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应用 ELISA 检测试剂盒检测伊氏锥虫(ESEA 抗原)排泄物/分泌蛋白在恰加斯病诊断中的开发和应用。

Development and Application of an ELISA Assay Using Excretion/Secretion Proteins from Epimastigote Forms of T. cruzi (ESEA Antigens) for the Diagnosis of Chagas Disease.

机构信息

Laboratorio de Diagnóstico Serológico en Enfermedades Infecciosas, Postgrado en Biología Aplicada, Universidad de Oriente, Núcleo de Sucre, Cumana 6101, Venezuela ; Instituto de Biomedicina y Ciencias Aplicadas, Universidad de Oriente, Núcleo de Sucre, Cumana 6101, Venezuela.

出版信息

J Trop Med. 2012;2012:875909. doi: 10.1155/2012/875909. Epub 2012 Sep 25.

Abstract

An indirect enzyme-linked immunoabsorbent assay (ELISA) for Trypanosoma cruzi was developed using epimastigote secretion/excretion proteins (ESEA antigens) obtained from axenic culture supernatants. A panel of 120 serum samples from subjects with confirmed Chagas disease (n = 50), healthy controls (n = 50), and patients with other parasitic diseases (n = 20) was used to evaluate the new ESEA-based ELISA (ELISA(ESEA)). This new test had excellent sensitivity (98%) and acceptable specificity (88%). Cross-reactivity was observed largely in sera from subjects with Leishmania and Ascaris infections. Using Western blotting and epimastigotes from two distinct T. cruzi isolates, several polypeptide bands with molecular masses ranging from 50 to 220 kDa were detected in pooled chagasic sera. However, the band pattern for each isolate was different. These data suggest that an inexpensive and technically simple ELISA based on ESEA antigens is a promising new tool for the diagnosis of Chagas disease.

摘要

本研究采用从体外培养上清液中获得的无鞭毛体分泌/排泄蛋白(ESEA 抗原),建立了一种用于检测克氏锥虫的间接酶联免疫吸附试验(ELISA)。使用了一组 120 份来自确诊的恰加斯病患者(n=50)、健康对照者(n=50)和其他寄生虫病患者(n=20)的血清样本,以评估新的基于 ESEA 的 ELISA(ELISA(ESEA))。该新试验具有优异的敏感性(98%)和可接受的特异性(88%)。交叉反应主要出现在患有利什曼病和蛔虫感染的患者血清中。使用 Western blot 技术和来自两个不同 T. cruzi 分离株的无鞭毛体,在混合的恰加斯病患者血清中检测到了分子量范围为 50 至 220 kDa 的多个多肽带。然而,每个分离株的带型不同。这些数据表明,基于 ESEA 抗原的廉价且技术简单的 ELISA 是一种有前途的新工具,可用于恰加斯病的诊断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5fab/3463186/eaf4423077d8/JTM2012-875909.001.jpg

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