Human immunodeficiency virus (HIV) antibodies detected by new assays that are enhanced for HIV-1 subtype O

BACKGROUND: Human immunodeficiency virus type 1 (HIV‐1) subtype O infections are not reliably detected by commonly used anti‐HIV‐1/2 screening assays. Therefore, anti‐HIV‐1/2 assays have been modified to increase their sensitivity in detecting antibodies to HIV‐1 subtype O. STUDY DESIGN AND METHODS:...

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Published in:Transfusion (Philadelphia, Pa.) Vol. 37; no. 8; pp. 841 - 844
Main Authors: Jongeriüs, John M., van der Poel, Cees L., Van Loon, Anton M., van den Akker, Ruud, Schaasberg, Wim, Van Leeuwen, Eleonore F.
Format: Journal Article
Language:English
Published: Edinburgh, UK Blackwell Science Ltd 01-08-1997
Blackwell Publishing
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Summary:BACKGROUND: Human immunodeficiency virus type 1 (HIV‐1) subtype O infections are not reliably detected by commonly used anti‐HIV‐1/2 screening assays. Therefore, anti‐HIV‐1/2 assays have been modified to increase their sensitivity in detecting antibodies to HIV‐1 subtype O. STUDY DESIGN AND METHODS: Two new anti‐HIV‐1/2 enzyme‐linked immunosorbent assays (ELISAs) (Abbott Plus and Ortho Enhanced) were compared with a currently used anti‐HIV‐1/2 ELISA (Abbott Recombinant) in various serum panels: 91 Western blot‐confirmed anti‐HIV‐1‐positive samples, 20 samples from Western blot‐confirmed HIV‐1‐infected patients in log3 serial dilutions, and 1463 samples from consecutive, volunteer, nonremunerated blood donors. RESULTS: Among 91 anti‐HIV‐1 Western blot‐ positive samples, 2 (2.2%) were missed by the Abbott Recombinant ELISA, but all 91 were detected by the Abbott Plus and Ortho Enhanced ELISAs. In contrast, two discrepant samples were found to react in viral lysate‐ based assays. In serial dilutions, Ortho Enhanced ELISA was significantly less sensitive than the Abbott Recombinant and Abbott Plus ELISAs, with the latter two being of comparable sensitivity. The specificities of Abbott Recombinant, Abbott Plus, and Ortho Enhanced ELISAs in 1463 blood donors were 100, 99.93, and 99.86 percent, respectively. Routine testing of 29,102 donations with the enhanced Abbott Plus ELISA revealed a specificity of 99.93 percent. CONCLUSION: Two Western blot‐confirmed anti‐HIV‐1‐positive samples were missed by the Abbott Recombinant ELISA but detected by the Abbott Plus and Ortho Enhanced ELISAs. The analytic sensitivity of the Ortho Enhanced ELISA was inferior to that of both Abbott ELISAs. The specificities of the Abbott Recombinant, Abbott Plus, and Ortho Enhanced ELISAs were comparable.
Bibliography:istex:03679D56CDD4930803C900DC1E4858C79EB93D94
ArticleID:TRF3790
ark:/67375/WNG-3JQWZVKG-9
Anton M. van Loon, PhD, Head, Laboratory of Virology, Department of Virology, Academic Hospital Utrecht, Utrecht, the Netherlands.
Eleonore F. van Leeuwen, MD, PhD, Medical Director, Red Cross Blood Bank Utrecht.
Cees L. van der Poel, MD, PhD, Consultant, Transfusion Medicine, and Epidemiologist, Red Cross Blood Bank Utrecht.
John M. Jongeriüs, MT, Head, Laboratory, Red Cross Blood Bank Utrecht, Rubenslaan 190, 3582 JJ Utrecht, the Netherlands. [Reprint requests]
Wim Schaasberg, MSc, Statistician, Central Laboratory of the Netherlands Red Cross Blood Transfusion Service Amsterdam, Amsterdam, the Netherlands.
Ruud van den Akker, MSc, Senior Scientist, National Institute of Public Health and Environmental Protection, Bilthoven, the Netherlands.
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ISSN:0041-1132
1537-2995
DOI:10.1046/j.1537-2995.1997.37897424408.x