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无细胞游离 DNA 检测肾移植排斥反应。

Cell-free DNA for the detection of kidney allograft rejection.

机构信息

Université Paris Cité, INSERM U970, Paris Institute for Transplantation and Organ Regeneration, Paris, France.

Department of Kidney Transplantation, Necker Hospital, Assistance Publique - Hôpitaux de Paris, Paris, France.

出版信息

Nat Med. 2024 Aug;30(8):2320-2327. doi: 10.1038/s41591-024-03087-3. Epub 2024 Jun 2.

DOI:10.1038/s41591-024-03087-3
PMID:38824959
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11333280/
Abstract

Donor-derived cell-free DNA (dd-cfDNA) is an emerging noninvasive biomarker that has the potential to detect allograft injury. The capacity of dd-cfDNA to detect kidney allograft rejection and its added clinical value beyond standard of care patient monitoring is unclear. We enrolled 2,882 kidney allograft recipients from 14 transplantation centers in Europe and the United States in an observational population-based study. The primary analysis included 1,134 patients. Donor-derived cell-free DNA levels strongly correlated with allograft rejection, including antibody-mediated rejection (P < 0.0001), T cell-mediated rejection (P < 0.0001) and mixed rejection (P < 0.0001). In multivariable analysis, circulating dd-cfDNA was significantly associated with allograft rejection (odds ratio 2.275; 95% confidence interval (CI) 1.902-2.739; P < 0.0001) independently of standard of care patient monitoring parameters. The inclusion of dd-cfDNA to a standard of care prediction model showed improved discrimination (area under the curve 0.777 (95% CI 0.741-0.811) to 0.821 (95% CI 0.784-0.852); P = 0.0011) and calibration. These results were confirmed in the external validation cohorts (n = 1,748) including a cohort of African American patients (n = 439). Finally, dd-cfDNA showed high predictive value to detect subclinical rejection in stable patients. Our study provides insights on the potential value of assessing dd-cfDNA, in addition to standard of care monitoring, to improve the detection of allograft rejection. ClinicalTrials.gov registration: NCT05995379 .

摘要

供体来源的无细胞游离 DNA(dd-cfDNA)是一种新兴的非侵入性生物标志物,有可能检测同种异体移植物损伤。dd-cfDNA 检测肾移植排斥反应的能力及其在标准护理患者监测之外的附加临床价值尚不清楚。我们在欧洲和美国的 14 个移植中心招募了 2882 名肾移植受者进行观察性基于人群的研究。主要分析包括 1134 名患者。供体来源的无细胞游离 DNA 水平与移植物排斥反应强烈相关,包括抗体介导的排斥反应(P<0.0001)、T 细胞介导的排斥反应(P<0.0001)和混合排斥反应(P<0.0001)。在多变量分析中,循环 dd-cfDNA 与移植物排斥反应显著相关(比值比 2.275;95%置信区间(CI)1.902-2.739;P<0.0001),独立于标准护理患者监测参数。将 dd-cfDNA 纳入标准护理预测模型显示出更好的区分度(曲线下面积 0.777(95%CI 0.741-0.811)至 0.821(95%CI 0.784-0.852);P=0.0011)和校准。这些结果在外部验证队列(n=1748)中得到了证实,包括一个非裔美国患者队列(n=439)。最后,dd-cfDNA 在稳定患者中检测亚临床排斥反应具有很高的预测价值。我们的研究提供了关于评估 dd-cfDNA 的潜在价值的见解,除了标准护理监测外,还可以提高同种异体移植物排斥反应的检测。临床试验注册:NCT05995379。

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