Clinical significance and evolution of hepatic HBsAg expression in HBeAg-positive patients receiving interferon therapy.

Abstract

BACKGROUND:

Serum hepatitis B surface antigen (HBsAg) level is important in the management of chronic hepatitis B (CHB). However, it is unclear whether serum HBsAg reflects its expression in liver and the hepatic HBsAg evolution following interferon therapy.

METHODS:

Forty-five HBeAg-positive CHB patients receiving interferon-based therapy within a randomized, controlled, multicenter study during 1998-1999 were included. The hepatic HBsAg expressions were categorized into cytoplasmic, inclusion, marginal and negative patterns by immunohistochemical staining. The HBsAg-positive hepatocytes were quantified by image-based cytometry and correlated to HBV serological and virological profiles for clinical implications. The evolution of hepatic HBsAg levels was analyzed among 22 patients with paired liver biopsies before and after interferon therapy, sequentially.

RESULTS:

There was a positive correlation between pretreatment serum HBsAg and hepatic HBsAg levels (r = 0.67, P < 0.0001). The hepatic HBsAg expression pattern significantly evolved from cytoplasmic/inclusion pattern to marginal/negative pattern after interferon treatment. The serum HBV-DNA, HBsAg and hepatic HBsAg levels all decreased significantly after interferon therapy. Among 36 % patients with HBeAg loss after therapy, pretreatment hepatic HBsAg levels were significantly lower compared with those without HBeAg loss. After multivariate analysis, low pretreatment hepatic HBsAg levels rather than serum HBsAg titers were associated with a higher rate of HBeAg loss (OR: 4.97, 95 % CI: 1.12-22.00, P = 0.035).

CONCLUSIONS:

The serum HBsAg level positively reflects the HBsAg level in liver which evolves significantly after interferon therapy. A lower hepatic HBsAg level is associated with HBeAg loss after interferon treatment. Hepatic HBsAg may have clinical significance in CHB patients receiving interferon treatment.

• Authors: Tung-Hung Su, Chun-Jen Liu, Hung-Chih Yang, Yung-Ming Jeng, Huei-Ru Cheng, Chen-Hua Liu, Tai-Chung Tseng, Thai-Yen Ling, Pei-Jer Chen, Ding-Shinn Chen, Jia-Horng Kao
• Journal: Journal of gastroenterology (J Gastroenterol) Vol. 49 Issue 2 Pg. 356-62 (Feb 2014) ISSN: 1435-5922 [Electronic] Japan
• PMID: 23736797 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antiviral Agents
• DNA, Viral
• Hepatitis B Surface Antigens
• Hepatitis B e Antigens
• Interferon alpha-2
• Interferon-alpha
• Recombinant Proteins
• Alanine Transaminase

Topics

• Adult
• Alanine Transaminase (blood)
• Antiviral Agents (therapeutic use)
• DNA, Viral (blood)
• Female
• Genotype
• Hepatitis B Surface Antigens (analysis, blood)
• Hepatitis B e Antigens (analysis)
• Hepatitis B virus (genetics, immunology)
• Hepatitis B, Chronic (drug therapy, immunology, pathology)
• Hepatocytes (chemistry)
• Humans
• Immunohistochemistry
• Interferon alpha-2
• Interferon-alpha (therapeutic use)
• Liver (chemistry)
• Male
• Recombinant Proteins (therapeutic use)
• Young Adult