Evaluation of the Genetic Systems Corp. Integra HIV-1 Pageblot system

Author:

Starkey C A1,Yen-Lieberman B1,Proffitt M R1

Affiliation:

1. Department of Microbiology, Cleveland Clinic Foundation, Ohio 44195.

Abstract

The Genetic Systems Corp. Integra HIV-1 Pageblot system was evaluated as a supplementary assay to confirm the presence of antibodies to human immunodeficiency virus type 1 in 57 specimens from individuals at high risk of infection with the virus. Forty-one specimens identified as reactive in the Genetic Systems Integra HIV-1 Pageblot system were likewise identified as reactive in a U.S. Food and Drug Administration-licensed (Biotech/Dupont) Western blot (immunoblot). Six specimens identified as indeterminate in either or both immunoblot assays were all identified as nonreactive in a U.S. Food and Drug Administration-licensed enzyme immunoassay with recombinant antigens.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

Reference20 articles.

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2. Serological diagnosis of human immunodeficiency virus infection by Western blot testing;Carlson J. R.;J. Am. Med. Assoc.,1988

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4. Centers for Disease Control. 1989. Interpretation and use of the Western blot assay for serodiagnosis of human immunodeficiency virus type 1 infections. Morbid. Mortal. Weekly Rep. 38(Suppl. S-7):1-7.

5. False-positive autoantibodies in HIV infection;Davenport A.;Lancet,1990

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