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Target Enzyme Activity as a Biomarker for Immunosuppression

机译:目标酶活性作为免疫抑制的生物标志物

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Pharmacokinetic drug monitoring has been used for many years to relate immunosuppressant dose to drug exposure in vivo. However, this conventional therapeutic drug monitoring of blood immunosuppressant levels may not necessarily predict the pharmacologic effects on immune cells. The direct determination of target enzyme activity (eg, calcineurin activity, inosine-5'-mono-phospahte dehydrogenase [IMPDH] activity, p70S6 kinase) may help to better assess the individual response to the immunosuppressant. However, its use is limited by the difficulties of the assay systems, which did not allow yet the prospective assessment of these enzymes in larger patient cohorts with the establishment of validated phar-macodynamic drug monitoring. The most progress regarding a robust and reproducible test system has been achieved with the determination of IMPDH activity as a specific pharmacodynamic parameter of mycophenolic acid activity. This recently validated and standardized assay allows the investigation of IMPDH activity in larger clinical studies. Although the determination of target enzyme activity, eg, by the determination of IMPDH activity, holds promise for a more individualized therapy in transplant medicine, more studies are needed to prospectively validate this approach.
机译:药代动力学药物监测已被使用多年,以将免疫抑制剂剂量与体内药物暴露联系起来。但是,这种对血液免疫抑制剂水平的常规治疗药物监测不一定能预测对免疫细胞的药理作用。目标酶活性(例如钙调神经磷酸酶活性,肌苷5'-单磷酸脱氢酶[IMPDH]活性,p70S6激酶)的直接测定可能有助于更好地评估个体对免疫抑制剂的反应。然而,由于检测系统的困难,其使用受到了限制,由于建立了有效的药动动力学药物监测,尚无法在较大的患者队列中对这些酶进行前瞻性评估。通过确定IMPDH活性作为麦考酚酸活性的特定药效学参数,已经获得了有关鲁棒性和可重复性测试系统的最新进展。最近经过验证和标准化的测定方法可用于大型临床研究中的IMPDH活性研究。尽管例如通过确定IMPDH活性的目标酶活性的测定为移植医学中的更加个体化的疗法带来希望,但是需要更多的研究来前瞻性地验证这种方法。

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