De Nicolò Amedeo, Pinon Michele, Palermiti Alice, Nonnato Antonello, Manca Alessandra, Mula Jacopo, Catalano Silvia, Tandoi Francesco, Romagnoli Renato, D'Avolio Antonio, Calvo Pier Luigi
Laboratory of Clinical Pharmacology and Pharmacogenetics, Department of Medical Sciences, University of Turin, Turin, Italy.
Pediatric Gastroenterology Unit, Regina Margherita Children's Hospital, Azienda Ospedaliera-Universitaria Città della Salute e della Scienza, Turin, Italy.
Front Pharmacol. 2021 Nov 5;12:750433. doi: 10.3389/fphar.2021.750433. eCollection 2021.
Tacrolimus (TAC) is a first-choice immunosuppressant for solid organ transplantation, characterized by high potential for drug-drug interactions, significant inter- and intra-patient variability, and narrow therapeutic index. Therapeutic drug monitoring (TDM) of TAC concentrations in whole blood (WB) is capable of reducing the incidence of adverse events. Since TAC acts within lymphocytes, its monitoring in peripheral blood mononuclear cells (PBMC) may represent a valid future alternative for TDM. Nevertheless, TAC intracellular concentrations and their variability are poorly described, particularly in the pediatric context. Therefore, our aim was describing TAC concentrations in WB and PBMC and their variability in a cohort of pediatric patients undergoing constant immunosuppressive maintenance therapy, after liver transplantation. TAC intra-PBMCs quantification was performed through a validated UHPLC-MS/MS assay over a period of 2-3 months. There were 27 patients included in this study. No significant TAC changes in intracellular concentrations were observed ( = 0.710), with a median percent change of -0.1% (IQR -22.4%-+46.9%) between timings: this intra-individual variability was similar to the one in WB, -2.9% (IQR -29.4-+42.1; = 0.902). Among different patients, TAC weight-adjusted dose and age appeared to be significant predictors of TAC concentrations in WB and PBMC. Intra-individual seasonal variation of TAC concentrations in WB, but not in PBMC, have been observed. These data show that the intra-individual variability in TAC intracellular exposure is comparable to the one observed in WB. This opens the way for further studies aiming at the identification of therapeutic ranges for TAC intra-PBMC concentrations.
他克莫司(TAC)是实体器官移植的首选免疫抑制剂,其特点是药物相互作用潜力高、患者间和患者内差异显著、治疗指数窄。监测全血(WB)中TAC浓度的治疗药物监测(TDM)能够降低不良事件的发生率。由于TAC在淋巴细胞内起作用,因此监测外周血单核细胞(PBMC)中的TAC可能是TDM未来有效的替代方法。然而,TAC细胞内浓度及其变异性描述较少,尤其是在儿科患者中。因此,我们的目的是描述肝移植后接受持续免疫抑制维持治疗的儿科患者队列中WB和PBMC中的TAC浓度及其变异性。通过经过验证的超高效液相色谱-串联质谱法(UHPLC-MS/MS)在2至3个月的时间内对PBMC中的TAC进行定量。本研究纳入了27名患者。未观察到细胞内浓度有显著的TAC变化(=0.710),两次测量之间的中位变化百分比为-0.1%(IQR -22.4%-+46.9%):这种个体内变异性与WB中的相似,为-2.9%(IQR -29.4-+42.1;=0.902)。在不同患者中,TAC体重调整剂量和年龄似乎是WB和PBMC中TAC浓度的重要预测因素。观察到WB中TAC浓度存在个体内季节性变化,但PBMC中未观察到。这些数据表明,TAC细胞内暴露的个体内变异性与WB中观察到的相当。这为进一步研究确定PBMC中TAC浓度的治疗范围开辟了道路。