Nissaisorakarn Voravech, Lee John Richard, Lubetzky Michelle, Suthanthiran Manikkam
Division of Nephrology and Hypertension, Department of Medicine, Weill Cornell Medical College, New York, NY 10065, USA; Department of Transplantation Medicine, New York Presbyterian Hospital - Weill Cornell Medical Center, New York, NY 10065, USA.
Division of Nephrology and Hypertension, Department of Medicine, Weill Cornell Medical College, New York, NY 10065, USA; Department of Transplantation Medicine, New York Presbyterian Hospital - Weill Cornell Medical Center, New York, NY 10065, USA.
Hum Immunol. 2018 May;79(5):343-355. doi: 10.1016/j.humimm.2018.01.006. Epub 2018 Jan 31.
We developed urinary cell messenger RNA (mRNA) profiling to monitor in vivo status of human kidney allografts based on our conceptualization that the kidney allograft may function as an in vivo flow cell sorter allowing access of graft infiltrating cells to the glomerular ultrafiltrate and that interrogation of urinary cells is informative of allograft status. For the profiling urinary cells, we developed a two-step preamplification enhanced real-time quantitative PCR (RT-QPCR) assays with a customized amplicon; preamplification compensating for the low RNA yield from urine and the customized amplicon facilitating absolute quantification of mRNA and overcoming the inherent limitations of relative quantification widely used in RT-QPCR assays. Herein, we review our discovery and validation of urinary cell mRNAs as noninvasive biomarkers prognostic and diagnostic of acute cellular rejection (ACR) in kidney allografts. We summarize our results reflecting the utility of urinary cell mRNA profiling for predicting reversal of ACR with anti-rejection therapy; differential diagnosis of kidney allograft dysfunction; and noninvasive diagnosis and prognosis of BK virus nephropathy. Messenger RNA profiles associated with human kidney allograft tolerance are also summarized in this review. Altogether, data supporting the idea that urinary cell mRNA profiles are informative of kidney allograft status and tolerance are reviewed in this report.
基于我们的概念,即同种异体肾移植可能起到体内流式细胞分选仪的作用,使移植物浸润细胞能够接触肾小球超滤液,并且对尿细胞的检测能够提供有关同种异体移植状态的信息,我们开发了尿细胞信使核糖核酸(mRNA)分析方法来监测人肾移植的体内状态。为了对尿细胞进行分析,我们开发了一种两步预扩增增强型实时定量聚合酶链反应(RT-QPCR)检测方法,该方法使用定制的扩增子;预扩增可补偿尿液中RNA产量低的问题,定制的扩增子有助于mRNA的绝对定量,并克服了RT-QPCR检测中广泛使用的相对定量的固有局限性。在此,我们回顾了我们对尿细胞mRNA作为肾移植急性细胞排斥反应(ACR)的非侵入性生物标志物进行预后和诊断的发现及验证。我们总结了我们的结果,这些结果反映了尿细胞mRNA分析在预测抗排斥治疗后ACR逆转、肾移植功能障碍的鉴别诊断以及BK病毒肾病的非侵入性诊断和预后方面的实用性。本综述还总结了与人类肾移植耐受相关的mRNA谱。总之,本报告回顾了支持尿细胞mRNA谱能够提供肾移植状态和耐受信息这一观点的数据。