ACR Meeting Abstracts

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Abstracts tagged "Autoantibody(ies)"

  • Abstract Number: 0847 • ACR Convergence 2020

    Impact of Hydroxychloroquine Treatment on Immunologic Markers in SLE Depends on Ethnicity

    Laurence Magder1, Daniel Goldman2 and Michelle Petri2, 1University of Maryland, Baltimore, Baltimore, MD, 2Johns Hopkins University School of Medicine, Timonium, MD

    Background/Purpose: SLE patients with certain immunological markers (i.e., anti-DNA, low complement) are at higher risk of lupus nephritis and those with antiphospholipid antibodies are at…
  • Abstract Number: 1250 • ACR Convergence 2020

    Early Sjögren Antibodies: Potential Biomarker for Abnormal Minor Labial Salivary Gland Biopsy in Juvenile Sjögren’s Syndrome

    Akaluck Thatayatikom1, Sthorn Thatayatikom1, Indraneel Bhattacharyya2, Melissa Elder1, Renee Modica1 and Seunghee Cha2, 1Department of Pediatrics, University of Florida, Gainesville, FL, 2College of Dentistry, University of Florida, Gainesville, FL

    Background/Purpose: Juvenile Sjögren’s Syndrome (jSS) is a perplexing systemic autoimmune disease in children presenting with positive autoantibodies, glandular, and/ or extraglandular symptoms. In pediatric practice,…
  • Abstract Number: 1524 • ACR Convergence 2020

    Interstitial Lung Disease, Kidney Inflammation and Myositis Are Induced by Transfer of PBMC Derived from Systemic Sclerosis Patients into Rag2-/-/ IL2rg-/- mice

    Xiaoyang Yue1, Frank Petersen1, Xinhua Yu1, Gabriela Riemekasten2, Peter Lamprecht3, Antje Müller3 and Junping Yin4, 1Priority Area Asthma & Allergy, Research Center Borstel, Airway Research Center North (ARCN), Members of the German Center for Lung Research (DZL), Borstel, Germany, 2University of Lübeck, Department of Rheumatology and Clinical Immunology,, Lübeck, Germany, 3University of Lübeck, Department of Rheumatology and Clinical Immunology, Lübeck, Germany, 41 Priority Area Asthma & Allergy, Research Center Borstel, Airway Research Center North (ARCN), Members of the German Center for Lung Research (DZL),, Borstel, Germany

    Background/Purpose: To explore the pathogenic potential of lymphocytes in systemic sclerosis (SSc) and granulomatosis with polyangiitis (GPA), a humanized mouse model was generated by transferring…
  • Abstract Number: 0296 • ACR Convergence 2020

    Investigating the Differences in ANA Specificities Between Asymptomatic and Symptomatic ANA+ Individuals

    Carolina Munoz-grajales1, Stephenie Prokopec2, Dennisse Bonilla3, Earl D. Silverman4, Sindhu Johnson3, Arthur Bookman5, Zahi Touma6, Zareen Ahmad7, Linda Hiraki8, Paul Boutros9, Andrzej Chruscinski10 and Joan Wither3, 1University of Toronto, Toronto, Canada, 2Ontario Institute for Cancer Research, Toronto, Canada, 3University of Toronto Lupus Clinic, Centre for Prognosis Studies in Rheumatic Diseases, Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 4Division of Rheumatology, The Hospital for Sick Children, Translational Medicine, Research Institute, The Hospital for Sick Children, and Department of Paediatrics, University of Toronto., Toronto, ON, Canada, 5Division of Rheumatology, University Health Network; 8Department of Medicine, University of Toronto; Division of Rheumatology, Toronto, Canada, 6University of Toronto Lupus Clinic, Centre for Prognosis Studies in Rheumatic Diseases, Toronto Western Hospital, University Health Network; Krembil Research Institute, Toronto, ON, Canada, 7Department of Medicine, University of Toronto; Division of Rheumatology, Mount Sinai Hospital, Toronto, Canada, 8Division of Rheumatology, The Hospital for Sick Children; Department of Medicine, University of Toronto, Toronto, Canada, 9Department of Immunology, University of Toronto; Department of Medical Biophysics, University of Toronto; Department of Pharmacology and Toxicology, University of Toronto; Department of Human Genetics, University of California; Department of Urology, University of California; Eli and Edythe Broad Center of Regenerative Medicine and Stem Cell Research, University of California; Institute for Precision Health, University of California; Jonsson Comprehensive Cancer Centre, University of California, Toronto, Canada, 10Multi-Organ Transplant Program, University Health Network, Toronto, Canada

    Background/Purpose: Within the Anti-Nuclear Antibody (ANA) associated Systemic Autoimmune Rheumatic Diseases (SARD), such as Systemic Lupus Erythematous (SLE), Sjögren’s Syndrome (SS), and Systemic Sclerosis (SSc),…
  • Abstract Number: 0916 • ACR Convergence 2020

    Validating Autoantibody Associations and Clinical Impact of Severe Gastrointestinal Involvement in Systemic Sclerosis

    Fiza Ahmed1, Svetlana Nihtyanova1, Stamatia Chatzinikolaou2, Voon Ong1, Charles Murray2 and Christopher Denton3, 1Centre for Rheumatology, Royal Free Campus, UCL Division of Medicine, UK, London, United Kingdom, 2Department of Gastroenterology, Royal Free London Foundation Trust, UK, London, United Kingdom, 3University College London, London, United Kingdom

    Background/Purpose: Patients with systemic sclerosis (SSc) frequently experience gastrointestinal (GI) symptoms, ranging from mild to debilitating in severity. Better prediction of those most at risk…
  • Abstract Number: 1261 • ACR Convergence 2020

    Antiphospholipid Patterns Predict the Risk of Thrombosis in Systemic Lupus Erythematosus

    Selcan Demir1, Jessica Li2, Laurence Magder3 and Michelle Petri4, 1Hacettepe University Faculty of Medicine, Ankara, Ankara, Turkey, 2Johns Hopkins University, Baltimore, MD, 3University of Maryland, Baltimore, Baltimore, MD, 4Johns Hopkins University School of Medicine, Timonium, MD

    Background/Purpose: Antiphospholipid syndrome (APS) has been classified as the development of venous and/or arterial thromboses, and/or pregnancy morbidity, in the presence of persistently raised levels…
  • Abstract Number: 1574 • ACR Convergence 2020

    Over Half of Patients with Immune Checkpoint Inhibitor-related Myositis, Myasthenia Gravis and/or Myocarditis Have Autoantibodies: Results from a Systematic Literature Review

    Nilasha Ghosh1, Karmela Kim Chan2, Bridget Jivanelli3 and Anne Bass1, 1Hospital for Special Surgery/Weill Cornell Medicine, New York, NY, 2Hospital For Special Surgery, New York, NY, 3Hospital for Special Surgery, New York

    Background/Purpose: Although immune checkpoint inhibitor (ICI) cancer treatments are known to activate cytotoxic T-cells, autoantibodies may also contribute to the development of immune-related adverse events…
  • Abstract Number: 0299 • ACR Convergence 2020

    The Minor Protective Allele at rs1876453 Is Associated with Increased Age of Onset of Systemic Lupus Erythematosus

    Ani Oganesyan1, Jennifer Kelly2, Stuart Glenn2, Adam Adler2, Adrienne Williams3, Mary Comeau4, Julia Ziegler5, Miranda Marion5, Marta Alarcón-Riquelme6, Graciela Alarcón7, Juan-Manuel Anaya8, Sang-Cheol Bae9, Dam Kim9, Lee Hye-Soon9, Lindsey Criswell10, Barry Freedman11, Gary Gilkeson12, Joel Guthridge13, Chaim Jacob14, Judith James15, Diane Kamen16, Joan Merrill17, Kathy Moser Silvis18, Timothy Niewold19, Michelle Petri20, Rosalind Ramsey-Goldman21, John Reveille22, Hal Scofield23, Anne Stevens24, Luis Vilá25, Timothy Vyse26, Kenneth Kaufman27, John Harley28, Carl Langefeld5, Patrick Gaffney2, Elizabeth Brown29, Jeffrey Edberg7, Robert Kimberly7, Betty Tsao12, Daniela Ulgiati30, Kenneth Jones31 and Susan Boackle32, 1Division of Rheumatology, University of Colorado School of Medicine, Aurora, CO, 2Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Department of Biostatistical Sciences and Center for Public Health Genomics Wake Forest School of Medicine, Winston-Salem,, NC, 4Department of Biostatistical Sciences and Center for Public Health Genomics, Wake Forest School of Medicine; MC Analytics, Winston-Salem, NC, 5Department of Biostatistical Sciences and Center for Public Health Genomics, Wake Forest School of Medicine, Winston-Salem, NC, 6Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation;Centro Pfizer-Universidad de Granada-Junta de Andalucía de Genómica e Investigación Oncológica, Granada (GENYO), Granada, Spain, 7Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 8Center for Autoimmune Diseases Research (CREA), Universidad del Rosario, Bogotá, Colombia, 9Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea, 10Rosalind Russell/Ephraim P. Engleman Rheumatology Research Center, University of California San Francisco, San Francisco, CA, 11Department of Internal Medicine, Wake Forest School of Medicine, Winston-Salem,, NC, 12Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 13Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oaklahoma, OK, 14Department of Medicine, University of Southern California, Los Angeles, CA, 15Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation;Department of Pathology, University of Oklahoma Health Sciences Center;Department of Medicine, University of Oklahoma Health Sciences Center, Edmond, OK, 16Medical University of South Carolina, Charleston, SC, 17Department of Clinical Pharmacology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 18Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation; Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 19Colton Center for Autoimmunity, NYU School of Medicine, New York, NY, 20Johns Hopkins University School of Medicine, Baltimore, 21Division of Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 22Department of Internal Medicine, University of Texas, Houston, TX, 23Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation; Department of Medicine, University of Oklahoma Health Sciences Center; US Department of Veterans Affairs Medical Center, Charleston, SD, 24Janssen Pharmaceuticals, Spring House, PA, 25Division of Rheumatology, Department of Medicine, University of Puerto Rico Medical Sciences Campus, San Juan, Puerto Rico, 26Division of Genetics and Molecular Medicine and Immunology, King’s College, London, United Kingdom, 27Cincinnati Children’s Hospital Medical Center;US Department of Veterans Affairs Medical Center, Cincinnati, OH, 28Cincinnati Children's Hospital Medical Center/Univ of Cincinnati College of Medicine, Cincinnati, OH, 29Department of Pathology, University of Alabama at Birmingham, Birmingham, AL, 30School of Pathology and Laboratory Medicine, Centre for Genetic Origins of Health and Disease, The University of Western Australia, Crawley, Australia, 31Harold Hamm Diabetes Center, University of Oklahoma Health Science Center, Oklahoma City, OK, 32Division of Rheumatology, University of Colorado School of Medicine; Denver Veterans Affairs Medical Center, Aurora, CO

    Background/Purpose: Systemic lupus erythematosus (SLE) is a clinically heterogenous autoimmune disease characterized by autoantibody- and complement-mediated inflammatory damage to multiple organ systems. We previously showed…
  • Abstract Number: 0922 • ACR Convergence 2020

    Cancer in Systemic Sclerosis: Analysis of Antibodies Against Components of the Th/To Complex

    Christopher Mecoli1, Brittany Adler2, Qingyuan Yang2, Laura Hummers3, Antony Rosen2, Livia Casciola-Rosen4 and Ami Shah5, 1Johns Hopkins University School of Medicine, Baltimore, MD, 2Johns Hopkins University, Baltimore, MD, 3Johns Hopkins Univerisity, Ellicott City, MD, 4Johns Hopkins University, Johns Hopkins University, MD, 5Johns Hopkins University School of Medicine, Ellicott City, MD

    Background/Purpose: The aim of this study is to describe four of the most common autoantibodies against components of the Th/To complex: hPOP1, RPP25, RPP30, and…
  • Abstract Number: 1262 • ACR Convergence 2020

    Single LAC Positivity versus Double and Triple Positivity for Thrombosis in SLE

    Selcan Demir1, Jessica Li2, Laurence Magder3 and Michelle Petri4, 1Hacettepe University Faculty of Medicine, Ankara, Ankara, Turkey, 2Johns Hopkins University, Baltimore, MD, 3University of Maryland, Baltimore, Baltimore, MD, 4Johns Hopkins University School of Medicine, Timonium, MD

    Background/Purpose:Antiphospholipid syndrome (APS) is classified as the development of venous and/or arterial thromboses, and pregnancy morbidity, in the presence of antiphospholipid antibodies (aPL); lupus anticoagulant,…
  • Abstract Number: 1606 • ACR Convergence 2020

    Mortality with Idiopathic Inflammatory Myositis in an Academic Hospital Setting: A Five-year Retrospective Study

    Jaspreet Kaler1, Zareen Vaghaiwalla2, Gurjit Kaeley3 and Myint Thway4, 1University of Florida - Jacksonville, Jacksonville, FL, 2University of Florida Jacksonville, Jacksonville, FL, 3University of Florida College of Medicine - Jacksonville, Jacksonville, FL, 4University of Florida- Jacksonville, ponte vedra, FL

    Background/Purpose: Idiopathic inflammatory myositis is a diverse group of muscle diseases characterized by muscle inflammation and dysfunction. Approximately 3-7/100,000 cases are diagnosed per year in…
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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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