Abstract
The kinetics of CD8(+) T cell epitope presentation contribute to the antiviral efficacy of these cells yet remain poorly defined. Here, we demonstrate presentation of virion-derived Vpr peptide epitopes early after viral penetration and prior to presentation of Vif-derived epitopes, which required de novo Vif synthesis. Two Rev epitopes exhibited differential presentation kinetics, with one Rev epitope presented within 1 h of infection. We also demonstrate that cytolytic activity mirrors the recognition kinetics of infected cells. These studies show for the first time that Vpr- and Rev-specific CD8(+) T cells recognize and kill simian immunodeficiency virus (SIV)-infected CD4(+) T cells early after SIV infection.
Publication types
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Research Support, N.I.H., Extramural
MeSH terms
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Amino Acid Sequence
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Animals
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Antigen Presentation
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CD4-Positive T-Lymphocytes / immunology
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CD4-Positive T-Lymphocytes / virology
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CD8-Positive T-Lymphocytes / immunology*
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CD8-Positive T-Lymphocytes / virology*
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Cytotoxicity, Immunologic
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Epitopes, T-Lymphocyte / genetics
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Epitopes, T-Lymphocyte / immunology
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Gene Products, rev / genetics
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Gene Products, rev / immunology*
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Gene Products, vpr / genetics
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Gene Products, vpr / immunology*
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Host-Pathogen Interactions / immunology
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In Vitro Techniques
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Kinetics
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Macaca mulatta
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Simian Acquired Immunodeficiency Syndrome / immunology
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Simian Acquired Immunodeficiency Syndrome / virology
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Simian Immunodeficiency Virus / enzymology
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Simian Immunodeficiency Virus / immunology*
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Simian Immunodeficiency Virus / pathogenicity
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Simian Immunodeficiency Virus / physiology
Substances
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Epitopes, T-Lymphocyte
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Gene Products, rev
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Gene Products, vpr