Immunosuppression status of liver transplant recipients with hepatitis C affects biopsy-proven acute rejection

Clin Mol Hepatol. 2016 Sep;22(3):366-371. doi: 10.3350/cmh.2016.0022. Epub 2016 Sep 25.

Abstract

Background/aims: The relationship between patient survival and biopsy-proven acute rejection (BPAR) in liver transplant recipients with hepatitis C remains unclear. The aims of this study were to compare the characteristics of patients with and without BPAR and to identify risk factors for BPAR.

Methods: We retrospectively reviewed the records of 169 HCV-RNA-positive patients who underwent LT at three centers.

Results: BPAR occurred in 39 (23.1%) of the HCV-RNA-positive recipients after LT. The 1-, 3-, and 5-year survival rates were 92.1%, 90.3%, and 88.5%, respectively, in patients without BPAR, and 75.7%, 63.4%, and 58.9% in patients with BPAR (P<0.001). Multivariate analyses showed that BPAR was associated with the non-use of basiliximab and tacrolimus and the use of cyclosporin in LT recipients with HCV RNA-positive.

Conclusion: The results of the present study suggest that the immunosuppression status of HCV-RNA-positive LT recipients should be carefully determined in order to prevent BPAR and to improve patient survival.

Keywords: Calcineurin antagonists; Hepatitis C virus; Immunosuppression; Outcome; Rejection; Tacrolimus.

MeSH terms

  • Antibodies, Monoclonal / therapeutic use
  • Basiliximab
  • Biopsy
  • Cyclosporine / therapeutic use
  • Drug Therapy, Combination
  • Genotype
  • Graft Rejection / mortality
  • Graft Rejection / prevention & control*
  • Hepacivirus / genetics
  • Hepacivirus / isolation & purification
  • Hepatitis C / drug therapy
  • Hepatitis C / virology*
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Liver Transplantation* / adverse effects
  • Polymerase Chain Reaction
  • RNA, Viral / blood
  • Recombinant Fusion Proteins / therapeutic use
  • Recurrence
  • Retrospective Studies
  • Survival Rate
  • Tacrolimus / therapeutic use

Substances

  • Antibodies, Monoclonal
  • Immunosuppressive Agents
  • RNA, Viral
  • Recombinant Fusion Proteins
  • Cyclosporine
  • Basiliximab
  • Tacrolimus