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Abstracts tagged "synovial fluid"

  • Abstract Number: 1330 • 2017 ACR/ARHP Annual Meeting

    Rhesus Theta Defensin 1 (RTD-1) Suppresses Disease-Associated Genes and Induces Anti-Inflammatory Expression Signature in Synovial Tissues of Rat Model of Rheumatoid Arthritis

    Prasad Tongaonkar1, Vasu Punj2, Akshay Subramanian3, Dat Tran3, Katie Trinh4, Justin Schaal1, Percio S. Gulko5, Andre Oullette3 and Michael Selsted3, 1Pathology and Laboratory Medicine, Keck School of Medicine University of Southern California, Los Angeles, CA, 2Medicine, Keck School of Medicine University of Southern California, Los Angeles, CA, 3Keck School of Medicine University of Southern California, Los Angeles, CA, 4Pathology, Keck School of Medicine University of Southern California, Los Angeles, CA, 5Medicine/Rheumatology, Icahn School of Medicine at Mount Sinai, New York, NY

    Background/Purpose: Theta (θ) defensins are the only known macrocyclic peptides found in the Animal kingdom and are exclusively expressed in Old World monkeys. θ-defensins were…
  • 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: 1413 • 2017 ACR/ARHP Annual Meeting

    Cytokine-Induced Aire Activity in Rheumatoid Arthritis Fibroblast-like Synoviocytes Regulates Expression of Interferon-γ Response Genes

    Beatrice Bergström1, Christina Lundqvist1, Hans Carlsten1, Olov Ekwall2 and Anna-Karin Hultgård Ekwall1, 1Rheumatology and Inflammation Research, Sahlgrenska Academy, Gothenburg University, Gothenburg, Sweden, 2Dept. of Rheumatology and Inflammation Research, Institute of Medicine, Sahlgrenska Academy University of Gothenburg, Göteborg, Sweden

    Background/Purpose: AIRE is a transcriptional regulator of tissue specific antigens in medullary thymic epithelial cells (mTEC). AIRE orchestrates the negative selection of self-reactive T cells…
  • Abstract Number: 1940 • 2017 ACR/ARHP Annual Meeting

    Immunologic Synovitis Score: A New Score for Synovial Membrane Characterization in Inflammatory and Non-Inflammatory Arthritis

    Aurélie Najm1,2, Benoît Le Goff MD PhD2,3, Frédéric Blanchard1, Jérome Amiaud4, Céline Charrier5 and Veit Krenn6, 1INSERM U1238 University of medicine, PHY-OS Laboratory, Nantes, France, 2Rheumatology, Nantes University Hospital, Nantes, France, 3UNR1238 University of medicine, PHY-OS Laboratory, Nantes, France, 4UMR1238 University of medicine, PHY-OS Laboratory, Nantes, France, 5UNMR1238 University of medicine, PHY-OS Laboratory, Nantes, France, 6Zytologie und Molekulare Diagnostik, MVZ-Zentrum für Histologie, Trier, Germany

    Background/Purpose: General Synovitis score (GSS) has been developed by Krenn et al in order to discriminate inflammatory arthritis (IA) and non-inflammatory arthritis (NIA) (1). This…
  • Abstract Number: 135 • 2017 Pediatric Rheumatology Symposium

    Epigenetic Profiling Of Juvenile Idiopathic Arthritis (JIA) Synovial Fluid Monocytes Points Towards a Role For Monocytes In Bone Damage

    Janneke Peeters1, Arjan Boltjes2,3, Stephin Vervoort4, Paul Coffer1, Bas Vastert2,5, Femke van Wijk2,3, Michal Mokry3, Teun de Vries6,7 and Jorg van Loosdregt3, 1Center for Molecular Medicine and Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, Netherlands, 2Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 3Division of Pediatrics, University Medical Center Utrecht, Utrecht, Netherlands, 4Peter MacCallum Cancer Centre, Melbourne, Australia, 5Division of Pediatric Rheumatology, University Medical Center Utrecht, Utrecht, Netherlands, 6Department of Oral Cell Biology and Functional Anatomy, Academic Centre for Dentistry Amsterdam, Amsterdam, Netherlands, 7Department of Periodontology, Academic Centre for Dentistry Amsterdam, Amsterdam, Netherlands

    Background/Purpose:  Juvenile Idiopathic Arthritis (JIA) is a multifactorial autoimmune disease characterized by the accumulation of various immune cells, including monocytes, in the joint synovial fluid…
  • Abstract Number: 144 • 2017 Pediatric Rheumatology Symposium

    Linear Discriminant Analysis of Cultured Fibroblast-like Synoviocytes Identifies 6 Candidate Genes Which Predict Extended Course in Juvenile Idiopathic Arthritis

    AnneMarie Brescia1, Megan Simonds2, Suzanne M. McCahan3, Timothy Bunnell3, Kathleen E. Sullivan4 and Carlos D. Rosé5, 1Pediatric Rheumatology, Nemours A.I. duPont Hospital for Children, Wilmington, DE, 2Nemours, Nemours Biomedical Research, Wilmington, DE, 3Nemours Biomedical Research, Wilmington, DE, 4Allergy Immunology, The Children's Hospital of Philadelphia, Philadelphia, PA, 5Pediatric Rheumatology, Nemours/Thomas Jefferson University, Wilmington, DE

    Background/Purpose: The goal of this project is the identification of informative synovial biomarkers to predict which children with oligoarticular juvenile idiopathic arthritis (JIA) will have…
  • Abstract Number: 141 • 2017 Pediatric Rheumatology Symposium

    Expression of Siglec-10 on Synovial Fluid CD14dim Monocytes Was Decreased in Juvenile Idiopathic Arthritis Patients

    Qianzi Zhao1, Yang Liu2, Pan Zheng2 and Lawrence Jung3, 1Rheumatology, Children's National Medical Center, Washington, DC, 2Cancer and Immunology Research Center, Children's National Medical Center, Washington, DC, 3Pediatric Rheumatology, Children's National Medical Center, Washington, DC

    Background/Purpose: Monocytes plays a role in juvenile idiopathic arthritis (JIA). CD14dim monocytes have modulatory effects in innate and adaptive immune responses. Siglec-10, which is highly…
  • Abstract Number: 310 • 2016 ACR/ARHP Annual Meeting

    A Novel One Stage Technique Applicable during Arthroscopy for the Mobilization of Synovial Mesenchymal Stromal Cells Towards Joint Regeneration

    Alam Khalil-Khan1, Thomas Baboolal2, Elena Jones3, Owen Wall4 and Dennis McGonagle3, 1Faculty of Medicine, Leeds institute of Rheumatic and Musculoskeletal Medicine,, Leeds, United Kingdom, 2PhD, Leeds, United Kingdom, 3Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 4Orthopaedic Surgery, Department of Trauma and Orthopaedics, Leeds, United Kingdom

    Background/Purpose: , The discovery of MSCs in the synovium and synovial fluid (SF) provided a potential mechanism for repairing cartilage “from the top down”. Indeed,…
  • Abstract Number: 380 • 2016 ACR/ARHP Annual Meeting

    Linear Discriminant Analysis of Cultured Fibroblast-like Synoviocytes Identifies 6 Candidate Genes Which Predict Extended Course in Juvenile Idiopathic Arthritis

    AnneMarie Brescia1, Megan Simonds2, Suzanne McCahan3, Tim Bunnell3, Kathleen E. Sullivan4 and Carlos D. Rosé1, 1Pediatric Rheumatology, Thomas Jefferson University/ AI duPont Hospital for Children, Wilmington, DE, 2Nemours, Nemours Biomedical Research, Wilmington, DE, 3Nemours Biomedical Research, Wilmington, DE, 4Allergy Immunology, The Children's Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: The goal of this project is the identification of informative synovial biomarkers to predict which children with oligoarticular juvenile idiopathic arthritis (JIA) will have…
  • Abstract Number: 1093 • 2016 ACR/ARHP Annual Meeting

    DNA Methylation Defines Joint Specific Differences in Synovial Fibroblasts  from OA and RA Patients

    Emmanuel Karouzakis1, Mojca Frank Bertoncelj2, Kerstin Klein1, Christoph Kolling3, Renate E. Gay1, Steffen Gay1 and Caroline Ospelt1, 1Center of Experimental Rheumatology, University Hospital Zurich, Zurich, Switzerland, 2Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 3Schulthess Clinic, Zurich, Switzerland

    Background/Purpose: Recent studies revealed epigenetic changes in DNA methylation associated with rheumatoid arthritis (RA) synovial fibroblasts (SF). In addition, we have shown that SF exhibit…
  • Abstract Number: 1096 • 2016 ACR/ARHP Annual Meeting

    Augmentation of Wnt Signaling By IL-1β in Fibroblast-like Synoviocytes

    Satoshi Yamasaki1, Yusuke Yoshida2 and Eiji Sugiyama2, 1Hiroshima University Hospital, Hiroshima, Japan, 2Department of Clinical Immunology and Rheumatology, Hiroshima University Hospital, Hiroshima, Japan

    Background/Purpose: Wnt family proteins canonically stabilize β-catenin to activate T-cell factor (TCF) for the transcription of several genes, including Runx2, which is important for osteoblastogenesis.…
  • 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…
  • Abstract Number: 1116 • 2016 ACR/ARHP Annual Meeting

    Anti-Citrullinated Protein Antibodies Promote Synovial Fibroblasts Migration and Adhesion through a Peptidylarginine Deiminases (PAD) Dependent Pathway

    Meng Sun1, Vijay Joshua1, Akilan Krishnamurthy1, Yanying Liu2, Aase Hensvold1, Sergiu-Bogdan Catrina3, Caroline Ospelt4, Vivianne Malmström5, Khaled Amara1, Johanna Steen1, Muhammad Sohel Mia1, Marianne Engström1, Heidi Wähämaa1, Jimmy Ytterberg1, Bence Rethi1 and Anca I Catrina1, 1Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden, 2Rheumatology Unit, Department of Medicine, Peking University People's Hospital, Beijing, China, 3Molecular Medicine and Surgery, Molecular Medicine and Surgery, Karolinska University Hospital, Karolinska Institute, Stockholm, Sweden, 4University Hospital Zurich, Center of Experimental Rheumatology, Switzerland, Zurich, Switzerland, 5Department of Medicine, Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden

    Background/Purpose: Synovial fibroblasts (SFs) contribute to rheumatoid arthritis (RA) pathogenesis by growing into the synovial space and by producing pro-angiogenic and tissue remodelling factors, chemokines…
  • Abstract Number: 1435 • 2016 ACR/ARHP Annual Meeting

    KCa1.1 Potassium Channels Are a Novel Therapeutic Target on Fibroblast-like Synoviocytes in Rheumatoid Arthritis

    Mark Tanner1, Redwan Huq1, Rajeev Tajhya1, Michael Pennington2, Teresina Laragione3, Pércio Gulko4 and Christine Beeton5, 1Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX, 2Peptides International, Louisville, KY, 3Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, 4Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, 5Department of Molecular Physiology & Biophysics, Baylor College of Medicine, Houston, TX

    Background/Purpose: Fibroblast-like synoviocytes (FLS) develop a high degree of invasiveness during rheumatoid arthritis (RA), leading to joint degradation. There are currently no therapeutics that specifically…
  • Abstract Number: 1557 • 2016 ACR/ARHP Annual Meeting

    3-D Explant Method Facilitates the Study of Lymphocytes in Synovium and Reveals a Population of Resident Memory-like T Cells in Rheumatoid Arthritis

    Lauren Henderson1, Deepak Rao2, Nikola Teslovich3,4, Sandra King5, Fumitaka Mizoguchi6, Sarah Ameri6, Allyn Morris7, Christopher Elco8, James Lederer9, Scott Martin10, Barry Simmons10, John Wright10, Michael Brenner2, Soumya Raychaudhuri11,12,13,14,15, Peter Nigrovic1,16 and Robert Fuhlbrigge17,18, 1Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, 2Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Divisions of Genetics and Rheumatology, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, 4Brigham and Women's Hospital and Harvard Medical School, Cambridge, MA, 5Department of Dermatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 6Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 7Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital, Boston, MA, 8Department of Dermatology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 9Department of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 10Department of Orthopedic Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 11Divisions of Genetics and Rheumatology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, 12Program in Medical and Population Genetics, Broad Institute of Massachusetts Technical Institute, Harvard University, Cambridge, MA, 13Partners Center for Personalized Genetic Medicine, Boston, MA, 14Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital Solna, Stockholm, Sweden, 15Institute of Inflammation and Repair, University of Manchester, Manchester, United Kingdom, 16Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 17Immunology, Boston Children's Hospital, Boston, MA, 18Dermatology, Brigham and Women’s Hospital, Boston, MA

    Background/Purpose: Tissue resident memory T (TRM) cells survive indefinitely in barrier tissues and mediate swift immunologic memory responses at sites of microbe entry. TRM cells…
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