H epatitis C virus (HCV) infection is a global health problem. The importance of HCV infection lies in its propensity to cause insidious and progressive liver damage, including chronic hepatitis, cirrhosis, and hepatocellular carcinoma. The clinical and financial impact of HCV infection on this nati
Influence of donor/recipient HLA-matching on outcome and recurrence of hepatitis C after liver transplantation
✍ Scribed by Jan Michael Langrehr; Gero Puhl; Marcus Bahra; Maximilian Schmeding; Antonino Spinelli; Thomas Berg; Constanze Schönemann; Veit Krenn; Peter Neuhaus; Ulf Peter Neumann
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 122 KB
- Volume
- 12
- Category
- Article
- ISSN
- 1527-6465
- DOI
- 10.1002/lt.20648
No coin nor oath required. For personal study only.
✦ Synopsis
The aim of this study was to analyze the effect of human leukocyte antigen (HLA) matching on outcome, severity of recurrent hepatitis C and risk of rejection in hepatitis C positive patients after liver transplantation (LT). In a retrospective analysis, 165 liver transplants in patients positive for hepatitis C virus (HCV) with complete donor/recipient HLA typing were reviewed for recurrence of HCV and outcome. Follow-up ranged from 1 to 158 months (median, 74.5 months). Immunosuppression consisted of either cyclosporine-A-or tacrolimus-based quadruple induction therapy including or an interleukin 2-receptor antagonist. Protocol liver biopsies were performed after 1, 3, 5, 7, and 10 years and staged according to the Scheuer scoring system. The overall 1-, 5-, and 10-year graft survival figures were 81.8%, 69.11 and 62%, respectively. There was no correlation in the study population between number of HLA mismatches and graft survival. The number of rejection episodes increased significantly in patients with more HLA mismatches (P Ͻ 0.05). In contrast to this, the fibrosis progression was significantly faster in patients with 0-5 HLA mismatches compared to patients with a complete HLA mismatch. In conclusion, HLA matching did not influence graft survival in patients after LT for end-stage HCV infection, however, despite less rejection episodes, the fibrosis progression increased in patients with less HLA mismatches within the first year after LT.
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