Viral Hepatitis
Copyright ©The Author(s) 2003. Published by Baishideng Publishing Group Inc. All rights reserved.
World J Gastroenterol. Jan 15, 2003; 9(1): 117-121
Published online Jan 15, 2003. doi: 10.3748/wjg.v9.i1.117
Changes in serum and histology of patients with chronic hepatitis B after interferon alpha-2b treatment
Hong-Lei Han, Zhen-Wei Lang
Hong-Lei Han, Zhen-Wei Lang, Department of Pathology, Beijing Youan Hospital, Beijing 100054, China
Author contributions: All authors contributed equally to the work.
Correspondence to: Professor Zhen-Wei Lang, Department of Pathology, Beijing Youan Hospital, Beijing 100054, China
Telephone: +86-10-63292211-2402
Received: July 19, 2001
Revised: August 29, 2001
Accepted: September 21, 2001
Published online: January 15, 2003
Abstract

AIM: Chronic hepatitis B is a serious health problem. Interferon has long been used to treat Chronic hepatitis B. To evaluate the effects of interferon on chronic hepatitis B better, we designed the study to investigate the changes in sera and liver histology of patients with chronic hepatitis B after interferon alpha-2b treatment.

METHODS: Twenty-four patients with chronic hepatitis B were enrolled in this study. They all received interferon alpha-2b treatment as following: 3 million units, i.m. t.i.w., for 18 weeks. Sera of all patients were obtained respectively for evaluation of ALT, HBsAg, HBcAg, HBeAg, HBV DNA and TIMP-1 before and after interferon treatment, also a liver biopsy pre- and post-treatment was performed for comparison of HAI, HBsAg, HBcAg, HBeAg, TIMP-1 and activated HSC in the liver tissue.

RESULTS: Patients who had normalization of serum ALT and seroconversion of HBeAg and/or HBV DNA (blot hybridization) after treatment were defined as responders. The response rate in this study group was 37.5% (7/24). Compared to pretreatment, the serum HBV DNA and TIMP-1 decreased significantly (P < 0.05), so did the HAI, HBcAg, HBeAg, TIMP-1 and activated HSC (P < 0.05).

CONCLUSION: The significant decrease in HBV DNA in sera, the seroconversion of HBeAg, and the decrease of viral expression in liver indicated that interferon alpha-2b treatment can inhibit viral replication. The normalization of ALT in sera and the improvement of HAI in liver showed that interferon alpha-2b can improve the liver histology of patients with chronic hepatitis B. At the same time, interferon alpha-2b treatment can reduce the TIMP-1 in serum and liver and decrease the number of activated HSC, which may allievate or inhibit hepatic fibrosis. Although the response rate was unsatisfactory, interferon play a benefical role on patients with chronic hepatitis B in other respects. We still need further studies to improve the therapy effects.

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