ACR Meeting Abstracts

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Abstracts tagged "Animal models"

  • Abstract Number: 408 • 2017 ACR/ARHP Annual Meeting

    CR6086 Is Highly Effective and Improves Methotrexate Effect in a Mouse Model of Rheumatoid Arthritis

    Gianfranco Caselli1, Flora Ferrari1, Eleonora Comi1, Marco Perrella1, Camilla Recordati2, Adriana Grotti1, Rosanna Cavagnoli1, Marco Lanza1 and Lucio C. Rovati3, 1Rottapharm Biotech, Monza, Italy, 2Mouse & Animal Pathology Lab,, Fondazione Filarete, Milano, Italy, Milano, Italy, 3Clinical Research Department, Rottapharm Biotech, Monza, Italy

    Background/Purpose: CR6086, a selective EP4 antagonist, dose-dependently improves disease features in rheumatoid arthritis (RA) models in rodents. Indeed, recent studies highlight the role of the…
  • Abstract Number: 1337 • 2017 ACR/ARHP Annual Meeting

    ASN002, a Novel Dual SYK/JAK Inhibitor, Demonstrates Strong Efficacy in a Rat Model of Collagen-Induced Arthritis

    David Zammit1, Sanjeeva Reddy1, Roger Smith1, Nitin Damle2 and Sandeep Gupta1, 1Asana BioSciences LLC, Lawrenceville, NJ, 2Preclinical R&D, Sun Pharma Advanced Research Co. Ltd, Mumbai, India

    Background/Purpose: Spleen tyrosine kinase (SYK) and Janus kinase (JAK) mediate signaling in immune cells and hematopoietic cells important for the initiation and progression of rheumatoid…
  • Abstract Number: 2563 • 2017 ACR/ARHP Annual Meeting

    SH3BP2 Gain-of-Function Mutation Ameliorates Lupus in B6.MRL-Faslpr Mice

    Akiko Nagasu1, Tomoyuki Mukai1, Masanori Iseki2, Hajime Nagasu3, Shunichi Fujita1, Takafumi Mito1, Shoko Kodama1, Yumi Sasae4, Naoki Kashihara3, Katsuhiko Ishihara2, Yasuyoshi Ueki5 and Yoshitaka Morita1, 1Department of Rheumatology, Kawasaki Medical School, Kurashiki, Okayama, Japan, 2Department of Immunology and Molecular Genetics, Kawasaki Medical School, Kurashiki, Okayama, Japan, 3Department of Nephrology and Hypertension, Kawasaki Medical School, Kurashiki, Okayama, Japan, 4Department of Rheumatology, Kawasaki Medical School, Kurashiki Okayama, Japan, 5Department of Oral and Craniofacial Sciences, School of Dentistry, University of Missouri-Kansas City, Missouri-Kansas City, MO

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by the production of autoantibodies, leading to multiple organ dysfunction. SH3BP2 (Src homology domain 3…
  • Abstract Number: 503 • 2017 ACR/ARHP Annual Meeting

    BMS-986195 Is a Highly Selective and Rapidly Acting Covalent Inhibitor of Bruton’s Tyrosine Kinase with Robust Efficacy at Low Doses in Preclinical Models of RA and Lupus Nephritis

    JR Burke, KM Gillooly, MA Pattoli, L Cheng, S Skala, EM Heimrich, TL Taylor, C Pulicicchio, DW Kukral, T Petrone, IM Catlett, N Zheng, W Li, SH Watterson and JA Tino, Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: BMS-986195 is a potent, covalent, irreversible inhibitor of Bruton’s tyrosine kinase (BTK), a member of the Tec family of non-receptor tyrosine kinases essential in…
  • Abstract Number: 1339 • 2017 ACR/ARHP Annual Meeting

    Role of Hexokinase-2 in Synovial Lining Hypertrophy in Murine Arthritis

    Marta Fernandez Bustmanate1, Jeffrey Smith2, Adam Paul Croft3, Gary S. Firestein4, Chris Buckley5, Shigeki Miyamoto2 and Monica Guma6, 1Medicine, UCSD, San Diego, CA, 2Pharmacology, UCSD, La Jolla, CA, 3Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom, 4Medicine, University of California San Diego, La Jolla, CA, 5University of Birmingham, Birmingham, United Kingdom, 6Medicine, UCSD, La Jolla, CA

    Background/Purpose: Recent studies indicate that fibroblast-like synoviocyte (FLS) glucose metabolism is altered in rheumatoid arthritis (RA). Hexokinases (HKs) catalyze the first step in glucose metabolism.…
  • Abstract Number: 2574 • 2017 ACR/ARHP Annual Meeting

    Interleukin-33 Ameliorates Murine Lupus Via Induction of Regulatory T Cells and M2 Macrophage Polarisation

    Mo Yin Mok1, Ka Sin Law2, Wing Yin Kong1, Ge Liu1, Wallace Lau2, C Luo2, FP Huang3, GC Chan4 and Kwok Wah Chan3, 1Department of Biomedical Sciences, City University of Hong Kong, Hong Kong, Hong Kong, 2Department of Medicine, Queen Mary Hospital, Hong Kong, Hong Kong, 3Department of Pathology, University of Hong Kong, Hong Kong, Hong Kong, 4Department of Paediatrics, University of Hong Kong, Hong Kong, Hong Kong

    Background/Purpose: The levels of IL-33, a Th2 promoting cytokine, and the soluble form of its receptor ST2 were reported to be elevated in serum of…
  • Abstract Number: 11L • 2016 ACR/ARHP Annual Meeting

    BMS-986165 Is a Highly Potent and Selective Allosteric Inhibitor of Tyk2, Blocks IL-12, IL-23 and Type I Interferon Signaling and Provides for Robust Efficacy in Preclinical Models of Systemic Lupus Erythematosus and Inflammatory Bowel Disease

    Kathleen Gillooly1, Yifan Zhang1, Xiaoxia Yang1, Adriana Zupa-Fernandez1, Lihong Cheng1, Joann Strnad1, Mark Cunningham2, Elizabeth Heimrich1, Xiadi Zhou1, Jing Chen3, Charu Chaudhry3, Sha Li3, Kim McIntyre1, Julie Carman4, Ryan Moslin5, Stephen Wrobleski5, David Weinstein5 and James Burke1, 1Immunosciences Discovery Biology, Bristol-Myers Squibb, Princeton, NJ, 2Bristol-Myers Squibb, Princeton, NJ, 3Leads Discovery & Optimization, Bristol-Myers Squibb, Princeton, NJ, 4Discovery Translational Sciences Group, Bristol-Myers Squibb, Princeton, NJ, 5Immunosciences Discovery Chemistry, Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: Tyk2 mediates signaling downstream of the receptors for IL-12, IL-23 and Type I interferons, all key drivers of autoimmune disorders such as SLE. BMS-986165,…
  • Abstract Number: 374 • 2016 ACR/ARHP Annual Meeting

    Anxiolytic Effects of the Novel α2δ Ligand Mirogabalin (DS-5565) in Sluka Model, an Experimental Animal Model of Fibromyalgia

    Yuki Domon1, Naohisa Arakawa1, Hiroyasu Murasawa2, Hiroyuki Kobayashi2, Kensuke Saeki2 and Yutaka Kitano1, 1Pain & Neuroscience Laboratories, Daiichi Sankyo Co., Ltd., Tokyo, Japan, 2Nihon Bioresearch Inc., Hashima, Japan

    Anxiolytic Effects of the Novel Alpha-2-Delta Ligand Mirogabalin (DS-5565) in Sluka Model, an Experimental Animal Model of Fibromyalgia Yuki Domona, Naohisa Arakawaa, Hiroyasu Murasawab, Hiroyuki…
  • Abstract Number: 1122 • 2016 ACR/ARHP Annual Meeting

    Infliximab Suppresses the Monocyte Chemotaxis in Human TNF-Transgenic Mice

    Qi Quan Huang1, Robert Birkett1, Elyssa L Roberts2 and Richard M. Pope3, 1Medicine/Rheumatology, Northwestern University Feinberg school of Medicine, Chicago, IL, 2northwestern University, Chicago, IL, 3Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: Macrophages in rheumatoid arthritis (RA) synovium produce high levels of inflammatory cytokines/chemokines and play the pivotal role in promoting inflammation and joint destruction. Treatment…
  • Abstract Number: 1851 • 2016 ACR/ARHP Annual Meeting

    The Effect of Narrow Band Ultraviolet A1 Light on Bleomycin-Induced Mouse Model of Scleroderma

    Diana Karpec1,2, Romualdas Rudys2, Laima Leonaviciene2, Zygmunt Mackiewicz2, Ruta Bradunaite2, Gailute Kirdaite2, Rita Rugiene2 and Algirdas Venalis2,3, 1Clinics of Rheumatology, Traumatology-Orthopedics and Reconstructive Surgery, Vilnius University Hospital Santariskiu Klinikos, Vilnius, Lithuania, 2State Research Institute Centre for Innovative Medicine, Vilnius, Lithuania, 3Vilnius University Hospital Santariskiu Klinikos, Vilnius, Lithuania

    Background/Purpose: Ultraviolet A1 (UVA1) phototherapy implications for systemic sclerosis still remain the area of research. The aim of the study was to evaluate narrow band…
  • Abstract Number: 457 • 2016 ACR/ARHP Annual Meeting

    Novel Mechanism Mediated By the IL-23/Th17 Axis Contributing to Auto-Immune Arthritis

    René Pfeifle1, Tobias Rothe1, Natacha Ipseiz1, Stephan Culemann1, Ulrike Harre2, Gerhard Krönke3 and Georg Schett4, 1Department of Internal Medicine 3 and Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany, 2Department of Internal Medicine 3 and Institute for Clinical Immunology, Friedrich-Alexander-University Erlangen-Nuremberg (FAU), Erlangen, Germany, 3Universitätsklinikum Erlangen, Erlangen, Austria, 4Department of Internal Medicine III, Institute for Clinical Immunology,, Friedrich-Alexander-University Erlangen-Nuremberg (FAU), Erlangen, Germany

    Background/Purpose: Checkpoints and mechanisms regulating the onset of rheumatoid arthritis (RA) remain largely elusive. Apart from B cells and auto-antibodies, Th17 cells were shown to…
  • Abstract Number: 1126 • 2016 ACR/ARHP Annual Meeting

    Interleukin-1 Is Not Involved in Synovial Inflammation and Cartilage Destruction in Collagenase-Induced Osteoarthritis

    Stephanie van Dalen1, Arjen Blom1, Annet Sloetjes1, Monique M. Helsen1, Johannes Roth2, Thomas Vogl2, Wim B. van den Berg1, Martijn van den Bosch1 and Peter L. E. M. van Lent1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2Institute of Immunology, University of Münster, Münster, Germany

    Background/Purpose: Osteoarthritis (OA) is characterized by severe cartilage destruction, with a putative role for synovial macrophages. Up to 50% of the patients also show low…
  • Abstract Number: 1859 • 2016 ACR/ARHP Annual Meeting

    Fucosyltransferase-1 Mediated Fucosylation of TGF-βR1 Is Critical to TGF-β Signaling in Scleroderma and in Bleomycin-Induced Fibrosis

    W. Alexander Stinson1, Pei-Suen Tsou1,2, Yuxuan Du3, Huadong Cui1, Ellen Cealey3, Nicholas Lepore4, Ray A. Ohara1, Gautam Edhayan1, Sarah Arwani1, Rachel Morgan1, Dinesh Khanna1,2, David A. Fox1 and M. Asif Amin5, 1Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 2University of Michigan Scleroderma Program, Ann Arbor, MI, 3Rheumatology, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 4University of Michigan, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI, 5Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose:  Systemic sclerosis (SSc) is a connective tissue disease characterized by systemic fibrosis. The dysregulation of transforming growth factor-β (TGF-β) signaling causes proliferation of myofibroblasts…
  • Abstract Number: 458 • 2016 ACR/ARHP Annual Meeting

    The TAM Receptors Axl and Mer Play a Protective Role in a Temporal and Spatial Manner in Inflammatory Arthritis

    Claire E.J. Waterborg1, Paqui G. Través2, Silke Beermann1, Marije I. Koenders1, Greg Lemke2 and Fons A.J. van de Loo1, 1Experimental Rheumatology, Radboudumc, Nijmegen, Netherlands, 2Molecular Neurobiology Laboratory, The Salk Institute for Biological Studies, La Jolla, CA

    Background/Purpose:  Rheumatoid arthritis (RA) is a chronic autoimmune disease characterized by an unrestrained inflammatory response in selective, anatomically distinct synovial joints. The innate immune system…
  • Abstract Number: 1128 • 2016 ACR/ARHP Annual Meeting

    Anti-Fractalkine Monoclonal Antibody Inhibits Cartilage Destruction and Bone Erosion in Collagen-Induced Arthritis Model

    Kana Hoshino1, Masayoshi Ohkuro2, Wataru Ikeda1, Tomoya Nakatani1, Yoshikazu Kuboi3, Naoto Ishii1, Toshihiko Yamauchi1, Nobuyuki Yasuda1 and Toshio Imai1, 1KAN Research Institute Inc., Chuo-ku, Kobe-shi, Japan, 2Research Project Promotion Group, EA Pharma Co., Ltd., Kawasaki-ku, Kawasaki-shi, Japan, 3Medicine Creation. Neuro Business Group, Eisai Co., Ltd., Tsukuba-shi, Japan

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic disease leading to joint destruction. In the previous Phase 1/2 clinical study, E6011, a novel humanized anti-fractalkine (FKN)…
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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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