Department of Urology and Transplantation, La Conception Hospital, Assistance Publique-Hôpitaux Marseille, Marseille, France.
Department of Urology, Assistance Publique-Hôpitaux de Marseille, Hopital Nord, Aix-Marseille University, Marseille, France.
Front Immunol. 2022 Aug 11;13:966951. doi: 10.3389/fimmu.2022.966951. eCollection 2022.
We aimed to evaluate whether donor-related inflammatory markers found in kidney transplant preservation fluid can associate with early development of kidney allograft dysfunction.
Our prospective study enrolled 74 consecutive donated organs who underwent kidney transplantation in our center between September 2020 and June 2021. Kidneys from 27 standard criteria donors were allocated to static cold storage and kidneys from 47 extended criteria donors to hypothermic machine perfusion. ELISA assessment of inflammatory biomarkers (IL-6, IL6-R, ICAM, VCAM, TNFα, IFN-g, CXCL1 and Fractalkine) was analyzed in view of a primary endpoint defined as the occurrence of delayed graft function or slow graft function during the first week following transplantation.
Soluble VCAM levels measured in transplant conservation fluid were significantly associated with recipient serum creatinine on day 7. Multivariate stepwise logistic regression analysis identified VCAM as an independent non-invasive predictor of early graft dysfunction, both at 1 week (OR: 3.57, = .04, 95% CI: 1.06-12.03) and 3 Months (OR: 4.039, = .034, 95% CI: 1.11-14.73) after transplant surgery.
This prospective pilot study suggests that pre-transplant evaluation of VCAM levels could constitute a valuable indicator of transplant health and identify the VCAM-CD49d pathway as a target to limit donor-related vascular injury of marginal transplants.
本研究旨在评估供体相关的炎症标志物是否可以与肾移植后早期肾功能障碍的发生相关。
本前瞻性研究纳入了 2020 年 9 月至 2021 年 6 月期间在我院接受肾移植的 74 例连续供体。将 27 例标准供体的肾脏分配到静态冷保存,将 47 例扩展标准供体的肾脏分配到低温机器灌注。ELISA 评估了炎症生物标志物(IL-6、IL6-R、ICAM、VCAM、TNFα、IFN-g、CXCL1 和 fractalkine),将延迟移植物功能障碍或移植后第 1 周内缓慢移植物功能障碍定义为主要终点进行分析。
保存液中可溶性 VCAM 水平与移植后第 7 天受体血清肌酐显著相关。多元逐步逻辑回归分析确定 VCAM 是早期移植物功能障碍的独立非侵入性预测因子,在移植后 1 周(OR:3.57,.04,95%CI:1.06-12.03)和 3 个月(OR:4.039,.034,95%CI:1.11-14.73)时均如此。
这项前瞻性初步研究表明,术前评估 VCAM 水平可能是移植健康的一个有价值的指标,并确定 VCAM-CD49d 途径是限制边缘供体相关血管损伤的靶点。