Abstract

ObjectiveHepatitis B virus (HBV) reinfection is a serious complication that arise in patients who undergo hepatitis B virus related liver transplantation. We aimed to use biomarkers to evaluate the HBV reinfection in patients after orthotopic liver transplantation.MethodsSeventy-nine patients who underwent liver transplantation between 2009 and 2015 were enrolled, and levels of biomarkers were analyzed at different time points. Cox regression and receiver operating characteristic (ROC) curves of different markers at baseline were used to analyze sustained hepatitis B surface antigen (HBsAg) loss. The Kaplan-Meier method was used to compare the levels of the biomarkers.ResultsAmong the 79 patients, 42 sustained HBsAg loss with a median time of 65.2 months (12.0-114.5, IQR 19.5) after liver transplantation and 37 patients exhibited HBsAg recurrence with a median time of 8.8 (0.47-59.53, IQR 19.47) months. In the ROC curve analysis, at baseline, 4.25 log10 IU/mL qHBcAb and 2.82 log10 IU/mL qHBsAg showed the maximum Youden’s index values with area under the curves (AUCs) of 0.685and 0.651, respectively. The Kaplan-Meier method indicated that qHBsAg and quantitative antibody against hepatitis B core antigen (qHBcAb) levels in the two groups were significantly different (p = 0.031 and 0.006, respectively). Furthermore, the Cox regression model confirmed the predictive ability of qHBcAb at baseline (AUC = 0.685).ConclusionLower pretransplantation qHBcAb is associated with HBV infection. The baseline concentration of qHBcAb is a promising predictor for the recurrence of HBV in patients undergoing liver transplantation and can be used to guide antiviral treatment for HBV infection.

Highlights

  • Hepatitis B virus (HBV) infection is a global health problem

  • A total of 363 patients were enrolled in this study, 79 patients were selected retrospectively, and 284 patients were excluded including 44 patients with hepatitis B surface antigen (HBsAg)-negative status, 53 patients with underlying diseases or other infectious diseases, 18 patients receiving an HBV-positive graft, 17 patients who died post Liver transplantation (LT), 5 patients who underwent retransplantation and 147 patients without sufficient serum samples or integrated follow-up time points (Supplementary Figure 1)

  • The characteristics of qHBcAb and qHBsAg were significantly different between the groups (p = 0.037 and 0.023, respectively)

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Summary

Introduction

Hepatitis B virus (HBV) infection is a global health problem. Liver transplantation (LT) is an established treatment option for serious liver disease caused by HBV infection. The therapeutic strategy of nucleos(t)ide analogs (NAs) combined with immune globulin has proven useful in preventing HBV reinfection after LT [9, 10]. This strategy does not completely protect against future recurrence of HBV infection. HBV reinfection is dependent on residual viral infection in extrahepatic organs, and individual immune responses.

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