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Abstracts tagged "interleukins (IL)"

  • Abstract Number: 2145 • 2015 ACR/ARHP Annual Meeting

    Ixekizumab Improves Physical Function, Quality of Life, and Work Productivity in Biologic Disease-Modifying Antirheumatic Drug-Naive Patients with Active Psoriatic Arthritis

    Alice B. Gottlieb1, Philip J. Mease2, Raquel S. Cuchacovich3,4, Catherine L. Shuler5, Chen-Yen Lin5, Russel T. Burge5, Suvajit Samanta5, Chin H. Lee5 and Dafna D. Gladman6, 1Dermatology, Tufts Medical Center, Boston, MA, 2Department of Rheumatology, Swedish Medical Center and University of Washington, Seattle, WA, 3School of Medicine, Rheumatology Division, Indiana University, Indianapolis, IN, 4Bio Medicines Business Unit/Autoimmune Medical, Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly and Company, Indianapolis, IN, 6Department of Medicine, Division of Rheumatology, University of Toronto, Toronto, ON, Canada

    Background/Purpose: Psoriatic arthritis (PsA) is a chronic immune-mediated inflammatory disease associated with psoriasis, peripheral arthritis, enthesitis, dactylitis, and spondylitis. PsA has a significant negative impact…
  • Abstract Number: 2460 • 2015 ACR/ARHP Annual Meeting

    B10 Cells May be Involved in Controlling Disease Activity in Polyarticular Juvenile Idiopathic Arthritis Patients

    Qianzi Zhao1 and Lawrence K. Jung2, 1Rheumatology, Children's National Medical Center, Washington, DC, 2Pediatric Rheumatology, Children's National Medical Center, Washington, DC

    Background/Purpose: In addition to antibodies production, B cells have been shown to have down-regulatory function on immune response in both mouse and human. The down-regulatory…
  • Abstract Number: 2848 • 2015 ACR/ARHP Annual Meeting

    Network Meta-Analysis of Tumor Necrosis Factor, Interleukins, and Phosphodiesterase-4 Inhibitor in the Treatment of Psoriatic Arthritis

    Vibeke Strand1, M. Elaine Husni2, William Reichmann3, Keith Betts4, Jenny Griffith5, Yan Song3, Marci Beppu6 and Arijit Ganguli5, 1Biopharmaceutical Consultant, Portola Valley, CA, 2Rheumatology Dept A50, Cleveland Clinic Foundation, Cleveland, OH, 3Analysis Group Inc., Boston, MA, 4Analysis Group, Inc., Boston, MA, 5AbbVie Inc., North Chicago, IL, 6Abbvie, Newcastle, WA

    Background/Purpose: Multiple disease-modifying therapies for treatment of psoriatic arthritis (PsA) are available. However, there are limited data directly comparing these biologic therapies and the recently…
  • Abstract Number: 2853 • 2015 ACR/ARHP Annual Meeting

    Secukinumab Improves Skin Symptoms and Physical Functioning Compared with Ustekinumab in Patients with Moderate to Severe Psoriasis with Concomitant Psoriatic Arthritis: Subanalysis of a Randomized, Double Blind, Parallel-Group, Active Comparator-Controlled Phase 3b Trial

    Alice B. Gottlieb1, Diamant Thaci2, Andrew Blauvelt3, Marina Milutinovic4 and Shephard Mpofu4, 1Tufts Medical Center and Tufts University School of Medicine, Boston, MA, 2Comprehensive Center for Inflammation Medicine, University Hospital Schleswig-Holstein, Lübeck, Germany, 3Research Excellence & Personalized Patient Care, Oregon Medical Research Center, Portland, OR, 4Novartis Pharma AG, Basel, Switzerland

    Background/Purpose: Psoriatic arthritis (PsA) is a common comorbidity in patients (pts) with psoriasis. In the ongoing Phase 3b CLEAR study (NCT02074982), secukinumab, a fully human…
  • Abstract Number: 2883 • 2015 ACR/ARHP Annual Meeting

    Relationship Between Improvements in Fatigue and Signs & Symptoms of Active Psoriatic: Arthritis a Sub-Analysis of a Phase 3 Study with Secukinumab

    Laure Gossec1, Tore K. Kvien2, Philip G. Conaghan3, Mikkel Østergaard4, Juan D. Cañete5, C. Gaillez6, Shephard Mpofu6, Bintu Sherif7 and Steffen Jugl8, 1Rheumatology Department, Paris 06 University,Hôpital Pitié Salpêtrière, Paris, France, 2Dept of Rheumatology, Diakonhjemmet Hospital, Oslo, Norway, 3University of Leeds & NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds, United Kingdom, 4Center for Rheumatology and Spine Diseases, Glostrup Hospital, Copenhagen Center for Arthritis Research (COPECARE), Center for Rheumatology and Spine Diseases, Rigshospitalet - Glostrup, University of Copenhagen, Denmark, Glostrup, Denmark, 5Rheumatology, Hospital Clinic and IDIBAPS, Barcelona, Spain, 6Novartis Pharma AG, Basel, Switzerland, 7RTI Health Solutions, Durham, NC, 8BF I&D GPA, Health Economics and Outcomes Research, Novartis Pharma AG, Basel, Switzerland

    Background/Purpose:  Fatigue is highly important to patients (pts) with psoriatic arthritis (PsA). Secukinumab, an anti-interleukin-17A monoclonal antibody, significantly improved the signs and symptoms of active…
  • Abstract Number: 2039 • 2014 ACR/ARHP Annual Meeting

    Among Persons Assayed with Lower Serum Interleukin-1 Beta (IL-1β) Levels, Serum Androstenedione (Δ4A) and Testosterone (T) Were Significantly Lower in a Community-Based Cohort of Rheumatoid Arthritis Multi-Years before Clinical Onset (Pre-RA) Than in Non-RA Matched Control (CN) Subjects

    Alfonse T. Masi, Azeem A. Rehman and Jean C. Aldag, Medicine, University of Illinois College of Medicine at Peoria, Peoria, IL

    Background/Purpose: Dysregulations in androgenic-anabolic (A-A) steroids and cytokines are recognized in RA and pre-RA subjects (Rheum Dis Clin N Am 2005; 31: 131-60). However, deviations…
  • Abstract Number: 81 • 2014 ACR/ARHP Annual Meeting

    Elevated Peripheral Blood Leukocyte Inflammatory Gene Expression in Radiographic Progressors with Symptomatic Knee Osteoarthritis: NYU and OAI Cohorts

    Mukundan Attur1, Alexander Statnikov2, Svetlana Krasnokutsky Samuels1, Virginia B. Kraus3, Joanne Jordan4, Braxton D. Mitchell5, Michelle Yau6, Jyoti Patel1, Constantin F. Aliferis2, Marc C. Hochberg7, Jonathan Samuels1 and Steven B. Abramson8, 1Rheumatology, NYU Langone Medical Center, New York, NY, 2Center for Health Informatics and Bioinformatics, NYU Langone Medical Center, New York, NY, 3Medicine/Rheumatology, Duke University Medical Center, Durham, NC, 4Thurston Arthritis Research Center, The University of North Carolina at Chapel Hill, Chapel Hill, NC, 5Departments of Medicine and Epidemiology & Public Health, University of Maryland School of Medicine, Baltimore, MD, 6Epidemiology and Public Health, University of Maryland, Baltimore,, MD, 7Medicine, University of Maryland School of Medicine, Baltimore, MD, 8Dept of Rheumatology/Medicine, NYU Langone Medical Center, New York, NY

    Background/Purpose: We and others have demonstrated low grade inflammation exists in OA joint tissues, where it may contribute to disease pathogenesis. In the current studies…
  • Abstract Number: 1816 • 2014 ACR/ARHP Annual Meeting

    Toll-like Receptor 4-Induced Interleukin-1 Defines the Intestinal Microbiome and Mucosal Immune Response in Arthritis-Prone IL-1 Receptor Antagonist Deficient Mice

    Tom Ederveen1, Rebecca Rogier2, Jos Boekhorst1, Harm Wopereis3, Johan Garssen3, Sacha van Hijum1, Fons A.J. van de Loo2, Marije I. Koenders2, Wim B. van den Berg2 and Shahla Abdollahi-Roodsaz4, 1Centre for Molecular Bioinformatics Nijmegen (CMBI), Radboud university medical center, Nijmegen, Netherlands, 2Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 3Danone Research, Wageningen, Netherlands, 4Rheumatology, Radboud university medical center, Nijmegen, Netherlands

    Background/Purpose Interleukin-1 (IL-1) plays a pivotal role in inflammation and autoimmunity. Mice deficient in the IL-1 receptor antagonist (IL-1Ra-/-) spontaneously develop a T cell-driven autoimmune…
  • Abstract Number: 1746 • 2014 ACR/ARHP Annual Meeting

    Involvement of IL-17-Producing MAIT Cells in the Pathogenesis of Rheumatoid Arthritis

    Eri Hayashi1, Asako Chiba2, Mie Kitagaichi3, Kurisu Tada3, Ken Yamaji4, Naoto Tamura1, Yoshinari Takasaki3 and Sachiko Miyake2, 1Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 2Immunology, Juntendo University School of Medicine, Tokyo, Japan, 3Department of Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 4Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Mucosal-associated invariant T (MAIT) cells are a subset of innate-like lymphocytes which are restricted by the MHC-related molecule-1 (MR1) and express a semi-invariant TCRα…
  • Abstract Number: 1732 • 2014 ACR/ARHP Annual Meeting

    Attenuation of Sclerodermatous Graft Versus Host Disease (sclGVHD) in IL4RA Receptor-Deficient Mice

    Katia Urso1, Kelly Tsang2, Robert Lafyatis3 and Antonios O. Aliprantis2, 1Rheumatology, Brigham and Women's Hospital, Boston, MA, 2Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 3Rheumatology, Boston University School of Medicine, Boston, MA

    Background/Purpose Scleroderma is a rare autoimmune disease characterized by the accumulation of fibrotic tissue in multiple organs including the skin, gut and lungs. To date,…
  • Abstract Number: 1511 • 2014 ACR/ARHP Annual Meeting

    COVA322: A Clinical Stage Bispecific TNF/IL-17A Inhibitor for the Treatment of Inflammatory Diseases

    Wibke Lembke, Bernd Schlereth, Julian Bertschinger, Dragan Grabulovski and Mathias Locher, Covagen AG, Schlieren, Switzerland

    Background/Purpose: Biologic therapeutics such as TNF inhibitors have revolutionized the treatment of inflammatory diseases, including rheumatoid arthritis (RA), psoriasis and psoriatic arthritis. However, there is still…
  • Abstract Number: 1491 • 2014 ACR/ARHP Annual Meeting

    Discovery and Characterization of COVA322, a Clinical Stage Bispecific TNF/IL-17A Inhibitor for the Treatment of Inflammatory Diseases

    Dragan Grabulovski, Michela Silacci, Wibke Lembke, Wenjuan Zha, Richard Woods, Roger Santimaria, Julian Bertschinger and Mathias Locher, Covagen AG, Schlieren, Switzerland

    Background/Purpose: Biologics such as TNF inhibitors have revolutionized the treatment of inflammatory diseases including rheumatoid arthritis (RA), psoriasis and psoriatic arthritis. However, recent data suggest that…
  • Abstract Number: 1492 • 2014 ACR/ARHP Annual Meeting

    Safety and Tolerability of NNC0114­0006, an Anti-IL-21 Monoclonal Antibody, at Multiple s.c. Dose Levels in Patients with Rheumatoid Arthritis

    Frank Wagner1, Birte Skrumsager2 and Sergey Fitilev3, 1Charité Research Org GmbH, Berlin, Germany, 2Novo Nordisk A/S, Søborg, Denmark, 3Department of Clinical Pharmacology, Municipal Clinic #2, Moscow, Russia

    Background/Purpose A phase 1, randomised, double-blind, placebo-controlled, dose-escalation trial was conducted to assess the safety and tolerability of the anti-IL-21-antibody NNC0114-0006, in patients with active…
  • Abstract Number: 1459 • 2014 ACR/ARHP Annual Meeting

    IL-22 Secreted By NKp44+NK Cells Promote the Proliferation of Synovium in Patients with Rheumatoid Arthritis By Activation of STAT3

    Junqing Zhu1, Juan Li1 and Xiaoguang Chen2, 1Nanfang Hospital, College of Traditional Chinese Medicine, Southern Medical University, Guangzhou, China, 2School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou, China

    Background/Purpose: Although CD3-CD56+NKp44+ natural Killer cells (NKp44+NK cells) have been linked to autoimmune diseases including inflammatory bowel disease, ankylosing spondylitis, and primary Sjogren's syndrome, the…
  • Abstract Number: 1253 • 2014 ACR/ARHP Annual Meeting

    Anakinra – a Promising New Therapy for Idiopathic Recurrent Pericarditis

    Sonia Jain1, Charat Thongprayoon2, Raul Espinosa1, Sharonne Hayes1, Kyle Klarich1, Kevin Moder3, Nandan Anavekar1, Jae Oh1 and Eric L. Matteson4, 1Division of Cardiovascular Diseases, Mayo Clinic, Rochester, MN, 2Department of Medicine, Mayo clinic, Rochester, MN, 3Division of Rheumatology, Mayo Clinic, Rochester, MN, 4Rheumatology, Mayo Clinic, Rochester, MN

    Background/Purpose Idiopathic recurrent pericarditis (IRP) is a debilitating condition that can be recalcitrant to conventional therapy. Some patients develop steroid dependency with the attendant risks…
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Embargo Policy

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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