2576:基于细胞因子差异谱的VCA急性排斥反应可靠诊断的无创诊断和预测工具的优化

Piul S. Rabbani, Rohini L Kadle, Nakul Rao, Chin Park, Daniel J Ceradini
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引用次数: 0

摘要

2576:Piul S. Rabbani博士,Rohini L. Kadle医学博士,Nakul Rao, Chin Park和Daniel Ceradini纽约大学医学院,纽约,NY当前检测早期急性移植排斥反应的方法依赖于侵入性组织活检和耗时的组织学分析。我们提出了一种替代方法,使用粘接盘分析血管复合异体移植(VCA)表皮细胞的分子变化,以检测急性排斥反应的标志物。我们的目的是验证皮肤剥离作为VCA急性排斥反应的非侵入性预测和敏感诊断测试的有效性。方法使用已建立的VCA大鼠模型,我们将供体布朗-挪威大鼠的复合皮瓣移植到年龄匹配的受体Lewis大鼠身上。在环孢素治疗5天后,我们每天检查临床排斥症状,并在排斥前的每个时间点用粘连的cuderm -disc取样移植皮肤。我们对取样细胞进行QRT-PCR检测与早期排斥相关的细胞因子,并对皮瓣进行活检和组织学检查以证实椎间盘数据。结果与免疫抑制期相比,MCP1、MIP1ⅰ§、MIP1ⅰ和CXCL10的表达在轻度和晚期排斥反应中逐渐升高(p < 0.05),轻度排斥反应时MIP3ⅰ§和CXCL9的表达显著上调(分别为19倍、70倍),晚期排斥反应时表达下调(分别为4倍、20倍)。我们通过比较VCA活检组织中mRNA的表达,验证了CuDerm-disc方法的敏感性和有效性,发现两种方法之间的细胞因子检测具有可比性。来自椎间盘的轻度和晚期排斥细胞因子谱也符合同种异体移植细胞排斥的Banff分类。结论:与传统的组织活检相比,皮肤剥离是一种可比较的可靠的分析工具,从皮肤剥离收集的细胞因子谱清晰,能够检测早期急性排斥反应,并区分晚期排斥反应。我们的研究结果清楚地表明,在晚期排斥反应发生之前,皮肤剥离作为一种无创工具预测和诊断早期排斥反应是有希望的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
2576: Optimization of a differential cytokine profile-based non-invasive diagnostic and predictive tool for reliable diagnosis of acute rejection in VCA
2576: Optimization of a differential cytokine profile-based non-invasive diagnostic and predictive tool for reliable diagnosis of acute rejection in VCA Piul S. Rabbani, PhD, Rohini L. Kadle, MD, Nakul Rao, Chin Park, and Daniel Ceradini New York University School of Medicine, New York, NY, USA Background Current methods of detection of early acute transplant rejection relies on invasive tissue biopsies and time-consuming histological analysis We propose an alternative method using adhesive discs to analyze molecular changes in cells sampled from the epidermis of a vascular composite allotransplant (VCA), to detect markers of acute rejection We aim to validate efficiency of skin stripping as a non-invasive predictor and sensitive diagnostic test for acute rejection in VCA. Methods Using an established VCA rat model, we transplanted composite flaps from donor Brown-Norway rats to age-matched recipient Lewis rats Following cyclosporine for 5 days, we inspected daily for clinical signs of rejection and sampled transplanted skin with adhesive CuDerm-discs at each time point up to rejection We performed QRT-PCR on sampled cells for cytokines associated with early rejection We sampled flaps for biopsies and histology to corroborate the disc data. Results CuDerm-disc-sourced PCR revealed that expressions of MCP1, MIP1̂I§, MIP1̂I and CXCL10 increased progressively with mild and advanced rejection, compared to the immunosuppressed stage (p < 005) MIP3̂I§ and CXCL9 showed significant upregulation at mild rejection (19-fold, 70-fold, respectively), but a downregulation during advanced rejection (4fold,20-fold, respectively, p < 005) Comparison of mild and advanced rejection showed highly significant differential cytokine expression (p < 001) We verified the sensitivity and validity of the CuDerm-disc method by comparison of mRNA expression in VCA biopsies and found cytokine detection comparable between both methods The mild and advanced rejection cytokine profiles from discs also corresponded with the Banff classification of cellular allograft rejection of the respective flap histologies. Conclusions Skin stripping, when compared to traditional tissue biopsy, is a comparable and reliable analytical tool The cytokine profiles gathered from skin stripping are distinct and capable of detecting the earliest stages of acute rejection, as well as distinguishing from advanced rejection, stages which are difficult to analyze definitively using traditional histology Our results clearly demonstrate the promise of skin stripping as a noninvasive tool in predicting and diagnosing early rejection, prior to onset of advanced rejection.
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