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使用基于重组溶组织内阿米巴抗原的酶联免疫吸附测定法对侵袭性阿米巴病进行血清学诊断。

Serodiagnosis of invasive amebiasis using a recombinant Entamoeba histolytica antigen-based ELISA.

作者信息

Myung K, Burch D, Jackson T F, Stanley S L

机构信息

Department of Medicine, Washington University School of Medicine, St. Louis, MO.

出版信息

Arch Med Res. 1992;23(2):285-8.

PMID:1340316
Abstract

Amebic serology remains a critical component in the diagnosis of invasive amebiasis. A recombinant serine rich-Entamoeba histolytica-protein/maltose binding protein (SREHP/MBP) fusion protein was evaluated as the target antigen in an ELISA test to detect acute invasive amebiasis. Retrospective analysis of 65 serum samples from patients with amebic liver abscess and 40 asymptomatic control patients showed the SREHP/MBP ELISA test had a sensitivity of 74% and specificity of only 55% for the diagnosis of amebic liver abscess. This study was repeated under identical conditions using a purified recombinant SREHP cleaved from the MBP component. The purified recombinant SREHP-based ELISA had a sensitivity of 79% and specificity of 87%. Our data suggest a purified recombinant SREHP-based ELISA could prove useful in the serodiagnosis of acute invasive amebiasis.

摘要

阿米巴血清学检测仍是侵袭性阿米巴病诊断的关键组成部分。一种重组富含丝氨酸的溶组织内阿米巴蛋白/麦芽糖结合蛋白(SREHP/MBP)融合蛋白被评估作为酶联免疫吸附测定(ELISA)试验中的靶抗原,用于检测急性侵袭性阿米巴病。对65例阿米巴肝脓肿患者和40例无症状对照患者的血清样本进行回顾性分析,结果显示SREHP/MBP ELISA试验诊断阿米巴肝脓肿的灵敏度为74%,特异性仅为55%。在相同条件下,使用从MBP成分切割得到的纯化重组SREHP重复了这项研究。基于纯化重组SREHP的ELISA灵敏度为79%,特异性为87%。我们的数据表明,基于纯化重组SREHP的ELISA可能在急性侵袭性阿米巴病的血清学诊断中具有实用价值。

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