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Long-term impact of hepatitis B, C virus infection on renal transplantation
1Division of Nephrology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan, ROC.
Insights
Hepatitis B virus (HBV) infection significantly increases risks for liver cirrhosis, hepatic failure, and death in renal transplant recipients. Hepatitis C virus (HCV) infection appears to have minimal impact on long-term transplant outcomes.
Area of Science:
- Nephrology
- Hepatology
- Transplantation Immunology
Background:
- Chronic liver disease poses significant challenges for renal transplant recipients.
- The influence of hepatitis B virus (HBV) and hepatitis C virus (HCV) on long-term renal transplant outcomes requires elucidation.
Purpose of the Study:
- To investigate the impact of HBV and HCV infections on the long-term outcomes of renal transplantation.
- To assess the risks of hepatoma, liver cirrhosis, hepatic failure, graft failure, and mortality in infected patients.
Main Methods:
- Retrospective analysis of 477 renal transplant recipients from January 1984 to December 1999.
- Detection of HBsAg and anti-HCV antibodies using RIA methods.
- Monitoring of liver enzymes (SGOT/SGPT), diagnosis of hepatoma, and survival analysis using Cox regression.
Main Results:
- Prevalence: HBV (9.9%), HCV (28.5%), coinfection (3.1%).
- Higher incidences of liver cirrhosis/hepatic failure (p < 0.001) and chronic liver disease (p < 0.001) in HBV-infected groups.
- HBV infection was a borderline independent risk factor for patient mortality and associated with increased hepatoma, hepatic failure, graft failure, and death.
Conclusions:
- HBV infection significantly worsens long-term outcomes in renal transplant recipients, necessitating careful pre-transplant evaluation.
- HCV infection demonstrated minimal impact on patient and graft survival in this cohort.
- Further long-term studies are required to fully understand HCV's role in renal transplant recipients.
Abstract:
Chronic liver disease and its complications are major problems in renal transplant recipients. Our aim was to elucidate the influence of hepatitis B, C virus infection on the long-term outcome of renal transplantation. Four hundred and seventy-seven patients who received renal transplantation between January 1984 and December 1999, and who were followed up at our hospital were enrolled. HBsAg was detected by the RIA method and anti-HCV Ab was assayed by the second-generation RIA kit. SGOT/ SGPT were checked every 3 months. Hepatoma was diagnosed by dynamic CT scan, elevated alpha-fetoprotein, hypervascularity by angiography and confirmed by pathological examination. The prevalence of HBV, HCV, coinfected HBV/HCV was 9.9% (n = 47), 28.5% ( n = 136), 3.1% (n = 15), respectively. The incidences of hepatoma in the HBV-/HCV-, HBV-/HCV+, HBV+/HCV-, HBV+/HCV+ groups were 1.4% (n = 4), 4.4% (n = 6), 6.4% (n = 3), 6.7% (n = 1), respectively (p = 0.114). The incidences of liver cirrhosis/hepatic failure were 3.2% (n = 9), 6.6% (n = 9), 21.3% (n = 10), 20% (n = 3), respectively (p < 0.001). The frequencies of chronic liver disease were 10.4% (n = 29), 45.6% (n = 62), 66% (n = 31), 80% (n = 12), respectively (p < 0.001). Patient and graft survival rates were lower in the HBV-infected group than in the other groups. Cox regression analysis revealed that HBV infection is likely an independent risk factor for patient mortality although the statistical significance was only borderline. Patients with HBV as well as HCV infection were not at risk of graft loss according to this model of analysis. Patients with HBV infection showed higher incidences of hepatoma, hepatic failure, graft failure and death. Therefore, HBV-infected patients who are candidates for renal transplantation should be carefully evaluated. It seems that HCV infection has little influence on the outcome of renal transplant recipients. A longer period of follow-up is needed to clarify the impact of HCV on renal transplant recipients.
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