Sebastian Alizée, Silvy Monique, Coiffard Benjamin, Reynaud-Gaubert Martine, Magdinier Frédérique, Chiaroni Jacques, Picard Christophe, Pedini Pascal
Aix-Marseille University, Centre National de la Recherche Scientifique (CNRS), Etablissement Français du Sang (EFS), Anthropologie Bio-Culturelle, Droit, Éthique et Santé (ADES), Marseille, France.
BeDia Genomics, Aix-en-Provence, France.
Front Transplant. 2024 Nov 15;3:1474920. doi: 10.3389/frtra.2024.1474920. eCollection 2024.
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.
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.
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.
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.
循环游离DNA(cfDNA)正在成为实体器官移植(SOT)监测中的一种非侵入性生物标志物,近年来其诊断潜力的数据不断增加。本综述旨在总结cfDNA在移植领域的技术、临床应用和未来前景的主要进展,并探讨表观遗传学在改善排斥反应特异性检测方面的作用。
系统回顾了将cfDNA作为移植排斥诊断生物标志物的已发表文献,特别是评估基于cfDNA分数预测排斥反应的算法测试性能的临床试验。还回顾了突出移植排斥表观遗传特征的文献,以概述表观基因组分析对排斥反应特异性诊断需求的潜在贡献。
共检索了40篇文章,并提取和总结了结果。16篇文章通过评估预测性测试对区分排斥与非排斥患者的诊断性能符合纳入标准(2例心脏移植、3例肝脏移植、4例肾脏移植和7例肺移植)。反复得出的结论是,dd-cfDNA水平的动力学在移植后立即大幅上升,数天至数周后达到基础水平,在非排斥患者中保持稳定。另一方面,排斥反应的特征是dd-cfDNA水平升高,这取决于移植的器官。此外,表观遗传特征可通过寻找与患者临床状态相关的特定表观遗传特征来帮助提高排斥反应诊断的特异性。
游离DNA是一种有前景的非侵入性生物标志物,但仍需要技术和方案的标准化以用于诊断目的。此外,尽管在临床应用中仍需进一步进展,但表观遗传分析的数据不断增加,可弥补该标志物缺乏特异性的问题。