Hepatitis B Virus Reactivation in Non‐Liver Solid Organ Transplantation: Incidence and Risk Analysis

Author:

Chiu Chia‐Yu1ORCID,Brumble Lisa M.2,Vikram Holenarasipur R.3ORCID,Watt Kymberly D.45,Beam Elena15ORCID

Affiliation:

1. Division of Public Health Infectious Diseases, and Occupational Medicine Department of Medicine Mayo Clinic Rochester Minnesota USA

2. Division of Infectious Diseases Mayo Clinic Jacksonville Florida USA

3. Division of Infectious Diseases Mayo Clinic Phoenix Arizona USA

4. Division of Gastroenterology and Hepatology Department of Medicine Mayo Clinic Rochester Minnesota USA

5. William J. von Liebig Center for Transplantation and Clinical Regeneration Mayo Clinic Rochester Minnesota USA

Abstract

ABSTRACTIntroductionHepatitis B virus reactivation (HBVr) can occur in solid organ transplant (SOT) recipients with previously inactive hepatitis B virus (HBV) infection. Previous studies have reported that HBVr is generally less than 10% in nonliver SOT recipients with past HBV infection.MethodsWe conducted a retrospective study from January 2018 to August 2023 at Mayo Clinic sites in Arizona, Florida, and Minnesota. We examined the antiviral prophylaxis strategy used and the characteristics of HBVr in hepatitis B core antibody‐positive (HBcAb +) nonliver SOT adult recipients. Past HBV infection was defined as HBcAb + / hepatitis B surface antigen (HBsAg) –. Chronic HBV infection was defined as HBcAb + / HBsAg +.ResultsA total of 180 nonliver SOT recipients were identified during the study period. Indefinite antiviral prophylaxis was utilized in 77 recipients, and none developed HBVr after transplantation. In 103 recipients without antiviral prophylaxis, the incidence of HBVr was 12% (12/97) and 33% (2/6) in those with past HBV infection and chronic HBV infection. The incidence of HBVr in patients with past HBV infection is 16% (8/50), 15% (3/20), and 5% (1/22) in kidney, heart, and lungs, respectively. HBVr was more frequent in those who received alemtuzumab. Among 14 recipients with HBVr, none had HBV‐associated liver failure or death.ConclusionsOur study observed a higher rate of HBVr (12%) in nonliver SOT recipients with past HBV infection compared to the previous studies. Further studies are needed to identify predictors of HBVr in nonliver SOT recipients and optimize antiviral prophylaxis guidance.

Publisher

Wiley

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