Overview of anti-Hepatitis B virus agents

Q4 Immunology and Microbiology Journal of Bacteriology and Virology Pub Date : 2020-01-01 DOI:10.4167/JBV.2020.50.3.141
Lee Hye-Won, Park Yong-Kwang, Choi Yong-Wook
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引用次数: 3

Abstract

ƒThis is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/ license/by-nc/3.0/). Since the first FDA approval of Lamivudine in 1998, many nucleo(t)side analogs such as Lamivudine, Adefovir, and Entecavir have been used. However, they only inhibit DNA synthesis, and if their administration is stopped a viral breakthrough can develop, making long-term administration necessary, ultimately followed by the development of resistance. Tenofovir has been developed and drug-resistant mutations have decreased significantly, but the problem of resistance due to long-term drug use still remains, along with the drug safety problem. In this review, we introduce the recent trend in the development of hepatitis B treatment agents and the Korea National Research Institute of Health (KNIH) research for the development of a novel treatment for hepatitis B (drug repositioning) without resistance and which targets the various life cycles of HBV.
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抗乙型肝炎病毒药物综述
这是一篇基于知识共享署名非商业许可协议(http://creativecommons.org/ License /by-nc/3.0/)的开放获取文章。自1998年FDA首次批准拉米夫定以来,许多核苷类似物如拉米夫定、阿德福韦和恩替卡韦已被使用。然而,它们只抑制DNA合成,如果停止给药,病毒就会出现突破,需要长期给药,最终会产生耐药性。替诺福韦已被开发出来,耐药突变已显著减少,但长期用药引起的耐药问题以及药物安全问题仍然存在。在这篇综述中,我们介绍了乙型肝炎治疗剂的最新发展趋势,以及韩国国立卫生研究院(KNIH)为开发一种无耐药性的乙型肝炎新疗法(药物重新定位)而进行的研究,该疗法针对HBV的各个生命周期。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Bacteriology and Virology
Journal of Bacteriology and Virology Immunology and Microbiology-Immunology
CiteScore
0.80
自引率
0.00%
发文量
16
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