Abstract
Rhesus macaques immunized with the HIV-1 SF162DeltaV2 gp140 envelope using the DNA-prime plus protein-boost vaccination methodology, developed HIV envelope-specific T-cell lymphoproliferative responses and potent neutralizing antibodies. To evaluate the protective potential of these antibodies during acute infection, the animals were depleted of their CD8+ T lymphocytes using specific monoclonal antibodies and subsequently challenged intravenously with the pathogenic SHIV(SF162P4) isolate. As compared to non-vaccinated animals (one of which died from AIDS 16 weeks post-exposure) the vaccinated macaques had lower levels of peak viremia, rapidly cleared virus from the periphery and developed delayed seroconversion to SIV core antigens.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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AIDS Vaccines / pharmacology*
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Animals
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CD8-Positive T-Lymphocytes / immunology
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Gene Products, env / genetics
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Gene Products, env / immunology*
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HIV Antibodies / biosynthesis*
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HIV-1 / genetics
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HIV-1 / immunology*
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HIV-1 / isolation & purification
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Lymphocyte Activation
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Lymphocyte Depletion
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Macaca mulatta / immunology*
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Neutralization Tests
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SAIDS Vaccines / pharmacology
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Sequence Deletion
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Simian Immunodeficiency Virus / immunology
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T-Lymphocytes / immunology
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Vaccines, DNA / pharmacology*
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env Gene Products, Human Immunodeficiency Virus
Substances
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AIDS Vaccines
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Gene Products, env
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HIV Antibodies
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SAIDS Vaccines
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Vaccines, DNA
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env Gene Products, Human Immunodeficiency Virus
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gp140 envelope protein, Human immunodeficiency virus 1