Abstract
Hepatitis C virus (HCV) is a major causative agent of parenterally transmitted non-A, non-B hepatitis. The genomic region encoding the virion-associated core protein is relatively conserved among HCV strains. To generate a DNA vaccine capable of expressing the HCV core protein, the genomic region encoding amino acid residues 1 to 191 of the HCV-1 strain was amplified and cloned into an eukaryotic expression vector. Intramuscular inoculation of recombinant plasmid DNA into BALB/c mice (H-2d) generated core-specific antibody responses, lymphoproliferative responses, and cytotoxic T-lymphocyte activity. Our results suggest that the HCV core polynucleotide warrants further investigation as a potential vaccine against HCV infection.
Publication types
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Research Support, U.S. Gov't, P.H.S.
MeSH terms
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3T3 Cells
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Amino Acid Sequence
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Animals
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Antibody Formation*
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Base Sequence
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Cloning, Molecular
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DNA Primers
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DNA, Viral / immunology*
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Enzyme-Linked Immunosorbent Assay
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Female
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Hepacivirus / genetics
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Hepacivirus / immunology*
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Lymphocyte Activation*
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Mice
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Mice, Inbred BALB C
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Molecular Sequence Data
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Peptide Fragments / chemical synthesis
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Peptide Fragments / chemistry
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Peptide Fragments / immunology
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Plasmids / immunology*
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Polymerase Chain Reaction
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Recombinant Proteins / biosynthesis
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Recombinant Proteins / immunology
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Transfection
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Vaccines, Synthetic / immunology
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Viral Core Proteins / biosynthesis
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Viral Core Proteins / immunology*
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Viral Vaccines / immunology*
Substances
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DNA Primers
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DNA, Viral
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Peptide Fragments
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Recombinant Proteins
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Vaccines, Synthetic
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Viral Core Proteins
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Viral Vaccines