ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings

Abstracts tagged "Animal models"

  • Abstract Number: 1639 • 2012 ACR/ARHP Annual Meeting

    FLIP in Macrophages Promotes the Progression of Serum Transfer-Induced Arthritis

    Qi Quan Huang1, Robert Birkett2, Renee E. Koessler1, G. Kenneth Haines III3, Harris R. Perlman4 and Richard M. Pope5, 1Medicine/Rheumatology, Northwestern University, Chicago, IL, 2Division of Rheumatology, Department od Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Department of Pathology, Yale University, New Haven, CT, 4Feinberg School of Medicine, Northwestern University, Chicago, IL, 5Rheumatology, Northwestern University Feinberg school of Medicine, Chicago, IL

    Background/Purpose: Flip is well known as an anti-apoptotic protein induced by chronic inflammation that protects against death receptor-mediated apoptosis. Employing a FLIP myeloid lineage knock-out…
  • Abstract Number: 856 • 2012 ACR/ARHP Annual Meeting

    Am80, a Retinoic Acid Receptor Agonist, Ameliorates Murine Vasculitisthrough the Suppression of Neutrophil Migration and Activation

    Chie Miyabe1, Yoshishige Miyabe1, Noriko Miura2, Kei Takahashi3, Yuya Terashima4, Etsuko Toda4, Fumiko Honda5, Tomohiro Morio5, Naohito Ohno2, Jun-ichi Suzuki6, Mitsuaki Isobe7, Kouji Matsushima4, Ryoji Tsuboi8, Nobuyuki Miyasaka1 and Toshihiro Nanki9, 1Department of Medicine and Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan, 2Laboratory for Immunopharmacology of Microbial Products, School of Pharmacy, Tokyo University of Pharmacy and Life Science, Tokyo, Japan, 3Department of Pathology, Toho University Ohashi Medical Center, Tokyo, Japan, 4Department of Molecular Preventive Medicine, The University of Tokyo, Tokyo, Japan, 5Department of Pediatrics and Developmental Biology, Tokyo Medical and Dental University, Tokyo, Japan, 6Department of Advanced Clinical Science and Therapeutics, The University of Tokyo, Tokyo, Japan, 7Department of Cardiovascular Medicine, Tokyo Medical and Dental University, Tokyo, Japan, 8Department of Dermatology, Tokyo Medical University, Tokyo, Japan, 9Department of Rheumatology, Tokyo Medical and Dental University, Tokyo, Japan

    Background/Purpose: Vasculitis is characterized by leukocyte infiltration in the vessel walls with destructive damage to mural structures. Retinoids are compounds that bind to retinoic acid…
  • Abstract Number: 311 • 2012 ACR/ARHP Annual Meeting

    The DEK Autoantigen Regulates Formation of Neutrophil Extracellular Traps and Zymosan Induced Arthritis in Mice

    Nirit Mor-Vaknin1, Anjan K. Saha2, Maureen Legendre1, Marta J. Gonzalez-Hernandez3, M. Asif Amin4, Bradley J. Rabquer5, Julie M. Jorns6, Mariana J. Kaplan7, Barbara S. Adams8, David A. Fox9, Alisa E. Koch10 and David Markovitz1, 1Internal Medicine, University of Michigan, Ann Arbor, MI, 2Medical School, University of Michigan, Ann Arbor, MI, 3Graduate Program in Immunology, University of Michigan, Ann Arbor, MI, 4Department of Medicine, University of Michigan Medical School, Ann Arbor, MI, 5University of Michigan Medical School, Ann Arbor, MI, 6Pathology, Ann Arbor, MI, 7Systemic Autoimmunity Branch, National Institutes of Health/NIAMS, Bethesda, MD, 8University of Michigan, Ann Arbor, MI, 9Rheumatology/Int Medicine, Univ of Michigan Med Ctr, Ann Arbor, MI, 10Internal Medicine - Rheumatology, University of Michigan Medical School, Ann Arbor, MI

    Background/Purpose: The nuclear oncoprotein DEK is a known autoantigen associated with juvenile idiopathic arthritis (JIA) and other autoimmune diseases. DEK is actively secreted by human…
  • Abstract Number: 2290 • 2012 ACR/ARHP Annual Meeting

    Type I Interferon Associated Gene IRF7 in the Pathogenesis of Fibrosis in Systemic Sclerosis (SSc)

    Minghua Wu1, Michael R. Blackburn2, Shervin Assassi1, Xiaochun Liu1, John D. Reveille1, Filemon K. Tan1, Sandeep K. Agarwal3 and Maureen D. Mayes1, 1Rheumatology, University of Texas Health Science Center at Houston, Houston, TX, 2Biochemistry and Molecular Biology, The University of Texas Medical School at Houston, Houston, TX, 3Medicine, Section of Immunology, Allergy and Rheumatology, Baylor College of Medicine, Houston, TX

    Background/Purpose: Fibrosis in Systemic Sclerosis is characterized by excessive collagen production and accumulation in the skin and lungs. It has been increasingly appreciated that a…
  • Abstract Number: 1634 • 2012 ACR/ARHP Annual Meeting

    Delivering Mesenchymal Stem Cells to Arthritic Joints with Nano-Fiber Scaffold Resulted in Inhibition of Arthritis and Joint Damage in Arthritis Models

    Xiangmei Zhang1, Kunihiro Yamaoka1, Koshiro Sonomoto1, Masahiro Kondo1, Shunsuke Fukuyo1, Makoto Satake2, Hiroaki Kaneko2, Kazuhisa Nakano1, Shingo Nakayamada3, Yosuke Okada1 and Yoshiya Tanaka1, 1The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2The Third Laboratory, Integrative Technology Research Institute, Teijin Limited, Tokyo, Japan, 3First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan

    Background/Purpose:   Even though treatment of rheumatoid arthritis (RA) has emerged, aiming bone repair is still a challenge. Mesenchymal stem cells (MSCs) possess immunoregulatory function with…
  • Abstract Number: 785 • 2012 ACR/ARHP Annual Meeting

    Resident Lung Fibroblast Gene Expression Signatures Predict Susceptibility or Resistance to Experimental Lung Fibrosis

    Emma Derrett-Smith1, Rachel Hoyles1, Korsa Khan2, David J. Abraham3 and Christopher P. Denton2, 1Centre for Rheumatology and Connective Tissue Diseases,, UCL Medical School, London, United Kingdom, 2Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 3UCL Medical School, London, United Kingdom

    Background/Purpose:    In scleroderma (SSc), lung fibrosis is linked to epithelial damage and dysregulated repair mechanisms. Resident lung fibroblasts may affect multiple cell types including…
  • Abstract Number: 326 • 2012 ACR/ARHP Annual Meeting

    Silencing Intraarticular Snail Expression Ameliorates Rat Collagen-Induced Arthritis Through Induction of Mesenchymal-Epithelial Transition in Synovial Fibroblasts

    Chrong-Reen Wang1, Shih-Yao Chen2, Ai-Li Shiau3, Yuan-Tsung Li4, Ming-Fei Liu5 and Chao-Liang Wu2, 1Section of Rheumatology and Immunology, Department of Internal Medicine, College of Medicine, National Cheng Kung University, Tainan, Taiwan, 2Biochemistry and Molecular Biology, National Cheng Kung University Medical College, Tainan, Taiwan, 3Microbiology and Immunology, National Cheng Kung University Medical College, Tainan, Taiwan, 4Biochemistry and Molecular Biology, College of Medicine, National Cheng Kung University, Tainan, Taiwan, 5Internal Medicine, National Cheng Kung University Medical College, Tainan, Taiwan

    Background/Purpose: Morphological characteristics of rheumatoid arthritis (RA) synovial fibroblasts (SF) are similar to transformed cells. We hypothesized that epithelial-mesenchymal transition (EMT) of SF regulated by…
  • « Previous Page
  • 1
  • …
  • 23
  • 24
  • 25
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology