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Janus kinase inhibitors for the treatment of rheumatoid arthritis demonstrate similar profiles of in vitro cytokine receptor inhibition

机译:Janus激酶抑制剂用于治疗类风湿性关节炎,展示了体外细胞因子受体抑制的类似谱

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Janus kinase (JAK) inhibitors have emerged as an effective class of therapies for various inflammatory diseases such as rheumatoid arthritis (RA). JAK inhibitors function intracellularly by modulating the catalytic activity of JAKs and disrupting the receptor-mediated signaling of multiple cytokines and growth factors, including those with pro-inflammatory activity. Understanding the inhibition profiles of different JAK inhibitors, based on the associated cytokine receptors and downstream inflammatory pathways affected, is important to identify the potential mechanisms for observed differences in efficacy and safety. This study applied an integrated modeling approach, using in vitro whole blood cytokine inhibition potencies and plasma pharmacokinetics, to determine JAK-dependent cytokine receptor inhibition profiles, in the context of doses estimated to provide a similar clinical response in RA clinical trials. The calculated profiles of cytokine receptor inhibition for the JAK inhibitors tofacitinib, baricitinib, upadacitinib, and filgotinib and its metabolite, were generally similar when clinically efficacious doses for RA were considered. Only minor numerical differences in percentage cytokine receptor inhibition were observed, suggesting limited differentiation of these inhibitors based on JAK pharmacology, with each showing a differential selectivity for JAK1 heterodimer inhibition. Nevertheless, only robust clinical testing involving head-to-head studies will ultimately determine whether there are clinically meaningful differences between these JAK inhibitors. Furthermore, ongoing and future research into inhibitors with alternative JAK selectivity remains of clinical importance. Thus, all JAK inhibitors should be characterized via thorough preclinical, metabolic and pharmacological evaluation, adequate long-term clinical data, and when available, real-world experience.? 2019 The Authors. Pharmacology Research & Perspectives published by John Wiley & Sons Ltd, British Pharmacological Society and American Society for Pharmacology and Experimental Therapeutics.
机译:Janus激酶(Jak)抑制剂已成为各种炎症性疾病如类风湿性关节炎(RA)的有效疗法。 jak抑制剂通过调节jaks的催化活性并破坏多种细胞因子和生长因子的受体介导的信号传导,包括具有促炎活性的受体介导的信令。理解不同JAK抑制剂的抑制曲线,基于相关的细胞因子受体和受影响的下游炎性途径是重要的,对于识别观察到的疗效和安全性差异的潜在机制是重要的。本研究应用了综合建模方法,使用体外全血细胞因子抑制效应和血浆药代动力学来确定jak依赖性细胞因子受体抑制曲线,在估计的剂量的背景下提供了在RA临床试验中提供了类似的临床反应。当考虑RA的临床有效剂量时,jak抑制剂Tofacitinib,Baricitinib,uPadacitinib和菲霉菌及其代谢物的计算曲线通常相似。仅观察到百分比细胞因子受体抑制百分比的次要数值差异,表明基于JAK药理学的这些抑制剂有限分化,每种抑制剂都显示出jak1异二聚体抑制的差异选择性。尽管如此,只有涉及头部对头研究的稳健临床测试将最终确定这些jak抑制剂之间是否存在临床上有意义的差异。此外,持续和未来的抑制剂与替代JAK选择性仍然具有临床重要性的抑制剂。因此,所有JAK抑制剂都应通过彻底的临床前,代谢和药理学评估,适当长期的临床数据,以及可用,现实世界经验。 2019年的作者。 John Wiley&Sons Ltd,英国药理学会和美国药理学学会和实验治疗学士发表的药理学研究与观点。

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