ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 2880 • 2016 ACR/ARHP Annual Meeting

    Distinct Metabolic Pathways Regulate Lipid Antigen Presentation By Monocytes and B Cells: Implications for SLE Patients with Pre-Clinical Atherosclerotic Plaque

    Kirsty Waddington1, Edward Smith2, Sara Croca3, David A. Isenberg4, Anisur Rahman5, Ines Pineda Torra6 and Elizabeth Jury7, 1Clinical Pharmacology and Rheumatology, University College London, London, United Kingdom, 2Centre for Rheumatology Research, University College London, London, United Kingdom, 3Rheumatology, University College London, London, United Kingdom, 4Centre for Rheumatology Research, University College Hospital London, UK, London, United Kingdom, 5Rayne Institute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom, 6Clinical Pharmacology, University College London, London, United Kingdom, 7Division of Medicine, Centre for Rheumatology Research, University College London, London, United Kingdom

    Background/Purpose:  Systemic lupus erythematosus (SLE) patients have an increased risk of developing clinically apparent cardiovascular disease (CVD) and subclinical atherosclerotic plaque, detectable by vascular ultrasound…
  • Abstract Number: 2881 • 2016 ACR/ARHP Annual Meeting

    Reduced Hippocampal-Thalamic Fiber Tracts in Systemic Lupus Erythematosus

    Meggan Mackay1, Pooneh Heshmati2, An Vo2, Cynthia Aranow2, Bruce Volpe2, Betty Diamond3 and David Eidelberg2, 1Autoimmune & Musculoskeletal Disorders, The Feinstein Institute for Medical Research, Manhasset, NY, 2The Feinstein Institute for Medical Research, Manhasset, NY, 3Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: SLE patients experience deterioration in cognitive function over time but attribution to disease-related mechanisms is confounded by medication effects, psychiatric disease, hormonal influences and…
  • Abstract Number: 2882 • 2016 ACR/ARHP Annual Meeting

    CD4+ T Helper Cells and Regulatory T Cells in Active Lupus Nephritis – an Imbalance Towards a Predominant Th1 Response?

    Danilo Mesquita Jr.1, Marcello Fabiano Franco2, Gianna Mastroianni Kirsztajn1, Luciana Aparecida Reis1, Sandro Perazzio3, Fernanda Vieira Mesquita1, Vanessa Ferreira1, Luis E C Andrade4 and Alexandre W.S. Souza5, 1Internal Medicine, Universidade Federal de São Paulo, São Paulo, Brazil, 2Pathology, Universidade Federal de São Paulo, São Paulo, Brazil, 3Rheumatology Division, Universidade Federal de São Paulo, Sao Paulo, Brazil, 4Pediatric Rheumatology Unit, Universidade Federal de São Paulo, São Paulo, Brazil, 5Universidade Federal de São Paulo, São Paulo, Brazil

    Background/Purpose:  Systemic lupus erythematosus (SLE) is a chronic inflammatory disease characterized by the involvement of multiple organs and systems with aberrations in T cell response,…
  • Abstract Number: 2883 • 2016 ACR/ARHP Annual Meeting

    The CD4+CD52low T Cell Contributes to the Development of Systemic Lupus Erythematosus through the CCR8/TARC Pathway

    Tomohito Sato1, Masataka Umeda1, Tomohiro Koga2, Takashi Igawa1, Syota Kurushima1, Ayuko Takatani1, Toshimasa Shimizu1, Shoichi Fukui1, Ayako Nishino1, Yoshiro Horai1, Shinya Kawashiri1, Naoki Iwamoto1, Yasuko Hirai1, Mami Tamai1, Hideki Nakamura1, Tomoki Origuchi3 and Atsushi Kawakami4, 1Department of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan, 2Department of Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan, 3Department of Rehabilitation Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 4Department of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki City, Japan

    Background/Purpose: CD52 is a cell-surface glycoprotein that is widely expressed in lymphocytes, monocytes and eosinophils. CD4+CD52high T cells inhibit the activation of CD4+CD52low T cells…
  • Abstract Number: 2884 • 2016 ACR/ARHP Annual Meeting

    Cell-Type Specific Epigenetic Features of Systemic Lupus Erythematosus

    Neelakshi R. Jog1, Richard C. Pelikan1, Melissa Bebak2, Joel M. Guthridge3, Judith A. James1 and Patrick M. Gaffney1, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma city, OK, 3Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a systemic autoimmune disease that involves multiple organ systems and periods of variable disease activity. Although SLE, especially in…
  • Abstract Number: 2885 • 2016 ACR/ARHP Annual Meeting

    Expression Levels and Function of the Inhibitory Molecule, Immunoglobulin like Transcript 7 (ILT7), Are Decreased on Circulating Plasmacytoid Dendritic Cells in SLE Patients with High ANA Titers

    Mark A. Jensen1, Jessica M. Dorschner2, Danielle Vsetecka2, Shreyasee Amin3, Ashima Makol3, Floranne C. Ernste4, Thomas Osborn3, Kevin Moder3, Vaidehi Chowdhary3 and Timothy B. Niewold5, 1Department of Immunology and Division of Rheumatology, Mayo Clinic, Rochester, MN, 2Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 3Rheumatology, Mayo Clinic, Rochester, MN, 4Division of Rheumatology, Mayo Clinic Rochester, Rochester, MN, 5Rheumatology and Immunology, Mayo Clinic, Rochester, MN

    Background/Purpose:  Systemic lupus erythematous (SLE) is a complex autoimmune disease often involving multiple organs. In SLE, immune complexes containing autoreactive antibody and nuclear material activate…
  • Abstract Number: 2886 • 2016 ACR/ARHP Annual Meeting

    Associations Between Type I Interferon and Antiphospholipid Antibody Status Differ Between Ancestral Backgrounds

    Taro Iwamoto1, Meenakshi Jolly2 and Timothy B. Niewold3, 1Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 2Rush, Chicago, IL, 3Rheumatology and Immunology, Mayo Clinic, Rochester, MN

    Background/Purpose:  Autoantibodies in SLE that bind to double-stranded DNA or RNA-binding proteins are strongly associated with high levels of type I interferon (IFN), likely via…
  • Abstract Number: 2887 • 2016 ACR/ARHP Annual Meeting

    Clinical Predictors for Development of Interstitial Lung Disease in Mixed Connective Tissue Disease

    Neha Narula1, Tathagat Narula2, Benjamin Wang1 and Andy Abril1, 1Division of Rheumatology, Mayo Clinic, Jacksonville, FL, 2Pulmonary and critical care medicine, Respiratory Critical Care & Sleep Medicine Associates, Jacksonville, FL

    Methods: We performed a retrospective case control study utilizing data from patients evaluated at a single tertiary care center from 2007-2014. Twenty-eight patients who met…
  • Abstract Number: 2888 • 2016 ACR/ARHP Annual Meeting

    Usefulness of Bosentan in the Prevention of Pulmonary Hypertension in Patients with Systemic Sclerosis

    Ivan Castellví1, Carmen Pilar Simeón2, Monica Paola Sarmiento1, Alfredo Guillen2, Cesar Diaz-Torné3, Josep Maria De Llobet Zubiaga1, Jordi Casademont4 and Vicent Fonollosa2, 1Rheumatology, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain, 2Internal Medicine, Hospital Universitari Vall d'Hebron, Barcelona, Spain, 3Rheumatology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain, 4Internal Medicine, Hospital Universitari de la Santa Creu i Sant Pau, Barcelona, Spain

    Background/Purpose:  Systemic sclerosis (SSc) is a systemic autoimmune disease in which the damage of microcirculation is critical to develop the disease. In SSc, vascular complications…
  • Abstract Number: 2889 • 2016 ACR/ARHP Annual Meeting

    Therapeutic Plasma Exchange for the Treatment of Raynaud’s and Digital Ulcers in Systemic Sclerosis: A Systematic Review

    Edward S Harris1, Herbert J Meiselman2, Patrick M Moriarty3 and Allan Metzger4, 1Scleroderma Education Project Ltd, Madison, WI, 2Keck School of Medicine, University of Southern California, Los Angeles, CA, 3Clinical Pharmacology, University of Kansas Medical Center, Kansas City, KS, 4RDL Reference Laboratory Inc, Los Angeles, CA

    Background/Purpose: Raynaud's phenomenon (RP) is an early marker of microvascular damage in systemic sclerosis (SSc) and digital ulcers (DU) are a serious complication of vascular…
  • Abstract Number: 2890 • 2016 ACR/ARHP Annual Meeting

    Feasibility of Same Day Adipose Tissue Harvest, Cell Processing and Subcutaneous Delivery of Adipose Derived Regenerative Cells into Fingers of Scleroderma Patients within a Randomized Double Blind Clinical Trial

    Dinesh Khanna1, Maureen D Mayes2, Robert W. Simms3, Virginia D. Steen4, Steven Cohen5, Paul Caldron6, Richard Martin7, Suzanne Kafaja8, Ankoor Shah9, Shadi Shahouri10, Robert F. Spiera11, John Ervin12, Vivien Hsu13, Robyn T. Domsic14, Laura K. Hummers15, John Yocum16, Soumya Chatterjee17, Chris T. Derk18, John Varga19, Mark Adams20, Eve M. Taylor21, Steven Kesten21 and Daniel E. Furst22, 1University of Michigan, Ann Arbor, MI, 2Rheumatology, University of Texas Medical School at Houston, Houston, TX, 3Rheumatology, Boston University School of Medicine, Boston, MA, 4Rheumatology, Georgetown University Medical Center, Washington, DC, 5FacesPlus, San Diego, CA, 6Arizona Arthritis and Rheumatology Associates, Phoenix, AZ, 7West Michigan Rheumatology, Grand Rapids, MI, 8Rheumatology, University of California Los Angeles, Los Angeles, CA, 9Medicine, Duke University Medical Center, Durham, NC, 10Heartland Research Associates, Wichitas, KS, 11Rheumatology, Hospital for Special Surgery, New York, NY, 12Center for Pharmaceutical Research, Kansas City, MO, 13RWJ Medical School, New Brunswick, NJ, 14Medicine - Rheumatology, University of Pittsburgh, Pittsburgh, PA, 15Johns Hopkins University School of Medicine, Baltimore, MD, 16Baptist Health Center for Clinical Research, Little Rock, AR, 17Rheumatic and Immunologic Ds, Cleveland Clinic, Cleveland, OH, 18Rheumatology, University of Pennsylvania, Philadelphia, PA, 19Rheumatology and Dermatology, Northwestern University, Feinberg School of Medicine Scleroderma Program, Chicago, IL, 20Central Kentucky Research, Lexington, KY, 21Cytori Therapeutics, Inc., San Diego, CA, 22Arthritis Associates of Southern California, Los Angeles, CA

    Background/Purpose:  Current medical therapy to improve hand function has had very limited benefit in patients with systemic sclerosis (SSc). Cells present within a person’s own…
  • Abstract Number: 2891 • 2016 ACR/ARHP Annual Meeting

    Prognostic Significance of Autoantibody Positivity in Interstitial Lung Disease: A Retrospective Case-Control Study

    Christos F Kampolis1, Aliki I Venetsanopoulou1, Fotini Karakontaki2, Vlassis Polychronopoulos2, Panayiotis G Vlachoyiannopoulos1 and Athanasios G. Tzioufas3, 1Pathophysiology, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece, 2Respiratory Medicine, “Hygeia” Hospital, Athens, Greece, 3School of Medicine, Pathophysiology Department, National and Kapodistrian University of Athens, Athens, Greece

    Background/Purpose:  Routine screening for circulating autoantibodies (AAbs) on the initial evaluation of interstitial lung disease (ILD) contributes to the diagnosis of underlying autoimmune disease. However,…
  • Abstract Number: 2892 • 2016 ACR/ARHP Annual Meeting

    Serum Level of KL-6, a Biomarker of Interstitial Lung Disease (ILD), Is Higher in Diffuse SSc Than in Limited SSc and RA Even When the Activity of ILD Is Low

    Tamao Nakashita1, Shinji Motojima2, Akira Jibatake2, Akira Yoshida2 and Yoshiki Yamamoto2, 1Department of Rheumatology and Allergy, Kameda Medical Center, Kamogawa-city, Japan, 2Department of Rheumatology and Allergy, Kameda Medical Center, Kamogawa city, Japan

    Background/Purpose:  KL-6 is a glycoprotein expressed on and released from type 2 alveolar cells and the measurement of KL-6 in serum was developed by Kohno…
  • Abstract Number: 2893 • 2016 ACR/ARHP Annual Meeting

    Usefulness of the Eustar Preliminary Criteria for Vey Early Systemic Sclerosis and Le Roy Criteria for Early-Systemic Sclerosis in Identifying Patients at Risk of Development of Systemic Sclerosis

    Francisco Miguel Ortiz-Sanjuán1, Jose Ivorra Cortes2, Luis Gonzalez Puig2, Inmaculada Chalmeta Verdejo2, Elena Grau Garcia2,3, Carlos Feced Olmos2, Eztizen Labrador Sanchez2, Karla Arevalo Ruales2, Rosa Negueroles Albuixech2, Jorge Fragio Gil2, Isabel Martinez Cordellat2, Jose Luis Valero Sanz2, Cristina Alcañiz Escandell2,3, Carmen Najera Herranz2, Gema Poveda Marin2,3 and Jose Andres Roman2, 1Department of Rheumatology, Hospital Universitario y Politecnico La Fe, Santander, Spain, 2Department of Rheumatology, Hospital Universitario y Politecnico La Fe, Valencia, Spain, 3IIS La Fe, Valencia, Spain

    Background/Purpose:  In our study, over the half of the patients initially classified as Early-SSc progressed to SSc during follow-up. EUSTAR preliminary criteria were more frequent…
  • Abstract Number: 2894 • 2016 ACR/ARHP Annual Meeting

    Efficacy of Rituximab in Systemic Sclerosis with Interstitial Lung Disease

    Ahmet Mesut Onat1, Orhan Zengin1, Savas Aksoy1, Mustafa Erkut Onder1, Koray Gorkem Sacıntı2 and Bunyamin Kisacik1, 1Rheumatology, Gaziantep University School of Medicine, Gaziantep, Turkey, 2Gaziantep University, School of Medicine, Gaziantep, Turkey

    Background/Purpose: Systemic sclerosis (SSc) is a progressive fibrotic and autoimmune disease, which results to severe systemic complications. Rituximab (Rtx), an anti CD-20 antibody, has recently…
  • « Previous Page
  • 1
  • …
  • 1607
  • 1608
  • 1609
  • 1610
  • 1611
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology