IgM antibody to a hepatitis C virus core peptide (CP14) for monitoring activity of liver disease in patients with acute or chronic hepatitis C

J Med Virol. 1994 Mar;42(3):311-7. doi: 10.1002/jmv.1890420320.

Abstract

Antibodies to the hepatitis C virus (HCV) core of various immunoglobulin classes were determined by enzyme immunoassays with three synthetic peptides, CP14 (amino acids 5-40 of the core protein), CP10 (5-23), and CP9 (39-74). In 135 patients with chronic type C liver disease, anti-CP14, anti-CP10, and anti-CP9 of IgG class were detected in 99%, 94%, 82%, respectively; those of IgM class in 86%, 69%, and 39%; and those of IgA class in 56%, 40%, and 4%. Thus anti-CP14 was more prevalent than anti-CP10 or anti-CP9 in every immunoglobulin class. The prevalence of IgM anti-CP14 was much higher (P < 0.001) in patients (116/135 or 86%) than in asymptomatic carriers of HCV (13/39 or 33%). In seven patients with acute hepatitis C, IgM anti-CP14 continued to decrease in two in whom hepatitis resolved, but increased in five in whom hepatitis once resolved and then exacerbated. IgM anti-CP14 was followed in 30 patients with chronic hepatitis C during 24 weeks while they received recombinant interferon alpha-2a. IgM anti-CP14 decreased remarkably within 8 weeks in all of them. Thereafter, it continued to decrease in nine patients who responded to interferon and lost HCV RNA from circulation, but started to increase in five non-responders who continued to have high titers of HCV RNA. In the remaining 16 patients in whom HCV RNA decreased once and then increased, IgM anti-CP14 continued to decrease till 20 weeks and then increased.(ABSTRACT TRUNCATED AT 250 WORDS)

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acute Disease
  • Amino Acid Sequence
  • Antigens, Viral / immunology*
  • Carcinoma, Hepatocellular / blood
  • Carcinoma, Hepatocellular / immunology
  • Carcinoma, Hepatocellular / microbiology
  • Carrier State / blood
  • Carrier State / immunology
  • Carrier State / microbiology
  • Epitopes / immunology
  • Female
  • Hepacivirus / immunology*
  • Hepatitis Antibodies / blood*
  • Hepatitis Antibodies / immunology
  • Hepatitis C / blood*
  • Hepatitis C / immunology
  • Hepatitis C / therapy
  • Hepatitis C Antibodies
  • Hepatitis C Antigens
  • Hepatitis, Chronic / blood
  • Hepatitis, Chronic / immunology
  • Hepatitis, Chronic / microbiology
  • Hepatitis, Chronic / therapy
  • Humans
  • Immunoglobulin A / blood
  • Immunoglobulin A / immunology
  • Immunoglobulin G / blood
  • Immunoglobulin G / immunology
  • Immunoglobulin M / blood*
  • Immunoglobulin M / immunology
  • Immunologic Factors / therapeutic use
  • Interferon alpha-2
  • Interferon-alpha / therapeutic use
  • Liver Cirrhosis / blood
  • Liver Cirrhosis / immunology
  • Liver Cirrhosis / microbiology
  • Liver Neoplasms / blood
  • Liver Neoplasms / immunology
  • Liver Neoplasms / microbiology
  • Male
  • Molecular Sequence Data
  • Monitoring, Immunologic
  • Peptide Fragments / chemical synthesis
  • Peptide Fragments / immunology
  • Recombinant Proteins
  • Treatment Outcome
  • Viral Core Proteins / immunology*

Substances

  • Antigens, Viral
  • Epitopes
  • Hepatitis Antibodies
  • Hepatitis C Antibodies
  • Hepatitis C Antigens
  • Immunoglobulin A
  • Immunoglobulin G
  • Immunoglobulin M
  • Immunologic Factors
  • Interferon alpha-2
  • Interferon-alpha
  • Peptide Fragments
  • Recombinant Proteins
  • Viral Core Proteins
  • nucleocapsid protein, Hepatitis C virus