evaluation of an enzyme-linked immunosorbent assay (ELISA) for the detection of antibodies to Entamoeba histolytica. Highly sensitive and reproducible results were obtained in antigen-coated plates prepared by air-drying at 37 degrees C. Comparison of the ELISA with indirect fluorescent antibody and indirect hemagglutination techniques showed that the former was slightly more sensitive than the two latter methods. The specificity was evaluated by testing specially chosen population groups. ELISA was negative in 96.4% of 693 normal adults and children and in 96.6% of 377 patients with various parasitic, bacterial, mycotic, and other clinical diseases. The assay was positive in 26% of 461 patients with suspected amebiasis and in all of 53 patients with amoebic liver abscess. The ELISA was found to be a specific, highly sensitive, and reliable procedure for detecting anti-E. histolytica antibodies in humans.

摘要

本报告描述了一种用于检测溶组织内阿米巴抗体的酶联免疫吸附测定(ELISA)的开发和评估。在37℃下空气干燥制备的抗原包被板中获得了高度灵敏且可重复的结果。ELISA与间接荧光抗体法和间接血凝技术的比较表明,前者比后两种方法稍灵敏。通过对特定选择的人群组进行检测来评估其特异性。在693名正常成人和儿童中,ELISA有96.4%呈阴性,在377名患有各种寄生虫、细菌、真菌及其他临床疾病的患者中,96.6%呈阴性。在461名疑似阿米巴病的患者中,26%的检测呈阳性,在53名阿米巴肝脓肿患者中全部呈阳性。ELISA被发现是一种检测人体抗溶组织内阿米巴抗体的特异性、高度灵敏且可靠的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8854/273270/153f07a749e4/jcm00185-0039-a.jpg

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