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酶联免疫吸附测定法在阿米巴肝脓肿血清学诊断中的评估

Evaluation of an enzyme-linked immunosorbent assay in the serodiagnosis of amoebic liver abscess.

作者信息

Sathar M A, Simjee A E, Nel J D, Bredenkamp B L, Gathiram V, Jackson T F

机构信息

Department of Medicine, University of Natal, Durban.

出版信息

S Afr Med J. 1988 Dec 17;74(12):625-8.

PMID:3144760
Abstract

An indirect enzyme-linked immunosorbent assay (ELISA) was evaluated for the detection of anti-amoebic IgG and IgM antibodies to assess its value in distinguishing past from current infection in invasive amoebiasis, particularly in amoebic liver abscess (ALA) patients. Using sera from 295 individuals, the ELISA was also compared with the amoebic gel diffusion (AGD) test. In 100 patients the IgG-ELISA at a single test dilution of 1/6,400 had a sensitivity of 99% for clinically diagnosed ALA. In these same patients the IgM-ELISA at a single dilution of 1/400, had a sensitivity of 64% and a specificity of 97.9%. No cross-reactions were observed in sera from patients with collagen vascular disease. In 121 patients without clinical invasive amoebiasis, 8 were AGD-positive and 12 were IgG-ELISA-positive, giving the latter assay a specificity of 91.7%. This is thought to be due to past infection with Entamoeba histolytica. In symptomless carriers of pathogenic zymodemes, 10/11 were seropositive by the IgG-ELISA and 11/11 by the AGD test. There was an excellent correlation between the IgG-ELISA and the AGD test (r = 0.99). The IgG-ELISA is a sensitive, specific, simple and rapid test. It has the clinical advantage that results are obtainable 2 1/2 hours after receipt of the specimen, compared with the 24-48 hours required for the AGD test. The prompt availability of IgG-ELISA results could prove advantageous for implementation of early therapy. The IgM-ELISA was not found to be sensitive enough to be used as an index of active amoebic infection.

摘要

评估了一种间接酶联免疫吸附测定(ELISA)用于检测抗阿米巴IgG和IgM抗体,以评估其在区分侵袭性阿米巴病(特别是阿米巴肝脓肿[ALA]患者)的既往感染和当前感染方面的价值。使用295名个体的血清,还将ELISA与阿米巴凝胶扩散(AGD)试验进行了比较。在100例临床诊断为ALA的患者中,IgG-ELISA在1/6400的单一检测稀释度下对临床诊断为ALA的敏感性为99%。在这些相同的患者中,IgM-ELISA在1/400的单一稀释度下,敏感性为64%,特异性为97.9%。在胶原血管病患者的血清中未观察到交叉反应。在121例无临床侵袭性阿米巴病的患者中,8例AGD阳性,12例IgG-ELISA阳性,后者的检测特异性为91.7%。这被认为是由于过去感染溶组织内阿米巴所致。在致病性酶型的无症状携带者中,10/11通过IgG-ELISA血清学阳性,11/11通过AGD试验血清学阳性。IgG-ELISA与AGD试验之间存在极好的相关性(r = 0.99)。IgG-ELISA是一种灵敏、特异、简单且快速的检测方法。它具有临床优势,与AGD试验所需的24 - 48小时相比,在收到标本后2.5小时即可获得结果。IgG-ELISA结果的快速可得性可能对早期治疗的实施具有优势。未发现IgM-ELISA足够灵敏,不能用作活动性阿米巴感染的指标。

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