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肺移植结局中的人类白细胞抗原错配。

Human leukocyte antigen mismatch on lung transplantation outcomes.

机构信息

Lewis Katz School of Medicine at Temple University, Philadelphia, PA, USA.

Department of Cardiovascular Surgery, Temple University Hospital, Philadelphia, PA, USA.

出版信息

Eur J Cardiothorac Surg. 2022 Jul 11;62(2). doi: 10.1093/ejcts/ezac132.

Abstract

OBJECTIVES

Human leucocyte antigen (HLA) mismatch is a known risk factor for renal transplantation; however, there are conflicting and limited data on its ramifications within lung transplantation (LTx). Therefore, our study evaluated the effects of total HLA, HLA-A, -B and -DR mismatches on LTx outcomes.

METHODS

We retrospectively examined the United Network for Organ Sharing database for adult patients who had undergone LTx for the first time between January 2005 and July 2021. Total HLA mismatch (0-3, 4, 5 and 6) and HLA locus mismatch (0-1 and 2) were analysed, with the end points of interest being mortality and bronchiolitis obliterans syndrome (BOS) development.

RESULTS

Kaplan-Meier curve analysis found a significant difference in both overall survival (n = 27 651; 11 830 events) and BOS development (n = 25 444; 8901 events) for the total number of HLA (P < 0.001, P < 0.001), HLA-A (P < 0.001, P = 0.006) and HLA-DR (P < 0.001, P < 0.001) mismatches. With reference to 0-3 total HLA mismatches, multivariable Cox regression model found that 6 mismatches had an increased risk of mortality (P = 0.002) while 4 (P = 0.010), 5 (P = 0.007) and 6 (P < 0.001) mismatches had an increased risk of BOS. HLA-B mismatch was not associated with an increased mortality (P = 0.975) or BOS risk (P = 0.512).

CONCLUSIONS

This study demonstrates a significant relationship between increased HLA mismatches and BOS development, with decreased overall survival only apparent with 6 mismatches. HLA-A and -DR mismatches were associated with an increased risk of mortality and BOS development compared to groups with at least 1 locus match.

摘要

目的

人类白细胞抗原(HLA)不匹配是肾移植的已知风险因素;然而,在肺移植(LTx)中,其结果存在相互矛盾且有限的数据。因此,我们的研究评估了总 HLA、HLA-A、-B 和 -DR 不匹配对 LTx 结果的影响。

方法

我们回顾性地检查了 2005 年 1 月至 2021 年 7 月期间首次接受 LTx 的成人患者的 United Network for Organ Sharing 数据库。分析了总 HLA 不匹配(0-3、4、5 和 6)和 HLA 基因座不匹配(0-1 和 2),感兴趣的终点是死亡率和细支气管炎闭塞综合征(BOS)的发展。

结果

Kaplan-Meier 曲线分析发现,在总 HLA 数量(n=27651;11830 例事件)和 BOS 发展(n=25444;8901 例事件)方面,HLA(P<0.001,P<0.001)、HLA-A(P<0.001,P=0.006)和 HLA-DR(P<0.001,P<0.001)不匹配均有显著差异。与 0-3 个总 HLA 不匹配相比,多变量 Cox 回归模型发现,6 个不匹配增加了死亡率的风险(P=0.002),而 4(P=0.010)、5(P=0.007)和 6(P<0.001)个不匹配增加了 BOS 的风险。HLA-B 不匹配与死亡率增加无关(P=0.975)或 BOS 风险增加无关(P=0.512)。

结论

本研究表明,HLA 不匹配增加与 BOS 发展之间存在显著关系,仅在存在 6 个不匹配时才出现总体生存率降低。与至少有 1 个基因座匹配的组相比,HLA-A 和 -DR 不匹配与死亡率和 BOS 发展的风险增加相关。

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