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.
MeSH Terms
3T3 Cells
Amino Acid Sequence
Animals
Antibody Formation
Base Sequence
Cloning, Molecular
DNA Primers
DNA, Viral/immunology
Enzyme-Linked Immunosorbent Assay
Female
Hepacivirus/genetics,immunology
Lymphocyte Activation
Mice
Mice, Inbred BALB C
Molecular Sequence Data
Peptide Fragments/chemical synthesis,chemistry,immunology
Plasmids/immunology
Polymerase Chain Reaction
Recombinant Proteins/biosynthesis,immunology
Transfection
Vaccines, Synthetic/immunology
Viral Core Proteins/biosynthesis,immunology
Viral Vaccines/immunology
Chemicals
DNA Primers
DNA, Viral
Peptide Fragments
Recombinant Proteins
Vaccines, Synthetic
Viral Core Proteins
Viral Vaccines
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Lagging L M
Division of Infectious Diseases and Immunology, Saint Louis University Health Sciences Center, MO 63104, USA.
Meyer K
Hoft D
Houghton M
Belshe R B
Ray R
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