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  • Abstract Number: 3034 • 2016 ACR/ARHP Annual Meeting

    A Selective JAK1 Inhibitor, Filgotinib Suppresses Lymphocytic Infiltration in Salivary Gland of Non Obese Diabetic Mice Via Suppression of BAFF and Chemokine Production of Salivary Gland Epithelial Cells

    Jennifer Lee1, Seo Hwa Kim2, Haneul Kim3, Seung-Ki Kwok4, Ji Hyeon Ju5 and Sung-Hwan Park5, 1Division of Rheumatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea, Republic of, 2Division of Rheumatology,, Division of Rheumatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea, The Republic of, 3Division of Rheumatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea, The Republic of, 4[email protected], Division of Rheumatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea, 5Division of Rheumatology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, South Korea

    Background/Purpose:  Interferon(IFN) signatures are upregulated in patients with primary Sjogren’s syndrome (pSS) and interferons are considered to play a pathogenic role in pSS. Therefore, Janus…
  • Abstract Number: 3035 • 2016 ACR/ARHP Annual Meeting

    Characterization of DC-STAMP+ T Cells, a CD3+CD4+ T Cell Subset Uniquely Present in Patients with Psoriatic Disease

    Yahui Grace Chiu1, Edward Schwarz2, Richard Bell3, Dongge Li4, Nelson Huertas4, Cristy Bell5, Sharon Moorehead5, Debbie Campbell5, Changyong Feng6 and Christopher T. Ritchlin7, 1Allergy, Immunology, and Rheumatology, University of Rochester Medical Center, Rochester, NY, 2Orthopedeatrics, University of Rochester, Rochester, NY, 3Pathology, University of Rochester, Rochester, NY, 4Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 5Allergy, Immunology & Rheumatology, University of Rochester, Rochester, NY, 6Statistics, University of Rochester, Rochester, NY, 7Allergy Immunology & Rheumatology, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Psoriatic arthritis (PsA) is an inflammatory joint disease that affects over 650,000 Americans. Bone damage occurs in half of these patients within the first…
  • Abstract Number: 3036 • 2016 ACR/ARHP Annual Meeting

    IL-22 Is Dysregulated in Psoriatic Arthritis and Acts to Limit IFN-γ Driven Inflammatory Chemokine Production

    Amara Ezeonyeji1, Helen Baldwin2, Milica Vukmanovic-Stejic3 and Michael R. Ehrenstein4, 1Rheumatology, Medicine, University College London, London, United Kingdom, 2Rheumatology, Centre for Rheumatology Research, University College London, london, United Kingdom, 3Infection & Immunity, University College London, london, United Kingdom, 4Medicine, University College London, London, United Kingdom

    Background/Purpose: IL-22 is an IL-10 family cytokine with both pro-inflammatory and anti-inflammatory effects and its dysregulation is associated with the development of autoimmune disease including…
  • Abstract Number: 3037 • 2016 ACR/ARHP Annual Meeting

    Calprotectin Is Highly Upregulated in Inflamed Axial Entheses in SKG Mice

    Zheni Stavre1, Yukiko Maeda2 and Ellen M. Gravallese3, 1Internal Medicine-Rheumatology, University of Massachusetts Medical School, Worcester, MA, 2Medicine, University of Massachusetts Medical School, Worcester, MA, 3Lazare Research Bldg, University of Massachusetts Medical School, Worcester, MA

    Background/Purpose:  SKG mice exhibit features of spondyloarthropathy (SpA) and inflammatory bowel disease (IBD). Their SpA-like phenotype is induced by a beta-glucan, curdlan, via the Dectin-1…
  • Abstract Number: 3038 • 2016 ACR/ARHP Annual Meeting

    Enumeration and Preliminary Characterisation of Peri-Entheseal Bone Type 3 Innate Lymphoid Cells

    Richard Cuthbert1, Yasser El-Sherbiny1, Evangelos M. Fragkakis1, Robert Dunsmuir2, Helena Marzo-Ortega3, Elena Jones1 and Dennis McGonagle1, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2Department of Spinal Surgery, National Health Service, Leeds, United Kingdom, 3NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals and University of Leeds, Leeds, United Kingdom

    Background/Purpose:  In an IL-23 overexpression animal model of spondyloarthropathy (SpA), primary entheseal disease is driven by innate like lymphocytes at peripheral and spinal enthesis with…
  • Abstract Number: 3039 • 2016 ACR/ARHP Annual Meeting

    Anti-IL-17A, but Not Anti-TNF, Can Halt Pathological New Bone Formation in Experimental Spondyloarthritis

    Melissa van Tok1, Leonie van Duivenvoorde1, Ina Kramer2, Peter Ingold2, Veronique Knaup1, Joel Taurog3, Frank Kolbinger4 and Dominique Baeten5, 1Academic Medical Center, Amsterdam, Netherlands, 2Novartis Institutes for Biomedical Research, Basel, Switzerland, 3Dept Int Med-Rheum Dis Div, University of Texas Southwestern Medical Center, Dallas, TX, 4Novartis Institutes for BioMedical Research, Novartis Pharma AG, Basel, Switzerland, 5Amsterdam Rheumatology and immunology Center, Amsterdam, Netherlands

    Background/Purpose: Secukinumab, a monocloncal antibody to IL-17A, suppresses signs and symptoms as well as inflammation in ankylosing spondylitis and psoriatic arthritis, and inhibits bone and…
  • Abstract Number: 3040 • 2016 ACR/ARHP Annual Meeting

    Th17 Migration into the Synovial Fluid of Patients with Active Psoriatic Arthritis Is Enhanced By Regulatory T Cells

    Helen Baldwin1, Amara Ezeonyeji2, Mohammed Rohan Butt2 and Michael R. Ehrenstein3, 1Rheumatology, University College London, London, United Kingdom, 2Rheumatology, Medicine, University College London, London, United Kingdom, 3Medicine, University College London, London, United Kingdom

    Background/Purpose: Uncontrolled migration of Th17 cells into the skin and joints is a major driver in the pathogenesis of psoriatic arthritis (PsA). Modulation of T…
  • Abstract Number: 3041 • 2016 ACR/ARHP Annual Meeting

    Age-Related Defects in the Immune System of Patients with GCA

    Zhenke Wen1, Yasuhiro Shimojima2, Gerald Berry3, Ebru Hosgur1, Joyce Liao4, Lindsy Forbess5, Michael Weisman6, Jorg Goronzy7 and Cornelia M. Weyand1, 1Medicine: Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 2Internal Medicine, Shinshu University School of Medicine, Matsumoto, Japan, 3Pathology, Stanford University School of Medicine, Stanford, CA, 4Byers Eye Institute at Stanford, Stanford University, Palo Alto, CA, 5Rheumatology, Cedars-Sinai, Los Angeles, CA, 6Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 7Medicine/Division of Immunology & Rheumatology, Stanford University School of Medicine, Stanford, CA

    Background/Purpose:  Advancing age is the strongest risk factor for GCA, a disease that exclusively affects individuals >50 years of age. The immune system undergoes dramatic…
  • Abstract Number: 3042 • 2016 ACR/ARHP Annual Meeting

    PD-1–Expressing T Cells in GCA Fail to Promote Immune Tolerance Functions

    Ryu Watanabe1, Hui Zhang2, Ebru Hosgur2, Gerald Berry3, Jorg Goronzy4 and Cornelia M. Weyand2, 1Medicine: Immunology/Rheumatology, Stanford University School of Medicine, Stanford, CA, 2Medicine: Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 3Pathology, Stanford University School of Medicine, Stanford, CA, 4Medicine/Division of Immunology & Rheumatology, Stanford University School of Medicine, Stanford, CA

    Background/Purpose:  The vasculitic lesions in GCA are filled with differentiated effector T cells that sustain granuloma formation, vessel wall restructuring, neoangiogenesis and intimal hyperplasia. Persistent…
  • Abstract Number: 3043 • 2016 ACR/ARHP Annual Meeting

    Dense Genotyping of Immune Related Loci in a Multi-Ethnic Behçet’s Disease Cohort Identifies Genetic Associations in a Long Noncoding RNA Near QSOX2, RASIP1/FUT2, and IL12A-AS1

    Paul Renauer1, Patrick Coit1, Travis Hughes2, Mikhail Ognenovski1, Adam Adler3, Lourdes Ortiz-Fernández4, Vuslat Yilmaz5, Kenan Aksu6, Nursen Duzgun7, Gokhan Keser8, Ayse Cefle9, Ayten Yazici10, Andac Ergen11, Erkan Alpsoy12, Carlo Salvarani13, Bruno Casali14, Ina Koetter15, Alexandra Zhernakova16, Cisca Wijmenga17, Fujio Takeuchi18, Shinji Harihara19, Toshikatsu Kaburaki20, Yeong Wook Song21, Francisco David Carmona22, Marta E. Alarcon Riquelme23, Javier Martín22, Güher Saruhan-Direskeneli24, María Francisca Gonzalez Escribano25, Haner Direskeneli26 and Amr H Sawalha1, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Division of Health Sciences and Technology, Harvard Medical School, Boston, MA, 3Oklahoma Medical Research Foundation, OK, OK, 4Immunology department, Hospital Universitario Virgen del Rocío, Sevilla, Spain, 5Istanbul University, Istanbul Faculty of Medicine, Department of Physiology, Istanbul, Turkey, 6İnternal Medicine Division of Rheumatology, Ege University Medical Faculty, Izmir, Turkey, 7Internal Medicines, Rheumatology Department, Ankara University School of Medicine, Ankara, Turkey, 8Rheumatology, Ege University Medical Faculty, Izmir, Turkey, 9Rheumatology, Kocaeli University Faculty of Medicine, Kocaeli, Turkey, 10Rheumatology, Kocaeli University School of Medicine, Kocaeli, Turkey, 11Okmeydaný Research and Education Hospital, Istanbul, Turkey, 12Department of Dermatology, Akdeniz University School of Medicine, Antalya, Turkey, 13Rheumatology, Azienda Ospedaliera ASMN, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy, 14Molecular Biology Laboratory, Azienda Ospedaliera Arcispedale Santa Maria Nuova, Istituto di Ricovero e Cura a Carattere Scientifico, Reggio Emilia, Italy, 15Internal Medicine IV Rheumatology, Asklepios Klinik Altona, Hamburg, Germany, 16Rheumatology and Clinical Immunology, University of Groningen, University Medical Center, Groningen, Netherlands, 17Genetics, University Medical Hospital Groningen, University of Groningen, Groningen, Netherlands, 18#504 Lab/ Dep of Internal Medicine (Allergy & Rheumatology), Faculty of Medicine, University of Toyko, Tokyo, Japan, 19Division of Anthropology, Department of Biological Science, The University of Tokyo Graduate School of Science, Tokyo, Japan, 20Ophthalmology, The University of Tokyo School of Medicine, Bunkyo-ku, Japan, 21Department of Molecular Medicine and Biopharmaceutical Sciences, Graduate School of Convergence Science and Technology, Seoul National University, Seoul, South Korea, 22Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, PTS-Granada, Granada, Spain, 23Centro de Genomica e Investigación Oncológica, Pfizer-University of Granada-Junta de Andalucía, Granada, Spain, 24Department of Physiology, Istanbul Faculty of Medicine, Istanbul University, Istanbul, Turkey, 25Hospital Universitario Virgen del Rocío (IBiS,CSIC,US), Sevilla, Spain, 26Rheumatology, Marmara University, School of Medicine, Istanbul, Turkey

    Background/Purpose:  Behçet’s disease is a chronic relapsing inflammatory disease characterized by recurrent mucocutaneous involvement. We performed dense genotyping in immune related loci in a large…
  • Abstract Number: 3044 • 2016 ACR/ARHP Annual Meeting

    Endothelin 1 Induces a Myofibroblastic Phenotype in Vascular Smooth Muscle Cells. A Mechanism Potentially Contributing to Vascular Remodeling and Intimal Hyperplasia in Giant Cell Arteritis

    Ester Planas-Rigol1, Nekane Terrades-Garcia2, Marc Corbera-Bellalta2, Ester Lozano2, Marco Antonio Alba2, Georgina Espígol-Frigolé3, Sergio Prieto-González2, Marta Segarra2, Jose Hernández-Rodríguez2, Sara Preciado4, Rodolfo Lavilla4 and Maria C. Cid2, 1Vasculitis research unit. Department of Autoimmune Diseases, Hospital Clínic. University of Barcelona. IDIBAPS, Barcelona, Spain, 2Vasculitis Research Unit. Department of Autoimmune Diseases, Hospital Clínic. University of Barcelona. IDIBAPS, Barcelona, Spain, 3Vasculitis Research Unit, Systemic Autoimmune Diseases, Hospital Clínic. University of Barcelona. IDIBAPS, Barcelona, Spain, 4Laboratory of Organic Chemistry, Faculty of Pharmacy. Barcelona Science Park, Barcelona, Spain

    Background/Purpose: Giant cell arteritis (GCA) is a vascular inflammatory disease involving large and medium sized arteries, particularly the cranial vessels. Inflammation-induced vascular remodeling leads to…
  • Abstract Number: 3045 • 2016 ACR/ARHP Annual Meeting

    Immunometabolism in ANCA-Associated Glomerulonephritis

    Peter C. Grayson1, Sean Eddy2, Viji Nair2, Hemang Parikh3, Maja Lindenmeyer4, Laura Mariani2, Huateng Huang2, Wenjun Ju3, Casey Greene5, Clemens Cohen4, Jeffrey Krischer3, Matthias Kretzler2, Peter A. Merkel6 and Felix H. Eichinger2, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Division of Nephrology, University of Michigan, Ann Arbor, MI, 3University of South Florida, Tampa, FL, 4University of Munich, Munich, Germany, 5Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, 6Division of Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Mounting an inflammatory response requires immune cells to undergo major changes in metabolism. Mediators such as cytokines can specifically alter the metabolism of different…
  • Abstract Number: 3046 • 2016 ACR/ARHP Annual Meeting

    Inflammatory Pathways As Shared Molecular Targets Across ANCA-Associated Vasculitis and Nephrotic Syndrome

    Sean Eddy1, Viji Nair1, Hemang Parikh2, Maja Lindenmeyer3, Laura Mariani1, Felix H. Eichinger1, Huateng Huang1, Wenjun Ju2, Casey Greene4, Peter C. Grayson5, Clemens Cohen3, Jeffrey Krischer2, Peter A. Merkel6 and Matthias Kretzler1, 1Division of Nephrology, University of Michigan, Ann Arbor, MI, 2University of South Florida, Tampa, FL, 3University of Munich, Munich, Germany, 4Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, PA, 5National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 6Division of Rheumatology, University of Pennsylvania, Philadelphia, PA

    Background/Purpose: Clinical trials in rare diseases typically test therapeutic efficacy in one disease defined by a particular clinical phenotype. Improved understanding of the molecular mechanisms…
  • Abstract Number: 3047 • 2016 ACR/ARHP Annual Meeting

    Diabetes and BMI Modify the Association Between Painful Hip OA and All-Cause Mortality

    Rebecca Cleveland1, Todd A. Schwartz2, Jordan B. Renner3, Leigh F. Callahan1 and Joanne M. Jordan1, 1Thurston Arthritis Research Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, 2Department of Biostatistics, Gillings School of Global Public Health, University of North Carolina at Chapel Hill, Chapel Hill, NC, 3Radiology, University of North Carolina at Chapel Hill, Chapel Hill, NC

    Background/Purpose: Individuals with specific comorbid conditions have increased risk of having hip osteoarthritis (OA). Some of these conditions are also associated with increased risk of…
  • Abstract Number: 3048 • 2016 ACR/ARHP Annual Meeting

    Pain Severity As a Mediator of the Effect of Depressive Symptoms on Physical Performance in Knee Osteoarthritis

    Alan Rathbun1, Michelle Shardell2, Michelle S. Yau3, Mona Baumgarten4, Elizabeth Stuart5 and Marc Hochberg6, 1Epidemiology and Public Health, University of Maryland School of Medicine, Baltimore, MD, 2Translational Gerontology Branch, National Institute on Aging, Baltimore, MD, 3Clinical Epidemiology Research and Training Unit, Boston University School of Medicine, Boston, MA, 4University of Maryland School of Medicine, Baltimore, MD, 5Mental Health, Biostatistics, and Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, 6Department of Medicine, University of Maryland School of Medicine, Baltimore, MD

    Background/Purpose: Depression is a significant comorbidity of knee osteoarthritis (OA) that occurs in approximately 20% of OA patients. Depressive symptoms are associated with both subsequent…
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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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