ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 1905 • 2015 ACR/ARHP Annual Meeting

    Stimulators of Soluble Guanylate Cyclase (sGC) Inhibit Experimental Skin Fibrosis of Different Aetiologies

    Peter Sandner1,2, Clara Dees3, Joerg H. W. Distler3, Christian Beyer3, Alfiya Distler3, Yun Zhang4, Katrin Palumbo-Zerr4, Georg A. Schett5, Alina Soare3,6, Oliver Distler7 and Emanuel Haasbach8, 1Bayer Health Care, Global Drug Discovery, Bayer Pharma AG, Wuppertal, Germany, 2Institute of Pharmacology, Hannover Medical School, Hannover, Germany, 3Department of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany, 4Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 5Department of Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany, 6Carol Davila University of Medicine and Pharmacy, Internal Medicine and Rheumatology, Cantacuzino Hospital, Bucharest, Romania, 7Research of Systemic Autoimmune Diseases, Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland, 8Bayer HealthCare, Bayer Pharma AG, Wuppertal, Germany

    Background/Purpose: Systemic sclerosis (SSc) is characterised by fibrosis and vascular alterations, both of which account for the high morbidity and mortality of SSc. Although several…
  • Abstract Number: 1906 • 2015 ACR/ARHP Annual Meeting

    Stimulators of Soluble Guanylate Cyclase (sGC) Improve Wound Healing in the Tsk-1 Mouse Skin Fibrosis Mode

    Peter Sandner1,2, Christian Beyer3, Joerg H. W. Distler3 and Emanuel Haasbach1, 1Bayer HealthCare, Bayer Pharma AG, Wuppertal, Germany, 2Institute of Pharmacology, Hannover Medical School, Hannover, Germany, 3Department of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany

    Background/Purpose: Systemic sclerosis (SSc) is a multisystem disorder characterized by thickening of the skin and distinctive involvement of multiple internal organs. In addition to skin…
  • Abstract Number: 1907 • 2015 ACR/ARHP Annual Meeting

    Inhibition of Phosphodiesterase 4 (PDE4) Reduces Dermal Fibrosis By Interfering with the Release of Pro-Fibrotic Cytokines from M2-Macrophages

    Christiane Maier, Christian Beyer, Jeorg HW Distler and Georg Schett, Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany

    Background/Purpose: PDE4 catalyses the breakdown of the second messengers cAMP and cGMP to modulate intracellular effects. PDE4 is mainly expressed in inflammatory cells, and its…
  • Abstract Number: 1908 • 2015 ACR/ARHP Annual Meeting

    Macitentan Responsiveness Supports the Validity of a Murine Model of Pulmonary Hypertension in Scleroderma Associated with Altered Tgfbeta/BMPR2 Signalling

    Emma C. Derrett-Smith1, Vincent Sobanski2, Adrian Gilbane2, Sarah Trinder3, Yasmina Bauer4, Berengère Renault4, Marc Iglarz4, David Abraham5, Alan M. Holmes6 and Christopher P. Denton7, 1Centre for Rheumatology and Connective Tissue Diseases,, UCL Division of Medicine, London, United Kingdom, 2UCL Division of Medicine, London, United Kingdom, 3Centre for Rheumatology and Connective Tissue Disease, UCL Division of Medicine, London, United Kingdom, 4Actelion Pharmaceuticals Ltd., Allschwil, Switzerland, 5Centre for Rheumatology and Connective Tissue Disease, University College London, London, United Kingdom, 6Centre for Rheumatology and Connective Tissue Diseases, UCL Division of Medicine, London, United Kingdom, 7Rheumatology and Connective Tissue Diseases, University College London, London, United Kingdom

    Background/Purpose: Pulmonary arterial hypertension (PAH) is an important complication of systemic sclerosis (SSc) that occurs in around 10% of cases.  We have previously shown that…
  • Abstract Number: 1909 • 2015 ACR/ARHP Annual Meeting

    Nailfold Capillaroscopic Assessment and Vascular Biomarkers in Systemic Sclerosis: Low CD40L Levels in Patients with Late Scleroderma Patterns

    Yasemin Yalcinkaya1, Suzan Cinar2, Sevil Kamali3, Ozlem Pehlivan4, Lale Ocal1, Gunnur Deniz2 and Murat Inanc3, 1Istanbul Medical Faculty, Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul, Turkey, 2Department of Immunology, Istanbul University, Institute of Experimental Medicine (DETAE), Istanbul, Turkey, 3Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 4Istanbul Faculty of Medicine, Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul, Turkey

    Background/Purpose: To determine the relationship between vascular biomarkers reflecting the vascular   injury and neoangiogenesis with nailfold capillaroscopic changes in systemic sclerosis (SSc). Methods: Seventy-two SSc…
  • Abstract Number: 1910 • 2015 ACR/ARHP Annual Meeting

    Increased Circulating CD204/CD206 Double Positive Monocyte/Macrophages in Systemic Sclerosis Patients with “Early” Capillaroscopic Pattern of Microvascular Damage

    Stefano Soldano1, Paola Contini2, Paola Montagna1, Renata Brizzolara1, Amelia Chiara Trombetta3, Barbara Ruaro3, Alberto Sulli3, Sabrina Paolino3, Carmen Pizzorni3, Bruno Seriolo1, Marco A. Cimmino3 and Maurizio Cutolo3, 1Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, University of Genova, Genoa, Italy, Genoa, Italy, 2Division of Clinical Immunology, Department of Internal Medicine, University of Genova, Genoa, Italy, Genoa, Italy, 3Research Laboratory and Academic Division of Clinical Rheumatology, Department of Internal Medicine, IRCCS A.O.U. San Martino-IST, University of Genova, Genoa, Italy, Genoa, Italy

    Background/Purpose: Immune-inflammatory cells participate together with endothelial cells and myofibroblasts in the tissue damage that characterizes fibrotic diseases, including systemic sclerosis (SSc) (1). Among immune…
  • Abstract Number: 1911 • 2015 ACR/ARHP Annual Meeting

    Monocyte Chemoattractant Protein-1 (MCP-1, CCL2) Is a Potential Local Marker of Renal Involvement in Scleroderma

    Edward Stern1,2, Cassandra Hong2, Voon H. Ong2, Aine Burns1, Robert Unwin3 and Christopher P. Denton4, 1Nephrology, Royal Free Hospital, London, United Kingdom, 2Rheumatology, UCL Division of Medicine, London, United Kingdom, 3Nephrology, UCL Division of Medicine, London, United Kingdom, 4Rheumatology and Connective Tissue Diseases, University College London, London, United Kingdom

    Background/Purpose: Renal disease in scleroderma (SSc), including scleroderma renal crisis (SRC), remains a major clinical challenge. Previous studies showed up to 50% of SSc patients…
  • Abstract Number: 1912 • 2015 ACR/ARHP Annual Meeting

    Glycyrrhizin Ameliorates Fibrosis, Vasculopathy, and Immune Abnormalities in Animal Models of Systemic Sclerosis

    Takashi Yamashita1, Yoshihide Asano2, Takashi Taniguchi1, Ryosuke Saigusa3, Kouki Nakamura1, Syunnsuke Miura2, Tetsuo Toyama1, Takehiro Takahashi1, Yohei Ichimura1, Ayumi Yoshizaki1, Maria Trojanowska4 and Shinichi Sato1, 1Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2University of Tokyo Graduate School of Medicine, Tokyo, Japan, 37-3-1 Hongo, Bunkyo-ku, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 4Arthritis Center, Boston University, Arthritis Center, Boston, MA

    Background/Purpose:  Systemic sclerosis (SSc) is a multisystem autoimmune disease characterized by vasculopathy and fibrosis of the skin and various internal organs. Glycyrrhizin, a triterpenoid saponin…
  • Abstract Number: 1913 • 2015 ACR/ARHP Annual Meeting

    Lysyl Oxidase Induces Fibrosis Via Upregulation of IL-6 and Serves As a Biomarker to Monitor Response to Therapy

    Tetsuya Nishimoto1, Takahisa Takihara2, Logan Mlakar3 and Carol Feghali-Bostwick3, 1Department of Medicine, Medical University of South Carolina, Charleston, SC, 2Tokai University School of Medicine, Kanagawa, Japan, 3Medical University of South Carolina, Charleston, SC

    Background/Purpose: Lysyl oxidase (LOX) is a copper-dependent amine oxidase whose primary function is the covalent crosslinking of collagens in the extracellular matrix (ECM). Fibrosis is…
  • Abstract Number: 1914 • 2015 ACR/ARHP Annual Meeting

    Oncostatin M As a Potential Molecular Target in Systemic Sclerosis

    Maria Feeney1, Farhat Syed2, Korsa Khan3, Xu Shiwen4, Katherine Sully5, Sarah Trinder6, Paul Wilson7, David Abraham6,8, Alan M. Holmes6 and Christopher P. Denton9, 1Biopharm Research, GlaxoSmithKline, Stevenage, United Kingdom, 2Immuno-Inflammation, GlaxoSmithKline, Stevenage, United Kingdom, 3Centre For Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 4UCL Medical School, London, United Kingdom, 5Biopharm Translational Medicine, GlaxoSmithKline, Stevenage, United Kingdom, 6Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 7Quantitative Sciences, GlaxoSmithKline, Stevenage, United Kingdom, 8Centre for Rheumatology and Connective Tissue Disease, University College London, London, United Kingdom, 9Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom

    Background/Purpose:   Oncostatin M (OSM) is a pleiotropic member of the gp130/ IL-6 cytokine family, produced by a variety of immune cells, including macrophages, neutrophils…
  • Abstract Number: 1915 • 2015 ACR/ARHP Annual Meeting

    Pathogenetic Overlap Between Localised and Systemic Scleroderma: A Study of Nodular and Keloidal Morphea Occurring in Systemic Sclerosis

    Emma C. Derrett-Smith1, Nataliya Gak2, Svetlana I. Nihtyanova3, Voon H. Ong3, Victoria Swale2, Cate Orteu2 and Christopher P. Denton4, 1Centre for Rheumatology and Connective Tissue Diseases,, UCL Division of Medicine, London, United Kingdom, 2Royal Free London NHS Foundation Trust, London, United Kingdom, 3Rheumatology, UCL Division of Medicine, London, United Kingdom, 4Rheumatology and Connective Tissue Diseases, University College London, London, United Kingdom

    Background/Purpose:  Localised scleroderma can occur in overlap with systemic sclerosis (SSc); nodular and keloidal morphea are rare subtypes but can be disfiguring and challenging to…
  • Abstract Number: 1916 • 2015 ACR/ARHP Annual Meeting

    Validation of Novel Biomarker Candidates for Systemic Sclerosis

    Johannes Schulte-Pelkum1, Petra Budde1, Hans-Dieter Zucht1, Daniel Wirtz1, Peter Schulz-Knappe1, Oliver Distler2, Suzana Jordan3, Nicolas Hunzelmann4, Matthias Schneider5 and Britta Maurer2, 1Protagen AG, Dortmund, Germany, 2Division of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 3Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 4Department of Dermatology, University of Cologne, Cologne, Germany, 5Rheumatology, Heinrich-Heine-University, Duesseldorf, Germany

    Background/Purpose: Systemic sclerosis (SSc) is a systemic autoimmune disease that manifests as progressive fibrosis of the skin and internal organs. SSc is associated with the…
  • Abstract Number: 1917 • 2015 ACR/ARHP Annual Meeting

    Developing and Validating a Serum Biomarker for the Extent of Skin Disease in Patients with Diffuse Cutaneous Systemic Sclerosis

    Lisa Rice1, Julio Mantero2, Giuseppina Stifano1, Jessica Ziemek3, Robyn T. Domsic4 and Robert Lafyatis1, 1Boston University School of Medicine, Boston, MA, 2Rheumatology, Boston University School of Medicine, Boston, MA, 3Rheumatology/Arthritis Center, Boston University School of Medicine, Boston, MA, 4Medicine - Rheumatology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: In this study we aimed to both agonistically investigate alterations in the serum proteome of patients with diffuse cutaneous systemic sclerosis (dcSSc), as well…
  • Abstract Number: 1918 • 2015 ACR/ARHP Annual Meeting

    Pharmacologic Targeting of Mitochondrial Dysfunction in Systemic Sclerosis: Enhanced SIRT3 Signaling

    Kaname Akamata1, Mitra Bhattacharyya1, Mahesh Gupta2, Jack Arbiser3, David Kamp4, Jun Wei1 and John Varga1, 1Division of Rheumatology, Northwestern University, Feinberg School of Medicine, Chicago, IL, 2University of Chicago, Departments of Surgery, Chicago, IL, 3Department of Dermatology, Emory University School of Medicine Winship Cancer Institute Atlanta Veterans Administration Health Center, Atlanta, GA, 4Department of Medicine, Division of Pulmonary & Critical Care Medicine, Jesse Brown VA Medical Center and Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Recent evidences suggest that cytosolic and mitochondrial reactive oxygen species (ROS), play pivotal roles in modulating TGF-β-induced profibrotic responses and are implicated in pathogenesis…
  • Abstract Number: 1919 • 2015 ACR/ARHP Annual Meeting

    Genetic Deletion of Toll-like Receptor 4 (Tlr4) Abrogates TGF-β1-Induced Endothelial-to-Mesenchymal Transition (EndoMT) in Murine Pulmonary Endothelial Cells

    Peter J. Wermuth1 and Sergio A. Jimenez2, 1Jefferson Institute of Molecular Medicine, Division of Connective Tissue Diseases and Scleroderma Center, Thomas Jefferson University, Philadelphia, PA, 2Jefferson Institute of Molecular Medicine, Division of Connective Tissue Diseases and Scleroderma Center,Thomas Jefferson University, Philadelphia, PA

    Background/Purpose: Systemic sclerosis (SSc) is a systemic autoimmune disease of unknown etiology whose pathogenesis involves the regulation of a diverse range of molecular pathways. The…
  • « Previous Page
  • 1
  • …
  • 1814
  • 1815
  • 1816
  • 1817
  • 1818
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

All abstracts accepted to ACR Convergence are under media embargo once the ACR has notified presenters of their abstract’s acceptance. They may be presented at other meetings or published as manuscripts after this time but should not be discussed in non-scholarly venues or outlets. The following embargo policies are strictly enforced by the ACR.

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of our scientific journal, Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. In an exception to the media embargo, academic institutions, private organizations, and companies with products whose value may be influenced by information contained in an abstract may issue a press release to coincide with the availability of an ACR abstract on the ACR website. However, the ACR continues to require that information that goes beyond that contained in the abstract (e.g., discussion of the abstract done as part of editorial news coverage) is under media embargo until 10:00 AM ET on November 14, 2024. Journalists with access to embargoed information cannot release articles or editorial news coverage before this time. Editorial news coverage is considered original articles/videos developed by employed journalists to report facts, commentary, and subject matter expert quotes in a narrative form using a variety of sources (e.g., research, announcements, press releases, events, etc.).

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying colleagues, institutions, communications firms, and all other stakeholders related to the development or promotion of the abstract about this policy. If you have questions about the ACR abstract embargo policy, please contact ACR abstracts staff at [email protected].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology