Loading…

Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions

Chronic hepatitis B virus (HBV) infection affects more than 250 million people worldwide, which greatly increases the risk for terminal liver diseases, such as liver cirrhosis and hepatocellular carcinoma (HCC). Even though current approved antiviral therapies, including pegylated type I interferon...

Full description

Saved in:
Bibliographic Details
Published in:Viruses 2021-04, Vol.13 (5), p.777
Main Authors: Liu, Yongzhen, Maya, Stephanie, Ploss, Alexander
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53
cites cdi_FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53
container_end_page
container_issue 5
container_start_page 777
container_title Viruses
container_volume 13
creator Liu, Yongzhen
Maya, Stephanie
Ploss, Alexander
description Chronic hepatitis B virus (HBV) infection affects more than 250 million people worldwide, which greatly increases the risk for terminal liver diseases, such as liver cirrhosis and hepatocellular carcinoma (HCC). Even though current approved antiviral therapies, including pegylated type I interferon (IFN) and nucleos(t)ide analogs, can effectively suppress viremia, HBV infection is rarely cured. Since HBV exhibits a narrow species tropism and robustly infects only humans and higher primates, progress in HBV research and preclinical testing of antiviral drugs has been hampered by the scarcity of suitable animal models. Fortunately, a series of surrogate animal models have been developed for the study of HBV. An increased understanding of the barriers towards interspecies transmission has aided in the development of human chimeric mice and has greatly paved the way for HBV research in vivo, and for evaluating potential therapies of chronic hepatitis B. In this review, we summarize the currently available animal models for research of HBV and HBV-related hepadnaviruses, and we discuss challenges and future directions for improvement.
doi_str_mv 10.3390/v13050777
format article
fullrecord <record><control><sourceid>proquest_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_92c0fe052a70400c9926ec713086c8c5</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_92c0fe052a70400c9926ec713086c8c5</doaj_id><sourcerecordid>2520870537</sourcerecordid><originalsourceid>FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53</originalsourceid><addsrcrecordid>eNpdkVtvFCEUgCdGYy_64B8wJL5o0qlnYIDhpUldW7tJjQ_eHgkLZ7ZsZmGFmSb997Ju3bR94gQ-vnOrqjcNnDKm4ONtw4CDlPJZddgopepWNfz5g_igOsp5BSCEAvmyOii_aCsVO6x-nwe_NgP5Gh0OmcSeXOHGjH70mXwiv3yaMpmHHu3oY6i_T9ZizidkdmOGAcMSS2yCI5fTOCUkn33akflV9aI3Q8bX9-dx9fPy4sfsqr7-9mU-O7-uLWd8rNF0bsGBC1go2iDtJBWNMOCckFgKbxtOOfa2swvWc96BE4JJZ2xLrZLI2XE133ldNCu9SaWZdKej8frfRUxLbdLo7YBaUQs9AqdGQgtglaICrSyz60RJsHWd7VybabFGZzGMyQyPpI9fgr_Ry3iru6YVktEieH8vSPHPhHnUa58tDoMJGKesKafQSeBMFvTdE3QVpxTKqArFaOlbiq3ww46yKeacsN8X04Derl7vV1_Ytw-r35P_d83-An7Epyk</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2532415762</pqid></control><display><type>article</type><title>Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions</title><source>Publicly Available Content Database</source><source>PubMed Central</source><creator>Liu, Yongzhen ; Maya, Stephanie ; Ploss, Alexander</creator><creatorcontrib>Liu, Yongzhen ; Maya, Stephanie ; Ploss, Alexander</creatorcontrib><description>Chronic hepatitis B virus (HBV) infection affects more than 250 million people worldwide, which greatly increases the risk for terminal liver diseases, such as liver cirrhosis and hepatocellular carcinoma (HCC). Even though current approved antiviral therapies, including pegylated type I interferon (IFN) and nucleos(t)ide analogs, can effectively suppress viremia, HBV infection is rarely cured. Since HBV exhibits a narrow species tropism and robustly infects only humans and higher primates, progress in HBV research and preclinical testing of antiviral drugs has been hampered by the scarcity of suitable animal models. Fortunately, a series of surrogate animal models have been developed for the study of HBV. An increased understanding of the barriers towards interspecies transmission has aided in the development of human chimeric mice and has greatly paved the way for HBV research in vivo, and for evaluating potential therapies of chronic hepatitis B. In this review, we summarize the currently available animal models for research of HBV and HBV-related hepadnaviruses, and we discuss challenges and future directions for improvement.</description><identifier>ISSN: 1999-4915</identifier><identifier>EISSN: 1999-4915</identifier><identifier>DOI: 10.3390/v13050777</identifier><identifier>PMID: 33924793</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>animal model ; Animal models ; Antigens ; Antiviral agents ; Chronic infection ; Cirrhosis ; Genomes ; Hepatitis B ; hepatitis B virus ; Hepatocellular carcinoma ; humanized mice ; Infections ; Interferon ; Liver ; Liver cancer ; Liver cirrhosis ; Liver diseases ; Pathogenesis ; Review ; species tropism ; Transgenic animals ; Tropism ; Viremia ; Viruses</subject><ispartof>Viruses, 2021-04, Vol.13 (5), p.777</ispartof><rights>2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2021 by the authors. 2021</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53</citedby><cites>FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53</cites><orcidid>0000-0001-7321-9706 ; 0000-0003-1087-9613</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2532415762/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2532415762?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33924793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Yongzhen</creatorcontrib><creatorcontrib>Maya, Stephanie</creatorcontrib><creatorcontrib>Ploss, Alexander</creatorcontrib><title>Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions</title><title>Viruses</title><addtitle>Viruses</addtitle><description>Chronic hepatitis B virus (HBV) infection affects more than 250 million people worldwide, which greatly increases the risk for terminal liver diseases, such as liver cirrhosis and hepatocellular carcinoma (HCC). Even though current approved antiviral therapies, including pegylated type I interferon (IFN) and nucleos(t)ide analogs, can effectively suppress viremia, HBV infection is rarely cured. Since HBV exhibits a narrow species tropism and robustly infects only humans and higher primates, progress in HBV research and preclinical testing of antiviral drugs has been hampered by the scarcity of suitable animal models. Fortunately, a series of surrogate animal models have been developed for the study of HBV. An increased understanding of the barriers towards interspecies transmission has aided in the development of human chimeric mice and has greatly paved the way for HBV research in vivo, and for evaluating potential therapies of chronic hepatitis B. In this review, we summarize the currently available animal models for research of HBV and HBV-related hepadnaviruses, and we discuss challenges and future directions for improvement.</description><subject>animal model</subject><subject>Animal models</subject><subject>Antigens</subject><subject>Antiviral agents</subject><subject>Chronic infection</subject><subject>Cirrhosis</subject><subject>Genomes</subject><subject>Hepatitis B</subject><subject>hepatitis B virus</subject><subject>Hepatocellular carcinoma</subject><subject>humanized mice</subject><subject>Infections</subject><subject>Interferon</subject><subject>Liver</subject><subject>Liver cancer</subject><subject>Liver cirrhosis</subject><subject>Liver diseases</subject><subject>Pathogenesis</subject><subject>Review</subject><subject>species tropism</subject><subject>Transgenic animals</subject><subject>Tropism</subject><subject>Viremia</subject><subject>Viruses</subject><issn>1999-4915</issn><issn>1999-4915</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNpdkVtvFCEUgCdGYy_64B8wJL5o0qlnYIDhpUldW7tJjQ_eHgkLZ7ZsZmGFmSb997Ju3bR94gQ-vnOrqjcNnDKm4ONtw4CDlPJZddgopepWNfz5g_igOsp5BSCEAvmyOii_aCsVO6x-nwe_NgP5Gh0OmcSeXOHGjH70mXwiv3yaMpmHHu3oY6i_T9ZizidkdmOGAcMSS2yCI5fTOCUkn33akflV9aI3Q8bX9-dx9fPy4sfsqr7-9mU-O7-uLWd8rNF0bsGBC1go2iDtJBWNMOCckFgKbxtOOfa2swvWc96BE4JJZ2xLrZLI2XE133ldNCu9SaWZdKej8frfRUxLbdLo7YBaUQs9AqdGQgtglaICrSyz60RJsHWd7VybabFGZzGMyQyPpI9fgr_Ry3iru6YVktEieH8vSPHPhHnUa58tDoMJGKesKafQSeBMFvTdE3QVpxTKqArFaOlbiq3ww46yKeacsN8X04Derl7vV1_Ytw-r35P_d83-An7Epyk</recordid><startdate>20210428</startdate><enddate>20210428</enddate><creator>Liu, Yongzhen</creator><creator>Maya, Stephanie</creator><creator>Ploss, Alexander</creator><general>MDPI AG</general><general>MDPI</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0001-7321-9706</orcidid><orcidid>https://orcid.org/0000-0003-1087-9613</orcidid></search><sort><creationdate>20210428</creationdate><title>Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions</title><author>Liu, Yongzhen ; Maya, Stephanie ; Ploss, Alexander</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>animal model</topic><topic>Animal models</topic><topic>Antigens</topic><topic>Antiviral agents</topic><topic>Chronic infection</topic><topic>Cirrhosis</topic><topic>Genomes</topic><topic>Hepatitis B</topic><topic>hepatitis B virus</topic><topic>Hepatocellular carcinoma</topic><topic>humanized mice</topic><topic>Infections</topic><topic>Interferon</topic><topic>Liver</topic><topic>Liver cancer</topic><topic>Liver cirrhosis</topic><topic>Liver diseases</topic><topic>Pathogenesis</topic><topic>Review</topic><topic>species tropism</topic><topic>Transgenic animals</topic><topic>Tropism</topic><topic>Viremia</topic><topic>Viruses</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Yongzhen</creatorcontrib><creatorcontrib>Maya, Stephanie</creatorcontrib><creatorcontrib>Ploss, Alexander</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Virology and AIDS Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Biological Sciences</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Biological Science Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Viruses</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Yongzhen</au><au>Maya, Stephanie</au><au>Ploss, Alexander</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions</atitle><jtitle>Viruses</jtitle><addtitle>Viruses</addtitle><date>2021-04-28</date><risdate>2021</risdate><volume>13</volume><issue>5</issue><spage>777</spage><pages>777-</pages><issn>1999-4915</issn><eissn>1999-4915</eissn><abstract>Chronic hepatitis B virus (HBV) infection affects more than 250 million people worldwide, which greatly increases the risk for terminal liver diseases, such as liver cirrhosis and hepatocellular carcinoma (HCC). Even though current approved antiviral therapies, including pegylated type I interferon (IFN) and nucleos(t)ide analogs, can effectively suppress viremia, HBV infection is rarely cured. Since HBV exhibits a narrow species tropism and robustly infects only humans and higher primates, progress in HBV research and preclinical testing of antiviral drugs has been hampered by the scarcity of suitable animal models. Fortunately, a series of surrogate animal models have been developed for the study of HBV. An increased understanding of the barriers towards interspecies transmission has aided in the development of human chimeric mice and has greatly paved the way for HBV research in vivo, and for evaluating potential therapies of chronic hepatitis B. In this review, we summarize the currently available animal models for research of HBV and HBV-related hepadnaviruses, and we discuss challenges and future directions for improvement.</abstract><cop>Switzerland</cop><pub>MDPI AG</pub><pmid>33924793</pmid><doi>10.3390/v13050777</doi><orcidid>https://orcid.org/0000-0001-7321-9706</orcidid><orcidid>https://orcid.org/0000-0003-1087-9613</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1999-4915
ispartof Viruses, 2021-04, Vol.13 (5), p.777
issn 1999-4915
1999-4915
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_92c0fe052a70400c9926ec713086c8c5
source Publicly Available Content Database; PubMed Central
subjects animal model
Animal models
Antigens
Antiviral agents
Chronic infection
Cirrhosis
Genomes
Hepatitis B
hepatitis B virus
Hepatocellular carcinoma
humanized mice
Infections
Interferon
Liver
Liver cancer
Liver cirrhosis
Liver diseases
Pathogenesis
Review
species tropism
Transgenic animals
Tropism
Viremia
Viruses
title Animal Models of Hepatitis B Virus Infection-Success, Challenges, and Future Directions
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-06T20%3A22%3A25IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Animal%20Models%20of%20Hepatitis%20B%20Virus%20Infection-Success,%20Challenges,%20and%20Future%20Directions&rft.jtitle=Viruses&rft.au=Liu,%20Yongzhen&rft.date=2021-04-28&rft.volume=13&rft.issue=5&rft.spage=777&rft.pages=777-&rft.issn=1999-4915&rft.eissn=1999-4915&rft_id=info:doi/10.3390/v13050777&rft_dat=%3Cproquest_doaj_%3E2520870537%3C/proquest_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c535t-ea8db50560b921e2872616a0dd67e91541525efc8cb3f5580d6637dac42c97e53%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2532415762&rft_id=info:pmid/33924793&rfr_iscdi=true