ACR Meeting Abstracts

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Abstracts tagged "Fibroblasts"

  • 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…
  • Abstract Number: 1131 • 2016 ACR/ARHP Annual Meeting

    Regulation of Rheumatoid Arthritis Synovial Fibroblast Cytokine Production By Inhibitor of DNA Binding-1 Via Crispr/Cas9 Transfection

    Ray A. Ohara1, Gautam Edhayan1, Thomas L. Saunders2, Thomas M. Lanigan3, Rachel Morgan1, W. Alexander Stinson4, Phillip L. Campbell5, Jerry Graham4, David A. Fox5 and Jeffrey H. Ruth5, 1Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 2Molecular Medicine and Genetics, University of Michigan Medical School, Ann Arbor, MI, 3Vector Core, University of Michigan Medical School, Ann Arbor, MI, 4Division of Rheumatology, University of Michigan Medical School, Ann Arbor, MI, 5Internal Medicine, Division of Rheumatology, University of Michigan Medical School, Ann Arbor, MI

    Background/Purpose: Inhibitor of DNA binding-1 (Id1) is a nuclear protein actively transcribed in endothelial progenitor cells (EPCs) and synovial fibroblasts. We previously identified Id1 as…
  • Abstract Number: 3146 • 2016 ACR/ARHP Annual Meeting

    Selective Deletion of a Pathogenic Subset Synovial Fibroblasts Attenuates Synovial Inflammation

    Adam Paul Croft, Joana Campos, Andrew Filer, Francesca Barone and Chris Buckley, Institute of Inflammation and Ageing (IIA), University of Birmingham, Birmingham, United Kingdom

    Background/Purpose:  Despite their role as key effector cells driving synovial inflammation and joint damage, fibroblast like synoviocytes (FLS) have yet to be targeted therapeutically. Fibroblast…
  • Abstract Number: 1435 • 2016 ACR/ARHP Annual Meeting

    KCa1.1 Potassium Channels Are a Novel Therapeutic Target on Fibroblast-like Synoviocytes in Rheumatoid Arthritis

    Mark Tanner1, Redwan Huq1, Rajeev Tajhya1, Michael Pennington2, Teresina Laragione3, Pércio Gulko4 and Christine Beeton5, 1Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX, 2Peptides International, Louisville, KY, 3Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, 4Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, 5Department of Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX

    Background/Purpose: Fibroblast-like synoviocytes (FLS) develop a high degree of invasiveness during rheumatoid arthritis (RA), leading to joint degradation. There are currently no therapeutics that specifically…
  • Abstract Number: 3178 • 2016 ACR/ARHP Annual Meeting

    Heart Dysfunction in Systemic Sclerosis: Involvement of a Novel Fibrogenic Stromal Cell Subset

    Mara Stellato1, Michal Rudnik1, Florian Renoux2, Elena Pachera1, Karl Sotlar3, Karin Klingel4, Joerg C. Henes5, Przemyslaw Blyszczuk6, Oliver Distler1 and Gabriela Kania1, 1Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Depertment of Rheumatology, University Hospital Zurich, Schlieren, Switzerland, 3Institute of Pathology, Ludwig Maximilians University, Munich, Germany, 4Department of Molecular Pathology, University Hospital Tuebingen, Tuebingen, Germany, 5Department of Internal Medicine II, Division of Rheumatology, University Hospital Tuebingen, Tuebingen, Germany, 6Cardioimmunology, Center of Molecular Cardiology, University of Zurich, 8952 Schlieren, Switzerland

    Background/Purpose: Cardiac dysfunction is a significant cause of the high mortality in systemic sclerosis (SSc). Heart involvement in SSc patients resembles inflammatory dilated cardiomyopathy (iDCM)…
  • Abstract Number: 1558 • 2016 ACR/ARHP Annual Meeting

    Lower Expression of a Novel Cytoplasmic Long Noncoding RNA NR_122076 Contributes to Proliferation, Migration and Invasion of Fibroblast-like Synoviocytes from Patients with Rheumatoid Arthritis

    Yaoyao Zou, Siqi Xu, Qian Qiu, Shan Zeng, Maohua Shi, Youjun Xiao, Mingcheng Huang and Hanshi Xu, Department of Rheumatology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China., Guangzhou, China

    Background/Purpose:  Emerging evidence indicates that long noncoding RNAs (lncRNAs) play critical regulatory roles in various human diseases, especially in cancers and inflammatory disorders. However, the…
  • Abstract Number: 3215 • 2016 ACR/ARHP Annual Meeting

    ASK1 Is Regulated By IL-1β and TNF and Modulates Key Rheumatoid Arthritis (RA) Fibroblast-like Synoviocyte Functions (FLS)

    Gyrid Nygaard1, Deepa Hammaker2, David L. Boyle3, Astrid Clarke4, Li Li5, Julie Dipaolo6 and Gary Firestein7, 1Medicine, UC San Diego, La Jolla, CA, 2Division of Rheumatology, Allergy and Immunology, UCSD School of Medicine, La Jolla, CA, 3Division of Rheumatology, Allergy and Immunology, University of California, San Diego, La Jolla, CA, 4GIlead, South San Francisco, CA, 5Gilead Sciences, South San Francisco, CA, 6Gilead, South San Francisco, CA, 7Medicine, UCSD, La Jolla, CA

    Background/Purpose: RA fibroblast-like synoviocytes (FLS) possess a unique aggressive phenotype characterized by increased cell growth, cytokine production and invasion. Previous unsuccessful attempts to target the…
  • Abstract Number: 1564 • 2016 ACR/ARHP Annual Meeting

    The Comprehensive Analysis for the Transcriptional Organization of Stimuli Responses in Fibroblast-like Synoviocytes from Rheumatoid Arthritis Patients

    Haruka Tsuchiya1, Shuji Sumitomo1, Kazuyoshi Ishigaki2, Akari Suzuki2, Yuta Kochi2, Mineto Ota1, Yumi Tsuchida1, Hiroshi Inui3, Shuji Taketomi3, Yuho Kadono4, Sakae Tanaka3, Keishi Fujio1 and Kazuhiko Yamamoto1,2, 1Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 2Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan, 3Department of Orthopaedic Surgery, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 4Department of Orthopaedic Surgery, Graduate School of Medicine, Saitama Medical University, Saitama, Japan

    Background/Purpose:   Fibroblast-like synoviocyte (FLS) is expected to be a novel therapeutic target for rheumatoid arthritis (RA) because of their contribution to pathogenesis. FLS expresses…
  • 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…
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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 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.).

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