Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up

Lamivudine is a nucleoside analogue with efficacy in the suppression of hepatitis B viral (HBV) replication. In a previously reported study, lamivudine was administered to patients with chronic, actively replicating HBV infection who subsequently underwent liver transplantation. Patients became seru...

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Main Authors: Eric M Yoshida, Mang M Ma, Jennifer E Davis, Karl P Fischer, Norman M Kneteman, Siegfried R Erb, D Lorne Tyrrell, Vincent G Bain
Format: Article
Language:English
Published: Hindawi Limited 1998-01-01
Series:Canadian Journal of Gastroenterology
Online Access:http://dx.doi.org/10.1155/1998/617039
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spelling doaj-dea9f93269d54174a06f9152f28898d72020-11-24T22:49:05ZengHindawi LimitedCanadian Journal of Gastroenterology0835-79001998-01-0112212512910.1155/1998/617039Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-upEric M Yoshida0Mang M Ma1Jennifer E Davis2Karl P Fischer3Norman M Kneteman4Siegfried R Erb5D Lorne Tyrrell6Vincent G Bain7Department of Medicine, University of British Columbia, CanadaDepartment of Medicine, University of Alberta, Edmonton, Alberta, CanadaDepartment of Medicine, University of British Columbia, CanadaDepartment of Medicine, University of Alberta, Edmonton, Alberta, CanadaDepartment of Surgery, University of Alberta, Edmonton, Alberta, CanadaDepartment of Medicine, University of British Columbia, CanadaDepartment of Medicine, University of British Columbia, CanadaDepartment of Medicine, University of Alberta, Edmonton, Alberta, CanadaLamivudine is a nucleoside analogue with efficacy in the suppression of hepatitis B viral (HBV) replication. In a previously reported study, lamivudine was administered to patients with chronic, actively replicating HBV infection who subsequently underwent liver transplantation. Patients became serum HBV DNA-negative in response to lamivudine before transplantation, which was continued in the post-transplant period. Two of four patients surviving the immediate postoperative period developed allograft reinfection 240 and 409 days post-transplant. The strain of the reinfecting virus was analyzed, and a mutation in the YMDD region of the viral polymerase conferring resistance to lamivudine was discovered. The long term follow-up of these two patients is reported. The first patient developed ascites 16.5 months after allograft reinfection. A transjugular liver biopsy performed 18 months after the emergence of the lamivudine-resistant strain revealed cirrhosis and lobular hepatitis without rejection. The gradient between hepatic vein wedged and free pressures was 13 mmHg, consistent with portal hypertension. The second patient, 16 months after allograft reinfection with the lamivudine-resistant strain, is without clinical evidence of portal hypertension, although liver enzymes remain elevated. Both patients were given a trial of famciclovir, which did not significantly suppress HBV viremia. In conclusion, lamivudine-resistant HBV strains with the YMDD mutation may have an aggressive clinical course with rapid progression to cirrhosis. Famciclovir did not appear to be an effective rescue agent in these two patients.http://dx.doi.org/10.1155/1998/617039
collection DOAJ
language English
format Article
sources DOAJ
author Eric M Yoshida
Mang M Ma
Jennifer E Davis
Karl P Fischer
Norman M Kneteman
Siegfried R Erb
D Lorne Tyrrell
Vincent G Bain
spellingShingle Eric M Yoshida
Mang M Ma
Jennifer E Davis
Karl P Fischer
Norman M Kneteman
Siegfried R Erb
D Lorne Tyrrell
Vincent G Bain
Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
Canadian Journal of Gastroenterology
author_facet Eric M Yoshida
Mang M Ma
Jennifer E Davis
Karl P Fischer
Norman M Kneteman
Siegfried R Erb
D Lorne Tyrrell
Vincent G Bain
author_sort Eric M Yoshida
title Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
title_short Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
title_full Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
title_fullStr Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
title_full_unstemmed Postliver Transplant Allograft Reinfection with a Lamivudine-Resistant Strain of Hepatitis B Virus: Long Term Follow-up
title_sort postliver transplant allograft reinfection with a lamivudine-resistant strain of hepatitis b virus: long term follow-up
publisher Hindawi Limited
series Canadian Journal of Gastroenterology
issn 0835-7900
publishDate 1998-01-01
description Lamivudine is a nucleoside analogue with efficacy in the suppression of hepatitis B viral (HBV) replication. In a previously reported study, lamivudine was administered to patients with chronic, actively replicating HBV infection who subsequently underwent liver transplantation. Patients became serum HBV DNA-negative in response to lamivudine before transplantation, which was continued in the post-transplant period. Two of four patients surviving the immediate postoperative period developed allograft reinfection 240 and 409 days post-transplant. The strain of the reinfecting virus was analyzed, and a mutation in the YMDD region of the viral polymerase conferring resistance to lamivudine was discovered. The long term follow-up of these two patients is reported. The first patient developed ascites 16.5 months after allograft reinfection. A transjugular liver biopsy performed 18 months after the emergence of the lamivudine-resistant strain revealed cirrhosis and lobular hepatitis without rejection. The gradient between hepatic vein wedged and free pressures was 13 mmHg, consistent with portal hypertension. The second patient, 16 months after allograft reinfection with the lamivudine-resistant strain, is without clinical evidence of portal hypertension, although liver enzymes remain elevated. Both patients were given a trial of famciclovir, which did not significantly suppress HBV viremia. In conclusion, lamivudine-resistant HBV strains with the YMDD mutation may have an aggressive clinical course with rapid progression to cirrhosis. Famciclovir did not appear to be an effective rescue agent in these two patients.
url http://dx.doi.org/10.1155/1998/617039
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