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- Publisher Website: 10.1016/j.jhep.2005.03.013
- Scopus: eid_2-s2.0-21844435779
- PMID: 15964658
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Article: Failure of hepatitis B vaccination in patients receiving lamivudine prophylaxis after liver transplantation for chronic hepatitis B
Title | Failure of hepatitis B vaccination in patients receiving lamivudine prophylaxis after liver transplantation for chronic hepatitis B |
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Authors | |
Keywords | Active immunization Antibody against hepatitis B surface antigen Immunity Recurrence |
Issue Date | 2005 |
Publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep |
Citation | Journal Of Hepatology, 2005, v. 43 n. 2, p. 283-287 How to Cite? |
Abstract | Background/Aims: Lamivudine prophylaxis against hepatitis B virus (HBV) reinfection after liver transplantation is associated with recurrence due to escape mutants. Methods: Fifty-two patients on lamivudine prophylaxis at a median of 412 days (median, 370-2040 days) after transplantation for chronic HBV-related liver disease received two courses of an accelerated schedule of double-dose recombinant HBV vaccine. Before vaccination, all patients were seronegative for HBsAg, anti-HBs and HBV DNA (by qPCR). Three intramuscular doses of vaccine (40 μg each) were administered monthly and another identical course was repeated after 3 months. Lamivudine (100 mg/day) was continued throughout the study. Results: After the first course, two patients developed a weak response (anti-HBs titre of 12 mIU/mL) that disappeared rapidly. One early responder developed anti-HBs (27 mIU/mL) again after the second course but the other did not. Two other patients developed response (anti-HBs titre of 17 and 103 mIU/mL, respectively) giving an overall response rate of 7.7%. The antibody level declined rapidly. At the end of the study, one patient who did not respond had developed viral breakthrough which was treated with adefovir dipivoxil therapy. Conclusions: Active immunization with two courses of double-dose recombinant HBV vaccine has limited efficacy in patients receiving lamividine prophylaxis after liver transplantation. © 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved. |
Persistent Identifier | http://hdl.handle.net/10722/83271 |
ISSN | 2023 Impact Factor: 26.8 2023 SCImago Journal Rankings: 9.857 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Chung, ML | en_HK |
dc.contributor.author | Chi, LL | en_HK |
dc.contributor.author | See, CC | en_HK |
dc.contributor.author | Lau, GK | en_HK |
dc.contributor.author | Sheung, TF | en_HK |
dc.date.accessioned | 2010-09-06T08:39:02Z | - |
dc.date.available | 2010-09-06T08:39:02Z | - |
dc.date.issued | 2005 | en_HK |
dc.identifier.citation | Journal Of Hepatology, 2005, v. 43 n. 2, p. 283-287 | en_HK |
dc.identifier.issn | 0168-8278 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/83271 | - |
dc.description.abstract | Background/Aims: Lamivudine prophylaxis against hepatitis B virus (HBV) reinfection after liver transplantation is associated with recurrence due to escape mutants. Methods: Fifty-two patients on lamivudine prophylaxis at a median of 412 days (median, 370-2040 days) after transplantation for chronic HBV-related liver disease received two courses of an accelerated schedule of double-dose recombinant HBV vaccine. Before vaccination, all patients were seronegative for HBsAg, anti-HBs and HBV DNA (by qPCR). Three intramuscular doses of vaccine (40 μg each) were administered monthly and another identical course was repeated after 3 months. Lamivudine (100 mg/day) was continued throughout the study. Results: After the first course, two patients developed a weak response (anti-HBs titre of 12 mIU/mL) that disappeared rapidly. One early responder developed anti-HBs (27 mIU/mL) again after the second course but the other did not. Two other patients developed response (anti-HBs titre of 17 and 103 mIU/mL, respectively) giving an overall response rate of 7.7%. The antibody level declined rapidly. At the end of the study, one patient who did not respond had developed viral breakthrough which was treated with adefovir dipivoxil therapy. Conclusions: Active immunization with two courses of double-dose recombinant HBV vaccine has limited efficacy in patients receiving lamividine prophylaxis after liver transplantation. © 2005 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved. | en_HK |
dc.language | eng | en_HK |
dc.publisher | Elsevier BV. The Journal's web site is located at http://www.elsevier.com/locate/jhep | en_HK |
dc.relation.ispartof | Journal of Hepatology | en_HK |
dc.rights | NOTICE: this is the author’s version of a work that was accepted for publication in Journal of Hepatology. Changes resulting from the publishing process, such as peer review, editing, corrections, structural formatting, and other quality control mechanisms may not be reflected in this document. Changes may have been made to this work since it was submitted for publication. A definitive version was subsequently published in Journal of Hepatology, [VOL 43, ISSUE 2, 2005] DOI 10.1016/j.jhep.2005.03.013 | en_HK |
dc.subject | Active immunization | en_HK |
dc.subject | Antibody against hepatitis B surface antigen | en_HK |
dc.subject | Immunity | en_HK |
dc.subject | Recurrence | en_HK |
dc.subject.mesh | Hepatitis B Vaccines - administration and dosage - therapeutic use | - |
dc.subject.mesh | Hepatitis B virus - genetics - immunology | - |
dc.subject.mesh | Hepatitis B, Chronic - prevention and control - surgery - virology | - |
dc.subject.mesh | Reverse Transcriptase Inhibitors - therapeutic use | - |
dc.subject.mesh | Vaccination | - |
dc.title | Failure of hepatitis B vaccination in patients receiving lamivudine prophylaxis after liver transplantation for chronic hepatitis B | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | See, CC: chanlsc@hkucc.hku.hk | en_HK |
dc.identifier.authority | See, CC=rp01568 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1016/j.jhep.2005.03.013 | en_HK |
dc.identifier.pmid | 15964658 | - |
dc.identifier.scopus | eid_2-s2.0-21844435779 | en_HK |
dc.identifier.hkuros | 138679 | en_HK |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-21844435779&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 43 | en_HK |
dc.identifier.issue | 2 | en_HK |
dc.identifier.spage | 283 | en_HK |
dc.identifier.epage | 287 | en_HK |
dc.identifier.isi | WOS:000230803900013 | - |
dc.publisher.place | Netherlands | en_HK |
dc.identifier.scopusauthorid | Chung, ML=8696033300 | en_HK |
dc.identifier.scopusauthorid | Chi, LL=7409789712 | en_HK |
dc.identifier.scopusauthorid | See, CC=7404255575 | en_HK |
dc.identifier.scopusauthorid | Lau, GK=7102301257 | en_HK |
dc.identifier.scopusauthorid | Sheung, TF=6506234707 | en_HK |
dc.identifier.issnl | 0168-8278 | - |