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Abstracts tagged "Animal models"

  • Abstract Number: 2080 • 2012 ACR/ARHP Annual Meeting

    IL-20 Is Not Involved in Mouse Collagen Induced Arthritis

    Christina Andersson1, Kyle Serikawa2, Hermann Pelzer3, Peter Thygesen3, Patricia Smith2, Kim Kruse2, Shameek Biswas2, Brian Fox2, Anders Milner4, Peter Kvist5, Josephine Hebsgaard6, Jesper Pass7 and John Rømer8, 1AID Models, Immunopharmacology, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark, 2Molecular Immunology, Biopharmaceutical Research Unit, Novo Nordisk A/S, Seattle, WA, 3Exploratory ADME, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark, 4DMPK, Cell and Antibody Analysis, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark, 5Histology, Novo Nordisk A/S, Måløv, Denmark, 6Histology, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark, 7Antibody Thechnology, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark, 8Inflammation Science, Biopharmaceutical Research Unit, Novo Nordisk A/S, Måløv, Denmark

    Background/Purpose: Interleukin-20 (IL-20) is a pro-inflammatory cytokine involved in the pathogenesis of rheumatoid arthritis (RA). Clinical phase 2a testing has shown that treatment with an…
  • Abstract Number: 1059 • 2012 ACR/ARHP Annual Meeting

    Endogenous Complement Factor H Plays an Important Role in Controlling Immune Complex-Induced Inflammatory Arthritis

    Nirmal K. Banda1, Gaurav Mehta2, Viviana P. Ferreira3, Claudio Cortes3, Michael K. Pangburn4, William P. Arend2 and V. Michael Holers2, 1University of Colorado School of Medicine, Aurora, CO, 2Division of Rheumatology, University of Colorado School of Medicine, Aurora, CO, 3Department of Medical Microbiology and Immunology, University of Toledo Health Science Campus, Toledo, OH, 4Department of Biochemistry, University of Texas Health Sciences Center, Tyler, TX

    Background/Purpose: The complement system, a major component of innate immunity, likely plays an important role in the pathogenesis of rheumatoid arthritis (RA).  Factor H (fH)…
  • Abstract Number: 335 • 2012 ACR/ARHP Annual Meeting

    Treatment with Bgp-15, a Novel Insulin Sensitizer Attenuates Collagen-Induced Arthritis in DBA/1 Mice

    Peter Mandl1, Silvia Hayer2, Stephan Blüml3, Victoria Saferding1, Despoina Sykoutri1, Kurt Redlich2 and Josef S. Smolen4, 1Rheumatology, Medical University of Vienna, Vienna, Austria, 2Department of Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 3Department of Rheumatology, Medical University of Vienna, Vienna, Austria, 4Department of Rheumatology, Medical University of Vienna and Hietzing Hospital, Vienna, Austria

    Background/Purpose: BGP-15, a small synthetic hydroxylamine derivative is a member of a new class of insulin-sensitizing medications also known as chaperone-inducers. Beside its beneficial effects…
  • Abstract Number: 2308 • 2012 ACR/ARHP Annual Meeting

    CD11c+ Cells Are Necessary for Myofibroblast Maintenance in Bleomycin-Induced Cutaneous Fibrosis

    Jennifer J. Chia1, Sha Tian2 and Theresa T. Lu2, 1Weill Cornell/Rockefeller/Sloan-Kettering Tri-Institutional MD-PhD Program, New York, NY, 2Research Division, Hospital for Special Surgery, New York, NY

    Background/Purpose: Systemic sclerosis (SSc) is a heterogeneous connective tissue disease that has significant mortality and morbidity secondary to internal and cutaneous fibrosis. Though the exact…
  • Abstract Number: 1810 • 2012 ACR/ARHP Annual Meeting

    Identification and Characterization of Synthetic Small Molecule Macrocycle Antagonists of Human IL17A

    David Livingston, Sethu Alexander, Julian Bond, Timothy Briggs, Andrew Fraley, Stephen Hale, Tanya Landsman, Richard Martinelli, Kelley Shortsleeves, Nick Terrett and Nathan Walsh, Ensemble Therapeutics, Cambridge, MA

    Background/Purpose: :  IL17A has been demonstrated to be a key pro-inflammatory cytokine in human rheumatoid arthritis and in several rodent models of arthritis.  Synthetic macrocycles…
  • Abstract Number: 1061 • 2012 ACR/ARHP Annual Meeting

    Generation of Myeloid-Derived Suppressor Cells in Vitro From Murine Bone Marrow Precursors

    Julia Kurko1, Beata Tryniszewska1, Tibor A. Rauch1, Colt Egelston2, Tibor T. Glant1 and Katalin Mikecz1, 1Orthopedic Surgery, Rush University Medical Center, Chicago, IL, 2Immunology, Rush University Medical Center, Chicago, IL

    Background/Purpose: Myeloid-derived suppressor cells (MDSCs) are innate immune cells that expand under pathological conditions (such as cancer and autoimmune diseases) in response to local growth…
  • Abstract Number: 340 • 2012 ACR/ARHP Annual Meeting

    Myeloid Deletion of SIRT1 Aggravates Inflammatory Arthritis Via Nuclear Factor-Kappab Activation in Animal Model of Rheumatoid Arthritis

    Sang-il Lee and Yun-Hong Cheon, Division of Rheumatology, Department of Internal Medicine, Gyeongsang National University School of Medicine, Jinju, South Korea

    Background/Purpose: The nuclear factor-kappaB (NF-kB) activation plays a pivotal role and macrophages are of central importance in the pathogenesis of rheumatoid arthritis (RA). The SirT1,…
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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.).

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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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