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An optimized mode of interferon intermittent therapy help improve HBsAg disappearance in chronic hepatitis B patients

乙型肝炎表面抗原 病毒学 医学 干扰素 慢性肝炎 免疫学 乙型肝炎病毒 病毒
作者
Minghui Li,Si Xie,Xiaoyue Bi,Fangfang Sun,Zhan Zeng,Wen Deng,Tingting Jiang,Yanjie Lin,Yang Liu,Yao Lu,Lu Zhang,Wei Yi,Yao Xie
出处
期刊:Frontiers in Microbiology [Frontiers Media]
卷期号:13 被引量:7
标识
DOI:10.3389/fmicb.2022.960589
摘要

To investigate the effect of intermittent interferon therapy mode on the disappearance of hepatitis B surface antigen (HBsAg) in chronic hepatitis B (CHB) patients. This is a retrospective cohort study in CHB patients who were suspended from pegylated interferon α (PEG-IFNα) therapy due to a plateau in HBsAg decline during the initial treatment period, and resumed interferon therapy after an interval of 3-6 months. Patients received entecavir or tenofovir during the interval period. Hepatitis B virus (HBV) virological and serological indexes, clinical biochemical indexes, and blood routine tests were performed at the baseline and every 3 months during follow-up of initial interferon treatment. A functional cure was analyzed as a primary outcome. A total of 304 patients treated with intermittent PEG-IFNα were included in the statistical analysis, including 215 men and 89 women, aged 37.97 ± 8.53 years, and 73 hepatitis B e antigen (HBeAg)-negative and 231 HBeAg positive patients. In total 59 patients (19.41%) achieved HBsAg disappearance through the initial, intermittent, and retreatment of PEG-IFNα treatment, of whom 43 patients (14.14%) achieved HBsAg seroconversion. Early HBsAg response to initial treatment was significantly associated with HBsAg response at 12 and 24 weeks of retreatment. After the intermission period, the incidence of HBsAg disappearance in patients with early HBsAg response in the retreatment period was 43.87%. The baseline HBsAg and 12-week HBsAg response in the retreatment period had higher predictive value than the initial treatment HBsAg response. The initial, intermittent, and retreatment mode of interferon can help to improve the HBsAg disappearance rate in CHB patients. [www.ClinicalTrials.gov], identifier [NCT04028856].
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