肺移植术后出现感染并发症时,CLAD 期间的供体细胞游离 DNA 分数会升高,而感染并发症期间则不会

Mirza Novo, R. Nordén, Johan Westin, Göran Dellgren, Jens Böhmer, A. Ricksten, Jesper M. Magnusson
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摘要

在过去几年中,无细胞 DNA(cfDNA)已成为预测肺移植术后并发症的一种可能的非侵入性生物标志物。我们曾发表过一项概念验证研究,使用基于数字液滴聚合酶链反应(ddPCR)的方法检测 cfDNA。在当前的研究中,我们旨在进一步评估使用三种不同的 ddPCR 应用程序测量和计算 cfDNA 的供体部分 (DF) 以及一种使用供体来源的 cfDNA 绝对量的方法检测慢性肺移植功能障碍 (CLAD) 的潜在临床实用性。我们分析了从 26 名肺移植受者身上采集的 246 份血清样本。其中有九名患者在随访期间的某个阶段持续存在 CLAD。与非 CLAD 样本相比,所有四种方法都显示 CLAD 样本中的测量变量在统计学上有显著升高。这些结果支持将 ddPCR 检测到的 cfDNA 用作预测 CLAD 的潜在生物标记物。这些发现需要在后续的前瞻性研究中加以验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Donor Fractions of Cell-Free DNA Are Elevated During CLAD But Not During Infectious Complications After Lung Transplantation
During the last few years, cell-free DNA (cfDNA) has emerged as a possible non-invasive biomarker for prediction of complications after lung transplantation. We previously published a proof-of-concept study using a digital droplet polymerase chain reaction (ddPCR)-based method for detection of cfDNA. In the current study, we aimed to further evaluate the potential clinical usefulness of detecting chronic lung allograft dysfunction (CLAD) using three different ddPCR applications measuring and calculating the donor fraction (DF) of cfDNA as well as one method using the absolute amount of donor-derived cfDNA. We analyzed 246 serum samples collected from 26 lung transplant recipients. Nine of the patients had ongoing CLAD at some point during follow-up. All four methods showed statistically significant elevation of the measured variable in the CLAD samples compared to the non-CLAD samples. The results support the use of ddPCR-detected cfDNA as a potential biomarker for prediction of CLAD. These findings need to be validated in a subsequent prospective study.
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