ACR Meeting Abstracts

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Abstracts tagged "Arthritis"

  • Abstract Number: 58 • 2017 Pediatric Rheumatology Symposium

    Analysis and Implications of Non-Invasive Knee Acoustical Emissions in Juvenile Idiopathic Arthritis

    Daniel Whittingslow1,2, Beren Semiz3, Lori Ponders4, Andrew Wiens5, Omer Inan3,6 and Sampath Prahalad7, 1Emory University School of Medicine, Atlanta, GA, 2Department of Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, 3Electrical and Computer Engineering, Georgia Institute of Technology, Atlanta, GA, 4Emory University, Atlanta, GA, 5Computer Science, Cornell University, Ithaca, NY, 6Biomedical Engineering, Georgia Institute of Technology, Atlanta, GA, 7Pediatrics, Emory Children's Center, Atlanta, GA

    Background/Purpose: Juvenile Idiopathic Arthritis (JIA), the most common chronic rheumatic disease occurring in childhood, is an important cause of disability.  Despite the persistence of disease…
  • Abstract Number: 1440 • 2016 ACR/ARHP Annual Meeting

    Anti-TNF Vaccination Protects from Experimental Arthritis without Affecting Resistance to Mycobacterium Tuberculosis or Listeria Monocytogenes infection

    Eric Assier1,2, Nadia Belmellat1,2, Luca Semerano1,2,3, Bernhard Ryffel4, Patrice Decker1,5, Valérie Quesniaux4 and Marie-Christophe Boissier1,5,6, 1UMR 1125, Inserm, Bobigny, France, 2EA4222, University of Paris 13, Sorbonne Paris Cité, Bobigny, France, 3Service de Rhumatologie, Assistance Publique – Hôpitaux de Paris (AP-HP) Groupe hospitalier Avicenne - Jean Verdier – René Muret, Bobigny, France, 4INEM, CNRS UMR7355, Orléans, France, 5Li2P, University of Paris 13, Sorbonne Paris Cité, Bobigny, France, 6Rheumatology Department, Assistance Publique – Hôpitaux de Paris (AP-HP), Avicenne Hospital, Bobigny, France

    Background/Purpose: Anti-TNF-alpha therapy has been a successful treatment strategy for rheumatoid arthritis (RA), but is associated with reduced resistance to infection. In mice, TNF is…
  • Abstract Number: 2927 • 2016 ACR/ARHP Annual Meeting

    Mechanisms Regulating the Loss of Tregs in CD11c-Flip-KO Mice That Contribute to the Spontaneous Development of Inflammatory Arthritis

    Qi Quan Huang1, Renee E. Doyle2, Robert Birkett1, Deyu Fang3 and Richard M. Pope2, 1Medicine/Rheumatology, Northwestern University Feinberg school of Medicine, Chicago, IL, 2Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 3Department of Pathology, Northwestern University Feinberg School of Medicine, Chicago, IL

    Background/Purpose: CD11c-Flip-KO (HUPO) mice spontaneously develop inflammatory, erosive arthritis. We previously demonstrated that T regulatory cells (Tregs) were reduced in HUPO mice and that the…
  • Abstract Number: 1441 • 2016 ACR/ARHP Annual Meeting

    Dendritic Cell-Specific Transmembrane Protein (DC-STAMP) Knockout Attenuates Arthritis Progression and Systemic Inflammation in TNF-Tg Arthritis Mouse Models

    Yahui Grace Chiu1, Richard Bell2, Dongge Li3, Edward Schwarz4 and Christopher T. Ritchlin5, 1Allergy, Immunology, and Rheumatology, University of Rochester Medical Center, Rochester, NY, 2Pathology, University of Rochester, Rochester, NY, 3Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 4Orthopedeatrics, University of Rochester, Rochester, NY, 5Allergy Immunology & Rheumatology, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Tumor necrosis factor-transgenic (TNF-Tg) mice develop systemic inflammatory polyarthritis. DC-STAMP, a multi-pass transmembrane protein, was originally identified from a dendritic cell library and required…
  • Abstract Number: 3049 • 2016 ACR/ARHP Annual Meeting

    Prevalence of Doctor-Diagnosed Arthritis Among Adults with Clinically Measured Pre-Diabetes— United States, 2009–2014

    Kamil E. Barbour1, Michael Boring1, Charles Hemlick2, Jennifer M. Hootman3, Louise Murphy1 and Giuseppina Imperatore4, 1Arthritis Program, Centers for Disease Control and Prevention, Atlanta, GA, 2Centers for Disease Control and Prevention, Atlanta, GA, 3Centers for Disease Control and Prevention, Kennesaw, GA, 4Division of Diabetes Translation, National Center for Chronic Disease Prevention and Health Promotion, Atlanta, GA

    Background/Purpose:   In the US, over 86 million adults have pre-diabetes; physical activity is recommended to reduce the high risk of developing diabetes.  Arthritis is…
  • Abstract Number: 1442 • 2016 ACR/ARHP Annual Meeting

    Suppression of Acute Arthritis By N-Methyl-3,4-Dichloropropionaniline (N-MeDCPA), a Reversible Orai Calcium Channel Inhibitor

    John Barnett1, Lisa Robinson2, Jonathan Soboloff3, Rosana Schafer4, Ida Holaskova5, Meenal Elliott1, Michelle Witt2, Raphael Hirsch6 and Harry Blair7, 1Microbiology, Immunology and Cell Biology, West Virginia University, Morgantown, WV, 2Pathology, West Virginia University, Morgantown, WV, 3Dept of Medical Genetics and Molecular Biochemistry, Temple University, Philadelphia, PA, 4Dept Micro, Immun & Cell Biol, West Virginia University, Morgantown, WV, 5West Virginia University, Morgantown, WV, 6Stead Family Department of Pediatrics, University of Iowa Carver College of Medicine, Iowa City, IA, 7pathology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose:  Bone maintenance is a balance between the removal of old bone by osteoclasts (OCL) and the production of new bone by osteoblasts. In the…
  • 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: 1443 • 2016 ACR/ARHP Annual Meeting

    A Therapeutic Peptide Vaccine Reduces Pro-Inflammatory Responses and Suppresses Arthritis in the Cartilage Proteoglycan G1 Domain-Induced Mouse Model of Rheumatoid Arthritis

    Daniel Zimmerman1, Harold Steiner III1, Roy Carambula1, Adrienn Markovics2, Alison Finnegan3, Katalin Mikecz2 and Tibor Glant4, 1Research and Development, Cellular Immunology, CEL-SCI Corporation, VIENNA, VA, 2Orthopedic Surgery, Rush University Medical Center, Chicago, IL, 3Dept of Medicine, Rush University Med Ctr, Chicago, IL, 4Orthopedic Surgery, Rush Med Ctr Cohn Bldg Rm 708, Chicago, IL

    Background/Purpose:  Rheumatoid arthritis (RA) is an autoimmune disease leading to inflammatory destruction of the peripheral joints. Although pro-inflammatory T helper 1 (Th1) and/or Th17 cell…
  • Abstract Number: 3147 • 2016 ACR/ARHP Annual Meeting

    Remote Inflammation Triggers Autoimmune Arthritis through Th17 Distribution

    Nina Chevalier1, Jian Tan2, Linda Mason2, Remy Robert2, Craig McKenzie2, Seth Masters3 and Charles Mackay2, 1University Freiburg Medical Center, Freiburg, Germany, 2Monash University, Melbourne, Australia, 3WEHI, Melbourne, Australia

    Background/Purpose: Autoimmune diseases, such as autoimmune inflammatory arthritis, result through breakdown of immune tolerance and development of self-reactive T cells, or autoantibody-producing B cells. Tolerance…
  • Abstract Number: 173 • 2016 ACR/ARHP Annual Meeting

    S100A8/A9, a Potent Serum and Molecular Imaging Biomarker for Synovial Inflammation and Joint Destruction in Seronegative Experimental Arthritis

    Edwin J. W. Geven1, Martijn H. J. van den Bosch1, Shahla Abdolahi-Roodsaz1, Annet W. Sloetjes1, Sven Hermann2, Michael Schäfers2, Marije I. Koenders1, Dirk Föll3, Johannes Roth4, Thomas Vogl4 and Peter L. E. M. van Lent1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2European Institute for Molecular Imaging, University of Münster, Münster, Germany, 3Department of Pediatric Rheumatology and Immunology, University of Münster, Münster, Germany, 4Institute of Immunology, University of Münster, Münster, Germany

    Background/Purpose: Seronegative joint diseases, including psoriatic arthritis and juvenile idiopathic arthritis, are characterized by the lack of autoantibodies, which are relevant biomarkers for predicting disease…
  • Abstract Number: 1450 • 2016 ACR/ARHP Annual Meeting

    Regulatory Mechanisms of Mesenchymal Stem Cell Transplantation on Systemic Osteoporosis in Collagen-Induced Arthritis Mice

    Chang Liu, Huayong Zhang, Xiaojun Tang, Ruihai Feng, Genhong Yao, Weiwei Chen, Wenchao Li and Lingyun Sun, Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China

    Background/Purpose:  To investigate the effects of umbilical cord-mesenchymal stem cell (UC-MSC) transplantation on joint damage and systemic osteoporosis in collagen induced arthritis (CIA) mice. Methods:…
  • Abstract Number: 3165 • 2016 ACR/ARHP Annual Meeting

    HLA-B27 Expression Is Accompanied By a Profoundly Altered IgA Response to the Intestinal Microbiota and Microbial Translocation to the Joint

    Mark Asquith1, Sean Davin1, Patrick Stauffer1, Claire Mitchell2 and James T. Rosenbaum1, 1Oregon Health & Science University, Portland, OR, 2Division of Arthritis and Rheumatology, Oregon Health & Science University, Portland, OR

    Background/Purpose:  HLA-B27 is the strongest known genetic risk factor for ankylosing spondylitis and other spondyloarthropathies (SpAs). We have shown previously that Fisher 344 rats that…
  • Abstract Number: 459 • 2016 ACR/ARHP Annual Meeting

    Resident Non-Classical Monocytes Are Critically Important for Tissue Destruction in Arthritis

    Antonia Puchner1, Victoria Saferding2, Michael Bonelli3, Carl-Walter Steiner2, Eliana Goncalves-Alves3, Silvia Hayer4, Yohei Mikami5, Marije M. Koenders6, Birgit Niederreiter7, Josef S. Smolen8, Kurt Redlich3, Stephan Blüml9 and Michael Bonelli and Stephan blueml, 1Department of Rheumatology, Medical University of Vienna, Vienna, Austria, 2Rheumatology, Medical University of Vienna, Vienna, Austria, 3Division of Rheumatology, Medical University of Vienna, Vienna, Austria, 4Waehringer Guertel 18-20 A-A09, Medical University of Vienna, Vienna, Austria, 5Molecular Immunology and Inflammation Branch, NIAMS, Bethesda, MD, 6Rheumatology Research and Advanced Therapeutics, Radboud University Nijmegen Medical Center, Nijmegen, Netherlands, 7Rheumatology, Internal Medicine III, Medical University of Vienna, Vienna, Austria, 8Medical University of Vienna, Vienna, Austria, 9Internal Medicine 3; Division of Rheumatology, Medical University of Vienna, Vienna, Austria

    Background/Purpose: Bone destruction in rheumatoid arthritis is mediated by osteoclasts, which are derived from precursor cells of the myeloid lineage. Although there is much known…
  • 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: 462 • 2016 ACR/ARHP Annual Meeting

    Selective Inhibition of MMP9 Using a Monoclonal Antibody As a Therapeutic Strategy for Rheumatoid Arthritis

    Sunhwa Kim1, Brian Carr1, Leah Tong1, Debi Jin1, Ruth Wang1, Derrek Marshall1, David Gossage2 and Victoria Smith1, 1Biology, Gilead Sciences, Inc., Foster city, CA, 2Biology, Gilead Sciences, Inc., foster city, CA

    Background/Purpose: Matrix metalloproteinase-9 (MMP9), highly expressed by infiltrating inflammatory cells, pannus tissue, and multinucleated cells in the synovium and subchondral bone tissue, including osteoclasts, participates…
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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.).

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