Sensitivities of radioimmunoprecipitation assay and PCR for detection of human T-lymphotropic type II infection.
AUTOR(ES)
Gallo, D
RESUMO
Five hundred forty-eight uncoagulated blood specimens from intravenous drug users infected with human T-lymphotropic virus type II (HTLV-II) were used to evaluate the sensitivities of the radioimmunoprecipitation assay (RIPA) and PCR for detecting HTLV-II-infected people. The sensitivities of both RIPA and PCR were found to be dependent on the HTLV-II antibody titer, as determined by the immunofluorescence assay. Neither of these recommended confirmatory methods was as sensitive for detecting weakly reactive HTLV-II specimens as the immunofluorescence assay, Western blotting (immunoblotting), or a modified licensed enzyme immunoassay. Use of RIPA and PCR to determine the reliabilities of other tests may sometimes give erroneous results.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=264084Documentos Relacionados
- Serologic confirmation of simian T-lymphotropic virus type I infection by using immunoassays developed for human T-lymphotropic virus antibody detection.
- Molecular Evidence for Transmission of Human T-Lymphotropic Virus Type II Infection by a Human Bite
- Human T-lymphotropic virus types I and II.
- Infection of human endothelial cells by human T-lymphotropic virus type I.
- Infection with the human T-lymphotropic virus type I. A review for clinicians.