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Virol Sin. 2010 Aug;25(4):294-300. doi: 10.1007/s12250-010-3138-9. Epub 2010 Jul 28.
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Non-antigen-specific and antigen-specific immune therapies for chronic hepatitis B: evidences from laboratory benches and patient's bedsides.慢性乙型肝炎的非抗原特异性和抗原特异性免疫治疗:来自实验室和患者病床的证据。
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Controllable inhibition of hepatitis B virus replication by a DR1-targeting short hairpin RNA (shRNA) expressed from a DOX-inducible lentiviral vector.通过从强力霉素诱导的慢病毒载体表达的靶向DR1的短发夹RNA(shRNA)对乙型肝炎病毒复制进行可控抑制。
Virus Genes. 2013 Jun;46(3):393-403. doi: 10.1007/s11262-013-0886-2. Epub 2013 Feb 9.

本文引用的文献

1
Control of hepatitis B virus replication by innate response of HepaRG cells.HepaRG 细胞的先天免疫反应对乙型肝炎病毒复制的控制。
Hepatology. 2010 Jan;51(1):63-72. doi: 10.1002/hep.23230.
2
Stimulation of the interleukin-1 receptor and Toll-like receptor 2 inhibits hepatitis B virus replication in hepatoma cell lines in vitro.白细胞介素-1受体和Toll样受体2的刺激在体外抑制肝癌细胞系中的乙型肝炎病毒复制。
Antivir Ther. 2009;14(6):797-808. doi: 10.3851/IMP1294.
3
Hepatitis B virus variants.乙型肝炎病毒变异体
Nat Rev Gastroenterol Hepatol. 2009 Aug;6(8):453-62. doi: 10.1038/nrgastro.2009.107. Epub 2009 Jul 7.
4
Benefits and risks of interferon therapy for hepatitis B.干扰素治疗乙型肝炎的益处与风险。
Hepatology. 2009 May;49(5 Suppl):S103-11. doi: 10.1002/hep.22956.
5
Inhibitory effect of the combination of CpG-induced cytokines with lamivudine against hepatitis B virus replication in vitro.CpG诱导的细胞因子与拉米夫定联合使用对体外乙型肝炎病毒复制的抑制作用。
Antivir Ther. 2009;14(1):131-5.
6
Hepatitis B virus infection.乙型肝炎病毒感染
N Engl J Med. 2008 Oct 2;359(14):1486-500. doi: 10.1056/NEJMra0801644.
7
A randomized controlled phase IIb trial of antigen-antibody immunogenic complex therapeutic vaccine in chronic hepatitis B patients.一项关于抗原 - 抗体免疫原性复合治疗性疫苗用于慢性乙型肝炎患者的随机对照IIb期试验。
PLoS One. 2008 Jul 2;3(7):e2565. doi: 10.1371/journal.pone.0002565.
8
Zinc finger proteins designed to specifically target duck hepatitis B virus covalently closed circular DNA inhibit viral transcription in tissue culture.设计用于特异性靶向鸭乙型肝炎病毒共价闭合环状DNA的锌指蛋白可在组织培养中抑制病毒转录。
J Virol. 2008 Aug;82(16):8013-21. doi: 10.1128/JVI.00366-08. Epub 2008 Jun 4.
9
Prevention of hepatitis B virus infection in vivo by entry inhibitors derived from the large envelope protein.源自大包膜蛋白的进入抑制剂在体内预防乙型肝炎病毒感染
Nat Biotechnol. 2008 Mar;26(3):335-41. doi: 10.1038/nbt1389. Epub 2008 Feb 24.
10
Low resistance to adefovir combined with lamivudine: a 3-year study of 145 lamivudine-resistant hepatitis B patients.阿德福韦联合拉米夫定的低耐药性:对145例拉米夫定耐药乙型肝炎患者的3年研究
Gastroenterology. 2007 Nov;133(5):1445-51. doi: 10.1053/j.gastro.2007.08.079. Epub 2007 Sep 2.

开发治疗慢性乙型肝炎的新疗法。

Development of novel therapeutics for chronic hepatitis B.

机构信息

Key Laboratory of Medical Molecular Virology, Shanghai Medical College, Fudan University, Shanghai, 200032, China.

出版信息

Virol Sin. 2010 Aug;25(4):294-300. doi: 10.1007/s12250-010-3138-9. Epub 2010 Jul 28.

DOI:10.1007/s12250-010-3138-9
PMID:20960302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8227944/
Abstract

Chronic infection of hepatitis B virus (HBV) presents one of the serious public health challenges worldwide. Current treatment of chronic hepatitis B (CHB) is limited, and is composed of interferon and nucleoside/nucleotide reverse transcriptase inhibitors (NRTI). Interferon is poorly tolerated and is only responsive in a small fraction of CHB patients and NRTIs often face the problem of emergence of drug resistance during long-term treatment. The current treatment of CHB can be improved in several ways including genotyping mutations associated with drug resistance before treatment to guide the choice of NRTIs and suitable combinations among NRTIs and interferon. It is important to continue research in the identification of novel therapeutic targets in the life cycle of HBV or in the host immune system to stimulate the development of new antiviral agents and immunotherapies. Several antiviral agents targeting HBV entry, cccDNA, capsid formation, viral morphogenesis and virion secretion, as well as two therapeutic vaccines are currently being evaluated in preclinical studies or in clinical trials to assess their anti-HBV efficacy.

摘要

乙型肝炎病毒(HBV)慢性感染是全球面临的严重公共卫生挑战之一。目前慢性乙型肝炎(CHB)的治疗方法有限,包括干扰素和核苷(酸)类似物逆转录酶抑制剂(NRTI)。干扰素的耐受性差,仅对一小部分 CHB 患者有效,而 NRTIs 在长期治疗中经常面临耐药性出现的问题。CHB 的当前治疗可以通过多种方式得到改善,包括在治疗前对与耐药性相关的基因分型突变进行检测,以指导 NRTI 的选择,以及 NRTI 和干扰素之间的合适组合。重要的是要继续研究 HBV 生命周期或宿主免疫系统中的新治疗靶点,以刺激新抗病毒药物和免疫疗法的开发。目前有几种针对 HBV 进入、cccDNA、衣壳形成、病毒形态发生和病毒分泌的抗病毒药物以及两种治疗性疫苗正在进行临床前研究或临床试验,以评估其抗 HBV 的疗效。