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Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets

Hepatitis Delta Virus (HDV) is the smallest mammalian single-stranded RNA virus. It requires host cells and hepatitis B virus (HBV) to complete its unique life cycle. The present review summarizes the specific regions on hepatitis D antigen (HDAg) and hepatitis B surface antigen (HBsAg) that drive H...

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Autores principales: Zi, Jun, Gao, Xiuzhu, Du, Juan, Xu, Hongqin, Niu, Junqi, Chi, Xiumei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022428/
https://www.ncbi.nlm.nih.gov/pubmed/35464929
http://dx.doi.org/10.3389/fmicb.2022.838382
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author Zi, Jun
Gao, Xiuzhu
Du, Juan
Xu, Hongqin
Niu, Junqi
Chi, Xiumei
author_facet Zi, Jun
Gao, Xiuzhu
Du, Juan
Xu, Hongqin
Niu, Junqi
Chi, Xiumei
author_sort Zi, Jun
collection PubMed
description Hepatitis Delta Virus (HDV) is the smallest mammalian single-stranded RNA virus. It requires host cells and hepatitis B virus (HBV) to complete its unique life cycle. The present review summarizes the specific regions on hepatitis D antigen (HDAg) and hepatitis B surface antigen (HBsAg) that drive HDV to utilize host cell machinery system to produce three types of RNA and two forms of HDAg, and hijack HBsAg for its secretion and de novo entry. Previously, interferon-α was the only recommended therapy for HDV infection. In recent years, some new therapies targeting these regions, such as Bulevirtide, Lonafarnib, Nucleic acid polymers have appeared, with better curative effects and fewer adverse reactions.
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spelling pubmed-90224282022-04-22 Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets Zi, Jun Gao, Xiuzhu Du, Juan Xu, Hongqin Niu, Junqi Chi, Xiumei Front Microbiol Microbiology Hepatitis Delta Virus (HDV) is the smallest mammalian single-stranded RNA virus. It requires host cells and hepatitis B virus (HBV) to complete its unique life cycle. The present review summarizes the specific regions on hepatitis D antigen (HDAg) and hepatitis B surface antigen (HBsAg) that drive HDV to utilize host cell machinery system to produce three types of RNA and two forms of HDAg, and hijack HBsAg for its secretion and de novo entry. Previously, interferon-α was the only recommended therapy for HDV infection. In recent years, some new therapies targeting these regions, such as Bulevirtide, Lonafarnib, Nucleic acid polymers have appeared, with better curative effects and fewer adverse reactions. Frontiers Media S.A. 2022-04-06 /pmc/articles/PMC9022428/ /pubmed/35464929 http://dx.doi.org/10.3389/fmicb.2022.838382 Text en Copyright © 2022 Zi, Gao, Du, Xu, Niu and Chi. 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 Microbiology
Zi, Jun
Gao, Xiuzhu
Du, Juan
Xu, Hongqin
Niu, Junqi
Chi, Xiumei
Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title_full Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title_fullStr Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title_full_unstemmed Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title_short Multiple Regions Drive Hepatitis Delta Virus Proliferation and Are Therapeutic Targets
title_sort multiple regions drive hepatitis delta virus proliferation and are therapeutic targets
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9022428/
https://www.ncbi.nlm.nih.gov/pubmed/35464929
http://dx.doi.org/10.3389/fmicb.2022.838382
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