ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 770 • 2014 ACR/ARHP Annual Meeting

    Detection of Proteins in Lung Tissues of Patients with Systemic Sclerosis Using Tissue Microarrays

    Frank Schneider1 and Carol A. Feghali-Bostwick2, 1Pathology, University of Pittsburgh, Pittsburghh, PA, 2Medicine, Medical University of South Carolina, Charleston, SC

    Background/Purpose: Research on systemic sclerosis (SSc)-associated interstitial lung disease (ILD) has been hindered by the paucity of lung tissues, as SSc patients with lung involvement…
  • Abstract Number: 768 • 2014 ACR/ARHP Annual Meeting

    Transforming Growth Factor Beta Induces anti  Angio and Vasculo-Genesis Phenotype in Dermal Fibroblasts through Secretion of Pigment Epithelium Derived Factor

    Vasiliki Liakouli1, Margherita Scarcia2, Giuseppina Abignano3, Emma C. Derrett-Smith4, Justin Gillespie5, Paola Cipriani6, Paul Emery7, Christopher P. Denton8, R Giacomelli9, Georgia Mavria2 and Francesco Del Galdo10, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine and Department of Biotechnological and Applied Clinical Science, Rheumatology Unit, School of Medicine, University of L’Aquila, Leeds, United Kingdom, 2Signal Transduction and Angiogenesis group, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK, Leeds, United Kingdom, 3Leeds Institute of Rheumatic and Musculoskeletal Medicine and Department of Biotechnological and LTHT Leeds Musculoskeletal Biomedical Research Unit, leeds, United Kingdom, 4Centre for Rheumatology and Connective Tissue Diseases,, UCL Medical School Royal Free Campus, London, United Kingdom, 5University of Leeds, Leeds Institue of Rheumatic and Musculoskeletal Medicine, Leeds, United Kingdom, 6Department of Biotechnological and Applied Clinical Science, Rheumatology Unit, School of Medicine, University of L’Aquila, L'Aquila, Italy, 7NIHR-Leeds Musculoskeletal Biomedical Research Unit and Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 8Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School Royal Free Campus, London, United Kingdom, 9Università degli Studi dell'Aquila, L'Aquila, Italy, 10Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom

    Background/Purpose: Systemic Sclerosis (SSc) is an autoimmune disorder characterized by tissue fibrosis and vasculopathy. A proteomic analysis of the secretome of SSc dermal fibroblasts (SSc-FBs)…
  • Abstract Number: 769 • 2014 ACR/ARHP Annual Meeting

    Anti-Fibrotic Effects of an Investigational Drug: Bis-Oxetanyl Sulfoxide

    Logan Mlakar1, Takahisa Takihara2, Melissa Sprachman3, Peter Wipf4 and Carol Feghali-Bostwick1, 1Medical University of South Carolina, Charleston, SC, 2Tokai University School of Medicine, Kanagawa, Japan, 3Massachusetts General Hospital, Boston, MA, 4Chemisry, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose:   The hallmark of pulmonary fibrosis is thickening and scarring of the tissue caused by increased deposition of extracellular matrix (ECM) proteins like collagen…
  • Abstract Number: 767 • 2014 ACR/ARHP Annual Meeting

    The Impact of Plasmacytoid Dendiritc Cells (pDCs) on Fibrosis in bleomycin–induced Murine Model of Systemic Sclerosis (SSc)

    Suzanne Kafaja1, Isela Valera1, Anagha Divekar2, Daniel E. Furst3 and Ram Singh1, 1Medicine/Rheumatology, University of California, Los Angeles, Los Angeles, CA, 2Biolegend, San Diego, CA, 3Medicine/ Rheumatology, University of California, Los Angeles, Department of Medicine, Los Angeles, CA

    Background/Purpose Pathogenesis of systemic sclerosis (SSc) remains unclear. Alterations in adaptive and innate immune responses, with increased T-cells that produce type 2 cytokines and impaired…
  • Abstract Number: 766 • 2014 ACR/ARHP Annual Meeting

    Endothelial Fli1 Deficiency Delays Wound Healing Due to Impaired Anastomosis of Newly Formed Vessels – a Possible Mechanism of Refractory Skin Ulcers in Systemic Sclerosis

    Yoshihide Asano1 and Maria Trojanowska2, 1Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2Arthritis Center, Boston University, Boston, MA

    Background/Purpose Systemic sclerosis (SSc) is a multisystem inflammatory and vascular disease resulting in fibrosis of the skin and certain internal organs. Although the pathogenesis of…
  • Abstract Number: 765 • 2014 ACR/ARHP Annual Meeting

    Gene-Gene Interaction of IRF5 and BLK Polymorphisms in US and Spanish Cohorts of Systemic Sclerosis (SSc)

    Pravitt Gourh1, Yoonhee Kim2, Sandeep K. Agarwal3, Filemon K. Tan4, Shervin Assassi4, Javier Martin5, Frank C. Arnett4 and Maureen D Mayes4, 1NIAMS-Rheumatology, National Institutes of Health, Bethesda, MD, 2NIH, Bethesda, MD, 3Medicine, Section of Immunology, Allergy and Rheumatology, Baylor College of Medicine, Houston, TX, 4Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 5Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla (Granada), Spain

    Background/Purpose Systemic sclerosis (SSc) is a complex autoimmune disease and several genetic loci increasing SSc susceptibility have been identified with small to modest effect sizes.…
  • Abstract Number: 764 • 2014 ACR/ARHP Annual Meeting

    ERG and FLI1 in Systemic Sclerosis-Associated Pulmonary Complications

    Rong Han and Maria Trojanowska, Arthritis Center, Boston University, Boston, MA

    Background/Purpose: Pulmonary arterial hypertension (PAH) and pulmonary fibrosis (PF) are the two major lung complications associated with the autoimmune disease systemic sclerosis (SSc), and constitute…
  • Abstract Number: 763 • 2014 ACR/ARHP Annual Meeting

    Caveolin-1 and Peroxisome Proliferator-Activated Receptor Gamma Co-Regulate the Differentiation of Monocytes to Adipocytes and Myofibroblasts in Vivo and in Vitro

    Rebecca Lee1, Charles Reese2, Michael Bonner1, Beth Perry3, Richard M. Silver4, Richard P. Visconti5, Stanley Hoffman3 and Elena Tourkina6, 1Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 2Medical University of South Carolina, Charleston, SC, 3Rheumatology, Medical University of South Carolina, Charleston, SC, 4Div Rheumatology & Immunology, Medical University of South Carolina,Charleston,USA, Charleston, SC, 5Cell Biology and Regenerative Medicine, Medical University of South Carolina, Charleston, SC, 6Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC

    Background/Purpose Skin fibrosis in scleroderma is associated with the loss of subcutaneous adipose tissue (lipodystrophy). The mechanisms underlying lipodystrophy and its relationship to fibrosis are…
  • Abstract Number: 762 • 2014 ACR/ARHP Annual Meeting

    IQGAP1 Enhances Contractility of Scleroderma Lung Fibroblasts and Promotes Bleomycin-Induced Pulmonary Fibrosis

    Tanjina Akter1, Ilia Atanelishvili2, Yuichiro Shirai3, Sybil Prince Nelson4, Alvaro Garcia-Martos5, Thomas A. Morinelli3, Richard M. Silver6 and Galina S. Bogatkevich1, 1Department of Rheumatology, Medical University of South Carolina,Charleston,USA, Charleston, SC, 2Division of Rheumatology & Immunology, Medical University of South Carolina,Charleston,USA, Charleston, SC, 3Medical University of South Carolina,Charleston,USA, chareston, SC, 4College of Graduate Studies, Medical University of South Carolina,Charleston,USA, chareston, SC, 5Hospital la Zarzuela,Madrid,Spain, Madrid, Spain, 6Div Rheumatology & Immunology, Medical University of South Carolina,Charleston,USA, Charleston, SC

    Background/Purpose Scleroderma associated interstitial lung disease (SSc-ILD) is an irreversible and progressive complication and a leading cause of death among SSc patients. Constitutive overexpression of…
  • Abstract Number: 761 • 2014 ACR/ARHP Annual Meeting

    Specific Autoantibody Profiles and Disease Subgroups Correlate with Circulating Micro-RNA in Systemic Sclerosis

    Dirk Wuttge1, Anting L. Carlsen2, Gabriel Teku3, Samantha Steen4, Marie Wildt1, Mauno Vihinen3, Roger Hesselstrand1 and Niels H. H. Heegaard4,5, 1Rheumatology, Lund University, Lund, Sweden, 2Clinical Biochemistry, Immunology & Genetics, Statens Serum Institut, Copenhagen, Denmark, 3Experimental Medical Science, Lund University, Lund, Sweden, 4Department of Clinical Biochemistry, Immunology & Genetics, Statens Serum Institut, Copenhagen, Denmark, 5Department of Clinical Biochemistry & Pharmacology, Odense University Hospital, Odense C, Denmark

    Background/Purpose: Systemic sclerosis (SSc) is a serious autoimmune disease with clinical phenotypes of different prognosis, progression rate, and different extent of involvement of internal organs.…
  • Abstract Number: 760 • 2014 ACR/ARHP Annual Meeting

    Use of Multiplex Cytokine Analysis of Dermal Blister Fluid to Assess Local Inflammatory and Immune Activity in Systemic Sclerosis

    Kristina E.N. Clark1, Henry Lopez2, Xu Shiwen1, Bahja Ahmed Abdi1, George Martin3, Korsa Khan4, David J. Abraham1, Christopher P. Denton5 and Richard J. Stratton1, 1Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 2Murigenics, Vallejo, CA, 3Aero Dap, Vallejo, CA, 4Centre for Rheumatology and Connective Tissue Diseases, UCL medical School, London, United Kingdom, 5Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School Royal Free Campus, London, United Kingdom

    Background/Purpose Clinical diversity in systemic sclerosis (SSc) suggests complex multifaceted pathogenesis involving interplay of growth factors or cytokines within the lesional microenvironment.  We analysed dermal…
  • Abstract Number: 778 • 2014 ACR/ARHP Annual Meeting

    PTPN22 rs2476601 and Susceptibility to Biopsy Proven Giant Cell Arteritis (GCA) in an Australian Sample

    Susan Lester1, Alex Hewitt2, Linda Bradbury3, Elisabeth De Smit4, Andrew Harrison5, Graeme Jones6, Geoffrey O. Littlejohn7, Tony R. Merriman8, Bain Shenstone9, Malcolm D. Smith10, Maureen Rischmueller11, Matthew A. Brown12 and Catherine L. Hill13,14, 1Rheumatology Unit, Queen Elizabeth Hospital, Woodville South, Australia, 2Lions Eye Institute, University of Western Australia, Perth, Australia, 3The University of Queensland, Brisbane, Australia, 4Centre for Eye Research, University of Melbourne, Melbourne, Australia, 5Medicine, University of Otago, Wellington, New Zealand, 6Menzies Research Institute Tasmania, University of Tasmania, HOBART, Australia, 7Rheumatology, Monash Medical Center, Melbourne, Australia, 8Department of Biochemistry, University of Otago, Dunedin, New Zealand, 9Concord Hospital, Sydney, Australia, 10Rheumatology Research Unit, Repatriation General Hospital, Adelaide SA, Australia, 11Department of Rheumatology, The Queen Elizabeth Hospital, SA, Australia, 12University of Queensland Diamantina Institute, Brisbane, Australia, 13Discipline of Medicine, University of Adelaide, Adelaide, Australia, 14Rheumatology Unit, The Queen Elizabeth Hospital, Woodville, Australia

    Background/Purpose: The aetiology and genetic background of GCA remains unclear, although genetic susceptibility is known to play a role. Recently, an association with the minor,…
  • Abstract Number: 779 • 2014 ACR/ARHP Annual Meeting

    Toll-like Receptor 2 Agonism Induces Inflammation, Angiogenesis and Cell Migration in Giant Cell Arteritis

    Lorraine O'Neill1, Aoife Maher1, Jennifer McCormick2, Conor Murphy3, Geraldine M. McCarthy4, Douglas J. Veale5, Ursula Fearon2 and Eamonn S. Molloy1, 1Rheumatology, St. Vincent's University Hospital, Dublin 4, Ireland, 2Dublin Academic Medical Centre, Translational Rheumatology Research Group, Dublin, Ireland, 3Department of Ophthalmology, Royal Victoria Eye and Ear Hospital, Dublin, Ireland, 4Medicine/Rheumatology, Mater Misericordiae University Hospital, Dublin 7, Ireland, 5Translational Rheumatology Research Group, St. Vincent's University Hospital, Dublin 4, Ireland

    Background/Purpose Activation of dendritic cells (DCs) is one of the earliest inciting events in Giant Cell Arteritis (GCA). TLR 2 is expressed on DCs in…
  • Abstract Number: 777 • 2014 ACR/ARHP Annual Meeting

    Influence of the IL17A Locus in Giant Cell Arteritis Susceptibility

    Javier Martin1, Ana Márquez2, José Hernández-Rodríguez3, Maria C. Cid4, Roser Solans5, Santos Castañeda6, Inmaculada C. Morado7, Javier Narváez8, Victor M. Martinez-Taboada9, Norberto Ortego-Centeno10, Bernardo Sopeña11, Jordi Monfort12, Maria Jesus Garcia-Villanueva13, Luis Caminal-Montero14, Eugenio De Miguel15, Ricardo Blanco16, Øyvind Palm17, Øyvind Molberg18, Joerg Latus19, Niko Braun19, Frank Moosig20, Torsten Witte21, Lorenzo Beretta22, Alessandro Santaniello23, Giulia Pazzola24, Luigi Boiardi25, Carlo Salvarani26 and Miguel A. Gonzalez-Gay9, 1Immunology, Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla (Granada), Spain, 2Instituto de Parasitologia y Biomedicina López-Neyra (IPBLN-CSIC) and Systemic Autoimmune Diseases Unit, Hospital Clínico San Cecilio, Granada, Spain, 3Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain, 4Vasculitis Research Unit, Department of Autoimmune Diseases, Hospital Clínic University of Barcelona, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036- Barcelona, Spain, 5Autoimmune Systemic Diseases Unit, Department of Internal Medicine, Hospital Vall d'Hebron, Autonomous University of Barcelona, Barcelona, Spain, 6Department of Rheumatology, Hospital de la Princesa, IIS-Princesa, Madrid, Spain, 7Department of Rheumatology, Hospital Clínico San Carlos, Madrid, Spain, 8Rheumatology, Hospital Universitario de Bellvitge. Barcelona. Spain, Barcelona, Spain, 9Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, IFIMAV, Santander, Spain, 10Systemic Autoimmune Diseases Unit, Hospital Clínico San Cecilio, Granada, Spain, 11Department of Internal Medicine, Complejo Hospitalario Universitario de Vigo, Vigo, Spain, 12Department of Rheumatology, Grup de recerca cel•lular en inflamació i cartílag. IMIM (Institut de Recerca Hospital del Mar), Barcelona, Spain, 13Department of Rheumatology, Hospital Ramón y Cajal, Madrid, Spain, 14Department of Internal Medicine, Hospital Universitario Central de Asturias, Oviedo, Spain, 15Department of Rheumatology, Hospital Universitario La Paz, Madrid, Spain, 16Hospital Marques de Valdecilla, Santander, Spain, 17Department of Rheumatology, Oslo University Hospital and University of Oslo, Oslo, Norway, 18Department of Rheumatology, Oslo University Hospital Rikshospitalet, Oslo, Norway, 19Department of Internal Medicine, Division of Nephrology, Robert-Bosch-Hospital, Stuttgart, Germany, 20Department of Clinical Immunology and Rheumatology, University of Luebeck, Bad Bramstedt, Germany, 21Clinic for Immunology and Rheumatology, Hannover Medical School, Hannover, Germany, 22Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy, 23Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico di Milano, Milan, Italy, 24Rheumatology Unit, Arcispedale S Maria Nuova, Reggio Emilia, Italy, 25Unita` Operativa di Reumatologia, Azienda Ospedaliera ASMN, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy, 26Rheumatology Unit, Department of Internal Medicine, Azienda Ospedaliera ASMN, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy

    Background/Purpose: A recent study has showed that the number of Th17 lymphocytes is significantly increased in patients with GCA, resulting in an imbalance between Th17…
  • Abstract Number: 744 • 2014 ACR/ARHP Annual Meeting

    Integrin Inhibitor Modulates Pulmonary Fibrosis in the Reactive Oxygen Species Murine Model of Systemic Sclerosis

    Gianluca Bagnato1, Alessandra Bitto2, Natasha Irrera2, Gabriele Pizzino2, Neal Roberts3, Domenica Altavilla2, Francesco Squadrito2, Antonino Saitta4 and Gianfilippo Bagnato5, 1Rheumatology, University of Messina, Messina, Italy, 2Pharmacology, University of Messina, Messina, Italy, 3University of Louisville, Louisville, KY, 4Internal Medicine, University of Messina, Messina, Italy, 5Via C. Colombo, 41, Universita Messina, Villafranca Tirrena, Italy

    Background/Purpose: Systemic sclerosis (SSc) is an acquired connective tissue disorder in which inflammation, immune dysregulation and vascular damage lead to fibroblast activation that results in…
  • « Previous Page
  • 1
  • …
  • 2180
  • 2181
  • 2182
  • 2183
  • 2184
  • …
  • 2607
  • 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 »

Embargo Policy

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 CT on October 25. 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