The role of quantitative hepatitis B surface antigen revisited
Summary In the past 10 years, there has been a lot of enthusiasm surrounding the use of serum hepatitis B surface antigen (HBsAg) quantification to predict disease activity and monitor treatment response in chronic hepatitis B. The measurement of HBsAg levels have been standardized in IU/ml, and now...
Gespeichert in:
Veröffentlicht in: | Journal of hepatology 2017-02, Vol.66 (2), p.398-411 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 411 |
---|---|
container_issue | 2 |
container_start_page | 398 |
container_title | Journal of hepatology |
container_volume | 66 |
creator | Cornberg, Markus Wong, Vincent Wai-Sun Locarnini, Stephen Brunetto, Maurizia Janssen, Harry L.A Chan, Henry Lik-Yuen |
description | Summary In the past 10 years, there has been a lot of enthusiasm surrounding the use of serum hepatitis B surface antigen (HBsAg) quantification to predict disease activity and monitor treatment response in chronic hepatitis B. The measurement of HBsAg levels have been standardized in IU/ml, and nowadays it is almost a mandatory measurement due to the development of new antiviral treatments aiming at HBsAg seroclearance, i.e., functional cure of hepatitis B. Recently, there has been an improved understanding of the molecular virology of HBsAg, and particularly the relative roles of covalently closed circular DNA and integrated hepatitis B virus (HBV) DNA. This has shed new light on the interpretation of HBsAg levels in different phases of chronic hepatitis B. HBsAg level can assist the differentiation of immune tolerance and immune clearance in hepatitis B e antigen (HBeAg)-positive patients, and it can predict inactive disease and spontaneous HBsAg seroclearance in HBeAg-negative patients. The determination of HBsAg level is pivotal to individualize pegylated interferon (PegIFN) treatment; it is the key investigation to decide early termination of PegIFN among non-responders. Among patients treated by nucleos(t)ide analogues, responders tend to have dramatic reduction of HBsAg to low levels, which may be followed by HBsAg seroclearance. With newer data on combination treatment of PegIFN and nucleos(t)ide analogues as well as emerging new antiviral agents, HBsAg quantification is expected to become increasingly important to monitor and guide antiviral therapy for chronic hepatitis B. |
doi_str_mv | 10.1016/j.jhep.2016.08.009 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1837287312</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S016882781630441X</els_id><sourcerecordid>2078811858</sourcerecordid><originalsourceid>FETCH-LOGICAL-c505t-714e935555f374ed9e974c92652946878f5b00d706e873279a2e206fad5501a93</originalsourceid><addsrcrecordid>eNp9kUFr3DAQhUVpabZJ_0APxdBLL3ZnJMuSoATS0DaFQA9JoTehyONGrtfeSPZC_n1lNs0hh8xlBua9h_QNY-8QKgRsPvVVf0u7iue5Al0BmBdsgw1ACU2NL9kmL3SpudJH7E1KPQAIMPVrdsSVVFIgbtjp9S0VcRqomLribnHjHGY3hz0VOToPc0jFlyItsXOeinX9h8Yi0j6kMFN7wl51bkj09qEfs1_fvl6fX5SXP7__OD-7LL0EOZcKazJC5uqEqqk1ZFTtDW8kN3Wjle7kDUCroCGtBFfGceLQdK6VEtAZccw-HnJ3cbpbKM12G5KnYXAjTUuyqIXi2Yo8Sz88kfbTEsf8OstBaY2opc4qflD5OKUUqbO7GLYu3lsEu9K1vV3p2pWuBW0z3Wx6_xC93GypfbT8x5kFnw8Cyiz2gaJNPtDoqQ2R_GzbKTyff_rE7ocwBu-Gv3RP6fEfaBO3YK_W-67nxUZAXeNv8Q969J1D</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2078811858</pqid></control><display><type>article</type><title>The role of quantitative hepatitis B surface antigen revisited</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Cornberg, Markus ; Wong, Vincent Wai-Sun ; Locarnini, Stephen ; Brunetto, Maurizia ; Janssen, Harry L.A ; Chan, Henry Lik-Yuen</creator><creatorcontrib>Cornberg, Markus ; Wong, Vincent Wai-Sun ; Locarnini, Stephen ; Brunetto, Maurizia ; Janssen, Harry L.A ; Chan, Henry Lik-Yuen</creatorcontrib><description>Summary In the past 10 years, there has been a lot of enthusiasm surrounding the use of serum hepatitis B surface antigen (HBsAg) quantification to predict disease activity and monitor treatment response in chronic hepatitis B. The measurement of HBsAg levels have been standardized in IU/ml, and nowadays it is almost a mandatory measurement due to the development of new antiviral treatments aiming at HBsAg seroclearance, i.e., functional cure of hepatitis B. Recently, there has been an improved understanding of the molecular virology of HBsAg, and particularly the relative roles of covalently closed circular DNA and integrated hepatitis B virus (HBV) DNA. This has shed new light on the interpretation of HBsAg levels in different phases of chronic hepatitis B. HBsAg level can assist the differentiation of immune tolerance and immune clearance in hepatitis B e antigen (HBeAg)-positive patients, and it can predict inactive disease and spontaneous HBsAg seroclearance in HBeAg-negative patients. The determination of HBsAg level is pivotal to individualize pegylated interferon (PegIFN) treatment; it is the key investigation to decide early termination of PegIFN among non-responders. Among patients treated by nucleos(t)ide analogues, responders tend to have dramatic reduction of HBsAg to low levels, which may be followed by HBsAg seroclearance. With newer data on combination treatment of PegIFN and nucleos(t)ide analogues as well as emerging new antiviral agents, HBsAg quantification is expected to become increasingly important to monitor and guide antiviral therapy for chronic hepatitis B.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2016.08.009</identifier><identifier>PMID: 27575311</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Antigens ; Antiviral agents ; Antiviral drugs ; Antiviral treatment ; Circular DNA ; Deoxyribonucleic acid ; Disease Management ; DNA ; Entecavir ; Gastroenterology and Hepatology ; HBsAg ; Hepatitis ; Hepatitis B ; Hepatitis B e antigen ; Hepatitis B e Antigens - analysis ; Hepatitis B surface antigen ; Hepatitis B Surface Antigens - analysis ; Hepatitis B virus - physiology ; Hepatitis B, Chronic - immunology ; Hepatitis B, Chronic - virology ; Humans ; Immune clearance ; Immunological tolerance ; Interferon ; Patients ; Pegylated interferon ; Serologic Tests - methods ; Tenofovir</subject><ispartof>Journal of hepatology, 2017-02, Vol.66 (2), p.398-411</ispartof><rights>European Association for the Study of the Liver</rights><rights>2016 European Association for the Study of the Liver</rights><rights>Copyright © 2016 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><rights>Copyright Elsevier Science Ltd. Feb 2017</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c505t-714e935555f374ed9e974c92652946878f5b00d706e873279a2e206fad5501a93</citedby><cites>FETCH-LOGICAL-c505t-714e935555f374ed9e974c92652946878f5b00d706e873279a2e206fad5501a93</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S016882781630441X$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/27575311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cornberg, Markus</creatorcontrib><creatorcontrib>Wong, Vincent Wai-Sun</creatorcontrib><creatorcontrib>Locarnini, Stephen</creatorcontrib><creatorcontrib>Brunetto, Maurizia</creatorcontrib><creatorcontrib>Janssen, Harry L.A</creatorcontrib><creatorcontrib>Chan, Henry Lik-Yuen</creatorcontrib><title>The role of quantitative hepatitis B surface antigen revisited</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>Summary In the past 10 years, there has been a lot of enthusiasm surrounding the use of serum hepatitis B surface antigen (HBsAg) quantification to predict disease activity and monitor treatment response in chronic hepatitis B. The measurement of HBsAg levels have been standardized in IU/ml, and nowadays it is almost a mandatory measurement due to the development of new antiviral treatments aiming at HBsAg seroclearance, i.e., functional cure of hepatitis B. Recently, there has been an improved understanding of the molecular virology of HBsAg, and particularly the relative roles of covalently closed circular DNA and integrated hepatitis B virus (HBV) DNA. This has shed new light on the interpretation of HBsAg levels in different phases of chronic hepatitis B. HBsAg level can assist the differentiation of immune tolerance and immune clearance in hepatitis B e antigen (HBeAg)-positive patients, and it can predict inactive disease and spontaneous HBsAg seroclearance in HBeAg-negative patients. The determination of HBsAg level is pivotal to individualize pegylated interferon (PegIFN) treatment; it is the key investigation to decide early termination of PegIFN among non-responders. Among patients treated by nucleos(t)ide analogues, responders tend to have dramatic reduction of HBsAg to low levels, which may be followed by HBsAg seroclearance. With newer data on combination treatment of PegIFN and nucleos(t)ide analogues as well as emerging new antiviral agents, HBsAg quantification is expected to become increasingly important to monitor and guide antiviral therapy for chronic hepatitis B.</description><subject>Antigens</subject><subject>Antiviral agents</subject><subject>Antiviral drugs</subject><subject>Antiviral treatment</subject><subject>Circular DNA</subject><subject>Deoxyribonucleic acid</subject><subject>Disease Management</subject><subject>DNA</subject><subject>Entecavir</subject><subject>Gastroenterology and Hepatology</subject><subject>HBsAg</subject><subject>Hepatitis</subject><subject>Hepatitis B</subject><subject>Hepatitis B e antigen</subject><subject>Hepatitis B e Antigens - analysis</subject><subject>Hepatitis B surface antigen</subject><subject>Hepatitis B Surface Antigens - analysis</subject><subject>Hepatitis B virus - physiology</subject><subject>Hepatitis B, Chronic - immunology</subject><subject>Hepatitis B, Chronic - virology</subject><subject>Humans</subject><subject>Immune clearance</subject><subject>Immunological tolerance</subject><subject>Interferon</subject><subject>Patients</subject><subject>Pegylated interferon</subject><subject>Serologic Tests - methods</subject><subject>Tenofovir</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUFr3DAQhUVpabZJ_0APxdBLL3ZnJMuSoATS0DaFQA9JoTehyONGrtfeSPZC_n1lNs0hh8xlBua9h_QNY-8QKgRsPvVVf0u7iue5Al0BmBdsgw1ACU2NL9kmL3SpudJH7E1KPQAIMPVrdsSVVFIgbtjp9S0VcRqomLribnHjHGY3hz0VOToPc0jFlyItsXOeinX9h8Yi0j6kMFN7wl51bkj09qEfs1_fvl6fX5SXP7__OD-7LL0EOZcKazJC5uqEqqk1ZFTtDW8kN3Wjle7kDUCroCGtBFfGceLQdK6VEtAZccw-HnJ3cbpbKM12G5KnYXAjTUuyqIXi2Yo8Sz88kfbTEsf8OstBaY2opc4qflD5OKUUqbO7GLYu3lsEu9K1vV3p2pWuBW0z3Wx6_xC93GypfbT8x5kFnw8Cyiz2gaJNPtDoqQ2R_GzbKTyff_rE7ocwBu-Gv3RP6fEfaBO3YK_W-67nxUZAXeNv8Q969J1D</recordid><startdate>20170201</startdate><enddate>20170201</enddate><creator>Cornberg, Markus</creator><creator>Wong, Vincent Wai-Sun</creator><creator>Locarnini, Stephen</creator><creator>Brunetto, Maurizia</creator><creator>Janssen, Harry L.A</creator><creator>Chan, Henry Lik-Yuen</creator><general>Elsevier B.V</general><general>Elsevier Science Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7T5</scope><scope>H94</scope><scope>7X8</scope></search><sort><creationdate>20170201</creationdate><title>The role of quantitative hepatitis B surface antigen revisited</title><author>Cornberg, Markus ; Wong, Vincent Wai-Sun ; Locarnini, Stephen ; Brunetto, Maurizia ; Janssen, Harry L.A ; Chan, Henry Lik-Yuen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c505t-714e935555f374ed9e974c92652946878f5b00d706e873279a2e206fad5501a93</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Antigens</topic><topic>Antiviral agents</topic><topic>Antiviral drugs</topic><topic>Antiviral treatment</topic><topic>Circular DNA</topic><topic>Deoxyribonucleic acid</topic><topic>Disease Management</topic><topic>DNA</topic><topic>Entecavir</topic><topic>Gastroenterology and Hepatology</topic><topic>HBsAg</topic><topic>Hepatitis</topic><topic>Hepatitis B</topic><topic>Hepatitis B e antigen</topic><topic>Hepatitis B e Antigens - analysis</topic><topic>Hepatitis B surface antigen</topic><topic>Hepatitis B Surface Antigens - analysis</topic><topic>Hepatitis B virus - physiology</topic><topic>Hepatitis B, Chronic - immunology</topic><topic>Hepatitis B, Chronic - virology</topic><topic>Humans</topic><topic>Immune clearance</topic><topic>Immunological tolerance</topic><topic>Interferon</topic><topic>Patients</topic><topic>Pegylated interferon</topic><topic>Serologic Tests - methods</topic><topic>Tenofovir</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cornberg, Markus</creatorcontrib><creatorcontrib>Wong, Vincent Wai-Sun</creatorcontrib><creatorcontrib>Locarnini, Stephen</creatorcontrib><creatorcontrib>Brunetto, Maurizia</creatorcontrib><creatorcontrib>Janssen, Harry L.A</creatorcontrib><creatorcontrib>Chan, Henry Lik-Yuen</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cornberg, Markus</au><au>Wong, Vincent Wai-Sun</au><au>Locarnini, Stephen</au><au>Brunetto, Maurizia</au><au>Janssen, Harry L.A</au><au>Chan, Henry Lik-Yuen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The role of quantitative hepatitis B surface antigen revisited</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2017-02-01</date><risdate>2017</risdate><volume>66</volume><issue>2</issue><spage>398</spage><epage>411</epage><pages>398-411</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><abstract>Summary In the past 10 years, there has been a lot of enthusiasm surrounding the use of serum hepatitis B surface antigen (HBsAg) quantification to predict disease activity and monitor treatment response in chronic hepatitis B. The measurement of HBsAg levels have been standardized in IU/ml, and nowadays it is almost a mandatory measurement due to the development of new antiviral treatments aiming at HBsAg seroclearance, i.e., functional cure of hepatitis B. Recently, there has been an improved understanding of the molecular virology of HBsAg, and particularly the relative roles of covalently closed circular DNA and integrated hepatitis B virus (HBV) DNA. This has shed new light on the interpretation of HBsAg levels in different phases of chronic hepatitis B. HBsAg level can assist the differentiation of immune tolerance and immune clearance in hepatitis B e antigen (HBeAg)-positive patients, and it can predict inactive disease and spontaneous HBsAg seroclearance in HBeAg-negative patients. The determination of HBsAg level is pivotal to individualize pegylated interferon (PegIFN) treatment; it is the key investigation to decide early termination of PegIFN among non-responders. Among patients treated by nucleos(t)ide analogues, responders tend to have dramatic reduction of HBsAg to low levels, which may be followed by HBsAg seroclearance. With newer data on combination treatment of PegIFN and nucleos(t)ide analogues as well as emerging new antiviral agents, HBsAg quantification is expected to become increasingly important to monitor and guide antiviral therapy for chronic hepatitis B.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>27575311</pmid><doi>10.1016/j.jhep.2016.08.009</doi><tpages>14</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0168-8278 |
ispartof | Journal of hepatology, 2017-02, Vol.66 (2), p.398-411 |
issn | 0168-8278 1600-0641 |
language | eng |
recordid | cdi_proquest_miscellaneous_1837287312 |
source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | Antigens Antiviral agents Antiviral drugs Antiviral treatment Circular DNA Deoxyribonucleic acid Disease Management DNA Entecavir Gastroenterology and Hepatology HBsAg Hepatitis Hepatitis B Hepatitis B e antigen Hepatitis B e Antigens - analysis Hepatitis B surface antigen Hepatitis B Surface Antigens - analysis Hepatitis B virus - physiology Hepatitis B, Chronic - immunology Hepatitis B, Chronic - virology Humans Immune clearance Immunological tolerance Interferon Patients Pegylated interferon Serologic Tests - methods Tenofovir |
title | The role of quantitative hepatitis B surface antigen revisited |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-08T12%3A51%3A46IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=The%20role%20of%20quantitative%20hepatitis%20B%20surface%20antigen%20revisited&rft.jtitle=Journal%20of%20hepatology&rft.au=Cornberg,%20Markus&rft.date=2017-02-01&rft.volume=66&rft.issue=2&rft.spage=398&rft.epage=411&rft.pages=398-411&rft.issn=0168-8278&rft.eissn=1600-0641&rft_id=info:doi/10.1016/j.jhep.2016.08.009&rft_dat=%3Cproquest_cross%3E2078811858%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2078811858&rft_id=info:pmid/27575311&rft_els_id=S016882781630441X&rfr_iscdi=true |