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pubmed-article:20028817pubmed:abstractTextRecombinant alpha interferon (IFN-alpha) 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-alpha 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-alpha 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.lld:pubmed
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pubmed-article:20028817pubmed:pagination1179-85lld:pubmed
pubmed-article:20028817pubmed:dateRevised2010-9-2lld:pubmed
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pubmed-article:20028817pubmed:articleTitlePharmacokinetic-pharmacodynamic modeling of alpha interferon response induced by a Toll-like 7 receptor agonist in mice.lld:pubmed
pubmed-article:20028817pubmed:affiliationDepartment of Pharmacokinetics, Pharmacodynamics and Metabolism, Pfizer Global Research and Development, Ramsgate Road, Sandwich, United Kingdom. neil.benson@pfizer.comlld:pubmed
pubmed-article:20028817pubmed:publicationTypeJournal Articlelld:pubmed
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