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: 1642 • 2013 ACR/ARHP Annual Meeting

    CD25+CD39+ Regulatory T Cells Are Enriched At The Site Of Inflammation Of Patients With Rheumatoid Arthritis and Impaired In Suppressing IL-17A Secretion

    Jessica Herrath1, Karine Chemin2, Inka Albrecht1, Anca Catrina2 and Vivianne Malmström3, 1Department of Medicine, Solna, Unit of Rheumatology, Karolinska University Hospital, Department of Medicine, Solna, Unit of Rheumatology, Stockholm, Sweden, 2Department of Medicine, Solna, Unit of Rheumatology, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 3Rheumatology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose: Regulatory T cells (Tregs) are important for the maintenance of self-tolerance and are implicated in the origin of autoimmunity. Despite enrichment of Tregs in…
  • Abstract Number: 1603 • 2013 ACR/ARHP Annual Meeting

    Sustained Reductions In Circulating B Cell Populations and Immunoglobulin G Levels With Long-Term Belimumab Treatment In Patients With Systemic Lupus Erythematosus

    Herbert Struemper1, William Freimuth2, Christi Kleoudis3, Thi-Sau Migone4, David Roth3 and William Stohl5, 1GlaxoSmithKline, Research Triangle Park, NC, 2Human Genome Sciences, Inc., Rockville, MD, 3GlaxoSmithKline, King of Prussia, PA, 4Igenica, Burlingame, CA, 5Division of Rheumatology, University of Southern California Keck School of Medicine, Los Angeles, CA

    Background/Purpose: Belimumab treatment in autoantibody-positive systemic lupus erythematosus (SLE) patients for up to 76 weeks results in sustained reduction in several circulating B cell subsets,…
  • Abstract Number: 1604 • 2013 ACR/ARHP Annual Meeting

    Effects Of Chronic Treatment With Blisibimod, An Inhibitor Of B Cell Activating Factor, On Renal and Inflammation Biomarkers In Patients With Systemic Lupus Erythematosus: Observations From The Placebo-Controlled Pearl-SC and Open-Label Extension Studies

    Richard A. Furie1, Matthew Thomas2, Alvina Chu3, Renee S. Martin3, Colin Hislop3 and Morton A. Scheinberg4, 1The Feinstein Institute for Medical Research and North Shore-Long Island Jewish Health System, Lake Success, NY, 2Health and Research Centre, Trivandrum, Kerala, India, 3Anthera Pharmaceuticals Inc, Hayward, CA, 4Rheumatology Hospital Abreu Sodre Pesquisa Clínica, São Paulo, Brazil

    Background/Purpose: To evaluate the effects of subcutaneously-administered blisibimod on renal and inflammation biomarkers in patients with SLE during the phase 2b clinical trial PEARL-SC (NCT01162681)…
  • Abstract Number: 1605 • 2013 ACR/ARHP Annual Meeting

    Post-Marketing Experience With Belimumab In U.S. Lupus Centers: Data From The Lupus Clinical Trials Consortium, Inc. (LCTC) National Patient Registry

    Jinoos Yazdany1, Doruk Erkan2, Jorge sanchez-Guerrero3, Bevra H. Hahn4, Alana B. Levine2, Galina Marder5, W. Joseph McCune6 and Ellen M. Ginzler7, 1Medicine, University of California, San Francisco, San Francisco, CA, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Rheumatology, Mount Sinai Hospital and University Health Network, Toronto Canada, Toronto, ON, Canada, 4Rheumatology, UCLA David Geffen School of Medicine, Los Angeles, CA, 5Medicine, North Shore Long Island Health System, Great Neck, NY, 6Int Med/ Rheum, University of Michigan, Ann Arbor, MI, 7Rheumatology, SUNY-Downstate Medical Center, Brooklyn, NY

    Background/Purpose:  Much of the published experience with belimumab in lupus patients has derived from clinical trials.   We examined the non-sponsored experience with belimumab in routine…
  • Abstract Number: 1606 • 2013 ACR/ARHP Annual Meeting

    Overview Of The Safety Of Epratuzumab In Systemic Lupus Erythematosus

    Daniel J. Wallace1, Josep Ordi-Ros2, C. Michael Neuwelt3, Kenneth Kalunian4, Michelle A. Petri5, Slawomir Jeka6, Ronald F. van Vollenhoven7, Brian Kilgallen8, Sabine Bongardt9, Caroline Gordon10 and Vibeke Strand11, 1Cedars-Sinai Medical Center, Los Angeles, CA, 2Internal Medicine, Vall De Hebron General Hospt, Barcelona, Spain, 3East Bay Rheumatology Research Institute, San Leandro, CA, 4UCSD School of Medicine, La Jolla, CA, 5Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 62nd University Hospital in Bydgoszcz Medical College of Nicolaus Copernicus University, Bydgoszcz, Poland, 7Clinical Trials Unit Department of Rheumatology, The Karolinska Institute, Stockholm, Sweden, 8UCB Pharma, Raleigh, NC, 9UCB Pharma, Brussels, Belgium, 10Rheumatology Research Group (East Wing), School of Immunity and Infection, University of Birmingham, Birmingham, United Kingdom, 11Adjunct, Division of Immunology / Rheumatology, Stanford University, Palo Alto, CA

    Background/Purpose: The efficacy and safety of epratuzumab, a monoclonal antibody targeting CD22, has been evaluated in patients with moderate-to-severe systemic lupus erythematosus (SLE). A pooled…
  • Abstract Number: 1607 • 2013 ACR/ARHP Annual Meeting

    Two Year Follow-Up On Biologics Use In 13 Centers- Data From The International Registry For Biologics In Systemic Lupus Erythematosus

    Ronald F. van Vollenhoven1, Melinda Mild2, Søren Jacobsen3, S. Bernatsky4, Daniel J. Wallace5, Sang-Cheol Bae6, Manuel Ramos-Casals7, Francisco J. García-Hernández8, R. Ramsey-Goldman9, Andrea Doria10, Marta Mosca11, Michelle A. Petri12, M Ayala-Gutiérrez13, J.G. Hanley14 and for The SLICC group15, 1Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), the Karolinska Institute, Stockholm, Sweden, 2Department of medicine, Karolinska Institutet, Stockholm, Sweden, 3Department of Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark, 4Divisions of Rheumatology and Clinical Epidemiology, McGill University Health Centre, Montreal, QC, Canada, 5Cedars-Sinai Medical Center, Los Angeles, CA, 6Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, South Korea, 7Laboratorio de Enfermedades Autoinmunes Josep Font, Hospital Clínic, Barcelona, Spain, 8Internal Medicine, Hospital Virgen del Rocío, Sevilla, Spain, 9Medicine, Northwestern University Feinberg School of Medicine, Chicago, IL, 10Rheumatology Unit - Department of Medicine, University of Padova, Padova, Italy, 11Rheumatology Unit, University of Pisa, Pisa, Italy, 12Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 13Unidad de Enfermedades Autoinmunes, Servicio de Medicina Interna, Hospital Carlos Haya, Malaga, Spain, 14Division of Rheumatology, Halifax, NS, Canada, 15Department of Medicine, the Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Only one biologic agent has been approved for use in SLE, but some are used off-label in various settings. To obtain systematic information regarding…
  • Abstract Number: 1608 • 2013 ACR/ARHP Annual Meeting

    A Phase I Single-Dose Crossover Study To Evaluate The Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Clinical Efficacy Of AMG 811 (anti-IFN-gamma) In Subjects With Discoid Lupus Erythematosus

    Victoria P. Werth1, David Fiorentino2, Stanley B. Cohen3, David Fivenson4, Chris Hansen5, Steve Zoog6, Greg Arnold7, Christine Wang8, Michael Boedigheimer6, Andrew Welcher6, James Chung6, Barbara Sullivan6 and David A. Martin9, 1Department of Dermatology, Veteran Affairs Medical Center, Philadelphia, PA, 2Dermatology, Stanford University School of Medicine, Redwood City, CA, 3Metroplex Clinical Research Center, Dallas, TX, 4David Fivenson, MD, Dermatology, PLLC, Ann Arbor, MI, 5University of Utah School of Medicine, Salt Lake City, UT, 6Amgen, Thousand Oaks, CA, 7Medical Sciences, Amgen, Thousand Oaks, CA, 8Biostatistics, Amgen, Thousand Oaks, CA, 9Medical Sciences, Amgen, Seattle, WA

    Background/Purpose: Discoid Lupus Erythematosus (DLE) is the most common form of chronic cutaneous LE (CCLE) and develops in up to a quarter of SLE patients.…
  • Abstract Number: 1609 • 2013 ACR/ARHP Annual Meeting

    AMG 811 (anti-IFN-gamma) Treatment Leads To a Reduction In The Whole Blood IFN-Signature and Serum CXCL10 In Subjects With Systemic Lupus Erythematosus:   Results Of Two Phase I Studies

    David A. Martin1, Andrew Welcher2, Michael Boedigheimer2, Zahir Amoura3, Alan Kivitz4, Jill P. Buyon5, Jorge Sanchez-Guerrero6, Juanita Romero-Diaz7, Alla Rudinskaya8, Kevin M. Latinis9, S Cohen10, Cynthia Aranow11, Mike Damore2, Winnie Sohn2, Kit Chiu2, Christine Wang12, Naren Chirmule2, Barbara Sullivan2 and James Chung2, 1Medical Sciences, Amgen, Seattle, WA, 2Amgen, Thousand Oaks, CA, 3Department of Internal Medicine 2. Referal center for SLE/APS, CHU Pitié-Salpêtrière, Paris, France, 4Altoona Center for Clinical Research, Duncansville, PA, 5Medicine, Division of Rheumatology, NYU School of Medicine, New York, NY, 6UHN Toronto Western Hospital, Toronto, ON, Canada, 7Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 8Danbury Hospital, Danbury, CT, 9Latinis Rheumatology, Leawood, KS, 10Metroplex Clinical Research Center, Dallas, TX, 11The Feinstein Institute, Manhasset, NY, 12Biostatistics, Amgen, Thousand Oaks, CA

    Background/Purpose: Interferon-gamma (IFN-g) is a major pro-inflammatory cytokine that modulates the function of several important populations of immune cells including B cells, T cells, and…
  • Abstract Number: 1610 • 2013 ACR/ARHP Annual Meeting

    Lymphoablation Including B Cell Depletion and Autologous Hematopoietic Stem Cell Transplantation Leads To Long Remissions In Treatment-Resistant Systemic Lupus Erythematosus Patients

    Sarfaraz A. Hasni1, Gabor G. Illei2, Nikolay P. Nikolov3, Francis Hakim4, Susan Leitman4, James E. Balow5, Howard A. Austin6, Juan Gea-Banacloche4, Unsong Oh7, Paulo Muraro8, Claude Sportes9, Peter E. Lipsky10, Ronald Gress9, Steve Pavletic9 and Amrie Grammer11, 1National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Sjogren's Clinic, NIDCR/ NIH, Bethesda, MD, 3NIDCR, NIH, Bethesda, MD, 4NCI, NIH, Bethesda, MD, 5Clinical Director, NIDDK, National Institutes of Health, Bethesda, MD, 6Kidney Disease Section, NIDDK/NIH, Bethesda, MD, 7NINDS, NIH, Bethesda, MD, 8NINDS/NIH, Bethesda, MD, 9NCI/NIH, Bethesda, MD, 10NIAMS/NIH, Bethesda, MD, 11AMPEL BioSolutions, Charlottesville, VA

    Background/Purpose: Over the past two decades, approximately 200 patients with severe systemic lupus erythematosus(SLE) have received autologous hematopoietic stem cell transplants (autoHSCT). More than half…
  • Abstract Number: 1611 • 2013 ACR/ARHP Annual Meeting

    Off-Label Use Of Rituximab For Systemic Lupus Erythematosus in Europe: Limited Use Mostly In Refractory Patients

    Ronald F. van Vollenhoven1, Melinda Mild2, Andrea Doria3, T. Dörner4, Gianfranco Ferraccioli5, Frederic Houssiau6, T.W.J. Huizinga7, David A. Isenberg8, László Kovács9, Guillermo Ruiz-Irastorza10, Danilo Squatrito11, Alexandre Voskuyl12, Marta Mosca13, G D Sebastiani14, Murat Inanç15, Gabriella Szücs16, Søren Jacobsen17, A. Castro18 and for The IRBIS-EMA group19, 1Unit for Clinical Therapy Research, Inflammatory Diseases (ClinTRID), the Karolinska Institute, Stockholm, Sweden, 2Department of medicine, Karolinska Institutet, Stockholm, Sweden, 3Rheumatology Unit - Department of Medicine, University of Padova, Padova, Italy, 4Charité University Medicine Berlin, Berlin, Germany, 5Division of Rheumatology, Institute of Rheumatology and Affine Sciences, Catholic University of the Sacred Heart, Rome, Italy, 6Department of Rheumatology, Université catholique de Louvain, Brussels, Belgium, 7Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 8Centre for Rheumatology Research, Rayne Building, 4th Floor, Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 9Department of Rheumatology, University of Szeged, Szeged, Hungary, 10Autoimmune Diseases Research Unit, Department of Internal Medicine, BioCruces Health Research Institute, Hospital Universitario Cruces, University of the Basque Country, Barakaldo, Spain, 11Center for Autoimmune Diseases, Department of Internal Medicine, Careggi Hospital- Florence, Florence, Italy, 12Department of Rheumatology, VU University Medical Center, Amsterdam, Netherlands, 13Rheumatology Unit, University of Pisa, Pisa, Italy, 14Rheumatology Unit, San Camillo-Forlanini Hospital, Rome, Rome, Italy, 15Department of Internal Medicine, Rheumatology Division, Istanbul University, Istanbul Faculty of Medicine, Istanbul, Turkey, 16Department of Rheumatology, University of Debrecen Medical and Health Sciences Center, Debrecen, Hungary, 17Department of Rheumatology, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark, 18Hospital Universitari de Reus, Spain, Reus, Spain, 19ClinTRID, Department of Medicine, Karolinska Institute, Stockholm, Sweden

    Background/Purpose: Rituximab (Rituxan, Mabthera; RTX) has not been approved for use in SLE, but uncontrolled observations have suggested efficacy in some patients and the medication…
  • Abstract Number: 1612 • 2013 ACR/ARHP Annual Meeting

    Rituximab For Treatment Of Refractory Auto-Immune Hepatitis

    Chadi Rakieh1, Edward M. Vital2, Paul Emery3 and Michael Martin1, 1Rheumatology, Division of Rheumatic and Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, LTHT, Leeds, United Kingdom, Leeds, United Kingdom, 2Section of Musculoskeletal Disease, Division of Rheumatic and Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, LTHT, Leeds, United Kingdom, Leeds, United Kingdom, 3Division of Rheumatic and Musculoskeletal Disease, Leeds Institute of Molecular Medicine, University of Leeds and NIHR Leeds Musculoskeletal Biomedical Research Unit, LTHT, Leeds, United Kingdom, Leeds, United Kingdom

    Background/Purpose: Auto-immune hepatitis (AIH), also known as lupoid hepatitis, is a chronic progressive disease of unknown aetiology. First-line therapy consists of corticosteroids alone or in…
  • Abstract Number: 1613 • 2013 ACR/ARHP Annual Meeting

    Anti-Malarial Drugs (hydroxychloroquine and quinacrine) Decrease The Production Of Interferon-Alfa Initiated By TLR-9 Agonist

    Ou Jin1, Xi Zhang1, Qiuxia Li1, Lingkai Fang1, Hongyue Huang1, Chengcheng Hou1, Zetao Liao1, Qiujing Wei1, Zhiming Lin2, Dongfang Lin1 and Jieruo Gu3, 1Rheumatology, The Affiliated Third Hospital of Sun Yat-san University, Rheumatology, Guangzhou, China, 2Rheumatology, third affiliated hospital of Sun Yat-sen Universtiy, Guangzhou, China, 3Medicine, Third Affiliated Hospital of Sun Yat-sen University, GuangZhou, China

    Background/Purpose: Toll-like receptor 9 (TLR-9) plays an important role in initiating innate immunity.  The recognition of self DNA fragments by TLR-9 may results in the…
  • Abstract Number: 1614 • 2013 ACR/ARHP Annual Meeting

    Hydroxychloroquine Reverse The Elevation Of Interferon-Alfa Initiated By TLR-9 Agonist Which Irresponsive To Glucocorticoid

    Ou Jin1, Xi Zhang1, Lingkai Fang1, Qiuxia Li1, Hongyue Huang1, Zhiming Lin2, Zetao Liao1, Dongfang Lin1, Chengcheng Hou1 and Jieruo Gu3, 1Rheumatology, The Affiliated Third Hospital of Sun Yat-san University, Rheumatology, Guangzhou, China, 2Rheumatology, third affiliated hospital of Sun Yat-sen Universtiy, Guangzhou, China, 3Medicine, Third Affiliated Hospital of Sun Yat-sen University, GuangZhou, China

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by chronic stimulation of the innate immune system by endogenous nucleic acids through toll-like receptors (TLRs) pathway, which…
  • Abstract Number: 1615 • 2013 ACR/ARHP Annual Meeting

    Type I Interferons As a Serum Biomarker Of Subclinical Atherosclerosis In Pediatric Systemic Lupus Erythematosus Patients

    Smriti Mohan1, Julie Barsalou2, Timothy J. Bradley3, Cameron Slorach3, Lawrence Ng4, Deborah M. Levy5, Earl D. Silverman2 and Mariana J. Kaplan6, 1Pediatric Rheumatology, University of Michigan, Ann Arbor, MI, 2Rheumatology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada, 3Cardiology, The Hospital for Sick Children, University of Toronto, Toronto, ON, Canada, 4Rheumatology, The Hospital for Sick Children, Toronto, ON, Canada, 5Rheumatology, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada, 6Systemic Autoimmunity Branch, National Institutes of Health/NIAMS, Bethesda, MD

    Background/Purpose: Systemic lupus erythematosus (SLE) is a heterogeneous autoimmune disorder with a marked increase in cardiovascular (CV) morbidity and mortality due to premature atherosclerosis, distinct…
  • Abstract Number: 1616 • 2013 ACR/ARHP Annual Meeting

    Interferon Regulatory Factors 3 and 5 As Key Elements Of The Interferon Signature On Plasmacytoid Dendritic Cells From Systemic Lupus Erythematosus Patients

    Diana Gómez-Martín1, Karina Santana-de Anda2, Adriana Elizabeth Monsivais-Urenda3, Sandra Rajme-Lopez4, Luis Aparicio-Vera4, Jorge Alcocer-Varela1 and Roberto González-Amaro3, 1Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 2Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico, 3Department of Immunology, Facultad de Medicina. UASLP, San Luis Potosí, Mexico, 4Department of Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico city, Mexico

    Background/Purpose: Plasmacytoid dendritic cells (pDC) are considered the main source of type-I interferon (IFN-I). The interferon signature has been widely associated to systemic lupus erythematosus…
  • « Previous Page
  • 1
  • …
  • 2141
  • 2142
  • 2143
  • 2144
  • 2145
  • …
  • 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