cccDNA
乙型肝炎表面抗原
医学
乙型肝炎病毒
乙型肝炎
环状DNA
免疫学
病毒学
病毒
基因组
基因
生物
遗传学
作者
Zilong Wang,Jia-Rui Zheng,Ruifeng Yang,Lin-Xiang Huang,Hongsong Chen,Bo Feng
出处
期刊:Journal of clinical and translational hepatology
[Xia & He Publishing]
日期:2022-08-22
卷期号:000 (000): 000-000
被引量:2
标识
DOI:10.14218/jcth.2022.00289
摘要
In the era of antiviral therapy, the main goal of treatment has shifted from the persistent inhibition of hepatitis B virus (HBV) replication to the pursuit of serological clearance of HBs surface antigen (HBsAg). Based on the life cycle of HBV, HBsAg originates from covalently closed circular DNA (cccDNA) and integrated HBV DNA, thus reflecting their transcriptional activity. Complete HBsAg loss may mean elimination or persistent inactivity of the HBV genome including cccDNA and integrated HBV DNA. HBsAg loss improves the recovery of abnormal immune function, which in turn, may further promote the clearance of residual viruses. Combined with functional cure and the great improvement of clinical outcomes, the continuous seroclearance of high-sensitivity quantitative HBsAg may represent the complete cure of chronic hepatitis B (CHB). For many other risk factors besides HBV itself, patients with HBsAg loss still need regular monitoring. In this review, we summarized the evolution of CHB treatment, the origin of serum HBsAg, the pattern of HBsAg seroclearance, and the effect of HBsAg loss on immune function and disease outcomes. In addition, we discuss the significance of high-sensitivity HBsAg detection and its possibility as a surrogate of complete cure.
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