Evaluation of enzyme-linked immunosorbent and alternative assays for detection of HIV antibodies using panels of Brazilian sera. NLM AIDSLINE Important note: Information in this article was accurate in 1991. The state of the art may have changed since the publication date.

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Evaluation of enzyme-linked immunosorbent and alternative assays for detection of HIV antibodies using panels of Brazilian sera.

Rev Inst Med Trop Sao Paulo. 1990 Mar-Apr;32(2):96-100. Unique Identifier : AIDSLINE MED/91252717
Ivo-Dos-Santos J; Mello DL; Couto-Fernandez JC; Passos RM; Dias-Carneiro LA; Castilho EA; Galvao-Castro B; Fundacao Oswaldo Cruz, WHO Collaborating Centre on AIDS, Bahia,; Brazil.


Abstract: Sera from 472 Brazilian subjects, confirmed to be either positive or negative for HIV antibodies and comprising the total clinical spectrum of HIV infection, were utilized in the evaluation of six commercially available enzyme-linked immunosorbent assays (ELISA), as well as of four alternative assays, namely indirect immunofluorescence (IIF), passive hemagglutination (PHA), dot blot and Karpas AIDS cell test. The sensitivities ranged from 100% (Abbott and Roche ELISA) to 84.2% (PHA) and the specificities ranged from 99.3% (IIF) to 80.2% (PHA). The sensitivity and specificity of the PHA and the sensitivity of the Karpas cell test were significantly lower than those of the other tests. Although the IFF and dot blot had good sensitivities and specificities, the six ELISA were more attractive than those tests when other parameters such as ease of reading and duration of assay were considered.
Keywords: Blotting, Western Brazil Enzyme-Linked Immunosorbent Assay Evaluation Studies Fluorescent Antibody Technique Hemagglutination Tests Human HIV Antibodies/*ANALYSIS Sensitivity and Specificity Support, Non-U.S. Gov't JOURNAL ARTICLEKWDblotting,westernbrazilenzyme-linkedimmunosorbentassayevaluationstudiesfluorescentantibodytechniquehemagglutinationtestshumanhivantibodies/KWDanalysissensitivityandspecificitysupport,non-uKWDsKWDgov'tjournalarticle
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M9190676

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