Antiviral strategies to eliminate hepatitis B virus covalently closed circular DNA (cccDNA)

被引:24
|
作者
Revill, Peter [1 ]
Locarnini, Stephen [1 ]
机构
[1] Peter Doherty Inst Infect & Immun, Victorian Infect Dis Reference Lab, Melbourne, Vic 3000, Australia
关键词
HEPATOCYTE TURNOVER; NONHEPATOTOXIC DEGRADATION; X PROTEIN; HBV; REPLICATION; REACTIVATION; INHIBITION; INFECTION; TRANSIENT; TRANSPLANTATION;
D O I
10.1016/j.coph.2016.08.015
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
It has been over 50 years since the discovery of hepatitis B virus (HBV), yet 240 million people worldwide live with chronic HBV, resulting in up to 800 000 deaths per year. A cure is yet to be achieved, due largely to a viral nuclear reservoir of transcriptionally active covalently closed circular DNA (cccDNA). While current antiviral therapies are effective at reducing viral replication, they have no impact on the existing cccDNA reservoir. Identifying mechanisms to either eliminate (complete cure) or inactivate (functional cure) HBV cccDNA are a major focus of HBV research worldwide. This review discusses recent advances in efforts to eliminate and/or regulate cccDNA, as well as future directions that may be considered in efforts to cure chronic HBV.
引用
收藏
页码:144 / 150
页数:7
相关论文
共 50 条
  • [1] Potential capacity of interferon-α to eliminate covalently closed circular DNA (cccDNA) in hepatocytes infected with hepatitis B virus
    Gang Wang
    Jun Guan
    Nazif U. Khan
    Guojun Li
    Junwei Shao
    Qihui Zhou
    Lichen Xu
    Chunhong Huang
    Jingwen Deng
    Haihong Zhu
    Zhi Chen
    Gut Pathogens, 13
  • [2] Potential capacity of interferon-α to eliminate covalently closed circular DNA (cccDNA) in hepatocytes infected with hepatitis B virus
    Wang, Gang
    Guan, Jun
    Khan, Nazif U.
    Li, Guojun
    Shao, Junwei
    Zhou, Qihui
    Xu, Lichen
    Huang, Chunhong
    Deng, Jingwen
    Zhu, Haihong
    Chen, Zhi
    GUT PATHOGENS, 2021, 13 (01)
  • [3] Research progress in hepatitis B virus covalently closed circular DNA
    Zhang, Xiaodong
    Wang, Yufei
    Yang, Guang
    CANCER BIOLOGY & MEDICINE, 2022, 19 (04) : 415 - 431
  • [4] Quantatitative assays for covalently closed circular DNA of hepatitis B virus
    Shi, Tianshu
    Cao, Jiali
    Yang, Yinan
    Yuan, Quan
    CHINESE SCIENCE BULLETIN-CHINESE, 2020, 65 (16): : 1529 - 1545
  • [5] Research progress in hepatitis B virus covalently closed circular DNA
    Xiaodong Zhang
    Yufei Wang
    Guang Yang
    Cancer Biology & Medicine, 2022, 19 (04) : 415 - 431
  • [6] Approaches to quantifying hepatitis B virus covalently closed circular DNA
    Zhang, Henrik
    Tu, Thomas
    CLINICAL AND MOLECULAR HEPATOLOGY, 2022, 28 (02) : 135 - 149
  • [7] Surrogate Markers for Hepatitis B Virus Covalently Closed Circular DNA
    Tu, Thomas
    van Bommel, Florian
    Berg, Thomas
    SEMINARS IN LIVER DISEASE, 2022, 42 (03) : 327 - 340
  • [8] Quantitation of covalently closed circular hepatitis B virus DNA in chronic hepatitis B patients
    Wong, DKH
    Yuen, MF
    Yuan, HJ
    Sum, SSM
    Hui, CK
    Hall, J
    Lai, CL
    HEPATOLOGY, 2004, 40 (03) : 727 - 737
  • [9] TRANSCRIPTIONAL ACTIVITY OF HEPATITS B VIRUS COVALENTLY CLOSED CIRCULAR DNA(HBV CCCDNA) IS REGULATED BY METHYLATION
    Kim, Jin-Wook
    Jeong, Sook-Hyang
    HEPATOLOGY, 2008, 48 (04) : 375A - 376A
  • [10] Recent advances in the study of hepatitis B virus covalently closed circular DNA
    Ji, Mengying
    Hu, Kanghong
    VIROLOGICA SINICA, 2017, 32 (06) : 454 - 464