The kinetics of the hepatitis B surface antigen level after the initiation of antiretroviral therapy for hepatitis B virus and human immunodeficiency virus coinfected patients
Abstract Background Hepatic flares (HF), which reflect hepatitis B virus (HBV)-related immune reconstitution inflammatory syndrome (IRIS), frequently occur in patients with HBV and human immunodeficiency virus (HIV) coinfection after the start of antiretoroviral therapy (ART). The rate of hepatitis...
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Veröffentlicht in: | Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy 2015-04, Vol.21 (4), p.264-271 |
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creator | Mitsumoto, Fujiko Murata, Masayuki Ura, Kazuya Takayama, Koji Hiramine, Satoshi Shimizu, Motohiro Toyoda, Kazuhiro Ogawa, Eiichi Furusyo, Norihiro Hayashi, Jun |
description | Abstract Background Hepatic flares (HF), which reflect hepatitis B virus (HBV)-related immune reconstitution inflammatory syndrome (IRIS), frequently occur in patients with HBV and human immunodeficiency virus (HIV) coinfection after the start of antiretoroviral therapy (ART). The rate of hepatitis B envelope antigen (HBeAg) and hepatitis B surface antigen (HBsAg) loss is higher for patients with HF after the initiation of ART. Methods We retrospectively examined the kinetics of the HBsAg and HBeAg levels of six HBV/HIV coinfected patients after the commencement of ART that included tenofovir. All were male and HBeAg positive. Results Three patients developed HF after the initiation of ART. All subsequently lost HBeAg and one of them lost HBsAg after HF. None who did not experience HF lost HBeAg. The HBsAg and HBeAg levels remarkably decreased when HF occurred, but the decline of HBsAg was very slow in the periods before and after HF. The median decline of the HBsAg level at 48 weeks was 2.20 Log IU/mL for patients with HF, but only 1.00 Log IU/ml for patients without HF. Little decline was seen for either group in the median decline of the HBsAg level from 48 weeks to 96 weeks, 0.28 Log IU/mL in the HF group and 0.06 Log IU/mL in the non-HF group. Conclusion The immune reconstitution of a HBV/HIV coinfected patient plays an important role in the clearance of HBV. If HBsAg and HBeAg levels decrease rapidly when HF occurs, the hepatic flare would be due to HBV-related IRIS. |
doi_str_mv | 10.1016/j.jiac.2014.12.003 |
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The rate of hepatitis B envelope antigen (HBeAg) and hepatitis B surface antigen (HBsAg) loss is higher for patients with HF after the initiation of ART. Methods We retrospectively examined the kinetics of the HBsAg and HBeAg levels of six HBV/HIV coinfected patients after the commencement of ART that included tenofovir. All were male and HBeAg positive. Results Three patients developed HF after the initiation of ART. All subsequently lost HBeAg and one of them lost HBsAg after HF. None who did not experience HF lost HBeAg. The HBsAg and HBeAg levels remarkably decreased when HF occurred, but the decline of HBsAg was very slow in the periods before and after HF. The median decline of the HBsAg level at 48 weeks was 2.20 Log IU/mL for patients with HF, but only 1.00 Log IU/ml for patients without HF. Little decline was seen for either group in the median decline of the HBsAg level from 48 weeks to 96 weeks, 0.28 Log IU/mL in the HF group and 0.06 Log IU/mL in the non-HF group. Conclusion The immune reconstitution of a HBV/HIV coinfected patient plays an important role in the clearance of HBV. If HBsAg and HBeAg levels decrease rapidly when HF occurs, the hepatic flare would be due to HBV-related IRIS.</description><identifier>ISSN: 1341-321X</identifier><identifier>EISSN: 1437-7780</identifier><identifier>DOI: 10.1016/j.jiac.2014.12.003</identifier><identifier>PMID: 25596071</identifier><language>eng</language><publisher>Netherlands: Elsevier Ltd</publisher><subject>Adult ; Anti-Retroviral Agents - administration & dosage ; Anti-Retroviral Agents - pharmacology ; Anti-Retroviral Agents - therapeutic use ; Coinfection - drug therapy ; Coinfection - epidemiology ; Coinfection - virology ; DNA, Viral - blood ; Female ; Hematology, Oncology and Palliative Medicine ; Hepatitis B - complications ; Hepatitis B - drug therapy ; Hepatitis B - epidemiology ; Hepatitis B - virology ; Hepatitis B e Antigens - blood ; Hepatitis B surface antigen ; Hepatitis B Surface Antigens - blood ; Hepatitis B virus ; HIV Infections - drug therapy ; HIV Infections - epidemiology ; Human immunodeficiency virus ; Humans ; Immune Reconstitution Inflammatory Syndrome ; Kinetics ; Male ; Middle Aged ; Retrospective Studies ; RNA, Viral - blood ; Tenofovir - administration & dosage ; Tenofovir - pharmacology ; Tenofovir - therapeutic use ; Viral Load ; Young Adult</subject><ispartof>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy, 2015-04, Vol.21 (4), p.264-271</ispartof><rights>Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases</rights><rights>2014 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases</rights><rights>Copyright © 2014 Japanese Society of Chemotherapy and The Japanese Association for Infectious Diseases. Published by Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c604t-6004bd48c6d9ea576eb57cc19361382bd690d1d41b7740d5e1a84a2a0ced432e3</citedby><cites>FETCH-LOGICAL-c604t-6004bd48c6d9ea576eb57cc19361382bd690d1d41b7740d5e1a84a2a0ced432e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>315,781,785,27929,27930</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25596071$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mitsumoto, Fujiko</creatorcontrib><creatorcontrib>Murata, Masayuki</creatorcontrib><creatorcontrib>Ura, Kazuya</creatorcontrib><creatorcontrib>Takayama, Koji</creatorcontrib><creatorcontrib>Hiramine, Satoshi</creatorcontrib><creatorcontrib>Shimizu, Motohiro</creatorcontrib><creatorcontrib>Toyoda, Kazuhiro</creatorcontrib><creatorcontrib>Ogawa, Eiichi</creatorcontrib><creatorcontrib>Furusyo, Norihiro</creatorcontrib><creatorcontrib>Hayashi, Jun</creatorcontrib><title>The kinetics of the hepatitis B surface antigen level after the initiation of antiretroviral therapy for hepatitis B virus and human immunodeficiency virus coinfected patients</title><title>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</title><addtitle>J Infect Chemother</addtitle><description>Abstract Background Hepatic flares (HF), which reflect hepatitis B virus (HBV)-related immune reconstitution inflammatory syndrome (IRIS), frequently occur in patients with HBV and human immunodeficiency virus (HIV) coinfection after the start of antiretoroviral therapy (ART). The rate of hepatitis B envelope antigen (HBeAg) and hepatitis B surface antigen (HBsAg) loss is higher for patients with HF after the initiation of ART. Methods We retrospectively examined the kinetics of the HBsAg and HBeAg levels of six HBV/HIV coinfected patients after the commencement of ART that included tenofovir. All were male and HBeAg positive. Results Three patients developed HF after the initiation of ART. All subsequently lost HBeAg and one of them lost HBsAg after HF. None who did not experience HF lost HBeAg. The HBsAg and HBeAg levels remarkably decreased when HF occurred, but the decline of HBsAg was very slow in the periods before and after HF. The median decline of the HBsAg level at 48 weeks was 2.20 Log IU/mL for patients with HF, but only 1.00 Log IU/ml for patients without HF. Little decline was seen for either group in the median decline of the HBsAg level from 48 weeks to 96 weeks, 0.28 Log IU/mL in the HF group and 0.06 Log IU/mL in the non-HF group. Conclusion The immune reconstitution of a HBV/HIV coinfected patient plays an important role in the clearance of HBV. If HBsAg and HBeAg levels decrease rapidly when HF occurs, the hepatic flare would be due to HBV-related IRIS.</description><subject>Adult</subject><subject>Anti-Retroviral Agents - administration & dosage</subject><subject>Anti-Retroviral Agents - pharmacology</subject><subject>Anti-Retroviral Agents - therapeutic use</subject><subject>Coinfection - drug therapy</subject><subject>Coinfection - epidemiology</subject><subject>Coinfection - virology</subject><subject>DNA, Viral - blood</subject><subject>Female</subject><subject>Hematology, Oncology and Palliative Medicine</subject><subject>Hepatitis B - complications</subject><subject>Hepatitis B - drug therapy</subject><subject>Hepatitis B - epidemiology</subject><subject>Hepatitis B - virology</subject><subject>Hepatitis B e Antigens - blood</subject><subject>Hepatitis B surface antigen</subject><subject>Hepatitis B Surface Antigens - blood</subject><subject>Hepatitis B virus</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - epidemiology</subject><subject>Human immunodeficiency virus</subject><subject>Humans</subject><subject>Immune Reconstitution Inflammatory Syndrome</subject><subject>Kinetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Retrospective Studies</subject><subject>RNA, Viral - blood</subject><subject>Tenofovir - administration & dosage</subject><subject>Tenofovir - pharmacology</subject><subject>Tenofovir - therapeutic use</subject><subject>Viral Load</subject><subject>Young Adult</subject><issn>1341-321X</issn><issn>1437-7780</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkk2L1TAUhosozof-AReSpZvWnDZNekEEHXQUBlw4gruQJqfedNrkmqQX7q_yL5rOvQq60FUS8rxn8T6nKJ4BrYACfzlWo1W6qimwCuqK0uZBcQ6sEaUQHX2Y7w2Dsqnh61lxEeNIKYi26x4XZ3XbbjgVcF78uN0iubMOk9WR-IGk_N7iTiWbbCRvSVzCoDQS5ZL9ho5MuMeJqCFhuGety2CmvVvTKxUwBb-3QU0rENTuQAYf_hiaf5eYYUO2y6wcsfO8OG9wsNqi04cToL11A-qEhqxZdCk-KR4Naor49HReFl_ev7u9-lDefLr-ePXmptScslRySllvWKe52aBqBce-FVrDpuHQdHVv-IYaMAx6IRg1LYLqmKoV1WhYU2NzWbw4zt0F_33BmORso8ZpUg79EiV0tOMdbaj4P8o5Y6xuOc1ofUR18DEGHOQu2FmFgwQqV6dylKtTuTqVUMvsNIeen-Yv_Yzmd-SXxAy8OgKYC9lbDDLe14gmu9BJGm__Pf_1X3E9ZataTXd4wDj6JbhctQQZc0B-XrdqXSpguWQQvPkJ_y7LZA</recordid><startdate>20150401</startdate><enddate>20150401</enddate><creator>Mitsumoto, Fujiko</creator><creator>Murata, Masayuki</creator><creator>Ura, Kazuya</creator><creator>Takayama, Koji</creator><creator>Hiramine, Satoshi</creator><creator>Shimizu, Motohiro</creator><creator>Toyoda, Kazuhiro</creator><creator>Ogawa, Eiichi</creator><creator>Furusyo, Norihiro</creator><creator>Hayashi, Jun</creator><general>Elsevier 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>7X8</scope><scope>7T5</scope><scope>7U9</scope><scope>H94</scope></search><sort><creationdate>20150401</creationdate><title>The kinetics of the hepatitis B surface antigen level after the initiation of antiretroviral therapy for hepatitis B virus and human immunodeficiency virus coinfected patients</title><author>Mitsumoto, Fujiko ; Murata, Masayuki ; Ura, Kazuya ; Takayama, Koji ; Hiramine, Satoshi ; Shimizu, Motohiro ; Toyoda, Kazuhiro ; Ogawa, Eiichi ; Furusyo, Norihiro ; Hayashi, Jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c604t-6004bd48c6d9ea576eb57cc19361382bd690d1d41b7740d5e1a84a2a0ced432e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Adult</topic><topic>Anti-Retroviral Agents - administration & dosage</topic><topic>Anti-Retroviral Agents - pharmacology</topic><topic>Anti-Retroviral Agents - therapeutic use</topic><topic>Coinfection - drug therapy</topic><topic>Coinfection - epidemiology</topic><topic>Coinfection - virology</topic><topic>DNA, Viral - blood</topic><topic>Female</topic><topic>Hematology, Oncology and Palliative Medicine</topic><topic>Hepatitis B - complications</topic><topic>Hepatitis B - drug therapy</topic><topic>Hepatitis B - epidemiology</topic><topic>Hepatitis B - virology</topic><topic>Hepatitis B e Antigens - blood</topic><topic>Hepatitis B surface antigen</topic><topic>Hepatitis B Surface Antigens - blood</topic><topic>Hepatitis B virus</topic><topic>HIV Infections - drug therapy</topic><topic>HIV Infections - epidemiology</topic><topic>Human immunodeficiency virus</topic><topic>Humans</topic><topic>Immune Reconstitution Inflammatory Syndrome</topic><topic>Kinetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Retrospective Studies</topic><topic>RNA, Viral - blood</topic><topic>Tenofovir - administration & dosage</topic><topic>Tenofovir - pharmacology</topic><topic>Tenofovir - therapeutic use</topic><topic>Viral Load</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mitsumoto, Fujiko</creatorcontrib><creatorcontrib>Murata, Masayuki</creatorcontrib><creatorcontrib>Ura, Kazuya</creatorcontrib><creatorcontrib>Takayama, Koji</creatorcontrib><creatorcontrib>Hiramine, Satoshi</creatorcontrib><creatorcontrib>Shimizu, Motohiro</creatorcontrib><creatorcontrib>Toyoda, Kazuhiro</creatorcontrib><creatorcontrib>Ogawa, Eiichi</creatorcontrib><creatorcontrib>Furusyo, Norihiro</creatorcontrib><creatorcontrib>Hayashi, Jun</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><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Mitsumoto, Fujiko</au><au>Murata, Masayuki</au><au>Ura, Kazuya</au><au>Takayama, Koji</au><au>Hiramine, Satoshi</au><au>Shimizu, Motohiro</au><au>Toyoda, Kazuhiro</au><au>Ogawa, Eiichi</au><au>Furusyo, Norihiro</au><au>Hayashi, Jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The kinetics of the hepatitis B surface antigen level after the initiation of antiretroviral therapy for hepatitis B virus and human immunodeficiency virus coinfected patients</atitle><jtitle>Journal of infection and chemotherapy : official journal of the Japan Society of Chemotherapy</jtitle><addtitle>J Infect Chemother</addtitle><date>2015-04-01</date><risdate>2015</risdate><volume>21</volume><issue>4</issue><spage>264</spage><epage>271</epage><pages>264-271</pages><issn>1341-321X</issn><eissn>1437-7780</eissn><abstract>Abstract Background Hepatic flares (HF), which reflect hepatitis B virus (HBV)-related immune reconstitution inflammatory syndrome (IRIS), frequently occur in patients with HBV and human immunodeficiency virus (HIV) coinfection after the start of antiretoroviral therapy (ART). The rate of hepatitis B envelope antigen (HBeAg) and hepatitis B surface antigen (HBsAg) loss is higher for patients with HF after the initiation of ART. Methods We retrospectively examined the kinetics of the HBsAg and HBeAg levels of six HBV/HIV coinfected patients after the commencement of ART that included tenofovir. All were male and HBeAg positive. Results Three patients developed HF after the initiation of ART. All subsequently lost HBeAg and one of them lost HBsAg after HF. None who did not experience HF lost HBeAg. The HBsAg and HBeAg levels remarkably decreased when HF occurred, but the decline of HBsAg was very slow in the periods before and after HF. The median decline of the HBsAg level at 48 weeks was 2.20 Log IU/mL for patients with HF, but only 1.00 Log IU/ml for patients without HF. Little decline was seen for either group in the median decline of the HBsAg level from 48 weeks to 96 weeks, 0.28 Log IU/mL in the HF group and 0.06 Log IU/mL in the non-HF group. Conclusion The immune reconstitution of a HBV/HIV coinfected patient plays an important role in the clearance of HBV. If HBsAg and HBeAg levels decrease rapidly when HF occurs, the hepatic flare would be due to HBV-related IRIS.</abstract><cop>Netherlands</cop><pub>Elsevier Ltd</pub><pmid>25596071</pmid><doi>10.1016/j.jiac.2014.12.003</doi><tpages>8</tpages></addata></record> |
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subjects | Adult Anti-Retroviral Agents - administration & dosage Anti-Retroviral Agents - pharmacology Anti-Retroviral Agents - therapeutic use Coinfection - drug therapy Coinfection - epidemiology Coinfection - virology DNA, Viral - blood Female Hematology, Oncology and Palliative Medicine Hepatitis B - complications Hepatitis B - drug therapy Hepatitis B - epidemiology Hepatitis B - virology Hepatitis B e Antigens - blood Hepatitis B surface antigen Hepatitis B Surface Antigens - blood Hepatitis B virus HIV Infections - drug therapy HIV Infections - epidemiology Human immunodeficiency virus Humans Immune Reconstitution Inflammatory Syndrome Kinetics Male Middle Aged Retrospective Studies RNA, Viral - blood Tenofovir - administration & dosage Tenofovir - pharmacology Tenofovir - therapeutic use Viral Load Young Adult |
title | The kinetics of the hepatitis B surface antigen level after the initiation of antiretroviral therapy for hepatitis B virus and human immunodeficiency virus coinfected patients |
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