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Abstracts tagged "T Cell"

  • Abstract Number: 1407 • ACR Convergence 2020

    Resolvin D5 Modulates Th17/Treg Cell Differentiation and Suppresses Osteoclastogenesis

    Hirotaka Yamada1, Jun Saegusa2, Sho Sendo3, Yo Ueda4, Takaichi Okano1, Yoshikazu Fujikawa5, Yuzuru Yamamoto6, Takumi Nagamoto1, Yoshihide Ichise1, Ikuko Naka1, Kengo Akashi7, Akira Onishi7, Masakazu Shinohara1 and Akio Morinobu7, 1Kobe University, Kobe, Japan, 2Department of Clinical Laboratory, Kobe University Hospital, Kobe, Japan, 3Kobe University, Kobe, 4Kobe UniversityRheumatology and Clinical Immunology, Kobe University Hospital, Kobe, Japan, 5Kobe University, Kobe city, Japan, 6Kobe University, Kobe-city, Japan, 7Rheumatology and Clinical Immunology, Kobe University Hospital, Kobe, Japan

    Background/Purpose: Over the last two decades, it has become increasingly clear that resolution of acute inflammation is not a passive process, but requires active modulation.…
  • Abstract Number: 1857 • ACR Convergence 2020

    KIR3DL2 Is Not Overexpressed on CD4+ T Cells and NK Cells in Patients with Axial Spondyloarthritis csDMARD and bDMARD Naive

    Guillaume Larid1, Sophie Trijau1, Clothilde Barral1, Pierre Lafforgue1 and Thao Pham2, 1Aix Marseille Univ, APHM, Rheumatology department, Marseille, France, 2Aix Marseille Univ, APHM, department of rheumatology, Marseille, France

    Background/Purpose: Overexpression of KIR3DL2 on CD4+ T-cells and NK-cells has been reported in patients with ankylosing spondylitis (AS) HLAB27+. We aimed to 1) analyse KIR3DL2…
  • Abstract Number: 0775 • ACR Convergence 2020

    T and B Cell Responses to Common Tenascin-C Peptides in RA

    JING Song1, Anja Schwenzer2, Sara Turcinov3, Alicia Wong2, Cliff Rims1, Lorena Rodriguez Martinez2, David Arribas-Layton4, Christina Gerstner5, Virginia Muir6, Jeffrey Carlin7, Kim Midwood2, Vivianne Malmström8, Eddie James1 and Jane Buckner1, 1Center for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, 2Kennedy Institute of Rheumatology, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom, 3Division of Rheumatology, Department of Medicine,Center for Molecular Medicine, Institutet, Stockholm, Sweden, 4Center for Translational Immunology, Benaroya Research Institute at Virginia Mason, Seattle, 5Division of Rheumatology, Department of Medicine,Center for Molecular Medicine, Karolinska Institutet, Stockholm, Sweden, 6Center for Systems Immunology, Benaroya Research Institute at Virginia Mason, Seattle, WA, 7Department of Rheumatology, Virginia Mason Medical Center, Seattle, WA, 8Karolinska Institutet, Stockholm, Stockholms Lan, Sweden

    Background/Purpose: Although autoreactive CD4+ T cell and antibody responses against citrullinated antigens are known to contribute to loss of immune tolerance in rheumatoid arthritis (RA),…
  • Abstract Number: 1408 • ACR Convergence 2020

    Metabolic Reprogramming in Memory CD4+ T Cells Is Associated with Immune Cell Dysfunction During Aging

    Yuling Chen1, Yuanchun Ye2, Hao Wu3, Pierre-Louis Krauß1, Pelle Löwe1, Moritz Pfeiffenberger1, Lisa Ehlers1, Thomas Buttgereit4, Paula Hoff5, Frank Buttgereit6 and Timo Gaber1, 1Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 2Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Hematology, Oncology and Tumor Immunology, Berlin, Germany, 3Julius-Maximilians Universität Würzburg, Institut für Systemimmunologie, Würzburg, Germany, 4Charité-Universitätsmedizin Berlin, corporate member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Department of Dermatology, Venerology, and Allergology, Berlin, Germany, 5Endokrinologikum Berlin, Rheumatologie, Berlin, Germany, 6Charité University Medicine, Berlin, Germany

    Background/Purpose: Inflamm-aging is a chronic, sterile, low-grade inflammatory status, characterized by an increase of proinflammatory cytokines which participate in the development of most age-related diseases…
  • Abstract Number: 1858 • ACR Convergence 2020

    Increased Proportion of TH17, TH22 and TC17 Cells and the Correlation to IL-22 and Clinical Parameters in Patients with Ankylosing Spondylitis from Northern Sweden

    Kristina Lejon1, Urban Hellman2, Lan Do2, Anjani Kumar2 and Helena Forsblad-d'Elia3, 1Department of Clinical microbiology, Infection and Immunology, Umeå University, Umeå, Sweden, 2Department of Public Health and Clinical Medicine, Rheumatology, Umeå, Sweden, 3Department of Public Health and Clinical Medicine/Rheumatology, Umeå University, Umeå, Vasterbottens Lan, Sweden

    Background/Purpose: Increased levels of TH17 and TH22 as well as TC17 and TC22 cells have previously been associated with ankylosing spondylitis (AS). The correlation between…
  • Abstract Number: 0837 • ACR Convergence 2020

    Deletion of miR-223 Exacerbates Lupus Nephritis by Targeting S1pr1 in Faslpr/lpr Mice

    Sumie Hiramatsu Asano1, Tomoyuki Mukai2, Yoshitaka Morita3 and Jun Wada4, 1Kawasaki Medical School/Department of Rheumatology, Kurashiki city, Japan, 2Kawasaki Medical School, Kurashiki-shi, Okayama, Japan, 3Kawasaki Medical School/Department of Rheumatology, Kurashiki, Okayama, Japan, 4Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences., Okayama city, Japan

    Background/Purpose: To identify new candidate genes regulated by micro RNAs (miRNAs) and involved in the pathogenesis of systemic lupus erythematosus (SLE), we integrated miRNA and…
  • Abstract Number: 1409 • ACR Convergence 2020

    Lack of Conventional Acinar Cells in the Salivary Gland Following Anti PD-L1 and anti-PD-1 Immune Checkpoint Inhibitor Therapy

    Sarah Pringle1, Bert van der Vegt1, Xiaoyan Wang1, Nico van Bakelen1, Arjan Vissink1, Frans Kroese2 and Hendrika Bootsma2, 1UMCG, Groningen, 2University Medical Centre Groningen, Groningen, Netherlands

    Background/Purpose: Salivary glands (SGs) can be damaged by immune checkpoint inhibitor (ICI) therapy. In patients with ICI-induced SG dysfunction, 60% progress to fulfill the ACR-EULAR…
  • Abstract Number: 1949 • ACR Convergence 2020

    CB2 Receptor Distribution and Effects of LenabasumTM in Dermatomyositis In Vitro

    Spandana Maddukuri1, Jay Patel2, Christina Bax3, Maria Wysocka3 and Victoria Werth4, 1University of Pennsylvania and the Michael J. Crescenz VA Medical Center, Montville, NJ, 2University of Pennsylvania and the Michael J. Crescenz VA Medical Center, Philadelphia, 3University of Pennsylvania, Department of Dermatology, Philadelphia, 4University of Pennsylvania and Corporal Michael J. Crescenz Veterans Administration Hospital, Philadelphia

    Background/Purpose: Dermatomyositis (DM) patients report poor quality of life due to disease activity and persistent itch. Lenabasum is an oral non-immunosuppressive, non-psychoactive cannabinoid type 2…
  • Abstract Number: 0030 • ACR Convergence 2020

    Distinct DNA Methylation Patterns of Rheumatoid Arthritis Peripheral Blood and Synovial Tissue T Cells

    Rizi Ai1, Gary Firestein2, David Boyle3 and Wei Wang4, 1University of California San Diego, San Diego, CA, 2University of California, San Diego, La Jolla, CA, 3UCSD, La Jolla, CA, 4UCSD, La Jolla

    Background/Purpose: To understand the epigenetic patterns of T cells accumulated in rheumatoid arthritis (RA) synovium, we characterized DNA methylation of CD3+ T cells in peripheral…
  • Abstract Number: 0838 • ACR Convergence 2020

    T Cell–Specific CaMKIV Deficiency Protects Mice from Imiquimod-induced Glomerulonephritis

    Milena Vukelic1, Masataka Umeda1, Andrew Ferretti2, Rhea Bhargava1, Nobuya Yoshida1 and George Tsokos3, 1Beth Israel Deaconess Medical Center Harvard Medical School, Boston, MA, 2Beth Israel Deaconess Medical Center Harvard Medical School, Boston, 3Division of Rheumatology & Clinical Immunology/Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by autoantibody production, immune complex deposition and multisystem involvement.  Calcium/calmodulin-dependent protein kinase type IV…
  • Abstract Number: 1410 • ACR Convergence 2020

    Resident Memory T Cells Persist in Joints of Anakinra-Treated Mice in Spontaneous Arthritis Model

    Anais Levescot1, Margaret Chang2, Alexandra Wactor1, Rachel Blaustein1, Nathan Nelson-Maney1, Robert Fuhlbrigge3 and Peter Nigrovic4, 1Brigham and Women's Hospital, Boston, MA, 2Boston Children's Hospital, Boston, MA, 3University of Colorado, Denver, CO, 4Division of Rheumatology, Inflammation and Immunity, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA, Boston

    Background/Purpose: Inflammatory arthritis is characterized by chronic inflammation of joints which can be suppressed with immunomodulatory therapy. However, two-thirds of patients will have an arthritis…
  • Abstract Number: 1952 • ACR Convergence 2020

    Activated Memory T Cells Produce Ligands That Cause NF-κB-dependent Inflammatory Activation of the Endothelium: Identification of Novel Therapeutic Targets

    Kim Jeucken1, Jan Piet van Hamburg1, Lotte Kocken1 and Sander Tas2, 1Amsterdam Rheumatology and Immunology Center (ARC), Department of Rheumatology and Clinical Immunology, Department of Experimental Immunology and Amsterdam Infection and Immunity Institute, Amsterdam UMC; location AMC, University of Amsterdam, Netherlands, Amsterdam, Netherlands, 2Amsterdam Rheumatology and Immunology Center (ARC), Department of Rheumatology and Clinical Immunology, Department of Experimental Immunology and Amsterdam Infection and Immunity Institute, Amsterdam UMC; location AMC, University of Amsterdam, Netherlands, Utrecht, Netherlands

    Background/Purpose: Endothelial cells (EC) are important contributors to inflammation via expression of inflammatory mediators, including cytokines, chemokines and adhesion molecules. Production of these inflammatory mediators…
  • Abstract Number: 0095 • ACR Convergence 2020

    Systematic Evaluation of Nine Monogenic Autoinflammatory Diseases Reveals Common and Disease-Specific Correlations with Allergy-Associated Features

    Moses Kitakule1, Brian Dizon2, Cristhian Gutierrez-Huerta1, Sarah Blackstone2, Aarohan Burma1, Aran Son1, Natalie Deuitch1, Sofia Rosenzweig1, Hirsh Komarow1, Deborah Stone3, Anne Jones4, Michele Nehrbecky1, Patrycja Hoffmann5, Tina Romeo6, Adriana de Jesus7, Sara Alehashemi8, Megha Garg9, Sofia Torreggiani10, Gina Montealegre Sanchez11, Katelin R. Honer10, Karyl Barron1, Ivona Aksentijevich4, Amanda Ombrello12, Raphaela Goldbach-Mansky13, Daniel Kastner14, Joshua Milner15, Pamela Frischmeyer-Guerrerio1 and Daniella Schwartz16, 1National Institutes of Health, Bethesda, 2National Institutes of Health, BETHESDA, MD, 3NIH, Bethesda, 4National Human Genome Research Institute, Bethesda, MD, 5NIH, Vienna, VA, 6NIH, Bethesda, MD, 7Translational Autoinflammatory Disease Section (TADS)/NIAID/NIH, Silver Spring, MD, 8Translational Autoinflammatory Disease Section (TADS)/NIAID/NIH, Clarksville, MD, 9NIH/NIAID, Rochester, NY, 10Translational Autoinflammatory Disease Section (TADS)/NIAID/NIH, Bethesda, MD, 11NIAID/NIH, Rockville, MD, 12National Human Genome Research Institute/National Institutes of Health, Bethesda, MD, 13Translational Autoinflammatory Disease Section (TADS)/NIAID/NIH, Potomac, MD, 14National Human Genome Research Institute (NHGRI), NIH, Bethesda, MD, 15Division of Allergy, Immunology and Rheumatology Columbia University Medical Center, New York, NY, 16National Institutes of Health Clinical Center, Bethesda, MD

    Background/Purpose: Monogenic autoinflammatory diseases (AID) are caused by mutations in innate immune signaling genes. The effect of these mutations on the risk of allergy is…
  • Abstract Number: 0840 • ACR Convergence 2020

    Amelioration of Immune Complex-Mediated Glomerulonephritis via CD6 Modulation

    Samantha Chalmers1, Sayra Garcia1, Leal Herlitz2, Jeanette Ampudia3, Cherie Ng4, Stephen Connelly3 and Chaim Putterman1, 1Albert Einstein College of Medicine, Bronx, NY, 2Cleveland Clinic, Cleveland, OH, 3Equillium, Inc, San Diego, CA, 4Equillium, Inc, La Jolla, CA

    Background/Purpose: CD6 is a co-stimulatory receptor, predominantly expressed on T cells, that binds to activated leukocyte cell adhesion molecule (ALCAM), a ligand expressed on antigen-presenting…
  • Abstract Number: 1411 • ACR Convergence 2020

    CD8+ T Cell Subsets and Immune Checkpoint Profiles in Ankylosing Spondylitis Implicate Dysregulation of Cytotoxic T Lymphocytes (CTL)

    Michael Tang1, Zoya Qaiyum2, Melissa Lim1 and Robert Inman2, 1UNIVERSITY HEALTH NETWORK, TORONTO, Canada, 2University Health Network, Toronto, ON, Canada

    Background/Purpose: Ankylosing Spondylitis (AS) is characterized by chronic inflammation which underlies the pain and precedes spinal ankylosis. The strongest genetic association with AS is the…
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Embargo Policy

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 CT on October 25. 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].

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