Effects of interferon beta on non-A, non-B acute hepatitis: a prospective, randomized, controlled-dose study. Japan Acute Hepatitis Cooperative Study Group

Gastroenterology. 1994 Sep;107(3):805-11. doi: 10.1016/0016-5085(94)90130-9.

Abstract

Background/aims: Non-A, non-B acute hepatitis progresses to a higher incidence of chronicity and hepatocellular carcinoma. To avoid the development of chronic liver disease, resolution of acute hepatitis C might be most effective. The aim was to establish the effect of interferon in disturbing progression to chronicity and to determine the most appropriate treatment protocol.

Methods: Ninety-seven acute non-A, non-B hepatitis cases were randomly assigned to six different protocols and treated with 8.4-336 MU of interferon; 90 cases were finally completely analyzed. Titers of hepatitis C virus (HCV) RNA and HCV genotypes were determined.

Results: Seventy-four cases were positive for second-generation anti-HCV. Of these, 65 (89%) were positive for HCV RNA. In these 65 cases, the resolution rate was 32%, and this rate was dependent on the total treatment dosage. Only the group treated with 336 MU showed a high (83%; 10/12) resolution rate; the other five groups had 0%-38% resolution.

Conclusions: Interferon treatment for acute hepatitis C could be regarded as a "vaccinelike" therapy by preventing the development of the virus carrier state.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Aged
  • Dose-Response Relationship, Drug
  • Female
  • Genotype
  • Hepacivirus / genetics
  • Hepacivirus / immunology
  • Hepatitis Antibodies / analysis
  • Hepatitis C / drug therapy*
  • Hepatitis C / genetics
  • Humans
  • Immunoenzyme Techniques
  • Interferon-beta / therapeutic use*
  • Male
  • Middle Aged
  • Prospective Studies
  • RNA, Viral / analysis
  • Sensitivity and Specificity

Substances

  • Hepatitis Antibodies
  • RNA, Viral
  • Interferon-beta