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恰加斯病的血清学诊断:一种使用克氏锥虫保存蛋白抗原的潜在确证检测方法。

Serological diagnosis of Chagas' disease: a potential confirmatory assay using preserved protein antigens of Trypanosoma cruzi.

作者信息

Mendes R P, Hoshino-Shimizu S, Moura da Silva A M, Mota I, Heredia R A, Luquetti A O, Leser P G

机构信息

Laboratory of Immunology, Federal University of Uberlândia, Minas Gerais, Brazil.

出版信息

J Clin Microbiol. 1997 Jul;35(7):1829-34. doi: 10.1128/jcm.35.7.1829-1834.1997.

Abstract

The diagnosis of Chagas' disease relies mostly on data provided by immunologic tests, but inconclusive results often require elucidation, especially in blood banks. When six different types of Trypanosoma cruzi epimastigote antigens were studied by an immunoblotting assay (IBA), a preserved protein antigen (Ag PP) was found to present the most interesting immunochemical features because of its high reactivity with anti-T. cruzi antibodies. Thus, the IBA with Ag PP (PP IBA) was assessed with panels of coded and noncoded serum samples prepared in different laboratories, including the Brazilian Reference Laboratory for Chagas' Disease. It was found that serum samples from patients proved (clinically, eletrocardiographically, serologically, and epidemiologically) to have Chagas' disease consistently recognized 12 bands (140, 100, 85, 78, 59, 57, 46, 35, 27, 23, 20, and 18 kDa) of Ag PP. In contrast, sera from nonchagasic patients, including patients with mucocutaneous leishmaniasis, were negative or reacted weakly, and one serum sample did not have more than five different bands. These bands were 78, 57, 46, 35, 27, 23, 20, or 18 kDa. A criterion was adopted to interpret the results obtained in the PP IBA. The criterion considered positive a serum sample recognizing all 12 bands and considered negative a serum sample that did not recognize any of the bands except the eight nonspecific bands mentioned above. The PP IBA indicated maximum sensitivity and specificity as well as high positive and negative predictive values. The data demonstrate that the PP IBA discriminates chagasic from nonchagasic infections and seems to be applicable as a confirmatory assay for elucidating inconclusive results obtained by standard serology.

摘要

恰加斯病的诊断主要依赖免疫检测提供的数据,但结果不确定时往往需要进一步阐明,尤其是在血库中。当通过免疫印迹分析(IBA)研究六种不同类型的克氏锥虫前鞭毛体抗原时,发现一种保存的蛋白抗原(Ag PP)因其与抗克氏锥虫抗体的高反应性而呈现出最有趣的免疫化学特征。因此,使用在不同实验室(包括巴西恰加斯病参考实验室)制备的编码和非编码血清样本对含Ag PP的IBA(PP IBA)进行了评估。结果发现,经临床、心电图、血清学和流行病学证实患有恰加斯病的患者血清样本始终能识别出Ag PP的12条带(140、100、85、78、59、57、46、35、27、23、20和18 kDa)。相比之下,非恰加斯病患者的血清,包括黏膜皮肤利什曼病患者的血清,呈阴性或反应较弱,且一份血清样本识别的不同条带不超过五条。这些条带为78、57、46、35、27、23、20或18 kDa。采用了一项标准来解释PP IBA获得的结果。该标准将识别所有12条带的血清样本判定为阳性,将除上述八条非特异性条带外未识别任何条带的血清样本判定为阴性。PP IBA显示出最高的敏感性和特异性以及较高的阳性和阴性预测值。数据表明,PP IBA能够区分恰加斯病感染和非恰加斯病感染,似乎可作为一种确证检测方法,用于阐明标准血清学获得的不确定结果。

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