ACR Meeting Abstracts

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  • Abstract Number: 1753 • 2014 ACR/ARHP Annual Meeting

    Human T-Cells Express RANKL in Response to Combination of ZAP-70, Calcineurin and Voltage-Gated K+-Channel Signaling Following Co-Ligation of the Adhesion Molecule CD2 and the T-Cell Receptor Complex

    Bohdan P. Harvey and Zehra Kaymakcalan, Biologics, AbbVie Bioresearch Center, Worcester, MA

    Background/Purpose Human T lymphocytes promote osteolysis in rheumatic diseases through the production of the osteoclastogenic cytokine RANKL.  We have previously demonstrated that RANKL secretion is…
  • Abstract Number: 1752 • 2014 ACR/ARHP Annual Meeting

    CD30 As a Target of Aptamers and Delivery Portal for Aptamer-shRNA to Block Th17 Cells

    Cong-Qiu Chu1, Pingfang Song2, Yuan K. Chou3 and Shao Tao2, 1Rheumatology, Oregon Health & Science Univ, Portland, OR, 2Oregon Health & Science University, Portland, OR, 3Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University, Portland, OR

    Background/Purpose Aptamers are single-stranded 20 –100 nucleotides (RNA or DNA) that bind to molecular targets with high affinity and specificity due to their stable three…
  • Abstract Number: 1751 • 2014 ACR/ARHP Annual Meeting

    CD4 Aptamer-RORγt shRNA Chimera Inhibits IL-17 Synthesis By Human CD4+ T cells

    Cong-Qiu Chu1, Pingfang Song2, Yuan K. Chou3, Xiaowei Zhang2, Roberto Meza-Romero2, Kentaro Yomogida3 and Gil Benedek2, 1Rheumatology, Oregon Health & Science Univ, Portland, OR, 2Oregon Health & Science University, Portland, OR, 3Division of Arthritis and Rheumatic Diseases, Oregon Health & Science University, Portland, OR

    Background/Purpose RNA interfering (RNAi)-mediated gene silencing holds great promise for manipulating T cells to study basic T cell biology and for developing potential T cell…
  • Abstract Number: 1750 • 2014 ACR/ARHP Annual Meeting

    The Effect of a Pro-Inflammatory Milieu on Tregalizumab (BT-061)-Induced Regulatory T-Cell Activity

    Jan Kubach1, Faiza Rharbaoui2, Martin Koenig2, Jörg Schüttrumpf2, Silke Aigner2, Benjamin Dälken2 and Helmut Jonuleit1, 1Department of Dermatology, University of Mainz Medical Center, Mainz, Germany, 2Biotest AG, Dreieich, Germany

    Background/Purpose Regulatory T cells (Tregs) are essential for maintaining normal immune homeostasis. We have previously reported that tregalizumab is a humanized, non-depleting, CD4 agonistic antibody…
  • Abstract Number: 1749 • 2014 ACR/ARHP Annual Meeting

    Molecular Mechanisms Underlying 1,25(OH)2D3-Mediated Suppression of Th17 Cell Activity

    Wendy Dankers1,2, Jan Piet van Hamburg2,3, Wida Razawy1,2, Nadine Davelaar1,2, Anne-Marie Mus1,2, Patrick Asmawidjaja1,2, Johannes van Leeuwen4, Edgar Colin5 and Erik Lubberts1,2, 1Rheumatology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 2Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, Rotterdam, Netherlands, 4Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 5Rheumatology, ZGT, Almelo, Netherlands

    Background/Purpose Vitamin D has suppressive effects on autoimmune diseases, such as rheumatoid arthritis (RA). Within these diseases, Th17 cells play a crucial role in the…
  • Abstract Number: 1748 • 2014 ACR/ARHP Annual Meeting

    CCR6+CD4+ Cells Are Counterparts of Follicular T-Cells Supporting Autoantibody Production in Rheumatoid Arthritis

    Karin ME Andersson1, Dan Hu2, Ron Cialic2, Nicola Cavallini3, Vijay K. Kuchroo4, Malin Erlandsson1, Howard Lee Weiner2 and Maria Bokarewa5, 1Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden, 2Center for Neurologic Diseases, Department of Neurology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 3Rheumatology and Inflammation Research, University of Göteborg, Göteborg, Sweden, 4Department of Neurology, Brigham and Women's Hospital, Boston, MA, 5Guldhedsgatan 10, University of Goteborg, Goteborg, Sweden

    Background/Purpose CCR6 has been associated with rheumatoid arthritis (RA) in genome-wide association studies. CCR6 expression characterises Th17 cells recruited to inflamed joints of RA patients.…
  • 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: 1745 • 2014 ACR/ARHP Annual Meeting

    Memory Stem T Cells Are Selectively Enriched in Patients with Rheumatoid Arthritis, Contract upon Anti-TNF Treatment, and May Provide a Long-Term Reservoir of Arthritogenic Lymphocytes

    Nicoletta Cieri1, Giacomo Oliveira1, Raffaella Greco2, Mattia Baldini3, Elena Baldissera4, Fabio Ciceri2 and Chiara Bonini1, 1Division of Immunology, Infectious Diseases and Transplants, Experimental Hematology Unit, San Raffaele Scientific Institute, Milan, Italy, 2Division of Regenerative Medicine, Gene Therapy and Stem Cells, Hematology and Bone Marrow Transplantation Unit, San Raffaele Scientific Institute, Milan, Italy, 3Division of Immunology, Infectious Diseases and Transplants, Clinical immunopathology and advanced medical therapeutics, San Raffaele Scientific Institute, Milan, Italy, 4Clinical immunopathology and advanced medical therapeutics, San Raffaele Scientific Institute, Milan, Italy

    Background/Purpose: the T-cell memory compartment is multi-faceted and encompasses multiple subsets with divergent properties. In addition to central memory (TCM) and effector memory (TEM) cells,…
  • Abstract Number: 1764 • 2014 ACR/ARHP Annual Meeting

    Clinical and Other Differences Observed Between Cocaine Induced and Non-Cocaine Induced Anti-Neutrophil Cytoplasmic Antibody Positive Vasculitis

    Santhi Penmetsa1, N. Suzanne Emil2, Joshua Duchesne1, Wilmer Sibbitt Jr.3, Arthur Bankhurst4 and Roderick Fields5, 1Rheumatology, University of New Mexico Health sciences center, Albuquerque, NM, 2Rheumatology, Presbyterian Medical Group, Rio Rancho, NM, 3Rheumatology, University of New mexico health sciences center, Albuquerque, NM, 4Rheum/ MSC 105550, University of NM Med Ctr, Albuquerque, NM, 5Division of Rheumatology, University of New Mexico health Sciences center, Albuquerque, NM

    Background/Purpose Objective: To compare various factors including clinical manifestations, laboratory data and mortality in between two groups of patients with anti-neutrophil cytoplasmic antibody (ANCA) positive…
  • Abstract Number: 1763 • 2014 ACR/ARHP Annual Meeting

    Tobacco Differentially Affects the Clinical-Biological Phenotype of ANCA-Associated Vasculitides at Diagnosis

    Lucas Benarous1, Benjamin Terrier2, Bertrand Dunogué3, Pascal Cohen4, Xavier Puéchal4, Claire Le Jeunne4, Luc Mouthon4 and Loïc Guillevin for the French Vasculitis Study Group4, 1Cochin Hospital, Paris, France, 2National Referral Center for Rare Systemic Autoimmune Diseases, Cochin Hospital, Paris, France, 3Internal Medicine, Hôpital Cochin, Paris, France, 4National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, Paris, France

    Background/Purpose Occupational and non-occupational exposures may play a role in the occurrence of ANCA-associated vasculitides (AAV) and affect their initial clinical-biological phenotype. Among these potential…
  • Abstract Number: 1762 • 2014 ACR/ARHP Annual Meeting

    The Muscle Biopsy Is a Useful and Noninvasive Procedure in Diagnosing Systemic Vasculitis Affecting Small-to-Medium-Sized Vessels: A Prospective Evaluation

    Takahiro Nunokawa1, Takayasu Kise1, Naoto Yokogawa2, Kota Shimada1 and Shoji Sugii2, 1Department of Rheumatic diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan, 2Department of Rheumatic Diseases, Tokyo Metropolitan Tama Medical Center, Tokyo, Japan

    Background/Purpose: Histopathological confirmation is required for the diagnosis of systemic vasculitis. However, patients suspected of vasculitis often only have lesions with a low diagnostic yield…
  • Abstract Number: 1761 • 2014 ACR/ARHP Annual Meeting

    Standardisation of Disease Assesment in Systemic Vasculitis: Use of a Novel Web-Based Software Training Application

    Jan Sznajd1,2, Joe Rosa1, David Gray3, Jennifer O'Donoghue1, Joanna Robson1, Surjeet Singh1, Richard Philipson4, Judith Brown4, Thor Ostenfeld4 and Raashid Luqmani5, 1Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom, 2Jagiellonian University Medical College, Krakow, Poland, 3Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, Nuffield Department of Orthopaedics Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom, 4GlaxoSmithKline R&D, Brentford, United Kingdom, 5Oxford NIHR Musculoskeletal Biomedical Research Unit, Oxford, United Kingdom

    Background/Purpose The Birmingham Vasculitis Activity Score (BVAS) and Vasculitis Damage Index (VDI) are validated clinical assessment tools for the systemic vasculitides. However use of BVAS…
  • Abstract Number: 1744 • 2014 ACR/ARHP Annual Meeting

    CD4+ T Cell Subpopulations in Blood and Synovial Fluid Defined By Differential Expression of Integrins

    Deepak A. Rao1, Adam Chicoine2, Peter A. Nigrovic3, Soumya Raychaudhuri4, Michael B. Brenner5 and ACR Authors 2014, 1Rheumatology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Rheumatology, Immunology, Allergy, Brigham and Women's Hospital, Boston, MA, 3Brigham and Women's Hospital/Harvard University, Cambridge, MA, 4Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 5Division of Rheumatology, Immunology, and Allergy, Brigham & Women's Hospital, Harvard Medical School, Boston, MA

    Background/Purpose CD4+ T cells are important mediators of inflammation in rheumatoid arthritis; however, the specific CD4+ T cell populations most important in driving disease pathology…
  • Abstract Number: 1743 • 2014 ACR/ARHP Annual Meeting

    Antigen-Specificity Regulates Peripheral Homeostasis of Regulatory T Cells

    Laura Su1 and Mark Davis2, 1Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Microbiology, Stanford, Stanford, CA

    Background/Purpose One key mechanism of peripheral tolerance involves regulatory T cells (Tregs).  Tregs are best known for the expression of the transcription factor Foxp3 that…
  • Abstract Number: 1742 • 2014 ACR/ARHP Annual Meeting

    Depletion of Reactive Oxygen Species Biases T Cells to Proinflammatory Cytokine Production in Rheumatoid Arthritis

    Zhen Yang1, Eric L. Matteson2, Jorg J. Goronzy1 and Cornelia M. Weyand3, 1Medicine: Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 2Rheumatology, Mayo Clinic, Rochester, MN, 3Medicine, Stanford University School of Medicine, Stanford, CA

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic inflammatory disease, genetically associated with polymorphisms in HLA class II molecules. CD4 cells produce proinflammatory cytokines and orchestrate…
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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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