Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Department of Pathology, Medical School of Shiraz University, Shiraz University of Medical Sciences, Shiraz, Iran.
Front Immunol. 2020 Dec 23;11:613128. doi: 10.3389/fimmu.2020.613128. eCollection 2020.
The impact of anti-HLA donor-specific alloantibodies (DSA) which develop after long-term liver transplantation (LT) remains controversial and unclear. The aim of this study was to investigate the role of DSAs on the outcome in LT.
We did a systematic review and meta-analysis of observational studies published until Dec 31, 2019, that reported DSA outcome data (≥1 year of follow-up) after liver transplant. A literature search in the MEDLINE/PubMed, EMBASE, Cochrane Library, Scopus and Web of Science Core Collection databases was performed.
Of 5,325 studies identified, 15 fulfilled our inclusion criteria. The studies which reported 2016 liver transplant recipients with DSAs showed an increased complication risk, i.e. graft loss and chronic rejection (OR 3.61; 95% CI 1.94-6.71, < 0.001; I 58.19%), and allograft rejection alone (OR 6.43; 95% CI: 3.17-13.04; < 0.001; I 49.77%); they were compared to patients without DSAs. The association between DSAs and overall outcome failure was consistent across all subgroups and sensitivity analysis.
Our study suggested that DSAs had a significant deleterious impact on the liver transplant risk of rejection. The routine detection of DSAs may be beneficial as noninvasive biomarker-guided risk stratification.
在长期肝移植(LT)后产生的抗 HLA 供体特异性抗体(DSA)的影响仍存在争议且尚未明确。本研究旨在探讨 DSA 在 LT 结局中的作用。
我们对截至 2019 年 12 月 31 日发表的观察性研究进行了系统评价和荟萃分析,这些研究报告了肝移植后 DSA 结局数据(随访时间≥1 年)。我们在 MEDLINE/PubMed、EMBASE、Cochrane 图书馆、Scopus 和 Web of Science 核心合集数据库中进行了文献检索。
在 5325 项研究中,有 15 项符合我们的纳入标准。报道 2016 年肝移植受者存在 DSA 的研究显示,并发症风险增加,即移植物丢失和慢性排斥反应(OR 3.61;95%CI 1.94-6.71, < 0.001;I 58.19%),以及单独的同种异体移植排斥反应(OR 6.43;95%CI:3.17-13.04; < 0.001;I 49.77%);与无 DSA 的患者相比。DSA 与整体移植失败结局之间的关联在所有亚组和敏感性分析中均一致。
我们的研究表明,DSA 对肝移植排斥风险有显著的不良影响。常规检测 DSA 可能有益于作为非侵入性生物标志物指导的风险分层。