van Dijk Fransien, Olinga Peter, Poelstra Klaas, Beljaars Leonie
Department of Pharmacokinetics, Toxicology and Targeting, Groningen Research Institute for Pharmacy , Groningen , Netherlands ; Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute for Pharmacy , Groningen , Netherlands.
Department of Pharmaceutical Technology and Biopharmacy, Groningen Research Institute for Pharmacy , Groningen , Netherlands.
Front Med (Lausanne). 2015 Oct 5;2:72. doi: 10.3389/fmed.2015.00072. eCollection 2015.
Cytokines, growth factors, and other locally produced mediators play key roles in the regulation of disease progression. During liver fibrosis, these mediators orchestrate the balance between pro- and antifibrotic activities as exerted by the hepatic cells. Two important players in this respect are the profibrotic mediator platelet-derived growth factor BB (PDGF-BB) and the antifibrotic cytokine interferon gamma (IFNγ). PDGF-BB, produced by many resident and infiltrating cells, causes extensive proliferation, migration, and contraction of hepatic stellate cells (HSCs) and myofibroblasts. These cells are the extracellular matrix-producing hepatic cells and they highly express the PDGFβ receptor. On the other hand, IFNγ is produced by natural killer cells in fibrotic livers and is endowed with proinflammatory, antiviral, and antifibrotic activities. This cytokine attracted much attention as a possible therapeutic compound in fibrosis. However, clinical trials yielded disappointing results because of low efficacy and adverse effects, most likely related to the dual role of IFNγ in fibrosis. In our studies, we targeted the antifibrotic IFNγ to the liver myofibroblasts. For that, we altered the cell binding properties of IFNγ, by delivery of the IFNγ-nuclear localization sequence to the highly expressed PDGFβ receptor using a PDGFβ receptor recognizing peptide, thereby creating a construct referred to as "Fibroferon" (i.e., fibroblast-targeted interferon γ). In recent years, we demonstrated that HSC-specific delivery of IFNγ increased its antifibrotic potency and improved its general safety profile in vivo, making Fibroferon highly suitable for the treatment of (fibrotic) diseases associated with elevated PDGFβ receptor expression. The present review summarizes the knowledge on these two key mediators, PDGF-BB and IFNγ, and outlines how we used this knowledge to create the cell-specific antifibrotic compound Fibroferon containing parts of both of these mediators.
细胞因子、生长因子及其他局部产生的介质在疾病进展的调控中发挥关键作用。在肝纤维化过程中,这些介质协调肝细胞所发挥的促纤维化和抗纤维化活性之间的平衡。在这方面的两个重要参与者是促纤维化介质血小板衍生生长因子BB(PDGF - BB)和抗纤维化细胞因子干扰素γ(IFNγ)。由许多驻留细胞和浸润细胞产生的PDGF - BB可导致肝星状细胞(HSC)和成肌纤维细胞广泛增殖、迁移和收缩。这些细胞是产生细胞外基质的肝细胞,它们高度表达PDGFβ受体。另一方面,IFNγ由纤维化肝脏中的自然杀伤细胞产生,具有促炎、抗病毒和抗纤维化活性。这种细胞因子作为纤维化的一种可能治疗化合物引起了广泛关注。然而,临床试验结果令人失望,原因是疗效低且有不良反应,这很可能与IFNγ在纤维化中的双重作用有关。在我们的研究中,我们将抗纤维化的IFNγ靶向肝成肌纤维细胞。为此,我们通过使用识别PDGFβ受体的肽将IFNγ - 核定位序列递送至高度表达的PDGFβ受体,从而改变IFNγ的细胞结合特性,由此创建了一种称为“Fibroferon”(即成纤维细胞靶向干扰素γ)的构建体。近年来,我们证明IFNγ在HSC特异性递送时可提高其抗纤维化效力并改善其在体内的总体安全性,使得Fibroferon非常适合用于治疗与PDGFβ受体表达升高相关的(纤维化)疾病。本综述总结了关于这两种关键介质PDGF - BB和IFNγ的知识,并概述了我们如何利用这些知识创建包含这两种介质部分成分的细胞特异性抗纤维化化合物Fibroferon。