Catić-Đorđević Aleksandra, Cvetković Tatjana, Stefanović Nikola, Veličković-Radovanović Radmila
Faculty of Medicine, University of Niš, Niš, Serbia.
Faculty of Medicine, University of Niš, and Clinic of Nephrology, Clinical Center Niš, Niš, Serbia.
J Med Biochem. 2017 Jan 25;36(1):1-7. doi: 10.1515/jomb-2016-0029. eCollection 2017 Jan.
Immunosuppressive drugs play a crucial role in the inhibition of immune reaction and prevention of graft rejection aswell as in the pharmacotherapy of autoimmune disorders. Effective immunosuppression should provide an adequate safety profile and improve treatment outcomes and the patients' quality of life. High-risk transplant recipients may be identified, but a definitive prediction model has still not been recognized. Therapeutic drug monitoring (TDM) for immunosuppressive drugs is an essential, but at the same time insufficient tool due to low predictability of drug exposition and marked pharmacokinetic variability. Parallel therapeutic, biochemical and clinical monitoring may successfully optimize and individualize therapy for transplanted recipients, providing optimal medical outcomes. Modern pharmacotherapy management should include new biomarkers with better sensitivity and specificity that can identify early cell damage. The aim of this study was to point out the importance of finding new biomarkers that would enable early detection of adverse drug events and cell damage in organ transplant recipients. We wanted to confirm the importance of routine biochemical monitoring in improving the safety of immunosuppressive treatment.
免疫抑制药物在抑制免疫反应、预防移植排斥以及自身免疫性疾病的药物治疗中发挥着关键作用。有效的免疫抑制应具备足够的安全性,并改善治疗效果和患者的生活质量。虽然可以识别高风险移植受者,但尚未建立确定的预测模型。免疫抑制药物的治疗药物监测(TDM)是一项重要但同时又不够充分的工具,因为药物暴露的可预测性低且药代动力学变异性显著。并行的治疗、生化和临床监测可成功优化移植受者的治疗并使其个体化,从而提供最佳医疗效果。现代药物治疗管理应包括具有更高敏感性和特异性的新生物标志物,这些生物标志物能够识别早期细胞损伤。本研究的目的是指出寻找新生物标志物的重要性,这些新生物标志物将能够早期检测器官移植受者的药物不良事件和细胞损伤。我们希望证实常规生化监测在提高免疫抑制治疗安全性方面的重要性。