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Abstracts tagged "Antibodies"

  • Abstract Number: 635 • 2015 ACR/ARHP Annual Meeting

    Seronegative Sjögren’s Syndrome Is Associated with a Higher Frequency of Patient-Reported Neuropathic Pain: An Analysis of the Sjögren’s International Collaborative Clinical Alliance Cohort

    Alan N. Baer1 and Julius Birnbaum2, 1Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 2Medicine (Rheumatology), Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Patients with Sjögren’s syndrome (SS) and negative SSA/SSB serology (ie. seronegative SS) have phenotypic characteristics different than seropositive ones, and thus may constitute a…
  • Abstract Number: 3112 • 2015 ACR/ARHP Annual Meeting

    Incidence of Anti-Drug Antibodies in Rheumatoid Arthritis Patients Treated with Adalimumab, Etanercept, or Infliximab in a Real-World Setting

    RJ Moots1, Ricardo Xavier2, Chi Chiu Mok3, Mahboob U Rahman4, Wen-Chan Tsai5, Mustafa Al Maini6, Karel Pavelka7, Ehab Mahgoub8, Sameer Kotak9, Joan Korth-Bradley10, Ronald Pedersen11, Linda Mele8, Qi Shen8 and Bonnie Vlahos8, 1Department of Musculoskeletal Biology, University of Liverpool, Liverpool, United Kingdom, 2Hospital de Clínicas de Porto Alegre, Porto Alegre, Brazil, 3Medicine, Tuen Mun Hospital, Hong Kong, Hong Kong, 4Perelman School of Medicine, University of Pennsylvania, Philadephia, PA, 5Kaohsiung Medical University, Kaohsiung, Taiwan, 6Rheumatology, Allergy and Clinical Immunology Division, Mafraq Hospital, Abu Dhabi, United Arab Emirates, 7Charles University, Prague, Czech Republic, 8GIPB - Clinical Sciences, Pfizer, Collegeville, PA, 9Global Health and Value, Pfizer, New York, NY, 10GIPB- Clinical Sciences, Pfizer, Collegeville, PA, 11Department of Biostatistics, Pfizer, Collegeville, PA

    Background/Purpose: Treatment with biologics can elicit unwanted immune responses such as antidrug antibodies (ADA), which may decrease their clinical efficacy and increase adverse events. However,…
  • Abstract Number: 809 • 2015 ACR/ARHP Annual Meeting

    Patients with SLE Who Are Anti-Factor Xa IgG Positive Are Less Likely to Have Atherosclerotic Plaque

    Claire-Louise Murphy1, Sara Croca1, Bahar Artim-Esen2, Laura Hanns3, Charis Pericleous1, Thomas McDonnell1, Yiannis Ioannou4, David A. Isenberg1, Anisur Rahman1 and Ian Giles5, 1Rayne Institute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom, 2Department of Internal Medicine, Division of Rheumatology, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 3Rheumatology, Arthritis Research UK Centre for Adolescent Rheumatology, UCL Division of Medicine, London, United Kingdom, 4Rayne Institute, Arthritis Research UK Centre for Adolescent Rheumatology, UCL Division of Medicine, London, United Kingdom, 5Rayne Intitiute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom

    Background/Purpose: Patients with SLE have an increased risk of cardiovascular disease (CVD), which is not fully explained by traditional risk factors and may be mediated…
  • Abstract Number: 823 • 2015 ACR/ARHP Annual Meeting

    Anti-IFI16 Antibodies in Scleroderma Are Associated with Digital Gangrene

    Zsuzsanna McMahan1, Ami A. Shah2, Dhananjay Vaidya3, Fredrick M. Wigley4, Antony Rosen5 and Livia Casciola-Rosen6, 1Rheumatology, Johns Hopkins University, Baltimore, MD, 2Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 3Medicine, School of Medicine, Johns Hopkins, Baltimore, MD, 4Rheum Div/Mason F Lord, Johns Hopkins University School of Medicine, Baltimore, MD, 5Mason Lord Bldg Ctr Tower, Johns Hopkins University, School of Medicine, Baltimore, MD, 6Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Our aim was to examine and confirm the association between anti-IFI16 antibodies and clinical features of scleroderma.   Methods: Sera from a discovery sample…
  • Abstract Number: 1151 • 2015 ACR/ARHP Annual Meeting

    The Proteomic Profile of Histological Samples Derived from a Surgical Mouse Model of Osteoarthritis Reveals an Unexpected Mode of Action for the Anti-Aggrecanase-2 Monoclonal Antibody CRB0017

    Gianfranco Caselli1, Riccardo Chiusaroli2, Michela Visintin3, Tiziana Piepoli2, Ornella Letari2, Adriana Grotti2, Marco Lanza2, Antonella De Palma4, Dario di Silvestre4, Pierluigi Mauri4 and Lucio Claudio Rovati2, 1Pharmacology & Toxicology, Rottapharm Biotech Srl, Monza, Italy, 2Rottapharm Biotech Srl, Monza, Italy, 3Rottapharm Biotech Srl, Trieste, Italy, 4Institute for Biomedical Technologies - CNR, Segrate, Italy

    Background/Purpose : CRB0017 is a novel therapeutic monoclonal antibody that recognizes the spacer domain of aggrecanase-2, a key enzyme in the degradation of extracellular matrix…
  • Abstract Number: 1366 • 2015 ACR/ARHP Annual Meeting

    Natural Antibodies, Not B Cells, Contribute to Acute Cell Death-Induced Inflammation

    Hiroshi Kataoka, Rheumatology and Clinical Immunology, Sapporo City General Hospital, Sapporo, Japan

    Background/Purpose: Alarmins, such as uric acid, released from dying cells activate inflammasomes and mediate dead cell-induced inflammation (Ref.). Since it is remains unknown whether or…
  • Abstract Number: 1772 • 2015 ACR/ARHP Annual Meeting

    Anti-Pentraxin 3 Antibodies Ameliorate Disease Manifestations and Lupus-like Nephritis in New Zealand Black/New Zealand White F1 Mice

    Mariele Gatto1, Nicola Bassi1, Anna Ghirardello1, Roberto Luisetto1, Silvano Bettio1, Luca Iaccarino1, Leonardo Punzi2 and Andrea Doria2, 1Department of Medicine-DIMED, University of Padova, Padova, Italy, 2Department of Medicine - DIMED, University of Padova, Padova, Italy

     Background/Purpose: Pentraxin 3 (PTX3) is an acute-phase protein released by different cell types including renal epithelial cells and immune-competent cells. PTX3 is able to either…
  • Abstract Number: 1858 • 2015 ACR/ARHP Annual Meeting

    Serum Tartrate Resistant Acid Phosphatase (TRAP) Levels Are Decreased and Associated with Anti-Maa Antibodies in Systemic Lupus Erythematosus (SLE) Patients

    Kathleen Borghoff1, Andy Hollins2, Michael J. Duryee1, Ted R. Mikuls2, Zhixin Zhang3, Kaihong Su4, Michelene Hearth-Holmes5 and Geoffrey M. Thiele6, 1Internal Medicine Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 2University of Nebraska Medical Center, Omaha, NE, 3Department of Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, 4Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, 5Division of Rheumatology, University of Nebraska College of Medicine and VA Nebraska Western Iowa Health Care System, Omaha, NE, 6Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE

    Background/Purpose:   Previous studies have shown that patients with systemic lupus erythematosus (SLE) are prone to systemic osteoporosis, bone loss and fracture.  Paradoxically, previous studies…
  • Abstract Number: 2019 • 2015 ACR/ARHP Annual Meeting

    Serum Biomarkers of Inflammatory Arthritis in First Degree Relatives of Patients with Rheumatoid Arthritis and Their Association with Lifestyle Risk Factors

    Jamie C Sergeant and RA-MAP Consortium, NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom, Arthritis Research UK Centre for Epidemiology, Centre for Musculoskeletal Research, Manchester Academic Health Science Centre, University of Manchester, Manchester, United Kingdom

    Background/Purpose: Rheumatoid factor (RF), anti-cyclic citrullinated peptide antibodies (anti-CCP) and C-reactive protein (CRP) are known serum biomarkers of inflammatory arthritis (IA) and have potential predictive…
  • Abstract Number: 2057 • 2015 ACR/ARHP Annual Meeting

    Antibodies to Infliximab in Remicade-Treated Rheumatic Patients Show Identical Reactivity Towards Biosimilars

    Begoña Ruiz-Argüello1, Ainara Maguregui1, Ainhoa Ruiz del Agua1, Dora Pascual-Salcedo2, Ana Martínez2, Teresa Jurado3, Chamaida Plasencia4, Alejandro Balsa5, Francisca Llinares-Tello6, José Rosas7, Nerea Torres1, Antonio Martínez1 and Daniel Nagore1, 1R&D, Progenika-Grifols, Derio, Spain, 2Immunology Unit, La Paz University Hospital-Immunology, Madrid, Spain, 3Immunology, La Paz University Hospital-Idipaz, Madrid, Spain, 4Rheumatology Unit, La Paz University Hospital-Rheumatology, Madrid, Spain, 5Rheumatology, La Paz University Hospital-Rheumatology Department, Madrid, Spain, 6Clinical Analysis, Hospital Marina Baixa, Clinical Analysis, Villajoyosa, Spain, 7Rheumatology, Hospital Marina Baixa, Villajoyosa, Spain

    Background/Purpose: Infliximab (IFX) is the most immunogenic of anti-TNFα drugs available to treat patients with rheumatic diseases. The recent approval of the first infliximab biosimilars in…
  • Abstract Number: 2362 • 2015 ACR/ARHP Annual Meeting

    Rituximab in the Treatment of Jo-1 Antibody-Associated Antisynthetase Syndrome: Anti-Ro52 Positivity As a Marker for Severity and Treatment Response

    Jutta Bauhammer1, Norbert Blank2, Hanns-Martin Lorenz3, Regina Max4, Dietmar Krause5 and Christoph Fiehn1, 1ACURA Centre for Rheumatic Diseases, Baden-Baden, Germany, 2Dept. of Internal Medicine 5, Division of Rheumatology, University of Heidelberg, Heidelberg, Germany, 3Department of Internal Medicine 5, Division of Rheumatology, University of Heidelberg, Heidelberg, Germany, 4Dept. of Internal Medicine 5, Division of Rheumatology, University of Heidelberg, Heidelberg, Germany, 5Dept. of Medical Informatics, Biometry and Epidemiology, Ruhr University Bochum, Bochum, Germany

    Background/Purpose: Rituximab (RIX) has successfully been used for the treatment of severe Jo-1 antibody-associated antisynthetase syndrome (Jo-1 ASS). The aim of this retrospective study was…
  • Abstract Number: 405 • 2015 ACR/ARHP Annual Meeting

    Anti-C1q Antibodies As Potential Diagnostic and Prognostic Biomarkers in Juvenile Systemic Lupus Erythematosus

    Thaschawee Arkachaisri1,2, Justin Hung Tiong Tan1, Manasita Tanya1, Sook Fun Hoh3, Lena Das4 and Jing Yao Leong5,6, 1Rheumatology and Immunology, KK Women's and Children's Hospital, Singapore, Singapore, 2Paediatrics, Duke-NUS Graduate Medical School, Singapore, Singapore, 3Nursing, KK Women's and Children's Hospital, Singapore, Singapore, 4Dept of Rheumatology, Cincinnati Children`s Hospital Medical Center, Cincinnati, OH, 5Duke-National University of Singapore Graduate Medical School, Singapore, Singapore, 6SingHealth Translational Immunology and Inflammation Centre, Singapore Health Services Pte Ltd, Singapore, Singapore

    Background/Purpose: Anti-C1q antibodies (AC1q) were shown to strongly correlate with the occurrence and activity of lupus nephritis in adult SLE. Data of the antibodies in…
  • Abstract Number: 2367 • 2015 ACR/ARHP Annual Meeting

    Risk of Malignancy in Dermatomyositis with Anti-CADM-140/ Melanoma Differentiation- Associated Gene 5 Autoantibody

    Shinji Sato1, Takayoshi Kurabayashi1, Sho Sasaki2, Yasushi Koyama2, Shinichi Nogi3, Naofumi Chinen1, Chiho Yamada1 and Yasuo Suzuki1, 1Internal Medicine/ Rheumatology, Tokai University School of Medicine, Isehara, Japan, 2Internal Medicine/Rheumatology, Tokai University School of Medicine, Isehara, Japan, 3Division of Rheumatology, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan

    Background/Purpose: Anti-CADM-140/ Melanoma Differentiation-Associated Gene 5 (MDA5) antibody is found specifically in patients with dermatomyositis (DM). This autoantibody is associated with clinically amyopathic DM (CADM)…
  • Abstract Number: 483 • 2015 ACR/ARHP Annual Meeting

    Antibody to Malondialdehyde-Acetaldehyde (MAA) Adducts Serve As Biomarkers of Treatment Response in Rheumatoid Arthritis

    Ted R. Mikuls1, Brian Coburn1, Harlan Sayles2, Fang Yu3, Mary Brophy4, James R. O'Dell1, Lynell W. Klassen5 and Geoffrey M. Thiele1, 1Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE, 2University of Nebraska Medical Center, Omaha, NE, 3Public Health, University of Nebraska Medical Center, Omaha, NE, 4VA Boston Heathcare System, Boston, MA, 5Dept of Internal Medicine, Omaha VA Medical Center and University of Nebraska Medical Center, Omaha, NE

    Background/Purpose:   Previous reports have demonstrated that malondialdehyde-acetaldehyde (MAA) adducts are produced as a byproduct of oxidative stress and lipid peroxidation and are expressed in…
  • Abstract Number: 2376 • 2015 ACR/ARHP Annual Meeting

    Clinical Features in Dermatomyositis Patients with Novel Autoantibody to Small Ubiquitin-like Modifier Activating Enzymes (Anti-SAE Antibody) and Relationship to Interstitial Lung Disease: A Systematic Review of 29 Cases

    Sirada Panupattanapong1, Jessica Sun2 and Kevin Baszis1, 1Pediatrics, Division of Rheumatology, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO, 2Pediatric, Division of Rheumatology, Washington University School of Medicine, St. Louis Children's Hospital, St. Louis, MO

    Background/Purpose: Anti-SAE antibody is a novel myositis-specific antibody first described in 2007. SAE is an enzyme that facilitates sumoylation, leading to the formation of stable…
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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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