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Short-term Peginterferon-Induced High Functional Cure Rate in Inactive Chronic Hepatitis B Virus Carriers With Low Surface Antigen Levels.

Authors :
Zeng, Qing-Lei
Yu, Zu-Jiang
Shang, Jia
Xu, Guang-Hua
Sun, Chang-Yu
Liu, Na
Li, Chun-Xia
Lv, Jun
Liu, Yan-Min
Liang, Hong-Xia
Li, Zhi-Qin
Pan, Ya-Jie
Hu, Qiu-Yue
Li, Wei
Zhang, Da-Wei
Wang, Fu-Sheng
Source :
Open Forum Infectious Diseases. Jun2020, Vol. 7 Issue 6, p1-7. 7p.
Publication Year :
2020

Abstract

Background None of the current guidelines recommend antiviral therapy for inactive hepatitis B virus (HBV) carriers (IHCs). Methods In this real-world, multicenter, nonrandomized study, 32 participants meeting the inclusion criteria were enrolled 1:1 for treatment with peginterferon α-2b or monitoring without treatment based on participant preference. The expected treatment duration was 48 weeks. The primary end point was hepatitis B surface antigen (HBsAg) loss. The HBV vaccine could be injected after HBsAg loss. Results All patients had HBsAg levels of <20 IU/mL. The mean baseline HBsAg levels were 6.6 IU/mL and 5.8 IU/mL in the treated and untreated groups, respectively. Fifteen (93.8%) participants achieved HBsAg loss, 5 obtained HBsAg seroconversion after undergoing a mean of 19.7 weeks of therapy in the treated group, and no one in the follow-up group achieved HBsAg loss during a mean follow-up time of 12.6 months (P <.0001). Generally, the therapy was well tolerated. Nine of 11 individuals who exhibited HBsAg loss benefited from receiving the HBV vaccine. Conclusions This study provides justification for further studies of short-course peginterferon α-2b for the functional cure of IHCs with low HBsAg levels. Additionally, HBV vaccine injection is beneficial after interferon-induced HBsAg loss. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
23288957
Volume :
7
Issue :
6
Database :
Academic Search Index
Journal :
Open Forum Infectious Diseases
Publication Type :
Academic Journal
Accession number :
144824593
Full Text :
https://doi.org/10.1093/ofid/ofaa208