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

Abstracts tagged "T cells"

  • Abstract Number: 1065 • 2017 ACR/ARHP Annual Meeting

    Mucosal-Associated Invariant T Cell Deficiency in Systemic Lupus Erythematosus Is Realted to an Intrinsic Defect in the Ca2+/Calcineurin/NFAT1 Signaling Pathway

    Yong-Wook Park1, Young-Nan Cho2, Hye-Mi Jin1, Tae-Jong Kim3 and Seung-Jung Kee4, 1Rheumatology, Chonnam National University Medical School and Hospital, Gwangju, Korea, Republic of (South), 2Rheumatology, Chonnam National University Hospital and Medical School, Gwangju, MN, Korea, Republic of (South), 3Chonnam Nat`l University Medical School&Hospital, Chonnam, Korea, Republic of (South), 4Laboratory Medicine, Chonnam National University Medical School and Hospital, Gwangju, Korea, Republic of (South)

    Background/Purpose: Mucosal-associated invariant T (MAIT) cells contribute to protection against certain microorganism infections and play an important role in mucosal immunity. However, the role of…
  • Abstract Number: 1745 • 2017 ACR/ARHP Annual Meeting

    Autophagic Memory in Stress Experienced Human T Cells

    Pavanish Kumar1, Jorg van Loosdregt2, Suzan Saidin1, Bhairav Paleja1 and Salvatore Albani1, 1SingHealth Translational Immunology and Inflammation Centre (STIIC), Duke-NUS Medical School, Singapore, Singapore, 2Laboratory for Translational immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: Autophagy is central to many key immune related pathways, disregulation of which has been associated with rheumatoid arthritis (RA), cancer and neurodegenerative diseases. Autophagy…
  • Abstract Number: 2711 • 2017 ACR/ARHP Annual Meeting

    Mucosal-Associated Invariant T Cells Are an Important Source of TNF in Rheumatoid Arthritis

    Diahann Jansen1, Elizabeth Klinken1, Hendrik Nel1, Soi Cheng Law1, Hester Koppejan2, Marjolijn Hameetman3, Ligong Liu4, Alexandra Corbett5, Sidonia Eckle5, David Fairlie4, Rene E.M. Toes6, Floris van Gaalen7, Jamie Rossjohn8,9,10, James McCluskey5 and Ranjeny Thomas1, 1The University of Queensland Diamantina Institute, Translational Research Institute, Woolloongabba, Australia, 2Department of Rheumatology, Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 3Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 4Institute for Molecular Bioscience, University of Queensland, Brisbane, Australia, 5Department of Microbiology & Immunology, Peter Doherty Institute for Infection and Immunity, University of Melbourne, Parkville, Australia, 6Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 7Rheumatology, Department of Rheumatology, Leiden University Medical Center, Leiden, Netherlands, 8Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Monash University, Clayton, Australia, 9Institute of Infection and Immunity, Cardiff University School of Medicine, Cardiff, United Kingdom, 10Infection and Immunity Program, Biomedicine Discovery Institute and Department of Biochemistry and Molecular Biology, Monash University, Clayton, Australia

    Background/Purpose: CD8+ T cells have been described to comprise up to 40% of the rheumatoid arthritis (RA) synovial T cell compartment but their pathogenic function…
  • Abstract Number: 393 • 2017 ACR/ARHP Annual Meeting

    The Role of Follicular Helper 17 T Cells in Glucose-6-Phosphate Isomerase Induced Arthritis

    Izumi Kurata, Isao Matsumoto, Atsumu Osada, Hiroshi Ebe, Hoshimi Kawaguchi, Yuya Kondo, Hiroto Tsuboi and Takayuki Sumida, Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

    Background/Purpose: Follicular helper T (Tfh) cell is a novel T cell subset which promotes follicular B cell activation, differentiation to plasma cell and antibody production.…
  • Abstract Number: 1325 • 2017 ACR/ARHP Annual Meeting

    Immune Responses to Peptides Containing Homocitrulline or Citrulline in the DR4-Transgenic Mouse Model of Rheumatoid Arthritis

    Patrick Lac1, Sheri Saunders1, Elena Tutunea-Fatan1, Lillian Barra2, David Bell3 and Ewa Cairns2, 1Microbiology and Immunology, The University of Western Ontario, London, ON, Canada, 2Medicine, Microbiology and Immunology, The University of Western Ontario, London, ON, Canada, 3Medicine, The University of Western Ontario, London, ON, Canada

    Background/Purpose: Antibodies to proteins/peptides containing citrulline (commonly measured using cyclic citrullinated peptide, CCP2) are hallmarks of Rheumatoid Arthritis (RA). These antibodies are strongly associated with…
  • Abstract Number: 1747 • 2017 ACR/ARHP Annual Meeting

    Human C-C Chemokine Receptor-6 (CCR6)+ Th Memory Cells, Including Th17 and Th17.1 Cells, Change into Anti-Inflammatory Cells with Regulatory Capacity upon Exposure to Vitamin D

    Wendy Dankers1, Nadine Davelaar2, Jan Piet van Hamburg3, Patrick Asmawidjaja2, Hoyan Wen2, Johannes van Leeuwen4, Edgar Colin5 and Erik Lubberts2, 1Rheumatology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 2Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, Rotterdam, Netherlands, 4Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 5ZGT Almelo, Deventer, Netherlands

    Background/Purpose: Autoimmune diseases such as RA are driven by an aberrantly activated immune system and an imbalance between pro- and anti-inflammatory cells, resulting in tissue…
  • Abstract Number: 2714 • 2017 ACR/ARHP Annual Meeting

    The Paracaspase MALT1 Plays a Central Role in the Pathogenesis of Rheumatoid Arthritis

    Elisabeth Gilis1, Jens Staal2, Rudi Beyaert2 and Dirk Elewaut3, 1Molecular Immunology and Inflammation Unit, VIB Inflammation Research Center, Ghent, Belgium, Gent, Belgium, 2Molecular Immunology and Inflammation Unit, VIB Inflammation Research Center, Ghent, Belgium, 3VIB Inflammation Research Center, University of Ghent, Ghent, Belgium

    Background/Purpose: One of the hallmarks of many inflammatory arthritides is their strong linkage with MHC-signalling, which is mirrored by the marked role for adaptive immunity.…
  • Abstract Number: 642 • 2017 ACR/ARHP Annual Meeting

    Downstream Effects of Apremilast in Human Arthritic Ex Vivo Models

    Tue Wenzel Kragstrup1,2, Søren Lomholt2, Morten Aagaard Nielsen2, Line Dam Heftdal2, Peter H. Schafer3 and Bent Deleuran2,4, 1Randers Regional Hospital, Randers, Denmark, 2Department of Biomedicine, Aarhus University, Aarhus, Denmark, 3Department of Translational Development, Celgene Corporation, Summit, NJ, 4Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark

    Background/Purpose: Apremilast (Otezla) is a PDE4 inhibitor approved for the treatment of psoriasis and psoriatic arthritis, but the mechanisms of action of apremilast are not…
  • Abstract Number: 1328 • 2017 ACR/ARHP Annual Meeting

    A Dual ICOS/CD28 Antagonist ICOSL Variant Ig Domain (vIgDTM) Potently Suppresses Mouse Collagen-Induced Arthritis and Human Xenograft Graft Vs. Host Disease (GvHD)

    Stacey Dillon1, Katherine Lewis1, Ryan Swanson2, Lawrence Evans2, Michael Kornacker3, Steve Levin2, Martin Wolfson4, Erika Rickel2, Susan Bort2, Sherri Mudri1, Aaron Moss1, Michelle Seaberg1, Janhavi Bhandari4, Sean MacNeil4, Joe Hoover4, Mark Rixon4 and Stanford Peng5, 1Translational Sciences, Alpine Immune Sciences, Seattle, WA, 2Immunology, Alpine Immune Sciences, Seattle, WA, 3Protein Engineering, Alpine Immune Sciences, Seattle, WA, 4Protein Therapeutics, Alpine Immune Sciences, Seattle, WA, 5Clinical, R&D, Alpine Immune Sciences, Seattle, WA

    Background/Purpose:   Our proprietary variant Ig domain (vIgD) platform creates novel, therapeutically-applicable protein domains with tailored specificity and affinity. These vIgDs are created through directed…
  • Abstract Number: 1832 • 2017 ACR/ARHP Annual Meeting

    Gut Dysbiosis Contributes to Autoimmune Pathogenesis in Lupus-Prone Mice

    Seung Chul Choi1, Josephine Brown1, Mansour Mohamadzadeh2, Byron Croker1 and Laurence Morel3, 1Pathology, University of Florida, Gainesville, FL, 2Infectious Diseases & Pathology, University of Florida, Gainesville, FL, 3Pathology, Immunology, and Laboratory Medicine, University of Florida, Gainesville, FL

    Background/Purpose: Multiple studies have demonstrated that commensal bacteria play an immunoregulatory role and that gut dysbiosis is associated with inflammatory diseases. This study was conducted…
  • Abstract Number: 2740 • 2017 ACR/ARHP Annual Meeting

    Cyclophosphamide Treatment Modulates Circulating Cell Populations in Patients with Vasculitis and Autoimmune Systemic Diseases

    Martina Skácelová1, Gabriela Gabčová2, Pavel Horak3, Zuzana Mikulková2, František Mrázek4, Eva Kriegová5 and Andrea Smržová6, 1III. Department of Internal Medicine, Faculty of Medicine and Dentistry, Palacký University of Olomouc, Olomouc, Czech Republic, 2Department of Immunology, Faculty of Medicine and Dentistry, Palacky University Olomouc, Olomouc, Czech Republic, 3III. Department of internal medicine, III. Department of Internal Medicine, Faculty of Medicine and Dentistry, Palacký University of Olomouc, Olomouc, Czech Republic, 4Department of Immunology, Faculty of Medicine and Dentistry, Palacky University of Olomouc, Olomouc, Czech Republic, 5Department of Immunology, Department of Immunology, Faculty of Medicine and Dentistry, Palacky University of Olomouc, Olomouc, Czech Republic, 6III. Department of Internal Medicine, III. Department of Internal Medicine, Faculty of Medicine and Dentistry, Palacký University of Olomouc, Olomouc, Czech Republic

    Background/Purpose: Although cyclophosphamide (CFA) remain the cornerstone for treatment of patients with severe manifestations of systemic autoimmune diseases, the knowledge about the effect of CFA…
  • Abstract Number: 645 • 2017 ACR/ARHP Annual Meeting

    An Oral Tyk2 Inhibitor Effectively Suppresses the Development of Murine Th17 Cells In Vivo and Prevents Joint Damage in Experimental Ankylosing Spondylitis

    Eric Gracey1,2, Melissa Lim2, Zoya Qaiyum1, Yuriy Baglaenko1,2, Wenyan Miao3, Craig Masse3, William Westlin3 and Robert D Inman1,4, 1Department of Immunology, University of Toronto, Toronto, ON, Canada, 2Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 3Nimbus Therapeutics, Cambridge, MA, 4Toronto Western Hospital, University Health Network, toronto, ON, Canada

    Background/Purpose: Th17 cells play an important role in the pathogenesis of ankylosing spondylitis (AS). Tyk2, a member of the Janus Kinase (JAK) family of signaling…
  • Abstract Number: 1567 • 2017 ACR/ARHP Annual Meeting

    A Mitogen-Associated Protein Kinase (MAPK) Associated Kinase 2 Inhibitor Decreases in Vitro Th17 and Monocyte Inflammatory Responses in Spondyloarthritis

    Davide Simone, Hui Shi, Nuha Ansar, Alison Davies, Karen Doig and Paul Bowness, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom

    Background/Purpose: The current biologic treatment for Ankylosing Spondylitis (AS) and Psoriatic Arthritis (PsA) are limited to TNF-a inhibitors (TNFi) and, more recently, IL-17A monoclonal antibodies.…
  • Abstract Number: 1911 • 2017 ACR/ARHP Annual Meeting

    Impaired Control of Autoreactive T Cell Expansion Is Coupled with Type-1 Regulatory T Cell Deficiency in BALB/c ZAP70W163C Mutant Mice

    M. Arifur Rahman1, Daphne Montizaan2, Zaied Ahmed Bhuyan3, Linda Rehaume3 and Ranjeny Thomas4, 1The University of Queensland Diamantina Institute, The University of Queensland, Brisbane, Australia, 2The University of Groningen, Groningen, Netherlands, 3The University of Queensland Diamantina Institute, Translational Research Institute, Brisbane, Australia, 4Dendright Pty Ltd, Brisbane, Australia

    Background/Purpose: In the context of reduced TCR signaling in the BALB/c ZAP70W163C mutant (SKG) mouse, development of arthritis, psoriasis-like skin inflammation and ileitis after intra-peritoneal…
  • Abstract Number: 2772 • 2017 ACR/ARHP Annual Meeting

    Unbound IL-18 Distinguishes Human Macrophage Activation Syndrome from Familial Hemophagocytic Lymphohistiocytosis and Affects Innate Versus Adaptive Murine Lymphocytes Differently

    Paul Tsoukas1, Eric Weiss2, Dirk Holzinger3, Charlotte Girard4, Dirk Foell5, Alexei A. Grom6, Sandra Ammann7, Stephan Ehl7, Eduardo Schiffrin8, Adriana Almeida de Jesus9, Raphaela Goldbach-Mansky9, Cem Gabay10 and Scott Canna11, 1Pediatric Rheumatology, Children’s Hospital of Pittsburgh, Pittsburgh, PA, 2RK Mellon Institute, Children’s Hospital of Pittsburgh, Pittsburgh, PA, 3Department of Pediatric Rheumatology and Immunology, University of Muenster, Muenster, Germany, 4Division of Rheumatology, Department of Internal Medicine Specialties, University Hospital of Geneva, Geneva, Switzerland, 5University of Muenster, Muenster, Germany, 6Pediatric Rheumatology, Cincinnati Children’s Hospital, Cincinnati, OH, 7Center for Chronic Immunodeficiency, Faculty of Medicine, University of Freiburg, Freiburg, Germany, 8AB2 Bio, Lausanne, Switzerland, 9Translational Autoinflammatory Disease Studies (TADS), Laboratory of Clinical Investigation and Microbiology (LCIM), NIAID/NIH, Bethesda, MD, 10SCQM, Geneva, Switzerland, Geneva, Switzerland, 11Richard King Mellon Foundation Institute for Pediatric Research, Children's Hospital of Pittsburgh, Pittsburrgh, PA

    Background/Purpose: Persistently and extremely elevated serum IL-18 has been associated with Macrophage Activation Syndrome (MAS). Chronic IL-18 is hypothesized to contribute to excessive interferon (IFN)-g…
  • « Previous Page
  • 1
  • …
  • 8
  • 9
  • 10
  • 11
  • 12
  • …
  • 32
  • 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