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Outcome of hepatitis B and C virus infection on graft function after renal transplantation
A Behzad-Behbahani1, A Mojiri, S Z Tabei
1Clinical Virology Section, Organ Transplant Research Center, Namazi Hospital, Shiraz University of Medical Sciences, Shiraz, Iran. behbahani_2000@yahoo.com
Insights
Hepatitis B and C infections do not appear to cause renal dysfunction in kidney transplant recipients within the first year. Long-term effects on liver disease or graft loss remain a possibility.
Area of Science:
- Nephrology
- Hepatology
- Transplantation Immunology
Background:
- Chronic liver disease from Hepatitis B Virus (HBV) and Hepatitis C Virus (HCV) is a significant concern in kidney transplant recipients.
- The impact of HBV and HCV infection status on renal dysfunction post-transplantation is not well understood.
Purpose of the Study:
- To investigate the incidence of HBV and HCV infections following renal transplantation.
- To determine if these viral infections are associated with altered graft function or renal dysfunction.
Main Methods:
- Serum samples from 58 renal transplant recipients and their living donors were analyzed.
- Tests included enzyme immunoassays for antibodies and viral markers, and RT-PCR for viral RNA/DNA.
- Serum creatinine and aminotransferase levels were monitored.
Main Results:
- Post-transplantation, 17.2% tested positive for anti-HCV, with 3.4% having detectable HCV-RNA.
- Hepatitis B core antibody (anti-HBc) was found in 13.8% of patients; HBsAg was detected in only 1.7% post-transplantation.
- No HBV DNA was detected, and no patients exhibited clinical signs of renal dysfunction during the study period.
Conclusions:
- Neither HBV nor HCV infection was found to cause or contribute to renal dysfunction in the early (1-year) post-transplant period.
- Long-term consequences, including chronic liver disease or graft loss due to HBV/HCV, cannot be ruled out in renal transplant recipients.
Introduction:
Chronic liver disease resulting from hepatitis B virus (HBV) and hepatitis C virus (HCV) infections is still a major concern in kidney recipients. It is unclear whether HCV antibody status and markers of HBV infection are associated with renal dysfunction. Thus, we designed a study to investigate the incidence of HBV and HCV infection after renal transplantation and whether these infections alter graft function.
Methods:
Fifty-eight patients who underwent renal transplantation participated in the study. Serum creatinine and aminotransferase levels were measured with standard automated analyzers. Anti-HCV antibodies were detected with an enzyme immunoassay, and a reverse transcriptase-polymerase chain reaction (RT-PCR) technique was used to test for HCV-RNA. Serological markers for HBV (HBsAg and anti-HBc antibody) were detected by enzyme immunoassay. All samples from patients who were seropositive for HBsAg or anti-HBc antibody were PCR-tested for HBV-DNA. A serum sample collected from living donors was tested for anti-HCV antibodies and serological markers for HBV. Serum creatinine and aminotransferase levels were also measured in living donors.
Results:
Anti-HCV was not detected in serum samples of any cases before transplantation. However, 10 (17.2%) tested positive after transplantation. HCV-RNA was detected in 2 of the 10 patients (3.4% of all patients). None of the pretransplantation serum samples tested positive for HBsAg. However, anti-HBc antibody was identified in 8 (13.8%) of the 58 patients.. No HBV DNA was detected in serum samples of the patients with anti-HBc or HBsAg-positive. HBsAg was only detected in 1 (1.7%) recipient after transplantation. None of the 58 patients showed clinical signs or symptoms of renal dysfunction during the study period.
Conclusion:
Our data suggest that, neither HBV nor HCV infection appears to cause or contribute to renal dysfunction in the early period (1 year) after renal transplantation. Nevertheless, a long-term consequence of chronic HBV or HCV liver disease or graft loss is not impossible in renal transplant recipients.
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