Li Li, Khush Kiran, Hsieh Szu-Chuan, Ying Lihua, Luikart Helen, Sigdel Tara, Roedder Silke, Yang Andrew, Valantine Hannah, Sarwal Minnie M
Department of Pediatrics, Stanford University, Palo Alto, California, United States of America.
Division of Cardiovascular Medicine, Department of Medicine, Stanford University, Palo Alto, California, United States of America.
PLoS One. 2013 Dec 16;8(12):e82153. doi: 10.1371/journal.pone.0082153. eCollection 2013.
To test, whether 10 genes, diagnostic of renal allograft rejection in blood, are able to diagnose and predict cardiac allograft rejection, we analyzed 250 blood samples from heart transplant recipients with and without acute rejection (AR) and with cytomegalovirus (CMV) infection by QPCR. A QPCR-based logistic regression model was built on 5 of these 10 genes (AR threshold composite score >37% = AR) and tested for AR prediction in an independent set of 109 samples, where it correctly diagnosed AR with 89% accuracy, with no misclassifications for AR ISHLT grade 1b. CMV infection did not confound the AR score. The genes correctly diagnosed AR in a blood sample within 6 months prior to biopsy diagnosis with 80% sensitivity and untreated grade 1b AR episodes had persistently elevated scores until 6 months after biopsy diagnosis. The gene score was also correlated with presence or absence of cardiac allograft vasculopathy (CAV) irrespective of rejection grade. In conclusion, there is a common transcriptional axis of immunological trafficking in peripheral blood in both renal and cardiac organ transplant rejection, across a diverse recipient age range. A common gene signature, initially identified in the setting of renal transplant rejection, can be utilized serially after cardiac transplantation, to diagnose and predict biopsy confirmed acute heart transplant rejection.
为了测试血液中用于诊断肾移植排斥反应的10个基因是否能够诊断和预测心脏移植排斥反应,我们通过定量聚合酶链反应(QPCR)分析了250份来自心脏移植受者的血样,这些受者有或没有急性排斥反应(AR)以及是否感染了巨细胞病毒(CMV)。基于这10个基因中的5个构建了一个基于QPCR的逻辑回归模型(AR阈值综合评分>37% = AR),并在一组独立的109份样本中测试其对AR的预测能力,该模型以89%的准确率正确诊断了AR,对于AR国际心脏和肺移植协会(ISHLT)1b级没有错误分类。CMV感染并未混淆AR评分。这些基因在活检诊断前6个月内的血样中以80%的灵敏度正确诊断了AR,未经治疗的1b级AR发作在活检诊断后6个月内评分持续升高。无论排斥反应分级如何,基因评分也与心脏移植血管病变(CAV)的有无相关。总之,在肾和心脏器官移植排斥反应中,在不同的受者年龄范围内,外周血中存在共同的免疫运输转录轴。最初在肾移植排斥反应中确定的共同基因特征,可在心脏移植后连续使用,以诊断和预测活检证实的急性心脏移植排斥反应。