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Abstracts tagged "Fibroblasts"

  • Abstract Number: 1661 • 2016 ACR/ARHP Annual Meeting

    Toll-like Receptor 4 Induced IL-20 and IL-24 Stimulate Osteoblast Mineralization and Are Increased in Spondyloarthritis

    Tue Wenzel Kragstrup1,2, Morten Nørgaard Andersen3, Berit Schiøttz-Christensen4, Anne Grethe Jurik5, Malene Hvid6 and Bent Deleuran1, 1Department of Biomedicine, Aarhus University, Aarhus, Denmark, 2Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 3Aarhus University, Aarhus, Denmark, 4Hospital Lillebaelt, Middelfart, Denmark, 5Aarhus University Hospital, Aarhus, Denmark, 6Department of Clinical Medicine, Aarhus University, Aarhus, Denmark

    Background/Purpose: The pathogenesis of spondyloarthritis (SpA) involves activation of the innate immune system, inflammation and new bone formation. The innate immune system is activated through…
  • Abstract Number: 1671 • 2016 ACR/ARHP Annual Meeting

    Pirfenidone Might Inhibit New Bone Formation in Spondyloarthritis: Proof of Concept Study Using Cell Culture Models

    Julie Laustsen1, Søren Lomholt1, Pernille Andersen2, Jens Kelsen3 and Tue Wenzel Kragstrup1,4, 1Department of Biomedicine, Aarhus University, Aarhus, Denmark, 2Interdisciplinary Nanoscience Center, Aarhus University, Aarhus, Denmark, 3Department of Gastroenterology, Aarhus University Hospital, Aarhus, Denmark, 4Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark

    Background/Purpose:  The pathogenesis of spondyloarthritis (SpA) involves both inflammation and new bone formation in the spine. In line with this, the disease has been characterized…
  • Abstract Number: 1852 • 2016 ACR/ARHP Annual Meeting

    Decreased Expression of Sirtuin 7 By Lung Fibroblasts from Patients with Scleroderma Contributes to Elevated Collagen Production

    Anne E. Wyman1,2, Zahid Noor1, Nevins W. Todd1,2, Irina G. Luzina1,2 and Sergei P. Atamas1,2, 1University of Maryland School of Medicine, Baltimore, MD, 2Baltimore VA Medical Center, Baltimore, MD

    Background/Purpose:  Pulmonary fibrosis is a severe complication of systemic sclerosis (SSc). Changes in the expression levels of sirtuins (SIRTs), a family of NAD+-dependent histone deacetylases,…
  • Abstract Number: 1855 • 2016 ACR/ARHP Annual Meeting

    Phosphodiesterase-5 Inhibitors Attenuate Fibrotic Phenotype and Restore Anti-Fibrotic Resopnses of Cutaneous Fibroblasts in Patients with Scleroderma

    Vikas Agarwal1, Mohit kumar Rai1, Vinita Agrawal2, Harshit Singh1 and Saurabh Chaturvedi1, 1Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 2Pathology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, Lucknow, India

    Background/Purpose:  Scleroderma (SSc) is a chronic autoimmune disease, characterized by excessive fibrosis of skin and internal organs due to uncontrolled proliferation of fibroblasts and deposition…
  • Abstract Number: 1857 • 2016 ACR/ARHP Annual Meeting

    A Novel Highly Selective 5-Hydroxytryptamine 2B (5-HT2B) Receptor Antagonist Ameliorating Fibrosis in Preclinical Models of Systemic Sclerosis

    Christina Wenglén1, Lars Pettersson2, Helena Arozenius2 and Gunilla Ekström1, 1R&D, AnaMar AB, Lund, Sweden, 2AnaMar AB, Lund, Sweden

    Background/Purpose:   Methods:   Results:   Conclusion: The results demonstrate that the 5-HT2B receptor antagonist AM1125 prevents pro-fibrotic events in human dermal fibroblasts and attenuates…
  • Abstract Number: 2071 • 2016 ACR/ARHP Annual Meeting

    Expression of Neuraminidase 1 (NEU1) Is Upregulated in the Lungs of Scleroderma Patients with Pulmonary Fibrosis, and Gene Delivery of NEU1 to Mouse Lungs Elicits Accumulation of CD8+ Lymphocytes and Collagen

    Irina G. Luzina1,2, Anne E. Wyman1,2, Virginia Lockatell2, Zahid Noor2, Nevins W. Todd1,2, Simeon E. Goldblum1,2 and Sergei P. Atamas1,2, 1Baltimore VA Medical Center, Baltimore, MD, 2University of Maryland School of Medicine, Baltimore, MD

    Background/Purpose:  We and others have previously reported that pulmonary fibrosis in patients with scleroderma is accompanied by pulmonary accumulation of predominantly CD8+ T lymphocytes. Earlier…
  • Abstract Number: 2072 • 2016 ACR/ARHP Annual Meeting

    Fli1-Haploinsufficient Dermal Fibroblasts Promote Skin-Localized Transdifferentiation of Th2- and Th17-like Regulatory T Cells

    Ryosuke Saigusa1, Yoshihide Asano2, Takuya Miyagawa2, Megumi Hirabayashi2, Kouki Nakamura1, Shunsuke Miura3, Takashi Yamashita2, Yohei Ichimura1, Takehiro Takahashi1, Tetsuo Toyama2, Takashi Taniguchi1, Ayumi Yoshizaki2, Maria Trojanowska4 and Shinichi Sato1, 1Dermatology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 3University of Tokyo Graduate School of Medicine, Tokyo, Japan, 4Arthritis Center, Boston University, Arthritis Center, Boston, MA

    Background/Purpose:  Systemic sclerosis (SSc) is a multisystem connective tissue disease characterized by autoimmunity/inflammation, vasculopathy, and tissue fibrosis. Fli1 is a member of Ets family transcription…
  • Abstract Number: 2155 • 2016 ACR/ARHP Annual Meeting

    Crosstalk Between IL-6 and TNF-Alpha Signaling Pathway in Rheumatoid Arthritis Synovial Fibroblasts

    Alvaro Valin1, Yolanda Ruano2, Manuel J. Del Rey3, Carmen M. García-Herrero3, Eduardo Martín-Guerrero1, Beatriz Bravo4, Juan D. Cañete5, José L. Rodríguez-Peralto2 and Jose L. Pablos3,6, 1Grupo de Enfermedades Inflamatorias y Autoimmunes, Instituto de Investigación Hospital 12 de Octubre (i+12), Madrid, Spain, 2Pathology Department, Instituto de Investigación Hospital 12 de Octubre (i+12), Madrid, Spain, 3Grupo de Enfermedades Inflamatorias y Autoinmunes, Instituto de Investigación Hospital 12 de Octubre (i+12), Madrid, Spain, 4Servicio de Traumatología y Cirugía Ortopédica, Hospital 12 de Octubre, Madrid, Spain, 5Rheumatology, Hospital Clinic and IDIBAPS, Barcelona, Spain, 6Servicio de Reumatología, Hospital 12 de Octubre, Madrid, Spain

    Background/Purpose:  Although elevated IL-6 and its soluble receptor (sIL6R) have been found in the serum and synovium of arthritic patients, the molecular mechanisms by which…
  • Abstract Number: 2157 • 2016 ACR/ARHP Annual Meeting

    Share the Fate: Fibroblast-like Synoviocyte Cell-to-Cell Organelle Transfer Is Directed By the Inflammatory Microenvironment

    Ruth Byrne1, Isabel Olmos Calvo2, Thomas Karonitsch3, Felix Kartnig4, Johannes Holinka5, Günter Steiner6, Peter Ertl7, Josef Smolen8 and Hans Peter Kiener9, 1Rheumatology, Internal Medicine III, Medical University of Vienna, Vienna, Austria, 2Nanotechnology, Austrian Institute for Technology, Vienna, Austria, 3Internal Medicine III, Vienna Medical University, Vienna, Austria, 4Department of Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 5Department of Orthopaedics, Medical University of Vienna, Vienna, Austria, 6Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 7Vienna University of Technology, Vienna, Austria, 8Medical University of Vienna and Hietzing Hospital, Vienna, Austria, 9Division of Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Fibroblast-like synoviocytes (FLS) form a complex tissue network via long-distance intercellular connections with wide intercellular matrix spaces. The adaptive synovial tissue response to inflammation…
  • Abstract Number: 806 • 2016 ACR/ARHP Annual Meeting

    Single Cell Rnaseq Defines a Unique Transcriptome Profile for Myofibroblasts in the Skin of Patients with Systemic Sclerosis

    Robert A. Lafyatis1, Lisa Rice2, Giuseppina Stifano2, Jeff Browning2,3 and Robert W. Simms4, 1Division of Rheumatology and Clinical Immunology, University of Pittsburgh School of Medicine, Pittsburgh, PA, 2Boston University School of Medicine, Boston, MA, 3Boston university, Cambridge, MA, 4Rheumatology, Boston University School of Medicine, Boston, MA

    Background/Purpose: Fibrosis in systemic sclerosis (SSc), as well as a wide variety of other fibrotic diseases, is largely driven by myofibroblasts. Myofibroblasts are known to…
  • Abstract Number: 2556 • 2016 ACR/ARHP Annual Meeting

    Deficient Expression of the Novel Rheumatoid Arthritis (RA) Risk Gene, LBH, Induces S Phase Arrest in RA Fibroblast-like Synoviocytes (FLS)

    Shinji Matsuda1, Deepa Hammaker2, Steven Dowdy3, David L. Boyle4 and Gary Firestein5, 1Medicine, UC San Diego, La Jolla, CA, 2Division of Rheumatology, Allergy and Immunology, UCSD School of Medicine, La Jolla, CA, 3UC San Diego School of Medicine, La Jolla, CA, 4Division of Rheumatology, Allergy and Immunology, University of California, San Diego, La Jolla, CA, 5Medicine, UCSD, La Jolla, CA

    Background/Purpose:  LBH (Limb-bud and heart development) was recently identified as an RA risk gene that has abnormally methylated loci and a functional enhancer SNP in…
  • Abstract Number: 819 • 2016 ACR/ARHP Annual Meeting

    Impaired Adiponectin Signaling in SSc Contributes to Myofibroblast Differentiation and Organ Fibrosis

    Roberta Goncalves Marangoni1, Benjamin Korman2, Feng Fang1, Monique Hinchcliff1, Laszlo Otvos3, Philipp E. Scherer4, Warren Tourtellotte5 and John Varga6, 1Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL, 2Department of Rheumatology, Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL, 3Temple University, Philadelphia, PA, 4University of Texas Southwestern Medical Center, Dallas, TX, 5Department of Pathology, Ward, Northwestern University, Chicago, IL, 6Rheumatology and Dermatology, Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL

    Background/Purpose:  In systemic sclerosis (SSc) patients, skin fibrosis is accompanied by involution of dermal white adipose tissue (dWAT), a prominent source of adiponectin (APN). We…
  • Abstract Number: 2566 • 2016 ACR/ARHP Annual Meeting

    Hexokinase 2 As a Novel Metabolic Target for Rheumatoid Arthritis

    Marta Fernandez Bustamante1, Ricard Garcia-Carbonell2, Jeffrey Smith2, Gary Firestein1, Shigeki Miyamoto2 and Monica Guma1, 1Medicine, UCSD, La Jolla, CA, 2Pharmacology, UCSD, La Jolla, CA

    Background/Purpose: Hexokinases (HKs) catalyze the first step in glucose metabolism. HK2 constitutes the principal inducible isoform with a restricted distribution in normal adult tissues. Up-regulated…
  • Abstract Number: 1010 • 2016 ACR/ARHP Annual Meeting

    Elucidating the Activation Profile of Systemic Sclerosis Macrophages

    Michael S. Ball1, Emilie P. Shipman1, Mohamed A. Eltanbouly1, Viktor Martyanov2, Kimberly A. Archambault3, Mary A. Carns4, Esperanza Arroyo4, Kathleen Aren4, Monique Hinchcliff5, Michael L. Whitfield2,3 and Patricia A. Pioli1, 1Microbiology and Immunology, Geisel School of Medicine at Dartmouth, Hanover, NH, 2Department of Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 3Molecular and Systems Biology, Geisel School of Medicine at Dartmouth, Hanover, NH, 4Department of Medicine, Division of Rheumatology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL, 5Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL

    Background/Purpose: Genome-wide gene expression studies implicate macrophages (MØs) as mediators of fibrosis in systemic sclerosis (SSc) and our data indicate that MØs constitute the dominant…
  • Abstract Number: 2926 • 2016 ACR/ARHP Annual Meeting

    Rorc Positive Th17, Th17/Th1, and Th17.1 Cells from the Blood of Treatment NaïVe RA Patients Differ in IL-17A but Are All Pathogenic When Co-Cultured with RA Synovial Fibroblasts

    Sandra M.J. Paulissen1, Jan Piet van Hamburg2, Nadine Davelaar2, Wendy Dankers3, Patrick Asmawidjaja2, Anne-Marie Otten-Mus2 and Erik Lubberts2, 1Room Nb-84, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 2Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, University Medical Center, Rotterdam, Netherlands

    Background/Purpose: T cells play a central role in the early stages of rheumatoid arthritis (RA). In this context, we have shown increased proportions of memory…
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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].

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