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Published on: May 2, 2013
DR antigens influence graft outcome and HCV recurrence after liver transplantation
1Medical College of Virginia Hospitals, Department of Transplant Surgery, Richmond, Virginia 23298, USA. pkimball@gems.vcu.edu
Insights
Recipient DR antigens influence Hepatitis C (HCV) recurrence after liver transplant. Specific DR types impact allograft survival and disease severity, suggesting host genetics predict outcomes.
Area of Science:
- Immunogenetics
- Transplantation Immunology
- Hepatology
Background:
- Hepatitis C virus (HCV) recurrence post-liver transplantation is common but variable.
- The role of human leukocyte antigen (HLA) -DR antigens in HCV recurrence severity and allograft survival is not fully understood.
Purpose of the Study:
- To investigate the impact of recipient HLA-DR antigens and DR mismatching on HCV recurrence and allograft survival after liver transplantation.
Main Methods:
- Comparison of clinical outcomes in HCV+ liver transplant recipients based on specific DR antigens (DR2, DR3, DR5) versus others.
- Analysis of allograft survival, HCV recurrence rates, liver disease severity, and acute rejection incidence.
Main Results:
- Recipients with DR3 showed reduced allograft survival, higher HCV recurrence, and more severe liver disease.
- Recipients with DR5 demonstrated superior allograft survival, low HCV recurrence, and benign liver disease.
- Zero DR mismatches correlated with better allograft survival, though DR mismatching level did not impact HCV recurrence or severity.
Conclusions:
- Host genetic factors, specifically recipient DR antigens, significantly influence HCV recurrence and allograft outcomes post-liver transplantation.
- Identifying DR antigens can help predict individual patient risk for severe HCV recurrence and inform post-transplant management.
Abstract:
Hepatitis C (HCV) recurrence following liver transplantation is universal. However, the severity of recurrence is highly variable between patients. We speculated that recipient DR antigens or the level of DR mismatching between the recipient and the donor might affect the severity of HCV recurrence and allograft survival. Clinical outcome was compared between HCV+ recipients with DR2, DR3, or DR5 versus HCV+ recipients with all other DR antigens. Recipients with DR3 had reduced allograft survival (P < .02), a higher rate of HCV recurrence (P < .05), and more severe liver disease (P < .05). Recipients with DR5 had superior allograft survival (P < .05), low rates of HCV recurrence (P < .05), and benign liver disease (P < .05). Clinical outcome of recipients with DR2 was equivalent (P = Ns) to the non-DR2, -3, -5 recipients. The incidence of acute rejection was equivalent (P = Ns) in all groups. The level of DR mismatching between donor and recipient did not affect HCV recurrence or severity. However, allograft survival was better (P < .05) in recipients with zero DR mismatches. The data show that host genetic factors play an important role in HCV recurrence and allograft outcome after liver transplantation. In addition, identification of DR antigens may help predict an HCV+ patient's relative risk for severe HCV recurrence.
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