Self-limited HBV infection of the recipient does not reactivate after liver transplantation: Observations from a 30-year liver transplant program.


Journal

Transplant infectious disease : an official journal of the Transplantation Society
ISSN: 1399-3062
Titre abrégé: Transpl Infect Dis
Pays: Denmark
ID NLM: 100883688

Informations de publication

Date de publication:
Feb 2021
Historique:
received: 13 06 2020
revised: 22 07 2020
accepted: 25 07 2020
pubmed: 5 8 2020
medline: 4 8 2021
entrez: 5 8 2020
Statut: ppublish

Résumé

A self-limited hepatitis B infection can reactivate in patients under immunosuppression or chemotherapy (reappearance of hepatitis B surface antigen (HBsAg) or HBV-DNA). Exact circumstances of HBV reactivation in patients undergoing liver transplantation (LT) for end-stage liver diseases (ESLD) unrelated to HBV are unknown, and recommendations on HBV prophylaxis remain unclear. Among 1273 liver transplants, 168 patients with a self-limited HBV hepatitis B infection prior to LT were identified from our prospective liver transplant database. Patients with underlying chronic HBV infection and recipients of an anti-HBc-positive liver were not included in the analysis. Demographic, laboratory, serological, and virological data were analyzed retrospectively. Appearance of HBsAg or HBV-DNA was defined as reactivation. The median follow-up after LT was 12.0 years (0.6-30.7 years). The rate of HBV reactivation was 0% independent of antiviral prophylaxis (n = 7; 4.2%), the etiology of ESLD, hepatitis C treatment, or the anti-HBs concentration. The overall patient survival with a history of a self-limited HBV infection before LT did not significantly differ from the rest of the cohort. Antiviral treatment with nucleos(t)ide analogues post-liver transplantation in order to prevent HBV reactivation in patients with a resolved self-limited hepatitis B infection prior to LT seems to be omittable since the main viral reservoir is removed by the hepatectomy. These findings may clarify the current uncertainty in the recommendations regarding the risk of HBV reactivation in patients with self-limited hepatitis B prior to LT.

Sections du résumé

BACKGROUND BACKGROUND
A self-limited hepatitis B infection can reactivate in patients under immunosuppression or chemotherapy (reappearance of hepatitis B surface antigen (HBsAg) or HBV-DNA). Exact circumstances of HBV reactivation in patients undergoing liver transplantation (LT) for end-stage liver diseases (ESLD) unrelated to HBV are unknown, and recommendations on HBV prophylaxis remain unclear.
PATIENTS AND METHODS METHODS
Among 1273 liver transplants, 168 patients with a self-limited HBV hepatitis B infection prior to LT were identified from our prospective liver transplant database. Patients with underlying chronic HBV infection and recipients of an anti-HBc-positive liver were not included in the analysis. Demographic, laboratory, serological, and virological data were analyzed retrospectively. Appearance of HBsAg or HBV-DNA was defined as reactivation.
RESULTS RESULTS
The median follow-up after LT was 12.0 years (0.6-30.7 years). The rate of HBV reactivation was 0% independent of antiviral prophylaxis (n = 7; 4.2%), the etiology of ESLD, hepatitis C treatment, or the anti-HBs concentration. The overall patient survival with a history of a self-limited HBV infection before LT did not significantly differ from the rest of the cohort.
CONCLUSION CONCLUSIONS
Antiviral treatment with nucleos(t)ide analogues post-liver transplantation in order to prevent HBV reactivation in patients with a resolved self-limited hepatitis B infection prior to LT seems to be omittable since the main viral reservoir is removed by the hepatectomy. These findings may clarify the current uncertainty in the recommendations regarding the risk of HBV reactivation in patients with self-limited hepatitis B prior to LT.

Identifiants

pubmed: 32748492
doi: 10.1111/tid.13436
doi:

Substances chimiques

Antiviral Agents 0
Hepatitis B Antibodies 0
Hepatitis B Surface Antigens 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13436

Informations de copyright

© 2020 The Authors. Transplant Infectious Disease published by Wiley Periodicals LLC.

Références

Goldstein ST, Zhou F, Hadler SC, Bell BP, Mast EE, Margolis HS. A mathematical model to estimate global hepatitis B disease burden and vaccination impact. Int J Epidemiol. 2005;34(6):1329-1339.
Ott JJ, Ullrich A, Mascarenhas M, Stevens GA. Global cancer incidence and mortality caused by behavior and infection. J Public Health (Oxf). 2011;33(2):223-233.
Trepo C, Chan HL, Lok A. Hepatitis B virus infection. Lancet. 2014;384(9959):2053-2063.
Yuki N, Nagaoka T, Yamashiro M, et al. Long-term histologic and virologic outcomes of acute self-limited hepatitis B. Hepatology. 2003;37(5):1172-1179.
European Association for the Study of the Liver. Electronic address eee, European Association for the Study of the L. EASL 2017 clinical practice guidelines on the management of hepatitis B virus infection. J Hepatol. 2017;67(2):370-398.
Perez-Grande R, Gutierrez-Zufiaurre N, Munoz-Criado S, et al. Hepatitis B reactivation in a hepatitis B surface antigen-negative patient after allogeneic bone marrow transplant: successful treatment with lamivudine and seroconversion. Diagn Microbiol Infect Dis. 2009;64(1):80-82.
Cholongitas E, Papatheodoridis GV, Burroughs AK. Liver grafts from anti-hepatitis B core positive donors: a systematic review. J Hepatol. 2010;52(2):272-279.
Poethko-Müller CZR, Hamouda O, Faber M, Stark K, Ross RS, Thamm T. Die Seroepidemiologie der Hepatitis A, B und C in Deutschland: Ergebnisse der Studie zur Gesundheit Erwachsener in Deutschland (DEGS1). Bundesgesundheitsblatt Gesundheitsforschung Gesundheitsschutz. 2013;2013(56):707-715.
Shepard CW, Simard EP, Finelli L, Fiore AE, Bell BP. Hepatitis B virus infection: epidemiology and vaccination. Epidemiol Rev. 2006;28:112-125.
Post A, Nagendra S. Reactivation of hepatitis B: pathogenesis and clinical implications. Curr Infect Dis Rep. 2009;11(2):113-119.
Rehermann B, Ferrari C, Pasquinelli C, Chisari FV. The hepatitis B virus persists for decades after patients' recovery from acute viral hepatitis despite active maintenance of a cytotoxic T-lymphocyte response. Nat Med. 1996;2(10):1104-1108.
Yotsuyanagi H, Yasuda K, Iino S, et al. Persistent viremia after recovery from self-limited acute hepatitis B. Hepatology. 1998;27(5):1377-1382.
Marusawa H, Uemoto S, Hijikata M, et al. Latent hepatitis B virus infection in healthy individuals with antibodies to hepatitis B core antigen. Hepatology. 2000;31(2):488-495.
Omata M. Significance of extrahepatic replication of hepatitis B virus. Hepatology. 1990;12(2):364-366.
Querido S, Weigert A, Adragao T, et al. Risk of hepatitis B reactivation in hepatitis B surface antigen seronegative and core antibody seropositive kidney transplant recipients. Transpl Infect Dis. 2019;21(1):e13009.
Maguire D, Heaton ND, Smith HM. Failure of reactivation of hepatitis B after liver transplantation in hepatitis B surface antigen-negative, core antibody-positive recipients. Transplantation. 2002;73(3):481-482.
Duhart BT Jr, Honaker MR, Shokouh-Amiri MH, et al. Retrospective evaluation of the risk of hepatitis B virus reactivation after transplantation. Transpl Infect Dis. 2003;5(3):126-131.
Vionnet J, Pascual M, Testoni B, et al. Late hepatitis B reactivation following direct-acting antiviral-based treatment of recurrent hepatitis C in an anti-HBc-positive liver transplant recipient. Hepatology. 2018;67(2):791-793.
Mucke VT, Mucke MM, Peiffer KH, et al. No evidence of hepatitis B virus reactivation in patients with resolved infection treated with direct-acting antivirals for hepatitis C in a large real-world cohort. Aliment Pharmacol Ther. 2017;46(4):432-439.
Teegen EM, Maurer MM, Globke B, Pratschke J, Eurich D. Liver transplantation for Hepatitis-B-associated liver disease - Three decades of experience. Transpl Infect Dis. 2019;21(1):e12997.

Auteurs

R R Ossami Saidy (RR)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Muenevver Demir (M)

Department of Gastroenterology and Hepatology CVK/CCM, Charité University Medicine Berlin, Berlin, Germany.

Pauline Nibbe (P)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Eva-Maria Dobrindt (EM)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Robert Oellinger (R)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Wenzel Schoening (W)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Johann Pratschke (J)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

Dennis Eurich (D)

Department of Surgery, Charité Universitätsmedizin Berlin, Berlin, Germany.

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