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供体脑死亡后表达的肾脏缺血损伤基因可预测肾移植的结果。

Kidney ischemic injury genes expressed after donor brain death are predictive for the outcome of kidney transplantation.

作者信息

Kamińska D, Kościelska-Kasprzak K, Drulis-Fajdasz D, Hałoń A, Polak W, Chudoba P, Jańczak D, Mazanowska O, Patrzałek D, Klinger M

机构信息

Department of Nephrology and Transplantation Medicine, Wroclaw Medical University, Wroclaw, Poland.

出版信息

Transplant Proc. 2011 Oct;43(8):2891-4. doi: 10.1016/j.transproceed.2011.08.062.

Abstract

The results of deceased donor kidney transplantation largely depend on the extent of organ injury induced by brain death and the transplantation procedure. In this study, we analyzed the preprocurement intragraft expression of 29 genes involved in apoptosis, tissue injury, immune cell migration, and activation. We also assessed their influence on allograft function. Before flushing with cold solution we obtained 50 kidney core biopsies of deceased donor kidneys immediately after organ retrieval. The control group included 18 biopsies obtained from living donors. Gene expression was analyzed with low-density arrays (Taqman). LCN2/lipocalin-2 is considered a biomarker of kidney epithelial ischemic injury with a renoprotective function. HAVCR1/KIM-1 is associated with acute tubular injury. Comparison of deceased donor kidneys to control organs revealed a significantly higher expression of LCN2 (8.0-fold P=.0006) and HAVCR1 (4.7-fold, P<.0001). Their expressions positively correlated with serum creatinine concentrations after 6 months after transplantation: LCN2 (r=.65, P<.0001), HAVCR1 (r=.44, P=.006). Kidneys displaying delayed graft function and/or an acute rejection episode in the first 6 months after showed higher LCN2 expression compared to event-free ones (1.7-fold, P=.027). A significantly higher increase in expression of TLR2 (5.2-fold), Interleukin (IL) 18 (4.6-fold), HMGB1 (4.1-fold), GUSB (2.4-fold), CASP3 (2.0-fold) FAS (1.8-fold), and TP53 (1.6-fold) was observed among deceased donor kidneys compared with the control group. Their expression levels were not related to clinical outcomes: however, they showed significant correlations with one another (r>.6, P<.0001). We also observed a slightly reduced expression of IL10 (0.6-fold, P=.004). Our data suggested that increased LCN2 and HAVCR1 expression observed in the kidneys after donor brain death were hallmarks of the organ injury process. LCN2 expression level in retrieved kidneys can predict kidney transplantation outcomes.

摘要

已故供体肾移植的结果很大程度上取决于脑死亡和移植手术所导致的器官损伤程度。在本研究中,我们分析了参与细胞凋亡、组织损伤、免疫细胞迁移及激活的29个基因在器官获取前的移植肾内表达情况。我们还评估了它们对同种异体移植肾功能的影响。在使用冷溶液冲洗前,器官获取后立即从已故供体肾中获取了50份肾芯活检组织。对照组包括从活体供体获取的18份活检组织。采用低密度阵列(Taqman)分析基因表达。LCN2/脂质运载蛋白-2被认为是具有肾脏保护功能的肾上皮缺血损伤生物标志物。HAVCR1/KIM-1与急性肾小管损伤相关。将已故供体肾与对照器官进行比较,发现LCN2(8.0倍,P = 0.0006)和HAVCR1(4.7倍,P < 0.0001)的表达显著更高。它们的表达与移植后6个月时的血清肌酐浓度呈正相关:LCN2(r = 0.65,P < 0.0001),HAVCR1(r = 0.44,P = 0.006)。与未发生相关事件的肾脏相比,在术后头6个月出现移植肾功能延迟和/或急性排斥反应的肾脏LCN2表达更高(1.7倍,P = 0.027)。与对照组相比,在已故供体肾中观察到TLR2(5.2倍)、白细胞介素(IL)18(4.6倍)、HMGB1(4.1倍)、GUSB(2.4倍)、CASP3(2.0倍)、FAS(1.8倍)和TP53(1.6倍)的表达显著更高。它们的表达水平与临床结局无关:然而,它们之间显示出显著的相关性(r > 0.6,P < 0.0001)。我们还观察到IL10的表达略有降低(0.6倍,P = 0.004)。我们的数据表明,供体脑死亡后肾内LCN2和HAVCR1表达增加是器官损伤过程的标志。获取的肾脏中LCN2表达水平可预测肾移植结局。

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