Purpose of reviewHepatitis B virus (HBV) causes a large proportion of chronic liver disease worldwide. The limited efficiency of current treatments based on the use of nucleotide/nucleoside analogues or interferon-alpha requires the development of new therapeutic tools for the treatment of chronic HBV. We summarize the most recent therapeutic strategies designed to directly target HBV-infected hepatocytes or to restore antiviral immunity during chronic HBV infection.Recent findingsNovel therapies directly target HBV-infected hepatocytes by inducing covalently closed circular DNA degradation or by inhibiting HBV entry or the expression of viral proteins. In addition, immunotherapeutic approaches may boost HBV-specific T-cell responses or stimulate the intrahepatic innate response.SummaryThese new therapeutic approaches have mainly been tested in animal models. In humans, therapeutic strategies could be tailored to different chronic HBV patients in relation to their clinical and virological disease profile.
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Duke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
ASTAR, Singapore Inst Clin Sci, Viral Hepatitis Unit, Singapore, SingaporeDuke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
Bertoletti, Antonio
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Gehring, Adam J.
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St Louis Univ, Sch Med, Mol Microbiol & Immunol Dept, St Louis, MO USADuke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
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Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Lin, Junyu
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Wang, Fan
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机构:
Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Fudan Univ, Shanghai Publ Hlth Clin Ctr, Shanghai 200433, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Wang, Fan
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Wu, Min
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Chen, Cuncun
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Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
机构:
Duke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
ASTAR, Singapore Inst Clin Sci, Viral Hepatitis Unit, Singapore, SingaporeDuke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
Bertoletti, Antonio
;
Gehring, Adam J.
论文数: 0引用数: 0
h-index: 0
机构:
St Louis Univ, Sch Med, Mol Microbiol & Immunol Dept, St Louis, MO USADuke NUS Grad Med Sch, Program Emerging Viral Dis, Singapore, Singapore
机构:
Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Lin, Junyu
;
Wang, Fan
论文数: 0引用数: 0
h-index: 0
机构:
Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Fudan Univ, Shanghai Publ Hlth Clin Ctr, Shanghai 200433, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China
Wang, Fan
;
论文数: 引用数:
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机构:
Wu, Min
;
Chen, Cuncun
论文数: 0引用数: 0
h-index: 0
机构:
Fudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R ChinaFudan Univ, Shanghai Med Coll, Sch Basic Med Sci, Key Lab Med Mol Virol, Shanghai 200032, Peoples R China