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The progress of molecules and strategies for the treatment of HBV infection

Hepatitis B virus infections have always been associated with high levels of mortality. In 2019, hepatitis B virus (HBV)-related diseases resulted in approximately 555,000 deaths globally. In view of its high lethality, the treatment of HBV infections has always presented a huge challenge. The World...

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Autores principales: Pan, Youlu, Xia, Heye, He, Yanwen, Zeng, Shenxin, Shen, Zhengrong, Huang, Wenhai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053227/
https://www.ncbi.nlm.nih.gov/pubmed/37009498
http://dx.doi.org/10.3389/fcimb.2023.1128807
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author Pan, Youlu
Xia, Heye
He, Yanwen
Zeng, Shenxin
Shen, Zhengrong
Huang, Wenhai
author_facet Pan, Youlu
Xia, Heye
He, Yanwen
Zeng, Shenxin
Shen, Zhengrong
Huang, Wenhai
author_sort Pan, Youlu
collection PubMed
description Hepatitis B virus infections have always been associated with high levels of mortality. In 2019, hepatitis B virus (HBV)-related diseases resulted in approximately 555,000 deaths globally. In view of its high lethality, the treatment of HBV infections has always presented a huge challenge. The World Health Organization (WHO) came up with ambitious targets for the elimination of hepatitis B as a major public health threat by 2030. To accomplish this goal, one of the WHO’s strategies is to develop curative treatments for HBV infections. Current treatments in a clinical setting included 1 year of pegylated interferon alpha (PEG-IFNα) and long-term nucleoside analogues (NAs). Although both treatments have demonstrated outstanding antiviral effects, it has been difficult to develop a cure for HBV. The reason for this is that covalently closed circular DNA (cccDNA), integrated HBV DNA, the high viral burden, and the impaired host immune responses all hinder the development of a cure for HBV. To overcome these problems, there are clinical trials on a number of antiviral molecules being carried out, all -showing promising results so far. In this review, we summarize the functions and mechanisms of action of various synthetic molecules, natural products, traditional Chinese herbal medicines, as clustered regularly interspaced short palindromic repeats and their associated proteins (CRISPR/Cas)-based systems, zinc finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), all of which could destroy the stability of the HBV life cycle. In addition, we discuss the functions of immune modulators, which can enhance or activate the host immune system, as well some representative natural products with anti-HBV effects.
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spelling pubmed-100532272023-03-30 The progress of molecules and strategies for the treatment of HBV infection Pan, Youlu Xia, Heye He, Yanwen Zeng, Shenxin Shen, Zhengrong Huang, Wenhai Front Cell Infect Microbiol Cellular and Infection Microbiology Hepatitis B virus infections have always been associated with high levels of mortality. In 2019, hepatitis B virus (HBV)-related diseases resulted in approximately 555,000 deaths globally. In view of its high lethality, the treatment of HBV infections has always presented a huge challenge. The World Health Organization (WHO) came up with ambitious targets for the elimination of hepatitis B as a major public health threat by 2030. To accomplish this goal, one of the WHO’s strategies is to develop curative treatments for HBV infections. Current treatments in a clinical setting included 1 year of pegylated interferon alpha (PEG-IFNα) and long-term nucleoside analogues (NAs). Although both treatments have demonstrated outstanding antiviral effects, it has been difficult to develop a cure for HBV. The reason for this is that covalently closed circular DNA (cccDNA), integrated HBV DNA, the high viral burden, and the impaired host immune responses all hinder the development of a cure for HBV. To overcome these problems, there are clinical trials on a number of antiviral molecules being carried out, all -showing promising results so far. In this review, we summarize the functions and mechanisms of action of various synthetic molecules, natural products, traditional Chinese herbal medicines, as clustered regularly interspaced short palindromic repeats and their associated proteins (CRISPR/Cas)-based systems, zinc finger nucleases (ZFNs), and transcription activator-like effector nucleases (TALENs), all of which could destroy the stability of the HBV life cycle. In addition, we discuss the functions of immune modulators, which can enhance or activate the host immune system, as well some representative natural products with anti-HBV effects. Frontiers Media S.A. 2023-03-15 /pmc/articles/PMC10053227/ /pubmed/37009498 http://dx.doi.org/10.3389/fcimb.2023.1128807 Text en Copyright © 2023 Pan, Xia, He, Zeng, Shen and Huang https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Cellular and Infection Microbiology
Pan, Youlu
Xia, Heye
He, Yanwen
Zeng, Shenxin
Shen, Zhengrong
Huang, Wenhai
The progress of molecules and strategies for the treatment of HBV infection
title The progress of molecules and strategies for the treatment of HBV infection
title_full The progress of molecules and strategies for the treatment of HBV infection
title_fullStr The progress of molecules and strategies for the treatment of HBV infection
title_full_unstemmed The progress of molecules and strategies for the treatment of HBV infection
title_short The progress of molecules and strategies for the treatment of HBV infection
title_sort progress of molecules and strategies for the treatment of hbv infection
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10053227/
https://www.ncbi.nlm.nih.gov/pubmed/37009498
http://dx.doi.org/10.3389/fcimb.2023.1128807
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