Published online Oct 21, 2015. doi: 10.3748/wjg.v21.i39.11112
Peer-review started: April 16, 2015
First decision: May 18, 2015
Revised: June 4, 2015
Accepted: September 13, 2015
Article in press: September 13, 2015
Published online: October 21, 2015
Processing time: 187 Days and 18.7 Hours
The shortage of organ donors mandates the use of liver allograft from anti-HBc(+) donors, especially in areas highly endemic for hepatitis B virus (HBV) infection. The incidence of de novo hepatitis B infection (DNH) is over 30%-70% among recipients of hepatitis B core antibody (HBcAb) (+) grafts without any prophylaxis after liver transplantation (LT). Systematic reviews showed that prophylactic therapy [lamivudine and/or hepatitits B immunoglobulin (HBIG)] dramatically reduces the probability of DNH. However, there are limited studies regarding the effects of active immunization to prevent DNH, and the role of active vaccination is not well-defined. This review focuses on the feasibility and efficacy of pre- and post-LT HBV vaccination to prevent DNH in HBsAg(-) recipient using HBcAb(+) grafts. The presence of HBsAb in combination with lamivudine or HBIG results in lower incidence of DNH and may reduce the requirement of HBIG. There was a trend towards decreasing incidence of DNH with higher titers of HBsAb. High titers of HBsAb (> 1000 IU/L) achieved after repeated vaccination could eliminate the necessity for additional antiviral prophylaxis in pediatric recipients. In summary, active vaccination with adequate HBsAb titer is a feasible, cost-effective strategy to prevent DNH in recipients of HBcAb(+) grafts. HBV vaccination is advised for candidates on waiting list and for recipients after withdrawal of steroids and onset of low dose immunosuppression after transplantation.
Core tip:De novo hepatitis B virus infection (DNH) can both result in significant morbidity and reduced graft survival after liver transplantation. Utilization of hepatitis B core antibody(+) grafts may increase the risk of DNH. Different approaches to mitigate this risk have been described. There is no widespread consensus regarding the prophylactic measures to reduce the incidence of DNH by active immunization. This review examines the important published studies on DNH, and presents the clinically relevant points in a lucid manner. It also presents an algorithm which is simple to follow, and which has been validated in pediatric patients at our center.