无细胞DNA和表观遗传学在实体器官移植无创诊断中的研究进展。

Frontiers in transplantation Pub Date : 2024-11-15 eCollection Date: 2024-01-01 DOI:10.3389/frtra.2024.1474920
Alizée Sebastian, Monique Silvy, Benjamin Coiffard, Martine Reynaud-Gaubert, Frédérique Magdinier, Jacques Chiaroni, Christophe Picard, Pascal Pedini
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引用次数: 0

摘要

近年来,循环无细胞DNA (cfDNA)作为一种非侵入性生物标志物在实体器官移植(SOT)监测中逐渐兴起,有关其诊断潜力的数据也越来越多。本文综述了cfDNA在移植中的主要技术进展、临床应用和未来前景,并探讨了表观遗传学对提高排斥反应特异性检测的贡献。方法:系统回顾已发表的研究cfDNA作为移植排斥反应诊断生物标志物的文献,特别是评估基于cfDNA分数预测排斥反应算法测试性能的临床试验。文献强调移植排斥反应的表观遗传特征也进行了回顾,概述了表观基因组分析对排斥特异性诊断的潜在贡献。结果:共查阅文献40篇,提取总结结果。16例符合纳入标准,通过评估排斥反应与非排斥反应患者区分的预测测试的诊断性能(2例心脏、3例肝脏、4例肾脏和7例肺移植)。反复出现的结论是dd-cfDNA水平的动力学,在移植后立即强烈增加,在数天至数周后达到基础水平,并在非排斥患者中保持稳定。另一方面,排斥反应的特点是dd-cfDNA水平的增加,这取决于移植的器官。此外,表观遗传标记可以通过寻找与患者临床状态相关的特异性表观遗传特征,帮助提高排斥诊断的特异性。结论:无细胞DNA是一种很有前途的无创生物标志物,但仍需要标准化的技术和方案来用于诊断目的。此外,该标记物特异性的缺乏可以通过表观遗传分析的贡献来弥补,表观遗传分析的数据正在增长,尽管其在临床背景下的使用仍需取得进展。
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A review of cell-free DNA and epigenetics for non-invasive diagnosis in solid organ transplantation.

Introduction: Circulating cell-free DNA (cfDNA) is emerging as a non-invasive biomarker in solid organ transplantation (SOT) monitoring and data on its diagnostic potential have been increasing in recent years. This review aims to summarize the main advances in technologies, clinical applications and future perspectives of cfDNA for transplantation, and to approach the contribution of epigenetics to improve the specific detection of rejection.

Methods: Published literature investigating cfDNA as a biomarker for the diagnosis of transplant rejection was systematically reviewed, specifically clinical trials evaluating the test performance of algorithms predicting rejection based on cfDNA fraction. Literature highlighting epigenetic features in transplant rejection was also reviewed to outline the potential contribution of the epigenomic analysis to the needs of rejection-specific diagnosis.

Results: 40 articles were reviewed, and results were extracted and summarized. 16 met the inclusion criteria by evaluating the diagnostic performance of a predictive test for the discrimination of rejection vs. non-rejection patients (2 heart, 3 liver, 4 kidney, and 7 lung transplantations). The recurring conclusion is the kinetics of dd-cfDNA levels, strongly increasing immediately after transplantation and reaching basal levels after days to weeks and remaining stable in non-rejection patients. On the other hand, rejection is characterized by an increase in dd-cfDNA levels, depending on the transplanted organs. In addition, the epigenetic signature can help improve the specificity of the diagnosis of rejection by searching for specific epigenetic features that are by the clinical status of patients.

Conclusion: Cell-free DNA is a promising non-invasive biomarker but still needs standardization of technologies and protocols to be used for diagnostic purposes. Moreover, the lack of specificity of this marker can be compensated by the contribution of epigenetic analysis for which data are growing, although progress is still needed for its use in a clinical context.

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