Hepatitis B e Antigen-Positive Chronic Hepatitis B: Natural History and Treatment
ABSTRACT The natural history of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B is very heterogeneous. Age at acquisition is a major factor in determining the natural history of chronic infection. The vigor of the host immune response to the virus, viral factors (genotype, core promoter m...
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Veröffentlicht in: | Seminars in liver disease 2006-05, Vol.26 (2), p.116-129 |
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creator | Feld, Jordan J Heathcote, E. Jenny |
description | ABSTRACT
The natural history of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B is very heterogeneous. Age at acquisition is a major factor in determining the natural history of chronic infection. The vigor of the host immune response to the virus, viral factors (genotype, core promoter mutations, and duration of viral replication) as well as exogenous factors (alcohol, immune suppression) all influence the severity of disease. The goal of antiviral therapy is HBeAg seroconversion, and preferably HB surface Ag seroconversion as this latter end-point is associated with sustained immune control and the halting of disease progression. Although peginterferon is now considered as the first line of therapy for HBeAg-positive chronic hepatitis B, in most cases there are circumstances where nucleos(t)ide analogues are indicated (e.g., decompensated liver disease) for those requiring cancer chemotherapy/other immunosuppressive agents and for those with contraindications to interferon. The major challenge for the clinician using these agents is the emergence of antiviral drug resistance. Long-term immune control of viral replication is key to improving patient outcome. |
doi_str_mv | 10.1055/s-2006-939750 |
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The natural history of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B is very heterogeneous. Age at acquisition is a major factor in determining the natural history of chronic infection. The vigor of the host immune response to the virus, viral factors (genotype, core promoter mutations, and duration of viral replication) as well as exogenous factors (alcohol, immune suppression) all influence the severity of disease. The goal of antiviral therapy is HBeAg seroconversion, and preferably HB surface Ag seroconversion as this latter end-point is associated with sustained immune control and the halting of disease progression. Although peginterferon is now considered as the first line of therapy for HBeAg-positive chronic hepatitis B, in most cases there are circumstances where nucleos(t)ide analogues are indicated (e.g., decompensated liver disease) for those requiring cancer chemotherapy/other immunosuppressive agents and for those with contraindications to interferon. The major challenge for the clinician using these agents is the emergence of antiviral drug resistance. Long-term immune control of viral replication is key to improving patient outcome.</description><identifier>ISSN: 0272-8087</identifier><identifier>EISSN: 1098-8971</identifier><identifier>DOI: 10.1055/s-2006-939750</identifier><identifier>PMID: 16673290</identifier><language>eng</language><publisher>United States</publisher><subject>Antiviral Agents - therapeutic use ; Disease Progression ; Hepatitis B Surface Antigens - immunology ; Hepatitis B virus - immunology ; Hepatitis B, Chronic - drug therapy ; Hepatitis B, Chronic - immunology ; Hepatitis B, Chronic - virology ; Humans ; Risk Factors ; Treatment Outcome</subject><ispartof>Seminars in liver disease, 2006-05, Vol.26 (2), p.116-129</ispartof><rights>Copyright © 2006 by Thieme Medical Publishers, Inc., 333 Seventh Avenue, New York, NY 10001, USA.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c328t-98c304defa6ff85f78e78aea1d83c88d743f7d789916a27e5e70d8f8bbf324f63</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.thieme-connect.de/products/ejournals/pdf/10.1055/s-2006-939750.pdf$$EPDF$$P50$$Gthieme$$H</linktopdf><linktohtml>$$Uhttps://www.thieme-connect.de/products/ejournals/html/10.1055/s-2006-939750$$EHTML$$P50$$Gthieme$$H</linktohtml><link.rule.ids>314,776,780,3004,3005,27901,27902,54534,54535</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16673290$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Feld, Jordan J</creatorcontrib><creatorcontrib>Heathcote, E. Jenny</creatorcontrib><title>Hepatitis B e Antigen-Positive Chronic Hepatitis B: Natural History and Treatment</title><title>Seminars in liver disease</title><addtitle>Semin Liver Dis</addtitle><description>ABSTRACT
The natural history of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B is very heterogeneous. Age at acquisition is a major factor in determining the natural history of chronic infection. The vigor of the host immune response to the virus, viral factors (genotype, core promoter mutations, and duration of viral replication) as well as exogenous factors (alcohol, immune suppression) all influence the severity of disease. The goal of antiviral therapy is HBeAg seroconversion, and preferably HB surface Ag seroconversion as this latter end-point is associated with sustained immune control and the halting of disease progression. Although peginterferon is now considered as the first line of therapy for HBeAg-positive chronic hepatitis B, in most cases there are circumstances where nucleos(t)ide analogues are indicated (e.g., decompensated liver disease) for those requiring cancer chemotherapy/other immunosuppressive agents and for those with contraindications to interferon. The major challenge for the clinician using these agents is the emergence of antiviral drug resistance. Long-term immune control of viral replication is key to improving patient outcome.</description><subject>Antiviral Agents - therapeutic use</subject><subject>Disease Progression</subject><subject>Hepatitis B Surface Antigens - immunology</subject><subject>Hepatitis B virus - immunology</subject><subject>Hepatitis B, Chronic - drug therapy</subject><subject>Hepatitis B, Chronic - immunology</subject><subject>Hepatitis B, Chronic - virology</subject><subject>Humans</subject><subject>Risk Factors</subject><subject>Treatment Outcome</subject><issn>0272-8087</issn><issn>1098-8971</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M1LwzAYx_EgipsvR6-SkyejT5q2SbzNoU4YvsA8h6x94jrWdiapsP_ejg304ikQPvzg-RJyweGGQ5bdBpYA5EwLLTM4IEMOWjGlJT8kQ0hkwhQoOSAnISwBINEpHJMBz3MpEg1D8j7BtY1VrAK9p0hHTaw-sWFvbej_vpGOF75tqoL-YXf0xcbO2xWdVCG2fkNtU9KZRxtrbOIZOXJ2FfB8_56Sj8eH2XjCpq9Pz-PRlBUiUZFpVQhIS3Q2d05lTiqUyqLlpRKFUqVMhZOlVFrz3CYSM5RQKqfmcyeS1OXilFztdte-_eowRFNXocDVyjbYdsHkUgsAnvaQ7WDh2xA8OrP2VW39xnAw24YmmG1Ds2vY-8v9cDevsfzV-2g9uN6BuKiwRrNsO9_0p_6z9wPDTXoA</recordid><startdate>200605</startdate><enddate>200605</enddate><creator>Feld, Jordan J</creator><creator>Heathcote, E. Jenny</creator><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>7X8</scope></search><sort><creationdate>200605</creationdate><title>Hepatitis B e Antigen-Positive Chronic Hepatitis B: Natural History and Treatment</title><author>Feld, Jordan J ; Heathcote, E. Jenny</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c328t-98c304defa6ff85f78e78aea1d83c88d743f7d789916a27e5e70d8f8bbf324f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Antiviral Agents - therapeutic use</topic><topic>Disease Progression</topic><topic>Hepatitis B Surface Antigens - immunology</topic><topic>Hepatitis B virus - immunology</topic><topic>Hepatitis B, Chronic - drug therapy</topic><topic>Hepatitis B, Chronic - immunology</topic><topic>Hepatitis B, Chronic - virology</topic><topic>Humans</topic><topic>Risk Factors</topic><topic>Treatment Outcome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Feld, Jordan J</creatorcontrib><creatorcontrib>Heathcote, E. Jenny</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Seminars in liver disease</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Feld, Jordan J</au><au>Heathcote, E. Jenny</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis B e Antigen-Positive Chronic Hepatitis B: Natural History and Treatment</atitle><jtitle>Seminars in liver disease</jtitle><addtitle>Semin Liver Dis</addtitle><date>2006-05</date><risdate>2006</risdate><volume>26</volume><issue>2</issue><spage>116</spage><epage>129</epage><pages>116-129</pages><issn>0272-8087</issn><eissn>1098-8971</eissn><abstract>ABSTRACT
The natural history of hepatitis B e antigen (HBeAg)-positive chronic hepatitis B is very heterogeneous. Age at acquisition is a major factor in determining the natural history of chronic infection. The vigor of the host immune response to the virus, viral factors (genotype, core promoter mutations, and duration of viral replication) as well as exogenous factors (alcohol, immune suppression) all influence the severity of disease. The goal of antiviral therapy is HBeAg seroconversion, and preferably HB surface Ag seroconversion as this latter end-point is associated with sustained immune control and the halting of disease progression. Although peginterferon is now considered as the first line of therapy for HBeAg-positive chronic hepatitis B, in most cases there are circumstances where nucleos(t)ide analogues are indicated (e.g., decompensated liver disease) for those requiring cancer chemotherapy/other immunosuppressive agents and for those with contraindications to interferon. The major challenge for the clinician using these agents is the emergence of antiviral drug resistance. Long-term immune control of viral replication is key to improving patient outcome.</abstract><cop>United States</cop><pmid>16673290</pmid><doi>10.1055/s-2006-939750</doi><tpages>14</tpages></addata></record> |
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subjects | Antiviral Agents - therapeutic use Disease Progression Hepatitis B Surface Antigens - immunology Hepatitis B virus - immunology Hepatitis B, Chronic - drug therapy Hepatitis B, Chronic - immunology Hepatitis B, Chronic - virology Humans Risk Factors Treatment Outcome |
title | Hepatitis B e Antigen-Positive Chronic Hepatitis B: Natural History and Treatment |
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