Document 0099 DOCN M9580099 TI Evaluation of an agglutination HIV-1 + 2 antibody assay. DT 9506 AU Vercauteren G; Beelaert G; van der Groen G; Institute of Tropical Medicine, Department of Microbiology,; Antwerp, Belgium. SO J Virol Methods. 1995 Jan;51(1):1-8. Unique Identifier : AIDSLINE MED/95247861 AB Studies have shown that an HIV (HIV-PA) agglutination assay (Serodia) for the detection of antibody to human immunodeficiency virus (HIV) can be as sensitive and as specific as enzyme-linked immunosorbent assay (ELISA). However, since this HIV assay was designed to detect antibody to the HIV-1 virus, a substantial number of HIV-2 positive sera are missed by this assay. Since the HIV-2 has now been found throughout the world this test is becoming less suitable. The new HIV-1 + 2 assay version (HIV-1 + 2 PA) was evaluated in 300 sera, which contained 50 HIV-1, 40 HIV-2 and 10 HIV-1/HIV-2 antibody positive samples, and a sensitivity and specificity of 100% and 99%, respectively, was obtained. Whereas all HIV-2 positive sera were detected by the new HIV-1 + 2 version, 26% (13/50) were missed by the old version of the agglutination test. It is concluded that the HIV-1 + 2 PA assay is a promising instrument free assay which can be used for screening purposes in areas where both HIV-1 and HIV-2 are present. DE Agglutination Tests/*METHODS/STATISTICS & NUMER DATA AIDS Serodiagnosis/*METHODS/STATISTICS & NUMER DATA Comparative Study Enzyme-Linked Immunosorbent Assay/METHODS/STATISTICS & NUMER DATA Evaluation Studies Human HIV Antibodies/*BLOOD HIV Seropositivity/DIAGNOSIS/IMMUNOLOGY HIV-1/*IMMUNOLOGY HIV-2/*IMMUNOLOGY Sensitivity and Specificity Virology/METHODS/STATISTICS & NUMER DATA JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).