Capron Arnaud, Lerut Jan, Verbaandert Catherine, Mathys Jules, Ciccarelli Olga, Vanbinst Roger, Roggen Francine, De Reyck Chantal, Lemaire Julien, Wallemacq Pierre E
Department of Clinical Chemistry, Laboratory of Toxicology and Therapeutic Drug Monitoring, University Hospital St Luc, Université Catholique de Louvain, Brussels, Belgium.
Ther Drug Monit. 2007 Jun;29(3):340-8. doi: 10.1097/FTD.0b013e31805c73f1.
The aims of this work were both to validate a sensitive and specific method to quantify tacrolimus (TAC) in liver biopsies after hepatic transplantation and to evaluate the predictive value of either tissue or blood TAC concentrations for rejection in 146 adult patients under a TAC-based immunosuppression. Trough blood levels were monitored daily during the hospital stay by immunoassay. Liver biopsies were routinely performed at day 7 posttransplantation. The tissue assay was developed by liquid chromatography-mass spectrometry. The limit of quantification was 5 pg/mg, with intra- and interassay precision ranging from 3.9% to 14.3% and 4.7% to 15.9%, respectively. The extraction efficiency was approximately 80%. TAC found in liver biopsies ranged from less than 5 up to 387 pg/mg. Blood TAC levels ranged from 2.7 to 19.3 ng/mL. Tissue levels displayed excellent correlation with liver histopathologic BANFF rejection score, whereas blood levels did not. Clinically significant rejections (BANFF scores > or = 6) were characterized by mean TAC tissue and blood concentration of 13.1 pg/mg and 7.6 ng/mL, respectively, whereas these mean values became, respectively, 74.9 pg/mg (P < 0.05) and 7.1 ng/mL (not significant) for nonclinically significant rejection episodes (BANFF < 6). In this study, hepatic tissue TAC concentrations were distributed in a wider range and displayed a significantly better correlation with the severity of the organ rejection than predose blood levels. A tissue TAC concentration less than 30 pg/mg is 89% sensitive and 98% specific to discriminate clinically significant cellular rejection. Further studies are required to better understand the factors affecting TAC distribution within liver tissue (such as carrier proteins and cytochrome genetic polymorphism, liver function, age, hepatic blood flow, type of organ transplanted, time posttransplantation) and to define its value in the treatment of liver allograft rejection.
这项工作的目的,一是验证一种灵敏且特异的方法,用于定量肝移植后肝活检组织中的他克莫司(TAC);二是评估在接受基于TAC的免疫抑制治疗的146例成年患者中,组织或血液TAC浓度对排斥反应的预测价值。住院期间每天通过免疫测定法监测血药谷浓度。肝活检通常在移植后第7天进行。组织测定采用液相色谱 - 质谱法。定量限为5 pg/mg,批内和批间精密度分别为3.9%至14.3%和4.7%至15.9%。提取效率约为80%。肝活检组织中发现的TAC范围为小于5至387 pg/mg。血TAC水平为2.7至19.3 ng/mL。组织水平与肝脏组织病理学班夫排斥反应评分显示出极好的相关性,而血药水平则不然。具有临床意义的排斥反应(班夫评分≥6)的特征是,TAC组织和血液浓度平均值分别为13.1 pg/mg和7.6 ng/mL,而对于无临床意义的排斥反应事件(班夫评分<6),这些平均值分别变为74.9 pg/mg(P<0.05)和7.1 ng/mL(无显著性差异)。在本研究中,肝组织TAC浓度分布范围更广,与器官排斥反应严重程度的相关性明显优于给药前血药水平。组织TAC浓度低于30 pg/mg时,鉴别具有临床意义的细胞排斥反应的敏感性为89%,特异性为98%。需要进一步研究以更好地理解影响TAC在肝组织内分布的因素(如载体蛋白和细胞色素基因多态性、肝功能、年龄、肝血流量、移植器官类型、移植后时间),并确定其在肝移植排斥反应治疗中的价值。