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Pharmacokinetic-Pharmacodynamic Modeling of Alpha Interferon Response Induced by a Toll-Like 7 Receptor Agonist in Mice▿

机译:Toll样7受体激动剂在小鼠体内诱发α干扰素反应的药代动力学药效学模型▿

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摘要

Recombinant alpha interferon (IFN-α) is used in the treatment of hepatitis C virus (HCV)-infected patients but is not optimal in terms of efficacy or tolerability. Toll-like 7 receptor (TLR-7) agonists stimulate the innate immune system to produce, among other cytokines, IFN-α and are being evaluated as alternative drugs to treat HCV infection. This paper describes the application of pharmacokinetic-pharmacodynamic (PK-PD) modeling to understanding the behavior of a TLR-7 agonist [9-benzyl-8-hydroxy-2-(2-methoxyethoxy) adenine (BHMA)] in mice, using IFN-α as a biomarker. This is the first report of such a PK-PD model, and the conclusions may be of utility in the clinical development of TLR-7 agonists for HCV infection.
机译:重组α干扰素(IFN-α)用于治疗丙型肝炎病毒(HCV)感染的患者,但就功效或耐受性而言并非最佳。 Toll样7受体(TLR-7)激动剂可刺激先天免疫系统产生IFN-α等其他细胞因子,并且正在被评估为治疗HCV感染的替代药物。本文描述了药代动力学-药效学(PK-PD)模型在理解TLR-7激动剂[9-苄基-8-羟基-2-(2-甲氧基乙氧基)腺嘌呤(BHMA)]在小鼠中的行为中的应用,使用IFN-α作为生物标志物。这是这种PK-PD模型的首次报道,其结论可能在针对HCV感染的TLR-7激动剂的临床开发中有用。

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