Proceedings of the National Academy of Sciences · 1987 · 71 citations · 32 references
Life SciencesImmunologyInfectious DiseasesAdaptive ImmunityMolecular VirologyVaccinologyAnimal VirusesAntiviral ImmunityCellular Immunity In InfectionMammalian ImmunologyViral InfectionsViral VaccinesCellular Immune Response To VirusesExperimental Animal Models Of Viral InfectionGlycoprotein VaccinesHiv Envelope Glycoprotein AntigensHiv Infection ModelsPeripheral Blood Lymphocyte AnalysisSubunit Vaccine ImmunogenicityT-cell Immune Responses
The major envelope glycoprotein of a human immunodeficiency virus (HIV) has been purified and was utilized as a prototype vaccine in chimpanzees. The 120,000-dalton glycoprotein (gp120) was purified from membranes of human T-lymphotropic virus (HTLV)-IIIB-infected cells and the final preparation contained low levels to no detectable HTLV-IIIB core antigen (p24) and low levels of endotoxin. Chimpanzees inoculated with gp120 responded by developing antibodies that precipitated radiolabeled gp120 and neutralized in vitro infection of HTLV-IIIB. Antibodies to HTLV-IIIB p24 were not detected in the gp120-immunized chimpanzees. Peripheral blood leukocytes from the vaccinated animals were examined for T4+ and T8+ cells, and no decrease in the T4/T8 ratio was found, indicating that immunization with a ligand (gp120) that binds to T4 has no detectable adverse effect on the population of T4+ cells. The only current animal model that can be reproducibly infected with HIV is the chimpanzee. Immunization of chimpanzees with HIV proteins will provide an experimental system for testing the effectiveness of prototype vaccines for preventing HIV infection in vivo.
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The CD4 (T4) antigen is an essential component of the receptor for the AIDS retrovirus
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