Systemic sclerosis and localized scleroderma—current concepts and novel targets for therapy
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  • 作者:Oliver Distler ; Antonio Cozzio
  • 关键词:Systemic sclerosis ; Localized scleroderma ; Serotonin ; Interleukin ; 6 ; Soluble guanylate cyclase ; Nintedanib
  • 刊名:Springer Seminars in Immunopathology
  • 出版年:2016
  • 出版时间:January 2016
  • 年:2016
  • 卷:38
  • 期:1
  • 页码:87-95
  • 全文大小:326 KB
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  • 作者单位:Oliver Distler (1)
    Antonio Cozzio (2)

    1. Division of Rheumatology, University Hospital Zurich, Gloriastr. 25, 8091, Zurich, Switzerland
    2. Division of Dermatology, University Hospital Zurich, Zurich, Switzerland
  • 刊物类别:Biomedical and Life Sciences
  • 刊物主题:Biomedicine
    Immunology
    Internal Medicine
  • 出版者:Springer Berlin / Heidelberg
  • ISSN:1863-2300
文摘
Systemic sclerosis (SSc) is a chronic autoimmune disease with a high morbidity and mortality. Skin and organ fibrosis are key manifestations of SSc, for which no generally accepted therapy is available. Thus, there is a high unmet need for novel anti-fibrotic therapeutic strategies in SSc. At the same time, important progress has been made in the identification and characterization of potential molecular targets in fibrotic diseases over the recent years. In this review, we have selected four targeted therapies, which are tested in clinical trials in SSc, for in depths discussion of their preclinical characterization. Soluble guanylate cyclase (sGC) stimulators such as riociguat might target both vascular remodeling and tissue fibrosis. Blockade of interleukin-6 might be particularly promising for early inflammatory stages of SSc. Inhibition of serotonin receptor 2b signaling links platelet activation to tissue fibrosis. Targeting simultaneously multiple key molecules with the multityrosine kinase-inhibitor nintedanib might be a promising approach in complex fibrotic diseases such as SSc, in which many partially independent pathways are activated. Herein, we also give a state of the art overview of the current classification, clinical presentation, diagnostic approach, and treatment options of localized scleroderma. Finally, we discuss whether the novel targeted therapies currently tested in SSc could be used for localized scleroderma. Keywords Systemic sclerosis Localized scleroderma Serotonin Interleukin-6 Soluble guanylate cyclase Nintedanib

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