Institut National de la Santé Et de la Recherche Médicale INSERM U1064 and Institut de Transplantation Urologie Néphrologie (ITUN), Nantes, France.
PLoS One. 2013;8(4):e60702. doi: 10.1371/journal.pone.0060702. Epub 2013 Apr 5.
In renal transplantation, the unresponsiveness of patients undergoing chronic antibody mediated rejection (CAMR) to classical treatment stress on the need for accurate biomarkers to improve its diagnosis. We aim to determine whether microRNA expression patterns may be associated with a diagnosis of CAMR. We performed expression profiling of miRNAs in peripheral blood mononuclear cells (PBMC) of kidney transplant recipients with CAMR or stable graft function. Among 257 expressed miRNAs, 10 miRNAs associated with CAMR were selected. Among them, miR-142-5p was increased in PBMC and biopsies of patients with CAMR as well as in a rodent model of CAMR. The lack of modulation of miR-142-5p in PBMC of patients with renal failure, suggests that its over-expression in CAMR was associated with immunological disorders rather than renal dysfunction. A ROC curve analysis performed on independent samples showed that miR-142-5p is a potential biomarker of CAMR allowing a very good discrimination of the patients with CAMR (AUC = 0.74; p = 0.0056). Moreover, its expression was decreased in PHA-activated blood cells and was not modulated in PBMC from patients with acute rejection, excluding a non-specific T cell activation expression. The absence of modulation of this miRNA in immunosuppressed patients suggests that its expression was not influenced by treatment. Finally, the analysis of miR-142-5p predicted targets under-expressed in CAMR PBMC in a published microarray dataset revealed an enrichment of immune-related genes. Altogether, these data suggest that miR-142-5p could be used as a biomarker in CAMR and these finding may improve our understanding of chronic rejection mechanisms.
在肾移植中,接受慢性抗体介导排斥反应(CAMR)治疗的患者的无反应性强调了需要准确的生物标志物来改善其诊断。我们旨在确定 miRNA 的表达模式是否与 CAMR 的诊断相关。我们对 CAMR 或稳定移植物功能的肾移植受者的外周血单核细胞(PBMC)进行了 miRNA 表达谱分析。在 257 个表达的 miRNA 中,选择了与 CAMR 相关的 10 个 miRNA。其中,miR-142-5p 在 CAMR 患者的 PBMC 和活检中以及在 CAMR 的啮齿动物模型中均增加。肾功能衰竭患者的 PBMC 中 miR-142-5p 缺乏调节,表明其在 CAMR 中的过度表达与免疫紊乱而不是肾功能障碍有关。对独立样本进行的 ROC 曲线分析表明,miR-142-5p 是 CAMR 的潜在生物标志物,能够很好地区分 CAMR 患者(AUC=0.74;p=0.0056)。此外,它在 PHA 激活的血细胞中的表达降低,并且在急性排斥反应患者的 PBMC 中没有调节,排除了非特异性 T 细胞激活表达。该 miRNA 在免疫抑制患者中无调节表明其表达不受治疗影响。最后,在发表的微阵列数据集分析 CAMR PBMC 中低表达的 miR-142-5p 的预测靶标显示免疫相关基因富集。总之,这些数据表明 miR-142-5p 可作为 CAMR 的生物标志物,这些发现可能有助于我们了解慢性排斥反应机制。