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Abstracts tagged "autoantigens"

  • Abstract Number: 2291 • 2018 ACR/ARHP Annual Meeting

    Longitudinal Course of the Disease in Anti-Mi2 Patients: More Intense Muscle Weakness, Good Response to Treatment and Progressive Reduction of Autoantibody Titers

    Iago Pinal-Fernandez1,2, Katherine Pak3, Maria Casal-Dominguez4,5, Wilson Huang4, Jemima Albayda6, Eleni Tiniakou7, Julie J. Paik1, Christopher A. Mecoli8, Sonye K. Danoff9, Lisa Christopher-Stine9 and Andrew Mammen3,10, 1Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 2Muscle Diseases Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases. National Institutes of Health, Bethesda, MD, 3National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 4NIAMS, NIH, Bethesda, MD, 5Johns Hopkins Medical School, Baltimore, MD, 6Johns Hopkins University School of Medicine, Baltimore, MD, 7Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 8Internal Medicine/Rheumatology, Johns Hopkins University, Baltimore, MD, 9Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, 10Center Tower Ste 5300, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Autoantibodies targeting the Mi-2 (Mi-2a and Mi-2b) nuclear antigen in patients with dermatomyositis (DM) were first described in 1985. However, little is known about…
  • Abstract Number: 4 • 2018 ACR/ARHP Annual Meeting

    Anti-Jo1 Positive Myositis Patients Display a Characteristic IgG Fc-Glycan Profile Which Is Further Enhanced in Anti-Jo1 Autoantibodies

    Catia Fernandes-Cerqueira1,2, Nuria Renard1,2, Antonella Notarnicola1,2, Edvard Wigren1,2,3, Susanne Graslund1,2,3, Roman Zubarev4, Ingrid E. Lundberg1,2 and Susanna L. Lundström4, 1Department of Medicine, Division of Rheumatology, Karolinska Institutet, Stockholm, Sweden, 2Center for Molecular Medicine, Stockholm, Sweden, 3Structural Genomics Consortium, Stockholm, Sweden, 4Department of Medical Biochemistry and Biophysics, Division of Physiological Chemistry I, Stockholm, Sweden

    Background/Purpose: IgG Fc-glycans affect IgG function and are altered in autoimmune diseases and autoantibodies. Anti-histidyl tRNA synthetase autoantibodies (anti-Jo1) are frequent in myositis associated with…
  • Abstract Number: 16 • 2018 ACR/ARHP Annual Meeting

    Comprehensive Antibody Profiling Using High Density Peptide Arrays Reveals Novel Citrullinated Protein Targets in Rheumatoid Arthritis Serum Samples

    Ken Lo1, Hanying Li2, Eric Sullivan2 and Jigar Patel2, 1Technology Innovation, Roche Sequencing Solutions - Madison, Madison, WI, 2Roche Sequencing Solutions - Madison, Madison, WI

    Background/Purpose: Autoantibodies against citrullinated proteins are found in 64-89% of rheumatoid arthritis (RA) patients, with a specificity of 88-99%. While citrullinated vimentin, fibrin and histone…
  • Abstract Number: 2010 • 2018 ACR/ARHP Annual Meeting

    Anti-Endothelial Cell Antibodies in Pediatric Rheumatic Diseases

    Rie Karasawa1, Toshiko Sato1, Megumi Tanaka1, Mayumi Tamaki1, Kazuo Yudoh1 and James Jarvis2, 1Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan, 2Pediatrics, University at Buffalo Jacobs School of Medicine & Biomedical Sciences, Buffalo, NY

    Background/Purpose: Anti-endothelial cell antibodies (AECA) are antibodies detected in multiple autoimmune and inflammatory diseases. Increased levels of such antibodies may be involved in disease activity…
  • Abstract Number: 2056 • 2018 ACR/ARHP Annual Meeting

    Citrullination Is Not a Determinant in the Lack of Tolerance to Peptidylarginine Deiminase 2 and 4 in Rheumatoid Arthritis

    Pooja Naik1, Ryan Davis2, Jon T. Giles3, Felipe Andrade4 and Erika Darrah5, 1Department of Medicine, Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 2Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 3Columbia University, New York, NY, 4Medicine/Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 5Department of Medicine/Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Peptidylarginine deiminase (PAD) 2 and 4 are targets of the humoral response in RA. However, the mechanisms by which these enzymes become immunogenic in…
  • Abstract Number: 26 • 2017 ACR/ARHP Annual Meeting

    Single B Cell Analysis Revealed the Relationship Among the Cytokine Profile, Antibody Affinity, and Pathogenic Roles of Autoantigen-Reactive B Cells in Systemic Sclerosis

    Takemichi Fukasawa1, Ayumi Yoshizaki2, Satoshi Ebata1, Kouki Nakamura1, Ryosuke Saigusa1, Takashi Yamashita1, Yoshihide Asano3, Yutaka Kazoe4, Kazuma Mawatari4, Takehiko Kitamori4 and Shinichi Sato5, 1Dermatology, University of Tokyo, Graduate School of Medicine, Tokyo, Japan, 2Department of Dermatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 3Applied Chemistry, University of Tokyo, Graduate School of Medicine, Tokyo, Japan, 4Applied Chemistry, University of Tokyo, Graduate School of Engineering, Tokyo, Japan, 5Department of Dermatology, Graduate School of Medicine, The University of Tokyo, Bunkyo-ku, Japan

    Background/Purpose: Recent studies have indicated that B cells play critical roles in systemic autoimmunity and disease expression through various functions such as induction of the…
  • Abstract Number: 39 • 2017 ACR/ARHP Annual Meeting

    Protein Array Technology Identifies Rituximab-Treated Non-Responder Rheumatoid Arthritis Patients to Generate New Autoantibody Repertoires during Treatment

    Zoltán Konthur1, Melvin Michael Wiemkes2, Thomas Häupl2, Gerd R. Burmester2 and Karl Skriner2, 1Department of Biomolecular Systems, Max Planck Institute of Colloids and Interfaces, Potsdam, Germany, 2Department of Rheumatology and Clinical Immunology, Charité - University Medicine Berlin, Free University and Humboldt University Berlin, Berlin, Germany

    Background/Purpose: Rituximab (RTX) has shown clinical efficacy but up to 40 % of RTX treated rheumatoid arthritis (RA) patients are poor responders (Ann-Rheum-Dis. 2005 Feb;64(2):246-52)…
  • Abstract Number: 44 • 2017 ACR/ARHP Annual Meeting

    Characterization of Novel Stromal-Derived Autoantigens Recognized By RA Synovial Monoclonal Antibodies

    Elisa Corsiero1, Lucas Jagemann1, Costantino Pitzalis2 and Michele Bombardieri3, 1Centre for Experimental Medicine & Rheumatology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom, 2Centre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Barts and The London, School of Medicine and Dentistry, Queen Mary University of London, London, United Kingdom, 3Centre for Experimental Medicine and Rheumatology, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom

    Background/Purpose: We previously showed that up to 40% of RA synovial recombinant monoclonal antibodies (RA-rmAbs) generated from germinal center-like structure (GC-LS+) RA synovium recognize citrullinated…
  • Abstract Number: 676 • 2017 ACR/ARHP Annual Meeting

    Immunosignature Autoantibody Profiles Provide Mechanistic Insight into Systemic Lupus Erythematosus and Differentiation from Symptomatically Overlapping Diseases

    Theodore M. Tarasow1, Robert Gerwien1, Jonathan Melnick1, Scott A. Melville1 and Chaim Putterman2, 1HealthTell, Inc., San Ramon, CA, 2Division of Rheumatology, Albert Einstein College of Medicine, Bronx, NY, USA, Bronx, NY

    Background/Purpose: Diagnosis and monitoring of patients with SLE usually requires careful evaluation by a rheumatologist. However, difficulties in accurately quantifing disease and treatment response can…
  • Abstract Number: 2335 • 2017 ACR/ARHP Annual Meeting

    Antiendothelial Cell Antibodies in Juvenile Dermatomyositis: A Proteomics-Based Approach

    Rie Karasawa1, Mayumi Tamaki1, Toshiko Sato1, Megumi Tanaka1, Kazuo Yudoh1 and James Jarvis2, 1Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan, 2Department of Genetics, Genomics & Bioinformatics, University at Buffalo, Buffalo, NY

    Background/Purpose: Juvenile dermatomyositis (JDM) is a systemic disorder of childhood characterized by muscle inflammation and vasculopathy. The mechanisms of the blood vessel injury in JDM…
  • Abstract Number: 2658 • 2017 ACR/ARHP Annual Meeting

    4-Hydroxy-2-Nonenal Serum Protein-Adducts and Anti-4-Hydroxy-2-Nonenal-Protein Adduct Antibodies in SLE

    Biji T Kurien1,2,3 and R. Hal Scofield4, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2U.S. Department of Veterans Affairs Medical Center, Oklahoma City, OK, 3College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 4Arthritis & Clinical Immunology Program, Oklahoma Medical Research Foundation; Department of Medicine, University of Oklahoma Health Sciences Center; US Department of Veterans Affairs Medical Center, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic, complex disease and autoantibodies to self-antigens are a characteristic feature of the disorder. Our group and others…
  • Abstract Number: 17 • 2017 Pediatric Rheumatology Symposium

    Anti-endothelial cell antibodies in juvenile dermatomyositis

    Rie Karasawa1, Mayumi Tamaki1, Toshiko Sato1, Megumi Tanaka1, Kazuo Yudoh2 and James Jarvis3, 1Institute of Medical Science, St. Marianna University School of Medicine, Kawasaki, Japan, 2Institute of Medical Science, St. Marianna University School of Medicine, Kanagawa, Japan, 3Pediatrics, SUNY Buffalo School of Medicine, Buffalo, NY

    Background/Purpose:  Juvenile dermatomyositis (JDM) is the most common form of inflammatory myopathy in children. Although classified as a myopathy, involved tissues in JDM are characterized…
  • Abstract Number: 1083 • 2016 ACR/ARHP Annual Meeting

    Discovery and Subsequent Diagnostic Verification of Autoantibodies Against the Major Vault Protein (MVP) in Systemic Lupus Erythematosus

    Petra Budde1, Johannes Schulte-Pelkum1, Daniel Wirtz1, Hans-Dieter Zucht1, Heike Göhler1, Stefan Vordenbäumen2, Peter Schulz-Knappe1 and Matthias Schneider3, 1Protagen AG, Dortmund, Germany, 2Rheumatology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany, 3Rheumatology, Heinrich-Heine-University, Duesseldorf, Germany

    Background/Purpose: In systemic lupus erythematosus (SLE), early diagnosis and prognostic stratification are still great challenges. The broad characterization of the autoantibody repertoire in SLE is…
  • Abstract Number: 1208 • 2016 ACR/ARHP Annual Meeting

    High-Throughput Screening Discovers Multiple Novel Autoantibodies in Rheumatoid Arthritis, Systemic Lupus, Systemic Sclerosis and Sjogrens Syndrome

    Peter Schulz-Knappe1, Hans-Dieter Zucht1, Petra Budde1, Heike Göhler1, Daniel Wirtz1, Johannes Schulte-Pelkum1, Stefan Vordenbäumen2, Torsten Witte3 and Prof. Dr. Matthias Schneider4, 1Protagen AG, Dortmund, Germany, 2Rheumatology, Heinrich-Heine-University Düsseldorf, Düsseldorf, Germany, 3Department of Clinical Immunology and Rheumatology, Hannover Medical School, Hannover, Germany, 4Department of Rheumatology & Hiller Research Unit, Heinrich-Heine University, Düsseldorf, Germany

    Background/Purpose: Diagnostic biomarkers are decision-making tools in clinical lab routine and are of growing importance for clinical management of patients. In autoimmune diseases, one important…
  • Abstract Number: 1834 • 2016 ACR/ARHP Annual Meeting

    Commensal Ro60 Autoantigen Ortholog Cross-Reactivity in Human Lupus and Gnotobiotic Models

    Teri Greiling1, Carina Dehner2, Stephen Renfroe3, Xinguo Chen4, Kevin Hughes4, Silvio M. Vieira3, William Ruff3, Marco Boccitto4, Andrew Goodman5, Sandra L. Wolin4 and Martin Kriegel3,6, 1Dermatology and Immunobiology, Yale School of Medicine, New Haven, CT, 2Immunobiology, Yale School of Medicine, new haven, CT, 3Immunobiology, Yale School of Medicine, New Haven, CT, 4Cell Biology, Yale School of Medicine, New Haven, CT, 5Microbial Pathogenesis, Yale School of Medicine, New Haven, CT, 6Medicine/Division of Rheumatology, Yale School of Medicine, New Haven, CT

    Background/Purpose: The earliest autoantibodies in lupus are directed against the autoantigen Ro60, an RNA binding protein with orthologs that we identified in a subset of…
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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 CT on October 25. 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].

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