Virologic and Clinical Outcomes of Hepatitis B Virus Infection in HIV‐HBV Coinfected Transplant Recipients

Liver transplantation (LT) is the treatment of choice for end‐stage liver disease, but is controversial in patients with human immunodeficiency virus (HIV) infection. Using a prospective cohort of HIV‐hepatitis B virus (HBV) coinfected patients transplanted between 2001–2007; outcomes including surv...

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Veröffentlicht in:American journal of transplantation 2010-05, Vol.10 (5), p.1268-1275
Hauptverfasser: Coffin, C. S., Stock, P. G., Dove, L. M., Berg, C. L., Nissen, N. N., Curry, M. P., Ragni, M., Regenstein, F. G., Sherman, K. E., Roland, M. E., Terrault, N. A.
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container_end_page 1275
container_issue 5
container_start_page 1268
container_title American journal of transplantation
container_volume 10
creator Coffin, C. S.
Stock, P. G.
Dove, L. M.
Berg, C. L.
Nissen, N. N.
Curry, M. P.
Ragni, M.
Regenstein, F. G.
Sherman, K. E.
Roland, M. E.
Terrault, N. A.
description Liver transplantation (LT) is the treatment of choice for end‐stage liver disease, but is controversial in patients with human immunodeficiency virus (HIV) infection. Using a prospective cohort of HIV‐hepatitis B virus (HBV) coinfected patients transplanted between 2001–2007; outcomes including survival and HBV clinical recurrence were determined. Twenty‐two coinfected patients underwent LT; 45% had detectable HBV DNA pre‐LT and 72% were receiving anti‐HBV drugs with efficacy against lamivudine‐resistant HBV. Post‐LT, all patients received hepatitis B immune globulin (HBIG) plus nucleos(t)ide analogues and remained HBsAg negative without clinical evidence of HBV recurrence, with a median follow‐up 3.5 years. Low‐level HBV viremia (median 108 IU/mL, range 9–789) was intermittently detected in 7/13 but not associated with HBsAg detection or ALT elevation. Compared with 20 HBV monoinfected patients on similar HBV prophylaxis and median follow‐up of 4.0 years, patient and graft survival were similar: 100% versus 85% in HBV mono‐ versus coinfected patients (p = 0.08, log rank test). LT is effective for HIV‐HBV coinfected patients with complications of cirrhosis, including those who are HBV DNA positive at the time of LT. Combination HBIG and antivirals is effective as prophylaxis with no clinical evidence of HBV recurrence but low‐level HBV DNA is detectable in ∼50% of recipients. Post‐transplant outcomes in HIV‐infected persons with HBV‐related liver disease are excellent and recurrent HBV can be prevented with use of combination HBIG and antiviral therapy as prophylaxis, even in those with HBV DNA detectable at the time of transplantation.
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S. ; Stock, P. G. ; Dove, L. M. ; Berg, C. L. ; Nissen, N. N. ; Curry, M. P. ; Ragni, M. ; Regenstein, F. G. ; Sherman, K. E. ; Roland, M. E. ; Terrault, N. A.</creator><creatorcontrib>Coffin, C. S. ; Stock, P. G. ; Dove, L. M. ; Berg, C. L. ; Nissen, N. N. ; Curry, M. P. ; Ragni, M. ; Regenstein, F. G. ; Sherman, K. E. ; Roland, M. E. ; Terrault, N. A.</creatorcontrib><description>Liver transplantation (LT) is the treatment of choice for end‐stage liver disease, but is controversial in patients with human immunodeficiency virus (HIV) infection. Using a prospective cohort of HIV‐hepatitis B virus (HBV) coinfected patients transplanted between 2001–2007; outcomes including survival and HBV clinical recurrence were determined. Twenty‐two coinfected patients underwent LT; 45% had detectable HBV DNA pre‐LT and 72% were receiving anti‐HBV drugs with efficacy against lamivudine‐resistant HBV. Post‐LT, all patients received hepatitis B immune globulin (HBIG) plus nucleos(t)ide analogues and remained HBsAg negative without clinical evidence of HBV recurrence, with a median follow‐up 3.5 years. Low‐level HBV viremia (median 108 IU/mL, range 9–789) was intermittently detected in 7/13 but not associated with HBsAg detection or ALT elevation. Compared with 20 HBV monoinfected patients on similar HBV prophylaxis and median follow‐up of 4.0 years, patient and graft survival were similar: 100% versus 85% in HBV mono‐ versus coinfected patients (p = 0.08, log rank test). LT is effective for HIV‐HBV coinfected patients with complications of cirrhosis, including those who are HBV DNA positive at the time of LT. Combination HBIG and antivirals is effective as prophylaxis with no clinical evidence of HBV recurrence but low‐level HBV DNA is detectable in ∼50% of recipients. Post‐transplant outcomes in HIV‐infected persons with HBV‐related liver disease are excellent and recurrent HBV can be prevented with use of combination HBIG and antiviral therapy as prophylaxis, even in those with HBV DNA detectable at the time of transplantation.</description><identifier>ISSN: 1600-6135</identifier><identifier>EISSN: 1600-6143</identifier><identifier>DOI: 10.1111/j.1600-6143.2010.03070.x</identifier><identifier>PMID: 20346065</identifier><language>eng</language><publisher>Malden, USA: Blackwell Publishing Inc</publisher><subject>Adult ; Aged ; Antiviral Agents - immunology ; Antiviral Agents - pharmacology ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Graft Survival - immunology ; Hepatitis - drug therapy ; Hepatitis - immunology ; Hepatitis - virology ; Hepatitis B - drug therapy ; Hepatitis B - immunology ; Hepatitis B - virology ; hepatitis B immunoglobulin ; Hepatitis B virus ; Hepatitis B virus (HBV) ; Hepatitis B virus - genetics ; Hepatitis B virus - immunology ; HIV - genetics ; HIV - immunology ; HIV Infections - drug therapy ; HIV Infections - immunology ; HIV Infections - virology ; Human viral diseases ; Humans ; immune deficiency ; Immunoglobulins ; Immunologic Deficiency Syndromes - drug therapy ; Immunologic Deficiency Syndromes - immunology ; Infections - drug therapy ; Infections - immunology ; Infections - virology ; Infectious diseases ; Lamivudine - immunology ; Lamivudine - pharmacology ; Lamivudine - therapeutic use ; Liver Cirrhosis - drug therapy ; Liver Cirrhosis - immunology ; Liver Cirrhosis - surgery ; Liver Failure - drug therapy ; Liver Failure - immunology ; Liver Failure - virology ; Liver Transplantation - adverse effects ; Liver Transplantation - immunology ; Longitudinal Studies ; Male ; Medical sciences ; Middle Aged ; polymerase chain reaction ; posttransplant ; posttransplant complications ; posttransplant mortality ; Secondary Prevention ; surface (S) gene ; Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases ; Treatment Outcome ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral hepatitis ; Virus Diseases - drug therapy ; Virus Diseases - immunology ; Virus Diseases - virology ; Viruses - genetics ; Viruses - immunology</subject><ispartof>American journal of transplantation, 2010-05, Vol.10 (5), p.1268-1275</ispartof><rights>©</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1600-6143.2010.03070.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1600-6143.2010.03070.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,776,780,881,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=22853206$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20346065$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Coffin, C. S.</creatorcontrib><creatorcontrib>Stock, P. G.</creatorcontrib><creatorcontrib>Dove, L. M.</creatorcontrib><creatorcontrib>Berg, C. L.</creatorcontrib><creatorcontrib>Nissen, N. N.</creatorcontrib><creatorcontrib>Curry, M. P.</creatorcontrib><creatorcontrib>Ragni, M.</creatorcontrib><creatorcontrib>Regenstein, F. G.</creatorcontrib><creatorcontrib>Sherman, K. E.</creatorcontrib><creatorcontrib>Roland, M. E.</creatorcontrib><creatorcontrib>Terrault, N. A.</creatorcontrib><title>Virologic and Clinical Outcomes of Hepatitis B Virus Infection in HIV‐HBV Coinfected Transplant Recipients</title><title>American journal of transplantation</title><addtitle>Am J Transplant</addtitle><description>Liver transplantation (LT) is the treatment of choice for end‐stage liver disease, but is controversial in patients with human immunodeficiency virus (HIV) infection. Using a prospective cohort of HIV‐hepatitis B virus (HBV) coinfected patients transplanted between 2001–2007; outcomes including survival and HBV clinical recurrence were determined. Twenty‐two coinfected patients underwent LT; 45% had detectable HBV DNA pre‐LT and 72% were receiving anti‐HBV drugs with efficacy against lamivudine‐resistant HBV. Post‐LT, all patients received hepatitis B immune globulin (HBIG) plus nucleos(t)ide analogues and remained HBsAg negative without clinical evidence of HBV recurrence, with a median follow‐up 3.5 years. Low‐level HBV viremia (median 108 IU/mL, range 9–789) was intermittently detected in 7/13 but not associated with HBsAg detection or ALT elevation. Compared with 20 HBV monoinfected patients on similar HBV prophylaxis and median follow‐up of 4.0 years, patient and graft survival were similar: 100% versus 85% in HBV mono‐ versus coinfected patients (p = 0.08, log rank test). LT is effective for HIV‐HBV coinfected patients with complications of cirrhosis, including those who are HBV DNA positive at the time of LT. Combination HBIG and antivirals is effective as prophylaxis with no clinical evidence of HBV recurrence but low‐level HBV DNA is detectable in ∼50% of recipients. Post‐transplant outcomes in HIV‐infected persons with HBV‐related liver disease are excellent and recurrent HBV can be prevented with use of combination HBIG and antiviral therapy as prophylaxis, even in those with HBV DNA detectable at the time of transplantation.</description><subject>Adult</subject><subject>Aged</subject><subject>Antiviral Agents - immunology</subject><subject>Antiviral Agents - pharmacology</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Graft Survival - immunology</subject><subject>Hepatitis - drug therapy</subject><subject>Hepatitis - immunology</subject><subject>Hepatitis - virology</subject><subject>Hepatitis B - drug therapy</subject><subject>Hepatitis B - immunology</subject><subject>Hepatitis B - virology</subject><subject>hepatitis B immunoglobulin</subject><subject>Hepatitis B virus</subject><subject>Hepatitis B virus (HBV)</subject><subject>Hepatitis B virus - genetics</subject><subject>Hepatitis B virus - immunology</subject><subject>HIV - genetics</subject><subject>HIV - immunology</subject><subject>HIV Infections - drug therapy</subject><subject>HIV Infections - immunology</subject><subject>HIV Infections - virology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>immune deficiency</subject><subject>Immunoglobulins</subject><subject>Immunologic Deficiency Syndromes - drug therapy</subject><subject>Immunologic Deficiency Syndromes - immunology</subject><subject>Infections - drug therapy</subject><subject>Infections - immunology</subject><subject>Infections - virology</subject><subject>Infectious diseases</subject><subject>Lamivudine - immunology</subject><subject>Lamivudine - pharmacology</subject><subject>Lamivudine - therapeutic use</subject><subject>Liver Cirrhosis - drug therapy</subject><subject>Liver Cirrhosis - immunology</subject><subject>Liver Cirrhosis - surgery</subject><subject>Liver Failure - drug therapy</subject><subject>Liver Failure - immunology</subject><subject>Liver Failure - virology</subject><subject>Liver Transplantation - adverse effects</subject><subject>Liver Transplantation - immunology</subject><subject>Longitudinal Studies</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>polymerase chain reaction</subject><subject>posttransplant</subject><subject>posttransplant complications</subject><subject>posttransplant mortality</subject><subject>Secondary Prevention</subject><subject>surface (S) gene</subject><subject>Surgery (general aspects). 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Aids</subject><subject>Viral hepatitis</subject><subject>Virus Diseases - drug therapy</subject><subject>Virus Diseases - immunology</subject><subject>Virus Diseases - virology</subject><subject>Viruses - genetics</subject><subject>Viruses - immunology</subject><issn>1600-6135</issn><issn>1600-6143</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFksFuEzEQhi0EoqXwCsgXxClh7PF6NweQ2ghIUKVKKORqeb3e4sixl_UutDcegWfkSfC2IcAJXzya_9PM2PMTQhnMWT6vdnMmAWaSCZxzyFlAKGF-84CcHoWHxxiLE_IkpR0AK3nFH5MTDigkyOKU-K3ro4_XzlAdGrr0LjijPb0aBxP3NtHY0pXt9OAGl-gFzfiY6Dq01gwuBuoCXa23P7__WF1s6TK6O8E2dNPrkDqvw0A_WuM6Z8OQnpJHrfbJPjvcZ-TTu7eb5Wp2efV-vTy_nHVYMZgtTC2axkpZa1ZJNCgq1Iu2NkxLFKaRRW0klsJyJjSUTVsZxiqwUNoauKzxjLy5r9uN9d42JvfutVdd7_a6v1VRO_WvEtxndR2_KmRFkTvmAi8PBfr4ZbRpUHuXjPX5PTaOSZVCIoAs-f9JxAVDVolMPv97qOM0v3eRgRcHQKe8gjb_oHHpD8erAjnIzL2-5745b2-POgM1eUPt1LR2NVlATd5Qd95QN-r8w2aK8BfUKa4B</recordid><startdate>201005</startdate><enddate>201005</enddate><creator>Coffin, C. 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identifier ISSN: 1600-6135
ispartof American journal of transplantation, 2010-05, Vol.10 (5), p.1268-1275
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; Alma/SFX Local Collection
subjects Adult
Aged
Antiviral Agents - immunology
Antiviral Agents - pharmacology
Antiviral Agents - therapeutic use
Biological and medical sciences
Graft Survival - immunology
Hepatitis - drug therapy
Hepatitis - immunology
Hepatitis - virology
Hepatitis B - drug therapy
Hepatitis B - immunology
Hepatitis B - virology
hepatitis B immunoglobulin
Hepatitis B virus
Hepatitis B virus (HBV)
Hepatitis B virus - genetics
Hepatitis B virus - immunology
HIV - genetics
HIV - immunology
HIV Infections - drug therapy
HIV Infections - immunology
HIV Infections - virology
Human viral diseases
Humans
immune deficiency
Immunoglobulins
Immunologic Deficiency Syndromes - drug therapy
Immunologic Deficiency Syndromes - immunology
Infections - drug therapy
Infections - immunology
Infections - virology
Infectious diseases
Lamivudine - immunology
Lamivudine - pharmacology
Lamivudine - therapeutic use
Liver Cirrhosis - drug therapy
Liver Cirrhosis - immunology
Liver Cirrhosis - surgery
Liver Failure - drug therapy
Liver Failure - immunology
Liver Failure - virology
Liver Transplantation - adverse effects
Liver Transplantation - immunology
Longitudinal Studies
Male
Medical sciences
Middle Aged
polymerase chain reaction
posttransplant
posttransplant complications
posttransplant mortality
Secondary Prevention
surface (S) gene
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Treatment Outcome
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral hepatitis
Virus Diseases - drug therapy
Virus Diseases - immunology
Virus Diseases - virology
Viruses - genetics
Viruses - immunology
title Virologic and Clinical Outcomes of Hepatitis B Virus Infection in HIV‐HBV Coinfected Transplant Recipients
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