Liver grafts from anti-hepatitis B core positive donors: a systematic review

J Hepatol. 2010 Feb;52(2):272-9. doi: 10.1016/j.jhep.2009.11.009. Epub 2010 Jan 19.

Abstract

Background & aims: Although hepatitis B virus (HBV) transmission after liver transplantation of grafts from HBsAg-negative, anti-HBc positive donors is well established, the growing organ shortage favours the use of such marginal grafts. We systematically evaluated the risk of HBV infection after liver transplantation with such grafts and the effect of anti-HBV prophylaxis.

Methods: We performed a literature review over the last 15 years identifying 39 studies including 903 recipients of anti-HBc positive liver grafts.

Results: Recurrent HBV infection developed in 11% of HBsAg-positive liver transplant recipients of anti-HBc positive grafts, while survival was similar (67-100%) to HBsAg-positive recipients of anti-HBc negative grafts. De novo HBV infection developed in 19% of HBsAg-negative recipients being less frequent in anti-HBc/anti-HBs positive than HBV naive cases without prophylaxis (15% vs 48%, p<0.001). Anti-HBV prophylaxis reduced de novo infection rates in both anti-HBc/anti-HBs positive (3%) and HBV naive recipients (12%). De novo infection rates were 19%, 2.6% and 2.8% in HBsAg-negative recipients under hepatitis B immunoglobulin, lamivudine and their combination, respectively.

Conclusions: Liver grafts from anti-HBc positive donors can be safely used, preferentially in HBsAg-positive or anti-HBc/anti-HBs positive recipients. HBsAg-negative recipients should receive prophylaxis with lamivudine, while both anti-HBc and anti-HBs positive recipients may need no prophylaxis at all.

Publication types

  • Review
  • Systematic Review

MeSH terms

  • Algorithms
  • Antiviral Agents / pharmacology
  • Hepatitis B / immunology
  • Hepatitis B / prevention & control
  • Hepatitis B / transmission*
  • Hepatitis B Antibodies / metabolism*
  • Hepatitis B Antibodies / therapeutic use
  • Hepatitis B Core Antigens
  • Hepatitis B Surface Antigens / metabolism
  • Humans
  • Lamivudine / pharmacology
  • Liver Transplantation / adverse effects*
  • Liver Transplantation / immunology
  • Recurrence
  • Risk Factors
  • Tissue Donors*
  • Treatment Outcome

Substances

  • Antiviral Agents
  • Hepatitis B Antibodies
  • Hepatitis B Core Antigens
  • Hepatitis B Surface Antigens
  • Lamivudine