Changes in virus loads and precore mutations in chronic hepatitis B patients treated with 4 weeks of daily interferon alfa-2a therapy

Abstract

Interferon (IFN) alfa-2a was administered to 23 patients with chronic hepatitis B daily for 4 weeks and the relation between the efficacy of the treatment and changes in total hepatitis B virus (HBV) DNA and precore mutant levels was investigated. At 6 and 12 months after the completion of IFN therapy, 39.1% (9/23) and 36.8% (7/19) of patients, respectively, showed alanine transaminase (ALT) normalization; 31.3% (5/16) and 50.0% (7/14), respectively, became negative for HBe-antigen (HBeAg); and 42.1% (8/19) and 41.2% (7/17), respectively, became undetectable for HBV DNA. All 18 of the patients who were positive for HBeAg at baseline nevertheless had the precore mutation. The level of precore mutant as a proportion of the total HBV DNA level was constant at baseline, and 3 and 6 months after the completion of therapy. Thus, the investigation showed that in chronic hepatitis B, the precore mutation occurs at a constant proportion beginning in the HBeAg-positive phase, and IFN therapy inhibits the growth of the wild-type and precore mutant viruses equally.