Abstract
In this study, a 178 amino acids long portion of the hepatitis C virus (HCV) core gene was cloned, sequenced, expressed in Escherichia coli, and purified. The resulting antigen (C178) was tested with human sera enzyme-linked immunosorbent assay (ELISA) in order to assess its ability to diagnose HCV. It was shown by ELISA that 92% of the patients sera, diagnosed previously by a 3rd generation enzyme immunoassay (EIA) as HCV-positive, had antibodies against the C178 antigen. This antigen gave no false positive results when tested with anti-HCV-negative sera.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Cloning, Molecular
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DNA, Viral / biosynthesis
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Enzyme-Linked Immunosorbent Assay / methods*
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Escherichia coli / genetics
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Hepacivirus / immunology
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Hepatitis C / virology*
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Hepatitis C Antibodies / blood*
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Hepatitis C Antigens / biosynthesis
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Hepatitis C Antigens / immunology*
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Humans
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Recombinant Proteins / biosynthesis
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Sensitivity and Specificity
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Serologic Tests
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Viral Core Proteins / biosynthesis
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Viral Core Proteins / genetics
Substances
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DNA, Viral
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Hepatitis C Antibodies
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Hepatitis C Antigens
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Recombinant Proteins
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Viral Core Proteins