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Personalized Peptide Arrays for Detection of HLA Alloantibodies in Organ Transplantation
Published on: September 6, 2017
HLA-DR matching improves survival after heart transplantation: is it time to change allocation policies?
Ingo Kaczmarek1, Marcus-Andre Deutsch, Maria-Elisabeth Rohrer
1Department of Cardiac Surgery, Grosshadern University Hospital, Munich, Munich, Germany.
Insights
Human Leukocyte Antigen (HLA)-DR matching significantly impacts long-term survival and reduces cardiac allograft vasculopathy after heart transplantation. Incorporating HLA-DR matching into organ allocation policies could improve patient outcomes.
Area of Science:
- Immunogenetics
- Transplantation immunology
- Cardiovascular surgery
Background:
- Human Leukocyte Antigen (HLA) matching is crucial for kidney transplant success but not standard in heart transplant allocation.
- This study investigates the long-term impact of HLA matching on heart transplant recipients.
- Current heart transplant allocation policies do not consider HLA matching.
Purpose of the Study:
- To assess the influence of HLA matching on long-term outcomes in heart transplantation.
- To determine if HLA-DR matching affects patient survival and graft vasculopathy.
Main Methods:
- Retrospective analysis of 240 heart transplant recipients (1995-2002).
- Calculation of HLA mismatches (MM) at HLA-A, HLA-B, and HLA-DR loci based on renal allocation policy.
- Exclusion of patients with primary graft failure from statistical analysis.
Main Results:
- Significant impact of HLA-DR mismatches on survival; 5-year survival decreased with increasing HLA-DR MM.
- Reduced freedom from cardiac allograft vasculopathy with higher HLA-DR mismatches.
- A trend towards higher risk of adverse outcomes with increased HLA mismatches at major loci.
Conclusions:
- HLA-DR matching significantly influences survival after heart transplantation.
- Inclusion of HLA-DR matching in organ allocation policies may enhance long-term heart transplant outcomes.
- Optimizing donor organ utilization through HLA-DR matching is recommended.
Background:
HLA matching has improved outcome in kidney transplantation but is not considered in current allocation policies in heart transplantation. The aim of this single-center study was to assess the impact of HLA matching on long- term outcome after heart transplantation.
Methods:
The records of 240 consecutive heart transplant recipients (time period 1995 to 2002; mean age 51.8 +/- 11.7 years; mean follow-up 5.9 +/- 1.8 years) were analyzed retrospectively. According to the renal allocation policy, HLA mismatches (MM) on the major antigen loci HLA-A, HLA-B and HLA-DR were calculated, demonstrating 0 to 6 MM. Patients with primary graft failure were excluded from statistical analysis.
Results:
Survival analysis revealed a statistically significant impact of HLA-DR MM on survival. Five-year survival was 90% in patients without HLA-DR MM (n = 10), 79% in patients with 1 HLA-DR MM (n = 113), and 68.1% in patients with 2 HLA-DR MM (n = 117) (1 MM vs 2 MM: p < 0.05). Freedom from cardiac allograft vasculopathy after 5 years was 89% in HLA-DR-identical recipients (n = 10), 61% in patients with 1 HLA-DR MM (n = 102), 54% in patients with 2 HLA-DR MM (n = 104). Conventional matching with 6 mismatches over the three major HLA antigen loci revealed a trend toward a higher relative risk for adverse outcome in patients with increased MM.
Conclusions:
HLA-DR matching had a significant impact on survival after heart transplantation (HTx) at our center. In the effort to achieve the best comparative use of scarce donor organs the inclusion of HLA-DR matching into allocation policies might improve long-term outcome after HTx.
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