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Abstracts tagged "Mouse model"

  • Abstract Number: 918 • 2013 ACR/ARHP Annual Meeting

    Regulatory B Cells Suppress Skin Inflammation in a Murine Model of Psoriasis

    Koichi Yanaba1 and Shinichi Sato2, 1Dermatology, The University of Tokyo, Tokyo, Japan, 2Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan

    Background/Purpose: Psoriasis is a cutaneous disorder characterized by widespread erythematous plaques with adherent scales. Recent studies have revealed that both T helper (Th) 17 and…
  • Abstract Number: 771 • 2013 ACR/ARHP Annual Meeting

    The S100A9 Inhibitor Paquinimod (ABR-215757) Reduces Synovial Activation, Osteophyte Formation and Cartilage Damage In Experimental Osteoarthritis

    Rik Schelbergen1, Arjen B. Blom1, Tomas Leanderson2, Helena Eriksson3, Wim B. van den Berg4 and Peter L.E.M. van Lent1, 1Rheumatology Research & Advanced Therapeutics, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands, 2Immunology Group, Lund University, Lund, Sweden, 3BioScience, Active Biotech AB, Lund, Sweden, 4Rheumatology Research and Advanced Therapeutics, Department of Rheumatology, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

    Background/Purpose: Synovial activation is present in a large subset of osteoarthritis (OA) patients and it is thought to play an important role in the development…
  • Abstract Number: 46 • 2013 ACR/ARHP Annual Meeting

    Alarmins S100A8/A9 Regulate Osteophyte Formation In Experimental Osteoarthritis With High Synovial Activation

    Rik Schelbergen1, Arjen B. Blom1, Wouter de Munter1, Annet W. Sloetjes2, Thomas Vogl3, Johannes Roth4, Wim B. van den Berg5 and Peter L.E.M. van Lent1, 1Rheumatology Research & Advanced Therapeutics, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands, 2Experimental Rheumatology (272), Radboud university medical center, Nijmegen, Netherlands, 3Institute of Immunology, University of Muenster, Muenster, Germany, 4Immunology, Institute of Immunology University of Muenster, Muenster, Germany, 5Rheumatology Research and Advanced Therapeutics, Department of Rheumatology, Radboud University Nijmegen Medical Centre, Nijmegen, Netherlands

    Background/Purpose: Osteophytes are cartilage capped, bony outgrowths that limit joint movement and originate from the periosteum or from ligaments during osteoarthritis (OA). There is increasing…
  • Abstract Number: 48 • 2013 ACR/ARHP Annual Meeting

    The In Vivo Role Of Bone Specific EphB4 Receptor Overexpression In Osteoarthritic Synovial Membrane

    Gladys Valverde-Franco1, David Hum1, Bertrand Lussier2, Koichi Matsuo3, Jean-Pierre Pelletier1, Mohit Kapoor1 and Johanne Martel-Pelletier1, 1Osteoarthritis Research Unit, University of Montreal Hospital Research Centre (CRCHUM), Montreal, QC, Canada, 2Department of Clinical Sciences, Faculty of Veterinary Medicine, University of Montreal, Saint-Hyacinthe, QC, Canada, 3Laboratory of Cell and Tissue Biology, School of Medicine, Keio University, Tokyo, Japan

    Background/Purpose: Osteoarthritis (OA) is characterized by progressive destruction of all joint tissues including inflammation of the synovial membrane. The histological changes that occur in OA…
  • Abstract Number: 2859 • 2013 ACR/ARHP Annual Meeting

    Pain Pathway Activation In Dorsal Root Ganglia and Dorsal Horn In a Murine Surgical Model Of Osteoarthritis

    Rachel E. Miller1, Phuong Tran2, Richard J. Miller3 and Anne-Marie Malfait4, 1Rheumatology/Biochemistry, Rush University Medical Center, Chicago, IL, 2Rheumatology, Rush University Medical Center, Chicago, IL, 3Molecular Biochemistry and Pharmacology, Northwestern University, Chicago, IL, 4Internal Medicine/Biochemistry, Rush University Medical Center, Chicago, IL

    Background/Purpose: Using a surgical mouse model of osteoarthritis (OA), destabilization of the medial meniscus (DMM), we monitor pain and associated pathways over a period of…
  • Abstract Number: 2733 • 2013 ACR/ARHP Annual Meeting

    Spontaneous Osteoarthritis In Mice By Genetic Deletion Of Nfatc1 and Nfatc2

    Susan Y. Ritter1, Matthew B. Greenblatt2, Kelly Tsang1, Dorothy Z. Hu3, John Wright4 and Antonios O. Aliprantis1, 1Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Pathology, Brigham and Women's Hospital, Boston, MA, 3Endocrine Unit, Massachusetts General Hospital, Boston, MA, 4Orthopedic Surgery, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Osteoarthritis (OA) was once viewed as a mechanical disease of “wear and tear”, but recent advances suggest that OA results from active dysregulation of…
  • Abstract Number: 2706 • 2013 ACR/ARHP Annual Meeting

    Fli1 Haploinsufficiency Exacerbates Dermal Fibrosis Via Activation Of Fibroblasts, Endothelial Cells and Macrophages In Bleomycin-Treated Mice

    Takashi Taniguchi1, Yoshihide Asano1, Kaname Akamata1, Shinji Noda1, Takehiro Takahashi1, Yohei Ichimura1, Tetsuo Toyama1, Maria Trojanowska2 and Shinichi Sato1, 1Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2Arthritis Center, Boston University, Boston, MA

    Background/Purpose: Systemic sclerosis (SSc) is a multisystem autoimmune disorder with clinical manifestations resulting from immune activation, vascular injuries and fibrosis development. Previous reports suggest that…
  • Abstract Number: 2316 • 2013 ACR/ARHP Annual Meeting

    Anti-Human TNF-Alpha Domain Antibody Construct, CEP-37247/Placulumab, Is As Efficacious As Other Leading TNF-Alpha-Blockade Therapies in a Humanized Mouse Model of Rheumatoid Arthritis

    Matthew M. Seavey1, Linglong Zou2, Adam Clarke3, Anthony G. Doyle3, Roberta Weiss4, Aric Orbach5, Brad McIntyre6 and Merav Bassan7, 1Nonclinical Development, Pharmacology, Teva Pharmaceuticals, Inc., West Chester, PA, 2GB&T, Teva Biopharmaceuticals, Rockville, MD, 3Discovery Biologics, Teva Pharmaceuticals, Inc., Sydney, Australia, 4Clinical Development, Teva Pharmaceuticals, Inc., Frazer, PA, 5Nonclinical Development, Pharmacology, Teva Pharmaceuticals, Inc., Netanya, Israel, 6Formulation, Teva Pharmaceuticals, Inc., West Cheater, PA, 7Teva R&D - Innovative Project Leadership, Teva Pharmaceuticals, Inc., Netanya, Israel

    Background/Purpose: The cytokine tumor necrosis factor (TNF)alpha is a potent pro-inflammatory mediator involved in several autoimmune diseases including rheumatic arthritis and for over a decade…
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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].

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