Malan Annette K, Stipanovich Priscilla J, Martins Thomas B, Hill Harry R, Litwin Christine M
Associated Regional and University Pathologists (ARUP), Institute for Clinical and Experimental Pathology, University of Utah School of Medicine, Salt Lake City, UT, USA.
Am J Clin Pathol. 2003 Apr;119(4):508-15. doi: 10.1309/WJJ7-UE42-DFHT-TF1X.
West Nile virus (WNV) had its first recorded appearance in the western hemisphere in 1999 and has continued to spread across the United States, necessitating the development of serologic procedures to diagnose infection. We developed an immunofluorescence assay (IFA) protocol for the detection of WNV-specific IgG and IgM antibodies in serum and cerebrospinal fluid (CSF) specimens. We tested 82 serum and 16 CSF samples and compared the results with WNV IgG enzyme-linked immunosorbent assay (ELISA) and IgM antibody-capture (MAC) ELISA results. Agreement, clinical sensitivity, and clinical specificity for the IgG IFA were 92%, 100%, and 90%, respectively, and 98%, 96%, and 100% for the IgM IFA, respectively. Extensive arbovirus cross-reactions occurred in the IgG assays, but only minimal cross-reactions were observed in the IgM assays. The IFA protocol described herein is a cost-effective and sensitive alternative to ELISA and MAC-ELISA for the serologic diagnosis of WNV infection.
西尼罗河病毒(WNV)于1999年在西半球首次有记录出现,并持续在美国传播,因此需要开发血清学检测方法来诊断感染情况。我们开发了一种免疫荧光测定法(IFA)方案,用于检测血清和脑脊液(CSF)标本中的WNV特异性IgG和IgM抗体。我们检测了82份血清样本和16份脑脊液样本,并将结果与WNV IgG酶联免疫吸附测定(ELISA)和IgM抗体捕获(MAC)ELISA结果进行比较。IgG IFA的一致性、临床敏感性和临床特异性分别为92%、100%和90%,IgM IFA的分别为98%、96%和100%。在IgG检测中出现了广泛的虫媒病毒交叉反应,但在IgM检测中仅观察到极少的交叉反应。本文所述的IFA方案是一种用于WNV感染血清学诊断的、具有成本效益且敏感的ELISA和MAC-ELISA替代方法。