Yoo Ashley, Riedel Alexandria, Qian Ian, Bartosic Amanda, Soltani Rudi, Kibria Gulam, Haririan Abdolreza, Drachenberg Cinthia B, Abrams Peter L, Odorico Jon S, Cooper Matthew, Bromberg Jonathan S, Scalea Joseph R
Division of Transplant Surgery, Department of Surgery, University of Maryland School of Medicine, Baltimore, MD.
Division of Transplantation, Department of Surgery, University of Wisconsin School of Medicine and Public Health, Madison, WI.
Transplant Direct. 2023 Mar 15;9(4):e1459. doi: 10.1097/TXD.0000000000001459. eCollection 2023 Apr.
Pancreas transplantation offers patients with diabetes an opportunity for glucose homeostasis. Current blood tests to surveil for rejection have poor sensitivity and specificity for identifying rejection, and pancreas biopsies are challenging and associated with morbidity and graft loss. Donor-derived cell-free DNA (dd-cfDNA) is shed from transplanted organs and detectable in peripheral blood. Thus, a potential dd-cfDNA blood test assessing rejection would be clinically advantageous.
One hundred eighty-one dd-cfDNA samples (n) were collected from 77 patients (N) up to 132 mo posttransplant.
The median dd-cfDNA level among all subjects was 0.28% (0.13%, 0.71%). In simultaneous pancreas-kidney (SPK) transplant recipients, the median dd-cfDNA level was 0.29% (0.13%, 0.71%), and it was 0.23% (0.08%, 0.71%) in pancreas transplant alone (PTA) recipients. When isolating for when without infection or rejection, the median dd-cfDNA level was 0.28% (0.13%, 0.64%) for SPK and 0.20% (0.00%, 0.32%) for PTA. Both transplant types approached 1.0% ≤1 mo posttransplant followed by a decrease in median dd-cfDNA. During episodes of rejection or infection, median dd-cfDNA levels were greater among all transplant types.
The mean dd-cfDNA level for all pancreas transplant recipients is <1.0%, consistent with the published kidney transplant rejection threshold (>1.0%), regardless of SPK or PTA. Early posttransplant dd-cfDNA levels are transiently higher than later measurements. Dd-cfDNA elevation also correlates with rejection and infection and thus is a promising biomarker for surveilling pancreas transplant dysfunction.
胰腺移植为糖尿病患者提供了实现血糖稳态的机会。目前用于监测排斥反应的血液检测在识别排斥反应方面敏感性和特异性较差,而胰腺活检具有挑战性且与发病率和移植物丢失相关。供体来源的游离DNA(dd-cfDNA)从移植器官中释放出来并可在外周血中检测到。因此,一种潜在的评估排斥反应的dd-cfDNA血液检测在临床上将具有优势。
从77例患者中收集了181份dd-cfDNA样本,时间跨度为移植后长达132个月。
所有受试者的dd-cfDNA水平中位数为0.28%(0.13%,0.71%)。在胰肾联合移植(SPK)受者中,dd-cfDNA水平中位数为0.29%(0.13%,0.71%),而单纯胰腺移植(PTA)受者中为0.23%(0.08%,0.71%)。在无感染或排斥反应时,SPK的dd-cfDNA水平中位数为0.28%(0.13%,0.64%),PTA为0.20%(0.00%,0.32%)。两种移植类型在移植后≤1个月时dd-cfDNA水平均接近1.0%,随后dd-cfDNA中位数下降。在排斥反应或感染发作期间,所有移植类型的dd-cfDNA水平中位数均更高。
所有胰腺移植受者的平均dd-cfDNA水平<1.0%,这与已公布的肾移植排斥阈值(>1.0%)一致,无论SPK还是PTA。移植后早期的dd-cfDNA水平暂时高于后期测量值。Dd-cfDNA升高也与排斥反应和感染相关,因此是监测胰腺移植功能障碍的有前景的生物标志物。