Haque R, Neville L M, Wood S, Petri W A
International Centre for Diarrhoeal Disease Research, Dhaka, Bangladesh.
Am J Trop Med Hyg. 1994 May;50(5):595-6. doi: 10.4269/ajtmh.1994.50.595.
Current diagnosis of Entamoeba histolytica infection requires the direct microscopic identification of the parasite, a technique that is insensitive and cannot distinguish pathogenic E. histolytica from noninvasive E. dispar. Enzyme-linked immunosorbent assay (ELISA) antigen detection tests were developed to distinguish E. histolytica from E. dispar infection in stool specimens. The ELISA result for E. histolytica antigen was positive in 26 of 27 E. histolytica-positive stool specimens, three of 25 E. dispar-positive stools, and one of 30 stools with other or no intestinal parasites, giving a specificity and sensitivity for the detection of E. histolytica infection of 93% and 96%, respectively. The assay result used to detect both E. dispar and E. histolytica was positive in 26 of 27 E. histolytica-positive stools, 19 of 25 E. dispar-positive stools, and one of 30 stools negative by microscopy and culture for Entamoeba, giving a specificity and sensitivity of 97% and 87%, respectively. Because these ELISAs can be completed in several hours, they offer promise as rapid and sensitive means of detecting amebic infection.
目前,溶组织内阿米巴感染的诊断需要直接在显微镜下识别该寄生虫,这一技术并不敏感,且无法区分致病性溶组织内阿米巴和非侵袭性的迪斯帕内阿米巴。酶联免疫吸附测定(ELISA)抗原检测试验被开发出来,用于区分粪便标本中的溶组织内阿米巴感染和迪斯帕内阿米巴感染。在27份溶组织内阿米巴阳性粪便标本中,有26份的溶组织内阿米巴抗原ELISA检测结果呈阳性;在25份迪斯帕内阿米巴阳性粪便中,有3份呈阳性;在30份有其他肠道寄生虫或无肠道寄生虫的粪便中,有1份呈阳性。检测溶组织内阿米巴感染的特异性和敏感性分别为93%和96%。用于检测迪斯帕内阿米巴和溶组织内阿米巴的检测结果,在27份溶组织内阿米巴阳性粪便中有26份呈阳性,在25份迪斯帕内阿米巴阳性粪便中有19份呈阳性,在30份经显微镜检查和培养未发现Entamoeba的阴性粪便中有1份呈阳性,特异性和敏感性分别为97%和87%。由于这些ELISA检测可以在数小时内完成,它们有望成为检测阿米巴感染的快速且灵敏的方法。