Direct-acting antivirals and hepatitis B virus (HBV) reactivation in co-infected HBV/HCV kidney-transplant recipients

Transpl Infect Dis. 2018 Jun;20(3):e12864. doi: 10.1111/tid.12864. Epub 2018 Mar 25.

Abstract

Direct-acting agents (DAAs) are highly efficient at treating hepatitis C virus (HCV) infections after kidney transplantation. Although drug agencies have recently warned of the risk of hepatitis B virus (HBV) reactivation after patients have received DAAs, reports have discrepant results in HBsAg-positive and HBsAg-negative patients. We report on 3 cases of HBV reactivation that were detected after achieving a DAA-associated sustained virological response in 3 kidney-transplant recipients initially HBsAg-negative. In the first case, retrospective virological analysis revealed that HBsAgs had become positive and HBV DNA was detectable before initiating DAA therapy. In the second and third cases, HBV reactivation occurred 2 months and more than 1 year after stopping anti-HCV therapy. These cases underline the discrepancies and highlight the need for comprehensive information before making definitive conclusions regarding the causal link between DAAs and HBV reactivation.

Keywords: HBsAg; direct-acting agents; hepatitis B virus; hepatitis C virus; kidney transplantation.

Publication types

  • Case Reports

MeSH terms

  • Antiviral Agents / administration & dosage
  • Antiviral Agents / therapeutic use*
  • Coinfection / drug therapy
  • Coinfection / virology*
  • DNA, Viral / blood
  • Female
  • Hepacivirus / drug effects
  • Hepatitis B / drug therapy
  • Hepatitis B / virology
  • Hepatitis B Surface Antigens / analysis
  • Hepatitis B virus / drug effects
  • Hepatitis B virus / physiology*
  • Hepatitis C / drug therapy
  • Hepatitis C / virology
  • Hepatitis C, Chronic / drug therapy
  • Hepatitis C, Chronic / virology
  • Humans
  • Kidney Transplantation / adverse effects*
  • Male
  • Middle Aged
  • Retrospective Studies
  • Sustained Virologic Response
  • Transplant Recipients
  • Virus Activation / drug effects*

Substances

  • Antiviral Agents
  • DNA, Viral
  • Hepatitis B Surface Antigens