Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Research, United States Food and Drug Administration, Silver Spring, Maryland 20993, USA.
Clin Pharmacokinet. 2010 May;49(5):295-310. doi: 10.2165/11319980-000000000-00000.
Therapeutic proteins (TPs) may affect the disposition of drugs that are metabolized by cytochrome P450 (CYP) enzymes, as is evident from a review of data in recently published literature and approved Biologic License Applications. Many TPs belonging to the cytokine class appear to differentially affect CYP activities. Cytokine modulators may affect CYP enzyme activities by altering cytokine effects on CYP enzymes. The alteration in CYP enzyme activities seems to result from changes in transcription factor activity for CYP enzyme expression or changes in CYP enzyme stability, which have been observed during altered immunological states such as infection and inflammation. Human growth hormone also appears to differentially affect CYP activities through unknown mechanisms. Because TP-drug interaction research is an evolving area, limited information is available during drug development on TP-drug interactions mediated by CYP inhibition or induction. The authors of this review suggest that effort be made to understand TP-drug interactions for the safe and effective use of TPs in combination with small-molecule drugs.
治疗性蛋白(TPs)可能会影响细胞色素 P450(CYP)酶代谢的药物的处置,这从最近发表的文献和已批准的生物制品许可申请中的数据综述中可以明显看出。许多属于细胞因子类的 TPs 似乎会对 CYP 活性产生不同的影响。细胞因子调节剂可能通过改变细胞因子对 CYP 酶的影响来影响 CYP 酶活性。CYP 酶活性的改变似乎是由于 CYP 酶表达的转录因子活性或 CYP 酶稳定性的改变所致,这种改变在感染和炎症等免疫状态改变时已经观察到。生长激素似乎也通过未知机制对 CYP 活性产生差异影响。由于 TP-药物相互作用研究是一个不断发展的领域,在药物开发过程中,关于 CYP 抑制或诱导介导的 TP-药物相互作用的信息有限。本文作者建议,努力了解 TP-药物相互作用,以确保 TPs 与小分子药物联合使用的安全性和有效性。