HLA matching between donors and recipients improves clinical liver transplant graft survival

医学 人类白细胞抗原 免疫抑制 内科学 倾向得分匹配 肝移植 组织相容性试验 多元分析 移植 回顾性队列研究 生存分析 比例危险模型 肿瘤科 免疫学 抗原
作者
Sarah Nabulsi,Afolarin Otunla,Justin D. Salciccioli,Dominic C. Marshall,Vincenzo Villani,Kumaran Shanmugarajah,Joseph Shalhoub
出处
期刊:Liver International [Wiley]
卷期号:44 (2): 411-421
标识
DOI:10.1111/liv.15774
摘要

Abstract Background and Aims The importance of human leukocyte antigen (HLA) matching between liver transplant donors and recipients on graft survival remains unclear and is not a clinical consideration in liver transplantation. This study aimed to determine the relationship between HLA matching and liver graft survival using a large‐scale multi‐centre database (UNOS/OPTN) and multivariate logistic analysis. The secondary aim was to determine whether this relationship was influenced by transplant indication and donor status. Methods This retrospective observational analysis was performed using 22 702 liver transplant recipients from the UNOS/OPTN database. Patients were divided into two groups based on number of HLA mismatches (0–3 mismatches vs. 4–6 mismatches) and then subcategorized by indication and donor status. Risk‐adjusted outcomes were assessed by multivariate Cox analysis adjusting for donor and recipient characteristics and visualized using Kaplan–Meier survival curves. Results Allograft survival and risk of acute rejection were associated with degree of HLA mismatch. This association between HLA mismatch and graft survival persisted in individuals who underwent transplant for hepatitis, metabolic, drug toxicity, and congenital indications. Donor status also influenced the relationship between HLA mismatch and graft survival. Graft survival in DBD recipients was longer than in DCD in the 4–6 HLA mismatch group, whereas no significant difference was found in the 0–3 HLA mismatch group. Conclusion HLA mismatch significantly reduced graft survival and increased risk of acute rejection. This association was noted only in specific indications. These findings are of potential clinical relevance to organ allocation, allograft matching algorithms, immunosuppression protocols, and transplant surveillance.

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