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核糖核苷酸还原酶单纯疱疹病毒特异性血清学检测的性能与应用

Performance and use of a ribonucleotide reductase herpes simplex virus type-specific serological assay.

作者信息

Wales S Q, Smith C C, Wachsman M, Calton G, Aurelian L

机构信息

AuRx, Inc., Glen Burnie, Maryland 21061, USA.

出版信息

Clin Diagn Lab Immunol. 2004 Jan;11(1):42-9. doi: 10.1128/cdli.11.1.42-49.2004.

Abstract

In response to the increasingly evident need for herpes simplex virus (HSV) serotype-specific serologic assays that rely on proteins other than glycoprotein-G (gG), we developed a rapid serologic assay that is based on type-specific epitopes within the large subunit of HSV ribonucleotide reductase (R1). The assay (Au-2 enzyme-linked immunosorbent assay [ELISA]) uses an HSV type 2 (HSV-2) R1 peptide antigen. It provides a reliable method for detecting serotype-specific antibody to a protein other than gG-2. The Au-2 ELISA has high sensitivity and specificity as determined by direct comparison to Western blotting, a widely accepted "gold standard," and to ELISA with an HSV-1 R1 peptide (Au-1). The use of the Au-2 ELISA in conjunction with the gG-2-based assays will improve the sensitivity and specificity of serologic diagnosis and patient management.

摘要

鉴于对单纯疱疹病毒(HSV)血清型特异性血清学检测方法的需求日益明显,这种检测方法依赖于糖蛋白-G(gG)以外的蛋白质,我们开发了一种基于HSV核糖核苷酸还原酶大亚基(R1)内型特异性表位的快速血清学检测方法。该检测方法(Au-2酶联免疫吸附测定法[ELISA])使用HSV 2型(HSV-2)R1肽抗原。它为检测针对gG-2以外蛋白质的血清型特异性抗体提供了一种可靠的方法。通过与广泛认可的“金标准”蛋白质印迹法以及使用HSV-1 R1肽的ELISA(Au-1)直接比较,确定Au-2 ELISA具有高灵敏度和特异性。将Au-2 ELISA与基于gG-2的检测方法结合使用,将提高血清学诊断和患者管理的灵敏度和特异性。

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