ACR Meeting Abstracts

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Abstracts tagged "fibroblasts and scleroderma"

  • Abstract Number: 1705 • 2017 ACR/ARHP Annual Meeting

    Inhibition of EZH2 Stops Fibrosis and Improves Angiogenesis in Scleroderma

    Pei-Suen Tsou1, Phillip L. Campbell2, M. Asif Amin3, Patrick Coit1, David Fox4, Dinesh Khanna5 and Amr H Sawalha1, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Rheumatology, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 3Division of Rheumatology and Clinical Autoimmune Center of Excellence, University of Michigan, Ann Arbor, MI, Ann Arbor, MI, 4Department of Medicine [Division of Rheumatology], University of Michigan Medical System, Ann Arbor, MI, 5University of Michigan, Ann Arbor, MI

    Background/Purpose: Scleroderma (SSc) is a complex disease that involves activation of the immune system, vascular complications, and tissue fibrosis. Although the pathogenesis of this disease…
  • Abstract Number: 3003 • 2015 ACR/ARHP Annual Meeting

    Increased Heparanase Expression in Keratinocytes Promotes Dermal Fibrosis in Scleroderma

    In-Woon Baek1, Wan-Uk Kim2, Chul-Soo Cho1 and Ki-Jo Kim3, 1Internal Medicine, Yeouido St. Mary's Hospital, The Catholic University of Korea, Seoul, South Korea, 2Internal Medicine, Seoul St. Mary’s Hospital, The Catholic University of Korea, Seoul, South Korea, 3Internal Medicine, St. Vincent’s Hospital, The Catholic University of Korea, Suwon, South Korea

    Background/Purpose: Interactions between keratinocyte and dermal fibroblast via paracrine loop play an important role in wound repair and keloid formation. In this study, we investigated…
  • Abstract Number: 657 • 2013 ACR/ARHP Annual Meeting

    Lipoic Acid Plays a Crucial Role In Scleroderma Dermal Fibroblasts

    Pei-Suen Tsou1, Beatrix Balogh2, Adam J. Pinney2, George Zakhem2, Ann Kendzicky2, Elena Schiopu3, Dinesh Khanna4, David A. Fox5 and Alisa E. Koch5,6, 1Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 2University of Michigan Medical School, Ann Arbor, MI, 3Rheumatology/Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, 4Division of Rheumatology, University of Michigan Medical School, Ann Arbor, MI, 5Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, 6VA Medical Service, Ann Arbor, MI

    Background/Purpose: Systemic sclerosis (SSc) is a connective tissue disease characterized by vasculopathy and fibrosis of the skin and organs. Increase in oxidative stress and platelet-derived…
  • Abstract Number: 1518 • 2012 ACR/ARHP Annual Meeting

    Damage-Associated Endogenous TLR4 Ligand Fibronectin-EDA Is Overexpressed in Scleroderma and Drives Persistent Fibrosis Via TLR4 and Inhibition of TLR4 Prevents and Reverses Experimental Dermal Fibrosis: Novel Target for Scleroderma Therapy

    Swati Bhattacharyya1, Zenshiro Tamaki2, Wenxia Wang3, Paul Hoover4, Adam Booth5, Alyssa Dreffs6, Monique E. Hinchcliff7, Feng Fang8, Spiro Getsios4, Hang Yin9, Eric S. White6 and John Varga10, 1Division of Rheumatology, Northwestern University, Feinberg School of Medicine, Chicago, IL, 2Medicine, Rheumatology, Northwestern Univ Med School, Chicago, IL, Chicago, IL, 3Medicine/Rheumatology, Northwestern University, Feinberg School of Medicine, Chicago, IL, 4Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL, 5Ann Arbor, MI, 6Pulmonary and Critical Care Medicine, University of Michigan Medical School, Ann Arbor, MI, 7Division of Rheumatology, Northwestern Univ Med School, Chicago, IL, 8Rheumatology Division, Northwestern University, Chicago, IL, 9University of Colorado at Boulder, Boulder, CO, 10Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Recent studies implicate innate immune signaling and Toll like receptor-4 (TLR4) in fibrogenesis. We hypothesized that injury in scleroderma leads to tissue accumulation of…
  • Abstract Number: 1520 • 2012 ACR/ARHP Annual Meeting

    Role of 12/15-Lipoxygenase(LOX) in Patients with Systemic Sclerosis

    Hirahito Endo, Makoto Kabraki, Koutarou Shikano, Sei Muraoka, Nahoko Tanaka, Tatsuhiro Yamamoto, Kanako Kitahara, Kaichi Kaneko, Yoshie Kusunoki, Natsuko Kusunoki, Kenji Takagi, Tomoko Hasunuma and Shinichi Kawai, Division of Rheumatology, Department of Internal Medicine, School of Medicine, Faculty of Medicine, Toho University, Tokyo, Japan

    Background/Purpose: Recently 12/15-lipoxygenase (LOX) and it’s metabolites have a prominent anti-fibrotic role during dermal fibrosis in scleroderma experimental model using 12/15-LOX deficient mice were reported…
  • Abstract Number: 1498 • 2012 ACR/ARHP Annual Meeting

    Wisp-1 Neutralization Reduces Gvhd-Induced Skin Fibrosis by Altering TSLP-OX40L Axis-Dependent Th2 Responses

    Raphael Lemaire, Tim Burwell, Rachel Griffin, Julie Bakken, Joseph Madary, Lynne Murray, Ronald Herbst and Jane Connor, Research, MedImmune LLC, Gaithersburg, MD

    Background/Purpose: There is accumulating evidence for a role of Wnt-signaling pathway activation in connective tissue disorders, including dermal and lung fibrosis. In particular, expression of…
  • Abstract Number: 1503 • 2012 ACR/ARHP Annual Meeting

    Effect of Thiol Antioxidants On the Profibrotic Phenotype of Scleroderma Dermal Fibroblasts

    Pei-Suen Tsou1, Beatrix Balogh2, Adam J. Pinney2, Elena Schiopu3, Dinesh Khanna4 and Alisa E. Koch5, 1Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 2University of Michigan Medical School, Ann Arbor, MI, 3Rheumatology/Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, 4Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 5Internal Medicine - Rheumatology, University of Michigan Medical School, Ann Arbor, MI

    Background/Purpose: Systemic sclerosis (Scleroderma, SSc) is a connective tissue disease characterized by vasculopathy and fibrosis of the skin and organs. Increase in superoxide production and…
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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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