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pubmed-article:10534733pubmed:abstractTextSeroepidemiology studies of herpes simplex virus type 2 (HSV-2) infections have been difficult to carry out because antibodies to HSV type 1 (HSV-1) show an extensive cross-reactivity with HSV-2 antigens. Many kits available currently are not entirely type specific for serodiagnosis of HSV-2 infections and therefore do not allow reliable discrimination of past exposure to these closely related alphaherpes viruses. Attempts to develop type-specific antigens have focused on the envelope glycoproteins, particularly glycoprotein G (gG). A cross-sectional study was carried out to examine the seroprevalence of antibodies to HSV-2 among healthy university students, using different methods: a whole cell lysate enzyme-linked immunosorbent assay (ELISA), two different ELISAs, and a newly developed immunoblot assay, the last three based on recombinant gG2. HSV-2 prevalence was 24 times higher with the whole cell lysate ELISA (31%; 95% confidence interval [CI]: 27-35%) than the ELISAs and the immunoblot assay based on recombinant gG2 (1.3%; 95% CI: 0.1-2.5%), thus showing the inaccuracy of commercial tests based on whole-antigen preparations for epidemiological studies. Laboratories should be cautious and ensure that commercial tests for HSV typing are based on type-specific glycoproteins.lld:pubmed
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pubmed-article:10534733pubmed:copyrightInfoCopyright 1999 Wiley-Liss, Inc.lld:pubmed
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pubmed-article:10534733pubmed:volume59lld:pubmed
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pubmed-article:10534733pubmed:pagination502-6lld:pubmed
pubmed-article:10534733pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10534733pubmed:articleTitleWhole cell lysate enzyme immunoassays vs. recombinant glycoprotein G2-based immunoassays for HSV-2 seroprevalence studies.lld:pubmed
pubmed-article:10534733pubmed:affiliationMedical Department, SmithKline Beecham Pharmaceuticals, Madrid, Spain.lld:pubmed
pubmed-article:10534733pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:10534733pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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