ACR Meeting Abstracts

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Abstracts tagged "T cells"

  • Abstract Number: 58 • 2018 ACR/ARHP Annual Meeting

    Inhibition of Lipid Phosphatase SHIP1 Expands Myeloid-Derived Suppressor Cells and Attenuates Rheumatoid Arthritis in Mice

    Eui Young So1, Changqi Sun2, Patrycja M Dubielecka1, Anthony M. Reginato3 and Olin D. Liang1, 1Division of Hematology/Oncology, Rhode Island Hospital, Providence, RI, 2Division of Rheumatology, Rhode Island Hosital/The Warren Alpert School of Medicine of Brown University, Providence, RI, 3Division of Rheumatology, Rhode Island Hospital, Providence, RI

    Background/Purpose: The SH2-containing inositol-5’-phosphatase-1 (SHIP1) controls PI3K initiated signaling by limiting membrane recruitment and activation of AKT. SHIP1 knockout in mice leads to an increase…
  • Abstract Number: 155 • 2018 ACR/ARHP Annual Meeting

    Polyfunctional Synovial T-Cell Responses and Synovial Invasiveness Repressed By Blockade of Phosphodiesterase 4

    Sarah M. Wade1, Mary Canavan1, Trudy McGarry1, Siobhan C. Wade1, Ronan Mullan2, Douglas J. Veale3 and Ursula Fearon1, 1Molecular Rheumatology, School of Medicine, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin, Ireland, 2Department of Rheumatology,, Tallaght Hospital, Dublin, Ireland, 3Centre for Arthritis and Rheumatic Diseases, Dublin Academic Medical Centre, University College Dublin, Dublin, Ireland

    Background/Purpose: Genetic and functional studies strongly support the role of T-cells in PsA pathophysiology. Effective targeting of T-cells requires a detailed understanding of their phenotypic…
  • Abstract Number: 1828 • 2018 ACR/ARHP Annual Meeting

    Gut-Joint T Cell Trafficking in a Model of Bacteria-Driven Murine IBD-Spa

    Eric Norman1, Adam Lefferts1 and Kristine A Kuhn1,2, 1Rheumatology, University of Colorado Denver, Aurora, CO, 2Mucosal Inflammation Program, University of Colorado Denver, Aurora, CO

    Background/Purpose: Significant bacterial dysbiosis occurs in individuals with IBD and SpA, and individuals with SpA have evidence of circulating intestinal-derived cells, lending credence to the…
  • Abstract Number: 2798 • 2018 ACR/ARHP Annual Meeting

    Expanded T-Cell Clones Are Present in the Synovium before the Clinical Onset of Rheumatoid Arthritis

    Giulia Balzaretti1,2,3, Paul L. Klarenbeek4, Marieke E. Doorenspleet5, Maria JH de Hair6, Barbera C.D. van Schaik7, Rebecca Esveldt2, Marleen van de Sande1, Danielle Gerlag8, Antoine H.C. van Kampen7, Frank Baas2,9, Paul-Peter Tak10 and Niek de Vries3,5, 1Clinical Immunology & Rheumatology, ARC | Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 2Dept. of Genome Analysis, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 3Dept. of Experimental Immunology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 4Amsterdam Rheumatology & immunology Center | Department of Experimental Immunology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 5Amsterdam Rheumatology and immunology Center | Academic Medical Center / University of Amsterdam, Amsterdam, Netherlands, 6Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, the Netherlands, Utrecht, Netherlands, 7Bioinformatics Laboratory, Department of Clinical Epidemiology, Biostatistics and Bioinformatics, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 8GlaxoSmithKline, Stevenage, United Kingdom, 9Dept. of Genome Diagnostics, Leiden University, Leiden, Netherlands, 10GlaxoSmithKline, Cambridge, United Kingdom

    Background/Purpose: In healthy individuals with arthralgia and RA-specific autoantibodies (so called at-risk individuals) the presence of expanded B-cell receptor (BCR) clones in peripheral blood (PB)…
  • Abstract Number: 62 • 2018 ACR/ARHP Annual Meeting

    CCR6+CD4+ T Cells Drive IL-23R Signaling-Dependent Progression of Antigen-Induced Arthritis

    W Razawy1, N Salioska2, P Asmawidjaja3, A Otten-Mus4, N Kops5, M Oukka6, V Kuchroo7 and Erik Lubberts3, 1Rheumatology and Immunology, Erasmus MC, Rotterdam, Netherlands, 2Rheumatology, Erasmus MC, Rotterdam, Netherlands, 3Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 4Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 5Orthopedics, Erasmus MC, Rotterdam, Netherlands, 6Pediatrics, Seattle Children's Research Institute, Seattle, WA, 7Center for Neurologic Diseases, Harvard Institute of Medicine, Boston, MA

    Background/Purpose: The IL-23/IL-17A immune pathway is important for the progression of T cell-mediated arthritis. However, it is not known where IL-23R+ T cells locate during…
  • Abstract Number: 358 • 2018 ACR/ARHP Annual Meeting

    Immunophenotypic Analysis of T Cells from Leukemia Patients with Immune Checkpoint Inhibitor-Associated Respiratory Complications

    Sang Kim1, Vickie Shannon2, Ajay Sheshardi2, Hagop Kantarjian3, Guillermo Garcia-Manero3, Farhad Ravandi3, Aung Naing4, Padmanee Sharma5, Jin Im6, Wilfredo Ruiz Vazquez6, Adi Diab7, Dimitrios Kontoyiannis8, Andrew Futreal9 and Naval Daver3, 1General Internal Medicine, MD Anderson Cancer Center, Houston, TX, 2Pulmonary Medicine, MD Anderson Cancer Center, Houston, TX, 3Leukemia, MD Anderson Cancer Center, Houston, TX, 4Investigational Cancer Therapeutics, MD Anderson Cancer Center, Houston, TX, 5Genitourinary Medical Oncology, MD Anderson Cancer Center, Houston, TX, 6Stem Cell Transplantation, MD Anderson Cancer Center, Houston, TX, 7Melanoma Medical Oncology, Department of Melanoma Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA, Houston, TX, 8Infectious Diseases, MD Anderson Cancer Center, Houston, TX, 9Genomic Medicine, MD Anderson Cancer Center, Houston, TX

    Background/Purpose: Immune checkpoint inhibitor (ICI)-based combinations are showing encouraging results in acute myeloid leukemia (AML) and myelodysplastic syndrome (MDS) treatment; however, ICIs can cause immune-related…
  • Abstract Number: 1831 • 2018 ACR/ARHP Annual Meeting

    Intestinal Inflammatory Regulation in Murine and Human Spondyloarthropathy Requires High-Affinity T Cell Receptor-Zeta Chain-Associated Protein (ZAP)70-Mediated Runt-Related Transcription Factor (Runx)3 Activity

    Zaied Ahmed Bhuyan1, M. Arifur Rahman2, Muralidhara Maradana1, Ahmed Mehdi3, Giuliana Guggino4, Paul Leo5, Linda Rehaume1, Matthew Brown5, Francesco Ciccia4 and Ranjeny Thomas1, 1The University of Queensland Diamantina Institute, Brisbane, Australia, 2Translational Research Institute, The University of Queensland Diamantina Institute, Brisbane, Australia, 3Diamantina Institute, The University of Queensland Diamantina Institute, Brisbane, Australia, 4Rheumatology Unit, University of Palermo, Palermo, Italy, 5Translational Genomics Group, Institute of Health and Biomedical Innovation, Queensland University of Technology, Translational Research Institute, Brisbane, Australia, Brisbane, Australia

    Background/Purpose: Loss of function RUNX3 variants are associated with ankylosing spondylitis (AS) risk but the mechanism is unknown. Disturbances in immune regulation, intestinal microbial dysbiosis…
  • Abstract Number: 2800 • 2018 ACR/ARHP Annual Meeting

    Adenosine 2a Receptor Signals Act to Limit Autoimmune Arthritis By Inhibiting Pathogenic Germinal Center T Follicular Helper (GC-Tfh) Cells

    Shirdi Schmiel and Daniel L. Mueller, Medicine/Rheumatic and Autoimmune Diseases, University of Minnesota Medical School, Minneapolis, MN

    Background/Purpose: CD4 germinal center (GC)-T follicular helper (Tfh) cells are important in the pathogenesis of autoimmune arthritis. Previous studies have shown that adenosine 2a receptor…
  • Abstract Number: 99 • 2018 ACR/ARHP Annual Meeting

    DC-Hil+ Myeloid-Derived Suppressor Cells Are Elevated in the Peripheral Blood and Lesional Skin of Cutaneous Lupus Patients

    Stephanie Florez-Pollack1, Lin-chiang Tseng1, Masato Kobayashi1, Gregory Hosler1,2, Kiyoshi Ariizumi1 and Benjamin F. Chong1, 1Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 2Propath, Dallas, TX

     Background/Purpose: Myeloid derived suppressor cells (MDSCs) are major T cell suppressors, and their dysfunction has been implicated in the pathophysiology of autoimmune diseases. MDSCs suppress…
  • Abstract Number: 359 • 2018 ACR/ARHP Annual Meeting

    Characterization of Lymphoid Cells in Synovial Fluid from Cancer Patients with Immunotherapy-Induced Arthritis

    Sang Kim1, Jean Tayar1, Huifang Lu1, Jennifer Wang2, Don Gibbons3, Guillermo Garcia-Manero4, Patrick Hwu5, Adi Diab5 and Roza Nurieva6, 1General Internal Medicine (Rheumatology), MD Anderson Cancer Center, Houston, TX, 2Genitourinary Medical Oncology, MD Anderson Cancer Center, Houston, TX, 3Thoracic/Head and Neck Medical Oncology, MD Anderson Cancer Center, Houston, TX, 4Leukemia, MD Anderson Cancer Center, Houston, TX, 5Melanoma Medical Oncology, MD Anderson Cancer Center, Houston, TX, 6Immunology, MD Anderson Cancer Center, Houston, TX

    Background/Purpose: Checkpoint inhibitors (ICIs) are revolutionizing cancer treatment; however, ICI therapy is associated with immune-related adverse events (irAEs). irAEs can be life-threatening and/or severely impair…
  • Abstract Number: 1833 • 2018 ACR/ARHP Annual Meeting

    The Vδ2 Subset of Γδt-Cells Are Present at Healthy Human Enthesis and Have Transcriptional and Functional Characteristics Consistent with a Capacity for IL- 17A Production in Response to IL-23

    Richard Cuthbert1, Evangelos M. Fragkakis1, Charlie Bridgewood1, Robert Dunsmuir2, Abdulla Watad3, Abhay Rao2, Almas Khan2, Helena Marzo-Ortega4, Darren Newton5 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, 3Department of Internal Medicine 'B', Sheba Medical Center, Ramat Gan, Ramat Gan, Israel, 4NIHR LBRC, LTHT and LIRMM, University of Leeds, Leeds, United Kingdom, 5Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, United Kingdom

    Background/Purpose: Recent mouse studies of SpA pathogenesis have suggested that γδT-cells accumulate at entheseal regions in an IL-23 overexpression model and that these cells are…
  • Abstract Number: 2898 • 2018 ACR/ARHP Annual Meeting

    Increased Frequency of Circulating CD4+CXCR5-PD1hi Peripheral Helper T (cTph) Cells in Patients with Seropositive Early Rheumatoid Arthritis (RA)

    Paula Fortea-Gordo1, Laura Nuño2, Alejandro Villalba2, Diana Peiteado3, Irene Monjo4, Paloma Sanchez-Mateos5, Amaya Puig-Kröger6, Alejandro Balsa1 and Maria Eugenia Miranda-Carus1, 1Rheumatology, Hospital La Paz - IdiPAZ, Madrid, Spain, 2Rheumatology, La Paz University Hospital, Madrid, Spain, 3Hospital Universitario La Paz, Madrid, Spain, 4Rheumatology, Rheumatology, La Paz University Hospital, Madrid, Spain, 5Immunology, Hospital Gregorio Marañon, Madrid, Spain, 6Immuno-oncology, Hospital Gregorio Marañon, Madrid, Spain

    Background/Purpose: A novel population of CD4+ T cells with B cell helping capacity has been described in the synovial tissues and peripheral blood of seropositive…
  • Abstract Number: 133 • 2018 ACR/ARHP Annual Meeting

    GBR830, a True OX40 Antagonist Antibody with Potent Suppressive Effects on T Cell-Mediated Pathological Responses

    Julie Macoin1, Stanislas Blein1, Thierry Monney1, Pavankumar Sancheti2, Venkateshwar Reddy3 and Jonathan Back1, 1Glenmark Pharmaceuticals SA, La Chaux-de-Fonds, Switzerland, 2Glenmark Pharmaceuticals Ltd, Mumbai, India, 3Glenmark Pharmaceuticals SA, Paramus, NJ

    Background/Purpose: OX40 (TNFRSF4, CD134) is a costimulatory receptor member of the NGFR/TNFR superfamily expressed predominantly on activated T lymphocytes. Ligation of OX40 by its ligand…
  • Abstract Number: 714 • 2018 ACR/ARHP Annual Meeting

    A Predictive Clinical-Immunological Index for Infections Unveils Novel Innate and Adaptive Immunity Abnormalities As Key Risk Factors for Infections in a Cohort of Patients with Systemic Lupus Erythematosus

    Diana Gómez-Martín1,2, Jiram Torres-Ruíz3, Nancy R Mejía-Domínguez4, Guillermo Juárez-Vega5, Javier Merayo-Chalico3, Ana Barrera-Vargas3 and Jorge Alcocer-Varela1, 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 and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición, Salvador Zubirán, Mexico City, Mexico, 4Bioinformatics, Biostatistics and Computational Biology Unit, Red de Apoyo a la Investigación. Coordinación de la Investigación Científica, Universidad Nacional Autónoma de México, Mexico, Mexico, 5Flow Cytometry Unit, Red de Apoyo a la Investigación. Coordinación de la Investigación Científica, Universidad Nacional Autónoma de México, Mexico, Mexico

    Background/Purpose: Patients with systemic lupus erythematosus (SLE) have multiple innate and adaptive immune response abnormalities. It is unknown whether they play a key role in…
  • Abstract Number: 2021 • 2018 ACR/ARHP Annual Meeting

    Th22 Cells in Peripheral Blood and Synovial Fluid of Patients with Enthesitis Related Arthritis

    Sandeep Kansurkar1, Ankita Singh2, Ramnath Misra3 and Amita Aggarwal3, 1Dept of Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 2Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 3Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India

    Background/Purpose: IL-17 and IL-22 are important cytokines in pathogenesis of spondyloarthropathy. In an IL-23 or IL-22 over-expressing mouse model it was shown that enthesitis is…
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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.

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.).

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Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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