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Abstracts tagged "autoantigens"

  • Abstract Number: 1730 • 2014 ACR/ARHP Annual Meeting

    Identification of Novel Scleroderma –associated Antigens and Development of an Autoantibody Assay Panel Enabling Their Subsequent Validation

    Hans-Dieter Zucht1, Petra Budde1, Peter Schulz-Knappe1, Nicolas Hunzelmann2, Karsten Conrad3 and Prof. Dr. Matthias Schneider4, 1Protagen AG, Dortmund, Germany, 2Department of Dermatology, University of Cologne, Cologne, Germany, 3Medizinische Fakultät Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany, 4Department of Rheumatology, Univ. Duesseldorf, Duesseldorf, Germany

    Background/Purpose: Scleroderma (systemic sclerosis or SSc) has a highly variable clinical presentation and course resulting in difficulties for disease management. When SSc is suspected, autoantibodies…
  • Abstract Number: 1610 • 2014 ACR/ARHP Annual Meeting

    New Autoantigens Associated with Lupus Nephritis

    Sachiko Onishi1, Yuki Tanaka2, Tatsuhiko Miyazaki3, Jun Ishizaki1, Takuya Matsumoto1, Endy Adnan1, Hitoshi Yamasaki4, Koichiro Suemori1, Takafumi Okura5, Masaki Yasukawa1 and Hitoshi Hasegawa6, 1Department of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, Toon, Japan, 2Integrated Center for Sciences, Ehime University, Toon, Japan, 3Division of Pathology, Gifu University Hospital, Gifu, Japan, 4Department of Hematology, Clinical Immunology, and Infectious Disease, Ehime University Graduate School of Medicine, Toon, Japan, 5Department of Cardiology, Pulmonology, Hypertension and Nephrology, Ehime University Graduate School of Medicine, Toon, Japan, 6Department of Hematology, Clinical Immunology and Infectious Diseases, Ehime University Graduate School of Medicine, Toon, Japan

    [Background/Purpose ] Systemic lupus erythematosus (SLE) is characterized by the production of a variety of autoantibodies and is considered a prototype immune complex disease. Anti-dsDNA…
  • Abstract Number: 878 • 2014 ACR/ARHP Annual Meeting

    Luminex and Autoantigen Microarray Analysis of Sera from Patients with Diffuse Cutaneous Systemic Sclerosis Reveals Changes Associated with Imatinib Mesylate Treatment

    D. James Haddon1, Hannah Wand2, Paul J. Utz1, Robert F. Spiera3, Jessica K. Gordon3 and Lorinda Chung4, 1Medicine, Stanford University School of Medicine, Stanford, CA, 2Stanford University School of Medicine, Stanford, CA, 3Rheumatology, Hospital for Special Surgery, New York, NY, 4Immunology and Rheumatology, Stanford University School of Medicine, Palo Alto, CA

    Background/Purpose Tyrosine kinase inhibitors (TKIs), including imatinib mesylate, have been studied for the treatment of diffuse cutaneous Systemic Sclerosis (dcSSc). In a previously reported single…
  • Abstract Number: 339 • 2014 ACR/ARHP Annual Meeting

    Toll-like Receptor Dependent Autoantigens and Vesicles from P.Gingivalis in Animal Models of RA to Modulate Collagen and Collagen Antibody Induced Arthritis

    Christina Grimm1, Bianka Marklein1, Gerd Burmester1,2 and Karl Skriner3, 1Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, 2Charité – University Medicine Berlin, Berlin, Germany, 3Department of Rheumatology and Clinical Immunology, Germany, Charité - Universitätsmedizin Berlin, Berlin, Germany

    Background/Purpose A variety of animal models suggest that TLR signaling is important in the pathogenesis of RA and the generation of specific autoantibodies. This study…
  • Abstract Number: 87 • 2014 ACR/ARHP Annual Meeting

    Association of TRIM21 (RO52) Polymorphisms with Systemic Lupus Erythematosus in a Japanese Population

    Misaki Hidaka1, Aya Kawasaki1, Hiroshi Furukawa2, Yuya Kondo3, Satoshi Ito4, Isao Matsumoto5, Makio Kusaoi6, Hirofumi Amano6, Akiko Suda7, Keigo Setoguchi8, Tatsuo Nagai9, Kota Shimada10, Shoji Sugii10, Akira Okamoto11, Noriyuki Chiba12, Eiichi Suematsu13, Masao Katayama14, Akiko Okamoto15, Hajime Kono15, Shigeru Ohno7, Shunsei Hirohata16, Shouhei Nagaoka17, Yoshinari Takasaki18, Hiroshi Hashimoto19, Shigeto Tohma2, Takayuki Sumida3 and Naoyuki Tsuchiya1, 1Molecular and Genetic Epidemiology Laboratory, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan, 2Clinical Research Center for Allergy and Rheumatology, Sagamihara Hospital, National Hospital Organization, Sagamihara, Japan, 3Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan, 4Department of Rheumatology, Niigata Rheumatic Center, Shibata, Japan, 5Department of Interenal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan, 6Department of Rheumatology and Internal Medicine, Juntendo University, Tokyo, Japan, 7Center for Rheumatic Diseases, Yokohama City University Medical Center, Yokohama, Japan, 8Allergy and Immunological Diseases, Tokyo Metropolitan Cancer and Infectious Diseases Center Komagome Hospital, Tokyo, Japan, 9Department of Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Sagamihara, Japan, 10Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan, 11Department of Rheumatology,, Himeji Medical Center, National Hospital Organization, Himeji, Japan, 12Department of Rheumatology, Morioka Hospital, National Hospital Organization, Morioka, Japan, 13Department of Internal Medicine and Rheumatology, Clinical Research Institute, Kyushu Medical Center, National Hospital Organization, Fukuoka, Japan, 14Division of Rheumatology, Department of Internal Medicine, Nagoya Medical Center, National Hospital Organization, Nagoya City, Aichi, Japan, 15Department of Internal Medicine, Teikyo University School of Medicine, Tokyo, Japan, 16Int Med/Rheumatol & Infec Dis, Kitasato University School of Medicine, Sagamihara, Japan, 17Department of Rheumatology, Yokohama Minami Kyousai Hospital, Yokohama, Japan, 18Department of Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 19Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose TRIM21, also referred to as Ro52 or SS-A1, belongs to the tripartite motif-containing (TRIM) family. TRIM21 is not only important as an autoantigen, but…
  • Abstract Number: 1778 • 2013 ACR/ARHP Annual Meeting

    Physical Interactions Between Histidyl-tRNA Synthetase and Endogenous/Exogenous Alarmins Enhance Immunogenicity In a Model Of Antigen-Induced Myositis

    Irina Fernandez1, Lisa Harlow2, William Ridgway3 and Dana P. Ascherman4, 1Rheumatology, University of Miami, Miami, FL, 2Rheumatology and Clinical Immunology, University of Miami Miller School of Medicine, Miami, FL, 3Immunology, Allergy and Rheumatology, University of Cincinnati, Cincinnati, OH, 4Medicine/Rheumatology, University of Miami Miller School of Medicine, Miami, FL

    Objective:  To assess the biological interplay between histidyl-tRNA synthetase (HRS) and different endogenous/exogenous ligands capable of generating signals through MyD88-dependent receptor systems in idiopathic inflammatory…
  • Abstract Number: 1575 • 2013 ACR/ARHP Annual Meeting

    Identification Of Novel Distinct Autoantigen Clusters Reflecting The Heterogeneity Of Systemic Lupus Erythematosus

    Petra Budde1, Angelika Lueking1, Stefan Vordenbäumen2, Heike Göhler1, Martin Gamer1, Klaus Marquardt1, Anna Telaar1, Daniel Chamrad1, Carmen Theek1, Peter Schulz-Knappe1 and Matthias Schneider2, 1Protagen AG, Dortmund, Germany, 2Department of Endocrinology, Diabetes and Rheumatology, Heinrich-Heine-University Duesseldorf, Duesseldorf, Germany

    Background/Purpose: Diagnosis of systemic lupus erythematosus (SLE) is based on a combination of clinical findings and laboratory evidence such as anti-nuclear autoantibodies (ANA), anti-Smith and…
  • Abstract Number: 913 • 2013 ACR/ARHP Annual Meeting

    High Throughput Epitope Mapping Of Autoantibodies In BXD2 Mice Reveals The Generation Of Autoantibodies Against Citrullinated Antigens At The Predicted Major Immunogenic Sites

    Jennie Hamilton1, Qi Wu2, PingAr Yang2, Hui-Chen Hsu3 and John D. Mountz4, 1University of Alabama at Birmingham, Birmingham, AL, 2Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 3Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Increased polyreactive B cells have been identified in patients with systemic lupus erythematous (SLE) and rheumatoid arthritis (RA).  Such autoantibodies (autoAbs) were also identified…
  • Abstract Number: 630 • 2013 ACR/ARHP Annual Meeting

    Galectin-3-Binding Protein Is Highly Increased On Circulating Microparticles In SLE Patients and Co-Localizes With IgG In Glomerular Deposits In Human Lupus Nephritis

    Christoffer T. Nielsen1,2, Ole Østergaard3, Ole Petter Rekvig4, Gunnar K. Sturfelt5, Søren Jacobsen6 and Niels H. H. Heegaard7, 1Department of Clinical Biochemistry, Immunology & Genetics, Statens Serum Institut, Copenhagen S, Denmark, 2Infectious Diseases and Rheumatology, University Hospital Rigshospitalet, Copenhagen, Denmark, 3Department of Clinical Biochemistry, Immunology & Genetics, Statens Serum Institute, Copenhagen S, Denmark, 4Department of Biochemistry and Medical Biology, University Hospital, Tromsø, Norway, 5Department of Rheumatology, University Hospital Lund, Lund, Sweden, 6Department of Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark, 7Department of Clinical Biochemistry, Immunology & Genetics, Statens Serum Institut, Copenhagen, Denmark

    Background/Purpose: The origin of autoantigens in glomerular immune complex (IC) deposits in lupus nephritis patients is unknown. They may derive from the circulation (microparticle (MP)-ICs…
  • Abstract Number: 37 • 2013 ACR/ARHP Annual Meeting

    Follicular Entry Of Lymphotoxin-Expressing B Cells Via Type I Interferon Disrupts Marginal Zone Barrier Integrity and Exacerbates Systemic Autoimmunity

    Hao Li1, Hui-Chen Hsu2, Qi Wu3, Jun Li3, PingAr Yang3, Yang-Xin Fu4 and John D. Mountz5, 1Dept. Med - Immunology/Rheumatology division, University of Alabama at Birmingham, Birmingham, AL, 2Birmingham VA Medical Center, Birmingham, AL, 3Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Department of Pathology, The University of Chicago, Chicago, IL, 5Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Marginal zone macrophages (MZMs), a small subset of specialized splenic macrophages located in the MZ, act as final follicular entry barrier to clear apoptotic…
  • Abstract Number: 713 • 2012 ACR/ARHP Annual Meeting

    Rpp25 Is a Major Target of Autoantibodies to the Th/to Complex As Measured by ELISA and a New Chemilumiscence Assay

    Michael Mahler1, Cristina Gascon2, Sima Patel2, Angela Ceribelli3, Edward K.L. Chan3 and Minoru Satoh4, 1Research, INOVA Diagnostics, San Diego, CA, 2Research, INOVA Diagnostics, Inc., San Diego, CA, 3Oral Biology, University of Florida, Gainesville, FL, 4Medicine, University of Florida, Gainesville, FL

    Background/Purpose: Anti-nuclear antibodies (ANA) play an important role in the diagnosis of systemic autoimmune diseases including systemic sclerosis (SSc). A significant portion of ANA in…
  • Abstract Number: 2577 • 2012 ACR/ARHP Annual Meeting

    Characterization of Circulating Human B Cells That Bind Cyclic Citrullinated Peptide Antigens in Clinically Active Rheumatoid Arthritis

    Gregg J. Silverman1, John Jung2, Jeffrey D. Greenberg3, Adam J. Pelzek4, Caroline Gronwall5 and Jaya Vas5, 1Medical and Pathology, NYU School of Medicine, New York, NY, 2School of Medicine, NYU, New York, NY, 3New York Hospital for Joint Disease, New York, NY, 4School of Medicine, NYU School of Medicine, New York, NY, 5Rheumatology, NYU School of Medicine, New York, NY

    Background/Purpose: Anti-citrullinated protein antibodies (ACPA) were first identified based on their high specificity for RA and now are commonly used as a diagnostic tool. Yet,…
  • Abstract Number: 1391 • 2012 ACR/ARHP Annual Meeting

    Anti-Ku Autoantibodies in Systemic Lupus Erythematosus Versus Autoimmune Myositis As Measured by a Novel Chemiluminescence Assay

    Michael Mahler1, Jason Wu2, Magdalena Szmyrka-Kaczmarek3, Andreas Swart4, Marvin J. Fritzler5, Jean-Luc Senécal6 and John G. Hanly7, 1Research, INOVA Diagnostics, San Diego, CA, 2Research, INOVA Diagnostics, San Diego, 3Rheumatology, Wroclaw Medical University, Wroclaw, Poland, 4Rheumatology clinic Neuss, Neuss, Germany, 5Medicine, University of Calgary, Calgary, AB, Canada, 6Rheumatology, Hôpital Notre-Dame du CHUM, Montréal, QC, Canada, 7Division of Rheumatology, Dalhousie University and Capital Health, Halifax, NS, Canada

    Background/Purpose: Autoantibodies targeting Ku, an abundant nuclear protein with DNA helicase activity, have been reported in patients with systemic autoimmune rheumatic diseases. Little is known…
  • Abstract Number: 1081 • 2012 ACR/ARHP Annual Meeting

    Toll-Like Receptor 7, 8 and 9 Activation of Primary Human Cells by Lupus Immune Complexes Is Dependent On Interleukin 1 Receptor Associated Kinase 4 Activity

    Aaron Winkler1, Weiyong Sun1, Ken Dower2, Elizabeth A. Murphy1, Julia Shin1, Michael Luong1, Michael J. Primiano1, Varenka A. Rodriguez2, Tatyana Souza1, Lih-Ling Lin3, J. Perry Hall1, Katherine Lee4, Vikram R. Rao1 and Margaret Fleming1, 1Inflammation & Remodeling, Pfizer, Cambridge, MA, 2Inflammation and Remodeling, Pfizer, Cambridge, MA, 3Inflammation and Remodeling Research Unit, Pfizer, Cambridge, MA, 4Worldwide Medicinal Chemistry, Pfizer, Cambridge, MA

    Background/Purpose: Genetic, in vitro and in vivo evidence strongly implicate the activation of nucleic acid sensing toll like receptors (TLR) 7, 8, and 9 in…
  • Abstract Number: 889 • 2012 ACR/ARHP Annual Meeting

    Modeling Environmental and Genetic Determinants to Identify the Association of Risk Genes in Anti-Ro60-Mediated Injury: Relaxin Receptor I and Tumor Necrosis Factor

    Joanne H. Reed1, Paula S. Ramos2, Jiri Zavadil3, Jill P. Buyon4 and Robert M. Clancy1, 1Medicine, New York University School of Medicine, New York, NY, 2Department of Medicine, Medical University of South Carolina, Charleston, SC, 3Pathology and Center for Health Informatics and Bioinformtics, New York University School of Medicine, New York, NY, 4Department of Medicine, New York University School of Medicine, New York, NY

    Background/Purpose: Fetuses exposed to maternal anti-Ro60 antibodies can develop cardiac conduction abnormalities and life threatening cardiomyopathy; manifestations of neonatal lupus (NL). Recent data support an injury…
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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.

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