ACR Meeting Abstracts

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Abstracts tagged "Animal models"

  • Abstract Number: 3018 • 2016 ACR/ARHP Annual Meeting

    The Analysis of Severity of Arthritis in the Intestinal Microbiota-Humanized Mice

    Yuichi Maeda1, Masato Matsushita2, Masashi Narazaki3, Yukihiko Saeki4,5, Atsushi Kumanogoh6 and Kiyoshi Takeda7, 1Department of Respiratory Medicine, Allergy and Rheumatic Diseases, Osaka University Graduate School of Medicine, Suita, Japan, 2Rheumatology, Osaka Minami Medical Center, Osaka, Japan, 3Osaka University Graduate School of Medicine, Suita, Japan, 4Dept of Clinical research, Osaka-Minami Medical Ctr, Osaka, Japan, 5Dept of Clinical Research, Osaka-Minami Medical Center, Kawachinagano City, Japan, 6Respiratory Medicine, Allergy and Rheumatic Diseases, Osaka University Graduate School of Medicine, Suita, Japan, 7Department of Microbiology and Immunology, Osaka University Graduate School of Medicine, Suita, Japan

    Background/Purpose: Although various genetic factors have been implicated in susceptibility to rheumatoid arthritis (RA), environmental factors including smoking, periodontal disease and hormones are also necessary…
  • Abstract Number: 1008 • 2016 ACR/ARHP Annual Meeting

    Advantageous Effect of an Endogenous Retroviral Envelope Protein in Systemic Lupus Erythematosus with Ex Vivo and In Vivo Anti-Inflammatory Potential

    Anne Troldborg1,2, Magdalena Janina Laska3, Ellen-Margrethe Hauge4,5, Shervin Bahrami6 and Kristian Stengaard-Pedersen7,8, 1clinical medicine, Aarhus University, Aarhus, Denmark, 2Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 3Biomedicine, Aarhus University, Aarhus, Denmark, 4Dept. of Anatomy, Aarhus University, Aarhus, Denmark, 5Rheumatology, Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 6Clinical Medicine, Aarhus University, Aarhus, Denmark, 7Clinical medicine, Aarhus University, Aarhus, Denmark, 8Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark

    Background/Purpose: Human Endogenous Retroviruses (HERVs) are remnants of retroviral infections in the human germline. Most, but not all, HERV genes have become inactive by accumulation…
  • Abstract Number: 1452 • 2016 ACR/ARHP Annual Meeting

      18 F-FDG PET Imaging: An In Vivo quantitative Drug Screening Tool for Novel Antiinflammatory Therapies

    Siba P. Raychaudhuri1, Smriti K. Raychaudhuri2, Anupam Mitra3 and Abhijit Chaudhari4, 1Davis, CA, 2Rheumatology/Immunology, VA Sacramento Medical Center, Davis, CA, 3Dermatology, UC Davis School of Medicine, Davis, CA, 4Radiology, UC Davis School of Medicine, Sacramento, CA

    Background/Purpose: Collagen induced arthritis (CIA) mouse model is used for screening of new drugs for autoimmune arthritis. The conventional read outs of this model are…
  • Abstract Number: 3124 • 2016 ACR/ARHP Annual Meeting

    Huntingtin Interacting Protein 1 (Hip1) Is a New Arthritis Severity Gene

    Teresina Laragione1, Percio Gulko1 and Max Brenner2, 1Medicine/Rheumatology, Icahn School of Medicine at Mount Sinai, New York, NY, 2Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose:  Cia25/Pia42 is an arthritis severity and joint damage quantitative trait locus on rat chromosome 12 previously identified in an intercross between MHC identical but…
  • Abstract Number: 1031 • 2016 ACR/ARHP Annual Meeting

    Glucocorticoid Receptor Dimerization in Stromal Cells Modulates Macrophage Polarization during Serum Transfer-Induced Arthritis

    Mascha Koenen1, Ulrike Baschant2,3, Stephan Culemann3,4, Tobias Kockmann5, Hans-Michael Kaltenbach6, Sabine Vettorazzi1,3, Paolo Nanni7, Bernd Roschitzki8, Ulrich Auf dem Keller9 and Jan P. Tuckermann1,3, 1Institute for Comparative Molecular Endocrinology, University of Ulm, Ulm, Germany, 2Dep. of Medicine III, TU Dresden, Dresden, Germany, 3Leibniz Institute on Aging, FLI Jena, Jena, Germany, 4Dep. of Internal Medicine 3, Universitätsklinikum Erlangen, Erlangen, Germany, 5Institute for Molecular Health Sciences, ETH Zürich, Zürich, Switzerland, 6Dep. of Biosystems Science and Engineering, ETH Zürich, Zürich, Germany, 7Functional Genomics Center Zurich, University and ETH Zurich, Zürich, Switzerland, 8Functional Genomics Center Zurich, University and ETH Zurich, Zurich, Switzerland, 9Institute for Molecular Health Sciences, ETH Zürich, Zürich, Germany

    Background/Purpose: Rheumatoid arthritis is commonly treated with potent anti-inflammatory glucocorticoids (GC), despite severe side effects such as osteoporosis and insulin resistance associated with chronic dosing…
  • Abstract Number: 1454 • 2016 ACR/ARHP Annual Meeting

    Combination of the SYK Inhibitor, GS-9876, with a JAK Inhibitor Increases Efficacy in a Chronic Rat Model of Collagen-Induced Arthritis

    Julie Di Paolo1, David Alonzo2, Christian Franci3, Terry Gentzler1, Li Li4, Bernard Murray5 and Jim Zheng5, 1Biology, Gilead Sciences, Foster City, CA, 2FPD, Gilead Sciences, Foster City, CA, 3Biology, Gilead Sciences, Foster, CA, 4Gilead Sciences, South San Francisco, CA, 5DMPK, Gilead Sciences, Foster City, CA

    Background/Purpose:   Here we demonstrate that 1) the single agent activity of GS-9876 is efficacious in a late stage rat model of collagen-induced arthritis (CIA);…
  • 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: 1032 • 2016 ACR/ARHP Annual Meeting

    Early In Vivo Induction of Mouse Interferon-alpha1 Overexpression Triggers an Expansion of Highly Suppressive Regulatory T Lymphocytes Protecting Against Experimental Arthritis

    Katarzyna Matyja1,2, Matthieu Ribon1,2, Roxane Hervé1,2, Delphine Lemeiter1,2, Ken Tsumiyama3, Natacha Bessis1,2, Shunichi Shiozawa3, Marie-Christophe Boissier1,2,4 and Patrice Decker1,2, 1Li2P, University of Paris 13, Sorbonne Paris Cité, Bobigny, France, 2UMR 1125, Inserm, Bobigny, France, 3Department of Medicine, Rheumatic Diseases Unit, Kyushu University Beppu Hospital, Beppu, Japan, 4Rheumatology Department, Assistance Publique – Hôpitaux de Paris (AP-HP), Avicenne Hospital, Bobigny, France

    Background/Purpose:  Type I interferons (IFN-I) can be both anti- and pro-inflammatory. Among them, IFN-α inhibits normal Th17 differentiation, whereas it is pathogenic in lupus. The…
  • Abstract Number: 1456 • 2016 ACR/ARHP Annual Meeting

    Identification of a Unique Population of B220hi B-Cells in Inflamed Lymph Nodes (Bin) As a Potential Biomarker of Arthritic Progression in the Tumor Necrosis Factor Transgenic Mouse Model of Rheumatoid Arthritis

    Megan Forney1, Richard Bell2, Edward Schwarz3 and Homaira Rahimi4, 1Orthopedics, University of Rochester, Rochester, NY, 2Pathology, University of Rochester, Rochester, NY, 3Orthopedeatrics, University of Rochester, Rochester, NY, 4Rheumatology, University of Rochester/Golisano Children's Hosp, Rochester, NY

    Background/Purpose: Using the tumor necrosis factor transgenic (TNF-Tg) mouse model of rheumatoid arthritis (RA), we have shown that during progression of knee synovitis, popliteal lymph…
  • Abstract Number: 3173 • 2016 ACR/ARHP Annual Meeting

    Pan-PPAR Agonist IVA337 Is Effective in the Prevention of Experimental Lung Fibrosis and Related Pulmonary Hypertension

    Jerome Avouac1, Irena Konstantinova2, Christophe Guignabert3, Sonia Pezet4, Anne Cauvet5, Jeremy Sadoine6, Thomas Guilbert4, Jean-Michel Luccarini7, Jean-Louis Junien7, Pierre Broqua7 and Yannick Allanore8, 1Rheumatology A department and INSERM U1016, Paris Descartes University, Cochin Hospital, Paris, France, 2Inventiva, Daix, France, 3Inserm UMR_S 999, Hôpital Marie Lannelongue, Le Plessis Robinson, France, 4Institut Cochin, INSERM U1016, Paris, France, 5INSERM U1016, Paris Descartes University, Cochin Hospital, Paris, France, 6Equipe d’Accueil (EA) 2496 Pathologie, Imagerie et Biothérapies Orofaciales, Faculty of Odontology, Paris Descartes University, Montrouge, France, 7Inventiva, DAIX, France, 8Rheumatology, Paris Descartes University, Paris, France

    Background/Purpose: Peroxisome proliferator-activated receptors (PPARs) are nuclear receptors known to modulate fibrosis. The pan-PPAR agonist IVA337 recently demonstrated efficacy in prevention and treatment of experimental…
  • Abstract Number: 1034 • 2016 ACR/ARHP Annual Meeting

    Microrna-146a Controls Local Bone Destruction By Regulating Fibroblast Induced Osteoclastogenesis in Inflammatory Arthritis

    Victoria Saferding1, Antonia Puchner2, Eliana Goncalves-Alves3, Melanie Hofmann3, Julia Brunner4, Emine Sahin4, Silvia Hayer5, Philippe Georgel6, Marije M. Koenders7, Gernot Schabbauer4, Josef S. Smolen8, Günter Steiner9, Kurt Redlich3 and Stephan Blüml10, 1Rheumatology, Medical University of Vienna, Vienna, Austria, 2Department of Rheumatology, Medical University of Vienna, Vienna, Austria, 3Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 4Vascular Biology and Thrombosis research, Medical University of Vienna, Vienna, Austria, 5Waehringer Guertel 18-20 A-A09, Medical University of Vienna, Vienna, Austria, 6Centre de Recherche en Immunologie et Hématologie, Université de Strasbourg, Strasbourg, France, 7Rheumatology Research and Advanced Therapeutics, Radboud University Nijmegen Medical Center, Nijmegen, Netherlands, 8Department of Internal Medicine 3, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 9Internal Medicine III, Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 10Internal Medicine 3; Division of Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: MicroRNA (MiR-) 146a plays an important role in the regulation of the innate immune response and has also been shown to suppress cancer development…
  • Abstract Number: 1458 • 2016 ACR/ARHP Annual Meeting

    Intraadrenal Dendritic Cells Inhibit Corticosterone Response during Collagen-Induced Arthritis – a Role for IL-1β and CXC Chemokines?

    Hubert Stangl, Christine Wolff, Martin Lesiak and Rainer Straub, Laboratory of Exp. Rheumatology and Neuroendocrino-Immunology, University Hospital Regensburg, Regensburg, Germany

    Background/Purpose: In rheumatoid arthritis (RA) and collagen-induced arthritis (CIA) the phenomenon of a relative insufficiency of adrenal glands to produce an adequate amount of anti-inflammatory…
  • Abstract Number: 3229 • 2016 ACR/ARHP Annual Meeting

    Bone Morphogenetic Protein 6 Receptor Inhibition Restores Salivary Gland Function in a Mouse Model of Primary Sjögren’s Syndrome

    Hongen Yin1, Lovika Kalra1, Arif Karim1, Zhennan Lai1, Maria Guimaro1, Lauren Aber1, Bill Swaim1, Sandra Afione1, Alexandria Voigt2, Cuong Nguyen3, Paul Yu4, Donald Bloch5 and John A. Chiorini1, 1Molecular Physiology and Therapeutics Branch, National Institute of Dental and Craniofacial Research, National Institutes of Health, Bethesda, MD, 2Department of Pathology and Infectious Diseases, University of Florida, Gainesville, FL, 3Department of Pathology and Infectious Diseases, University of Florida, Bethesda, MD, 4Cardiovascular Division, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 5Center for Immunology and Inflammatory Diseases and the Division of Rheumatology, Allergy, and Immunology of the Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA

    Background/Purpose:   Methods:   Results: Elevated BMP6 was found in 63/80 (78.8%) of pSS patients examined in this study. In humans, ALK2 and ALK3 receptors…
  • Abstract Number: 181 • 2016 ACR/ARHP Annual Meeting

    Functional and Quantitative Changes of CCR6+ type3 Innate Lymphoid Cells in Murine Collagen-Induced Arthritis

    Ayako Takaki1, Yojiro Arinobu1, Kensuke Irino1, Hirofumi Tsuzuki1, Yuri Ota1, Daisuke Oroji1, Masahiro Ayano1, Yashitaka Kimoto2, Hiroki Mitoma1, Mitsuteru Akahoshi1, Hiroaki Niro1, Hiroshi Tsukamoto1, Takahiko Horiuchi2 and Koichi Akashi1, 1Department of medicine and biosystemic science, Kyushu University Hospital, Fukuoka, Japan, 2Department of internal medicine, Kyushu University Beppu Hospital, Beppu, Japan

    Background/Purpose: Innate lymphoid cells (ILCs) are a group of lymphocytes that lack antigen-specific receptors and have important roles in mediating immune responses and in regulating…
  • Abstract Number: 1111 • 2016 ACR/ARHP Annual Meeting

    Huntingtin Interactin Protein 1 (HIP1) Regulates Receptor Tyrosine Kinases Mediated Activity and Cell Invasiness in Fibroblast-like Synoviocytes

    Teresina Laragione, Nasim Azizgolshani, Carolyn Harris, Erjing Gao and Percio Gulko, Medicine/Rheumatology, Icahn School of Medicine at Mount Sinai, New York, NY

    Background/Purpose: Huntingtin-interacting protein 1 (Hip1) is a new arthritis severity gene recently identified in the Pristane and Collagen-induced arthritis (PIA, CIA) quantitative trait locus Cia25/Pia42…
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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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