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供者来源的无细胞 DNA(dd-cfDNA)在有指征性肾移植活检结果的受者中的应用:一项前瞻性单中心试验的结果。

Donor-Derived Cell-Free DNA (dd-cfDNA) in Kidney Transplant Recipients With Indication Biopsy-Results of a Prospective Single-Center Trial.

机构信息

Department of Nephrology, Heidelberg University Hospital, Heidelberg, Germany.

Institute of Immunology, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

Transpl Int. 2023 Nov 3;36:11899. doi: 10.3389/ti.2023.11899. eCollection 2023.

Abstract

Donor-derived cell-free DNA (dd-cfDNA) identifies allograft injury and discriminates active rejection from no rejection. In this prospective study, 106 kidney transplant recipients with 108 clinically indicated biopsies were enrolled at Heidelberg University Hospital between November 2020 and December 2022 to validate the clinical value of dd-cfDNA in a cohort of German patients. dd-cfDNA was quantified at biopsy and correlated to histopathology. Additionally, dd-cfDNA was determined on days 7, 30, and 90 post-biopsy and analyzed for potential use to monitor response to anti-rejection treatment. dd-cfDNA levels were with a median (IQR) % of 2.00 (0.48-3.20) highest in patients with ABMR, followed by 0.92 (0.19-11.25) in patients with TCMR, 0.44 (0.20-1.10) in patients with borderline changes and 0.20 (0.11-0.53) in patients with no signs of rejection. The AUC for dd-cfDNA to discriminate any type of rejection including borderline changes from no rejection was at 0.72 (95% CI 0.62-0.83). In patients receiving anti-rejection treatment, dd-cfDNA levels significantly decreased during the 7, 30, and 90 days follow-up compared to levels at the time of biopsy ( = 0.006, = 0.002, and < 0.001, respectively). In conclusion, dd-cfDNA significantly discriminates active rejection from no rejection. Decreasing dd-cfDNA following anti-rejection treatment may indicate response to therapy. : https://drks.de/search/de/trial/DRKS00023604, identifier DRKS00023604.

摘要

供体来源的无细胞游离 DNA(dd-cfDNA)可识别移植物损伤,并区分急性排斥反应与无排斥反应。在这项前瞻性研究中,2020 年 11 月至 2022 年 12 月期间,海德堡大学医院纳入了 106 例接受 108 例临床指征活检的肾移植受者,以验证 dd-cfDNA 在德国患者队列中的临床价值。在活检时定量测定 dd-cfDNA,并与组织病理学相关联。此外,在活检后第 7、30 和 90 天测定 dd-cfDNA,并分析其用于监测抗排斥治疗反应的潜力。dd-cfDNA 水平以中位数(IQR)%表示,ABMR 患者最高(2.00%[0.48-3.20]),TCMR 患者次之(0.92%[0.19-11.25]),边界改变患者为 0.44%[0.20-1.10],无排斥反应患者为 0.20%[0.11-0.53]。dd-cfDNA 鉴别包括边界改变在内的任何类型排斥反应与无排斥反应的 AUC 为 0.72(95%CI 0.62-0.83)。在接受抗排斥治疗的患者中,与活检时的水平相比,dd-cfDNA 水平在 7、30 和 90 天随访期间显著降低(=0.006,=0.002 和<0.001)。总之,dd-cfDNA 可显著区分急性排斥反应与无排斥反应。抗排斥治疗后 dd-cfDNA 的降低可能表明对治疗有反应。 : https://drks.de/search/de/trial/DRKS00023604,标识符 DRKS00023604。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c90f/10654198/f021fe87f98b/ti-36-11899-g001.jpg

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