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: 660 • 2016 ACR/ARHP Annual Meeting

    Expression of the Chemokine Receptor CXCR5 Is Decreased in the Periphery of Patients with Primary Sjogren’s Syndrome

    Marie Wahren-Herlenius1, Lara Adnan Aqrawi1, Margarita Ivanchenko1, Albin Björk1, Jorge Ramírez1, Marika Kvarnström1, Janicke Cecilie Liaaen Jensen2 and Kathrine Skarstein3, 1Karolinska Institutet, Stockholm, Sweden, 2University of Oslo, Oslo, Norway, 3University of Bergen, Bergen, Norway

    Background/Purpose: CXCR5 is a chemokine receptor expressed on B and T cell subsets, which binds the CXCL13 ligand produced by follicular dendritic cells. It is…
  • Abstract Number: 1905 • 2016 ACR/ARHP Annual Meeting

    Therapeutic Targeting of JAK/STAT Pathway Inhibits Follicular Helper T Cell Maturation and Function

    Flora Sagez and Jacques-Eric Gottenberg, Department of Rheumatology, Strasbourg University Hospital, Strasbourg, France

    Background/Purpose:  T follicular helper (Tfh) cells represent a CD4+T cell subset specialized to provide help to B cells and to induce memory B cell and…
  • Abstract Number: 1986 • 2016 ACR/ARHP Annual Meeting

    Murine Model of Arthritis Flare Identifies Tissue Resident Memory T Cells in Recurrent Synovitis

    Margaret H Chang1, Anais Levescot2, Allyn Morris2, Robert Fuhlbrigge1,3 and Peter Nigrovic1,2, 1Immunology, Boston Children's Hospital, Boston, MA, 2Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 3Dermatology, Brigham and Women’s Hospital, Boston, MA

    Background/Purpose:  There are 75,000 children affected by JIA in the United States. Despite recent therapeutic advances, treatment often requires chronic therapy and is associated with…
  • Abstract Number: 2923 • 2016 ACR/ARHP Annual Meeting

    T-Cell Receptor Signaling Inhibition By CC-90005, a Selective Protein Kinase C Theta Antagonist, Reduces Antigen Mediated T-Cell Activation and Arthritis Pathology in the Mouse CIA Model

    Garth Ringheim1, Jolanta Kosek1, Lori Capone2, Eun Mi Hur1 and Peter H. Schafer3, 1Inflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ, 2Celgene Corporation, Summit, NJ, 3Department of Translational Development, Celgene Corporation, Summit, NJ

    Background/Purpose:  PKC-θ is a member of the Ca2+-independent novel PKC subfamily, most abundantly expressed in T-cells, and mediates early antigen recognition signal transduction and cell…
  • Abstract Number: 3216 • 2016 ACR/ARHP Annual Meeting

    Integrated High-Dimensional Analyses Reveal a Pathologically Expanded ‘Peripheral’ B Cell-Helper T Cell Population in Rheumatoid Arthritis

    Deepak Rao1, Michael Gurish2, Kamil Slowikowski3, Chamith Fonseka2, Jennifer Marshall4, Yanyan Liu5, Laura T. Donlin6, Lauren Henderson7, Fumitaka Mizoguchi8, Nikola Teslovich9, Michael Weinblatt10, Elena Massarotti10, Jonathan Coblyn11, Simon M. Helfgott10, Yvonne C. Lee12, Derrick J. Todd10, Vivian P. Bykerk13, Susan M. Goodman14, Alessandra B. Pernis15, Lionel Ivashkiv14, Elizabeth W. Karlson10, Peter Nigrovic9, Andrew Filer16, Christopher Buckley17, James Lederer18, Soumya Raychaudhuri19 and Michael Brenner1, 1Division of Rheumatology, Immunology, and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 2Division of Rheumatology, Immunology, Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 3Divisions of Rheumatology and Genetics, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 4Rheumatology Research Group, Institute of Inflammation and Ageing, University of Birmingham, Birmingham, United Kingdom, 5Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 6Arthritis and Tissue Degeneration Program and the David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, 7Division of Immunology, Boston Children's Hospital, Harvard Medical School, Boston, MA, 8Department of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan, 9Brigham and Women's Hospital and Harvard Medical School, Cambridge, MA, 10Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 11Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 12Rheumatology Immunology & Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 13Divison of Rheumatology, Hospital for Special Surgery, New York, NY, 14Medicine, Hospital for Special Surgery, New York, NY, 15David Z. Rosensweig Genomics Research Center, Hospital for Special Surgery, New York, NY, 16University of Birmingham, Birmingham, United Kingdom, 17Rheumatology, University of Birmingham, Birmingham, United Kingdom, 18Department of Surgery, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 19Brigham and Women's Hospital, Boston, MA

    Background/Purpose: Determining the pathologic functions of T cells that infiltrate target tissues remains a central challenge in autoimmune diseases. In rheumatoid arthritis (RA), the formation…
  • Abstract Number: 674 • 2016 ACR/ARHP Annual Meeting

    Targeting Glandular IL-21-Production in Primary Sjogren′s Syndrome Patients By Immunomodulatory Treatment

    Gwenny M. Verstappen1, Hendrik L.F. Broekman1, Erlin A. Haacke2, Petra M. Meiners3, Fred K.L. Spijkervet3, Arjan Vissink4, Hendrika Bootsma5 and Frans G.M. Kroese1, 1Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 2Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 3Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 4Department of Oral and Maxillofacial Surgery, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 5Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, The Netherlands, Groningen, Netherlands

    Background/Purpose:  Interleukin-21 plays a central role in plasma cell differentiation and germinal center (GC) formation and is likely involved in the pathogenesis of primary Sjögren’s…
  • Abstract Number: 1908 • 2016 ACR/ARHP Annual Meeting

    Identification of a Novel Pro-Inflammatory T Cell Epitope from His-tRNA-Synthetase Associated with Interstitial Lung Disease in Anti-Jo-1 Positive Patients

    Angeles Shunashy Galindo-Feria1, Inka Albrecht2, Antonella Notarnicola2, Maryam Dastmalchi2, Anatoly Dubnovitsky3, Tatiana Sandalova3, Genadiy Kozhukh3, Lars Rönnblom4, Adnane Achour5, Vivianne Malmström6 and Ingrid E. Lundberg2, 1Department of Medicine., Rheumatology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 2Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 3Department of Medicine Solna and Department of Infectious Diseases,, Science for Life Laboratory, Karolinska Institutet and Karolinska University Hospital, Solna, Sweden, 4Uppsala University, Department of Medical Sciences, Rheumatology and Science for Life Laboratory, Uppsala, Sweden, 5Science for Life Laboratory, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, 6Department of Medicine, Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden

    Background/Purpose: Previous studies have demonstrated that CD4+ T cells from peripheral blood of anti-histidyl-tRNA synthetase (anti-His-tRNA) also known as anti-Jo-1 positive patients proliferate in response…
  • Abstract Number: 2008 • 2016 ACR/ARHP Annual Meeting

    Rapamycin Elicits Rapid and Lasting Improvement of Disease Activity through Blocking Pro-Inflammatory T Cell Lineage Specification in Patients with Active SLE

    Zhi-Wei Lai1, Ivan Marchena2, Hajra Tily2, Ricardo Garcia1, Julie Yu2, Lisa Francis2, Maha Dawood2, Ryan Kelly2, Stephen Faraone2, Paul E. Phillips3 and Andras Perl4, 1Medicine, SUNY, Syracuse, NY, 2SUNY, Syracuse, NY, 3Dept of Medicine/Div of Rheum, SUNY-Upstate Medical Univ, Syracuse, NY, 4Department of Medicine, Upstate Medical University, Syracuse, NY

    Background/Purpose:  The rationale for this prospective, biomarker-driven, open-label clinical trial of rapamycin (ClinicalTrials.gov Identifier: NCT00779194) has been based on growing evidence for involvement of the…
  • Abstract Number: 2926 • 2016 ACR/ARHP Annual Meeting

    Rorc Positive Th17, Th17/Th1, and Th17.1 Cells from the Blood of Treatment NaïVe RA Patients Differ in IL-17A but Are All Pathogenic When Co-Cultured with RA Synovial Fibroblasts

    Sandra M.J. Paulissen1, Jan Piet van Hamburg2, Nadine Davelaar2, Wendy Dankers3, Patrick Asmawidjaja2, Anne-Marie Otten-Mus2 and Erik Lubberts2, 1Room Nb-84, Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands, 2Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 3Rheumatology, Erasmus MC, University Medical Center, Rotterdam, Netherlands

    Background/Purpose: T cells play a central role in the early stages of rheumatoid arthritis (RA). In this context, we have shown increased proportions of memory…
  • Abstract Number: 918 • 2016 ACR/ARHP Annual Meeting

    Anergic B Cells May Preserve Peripheral Tolerance in Lupus-Prone Congenic Mice

    Kieran Manion1,2, Yuriy Baglaenko1,2, Nan-Hua Chang2, Nafiseh Talaei3 and Joan Wither4, 1Immunology, University of Toronto, Toronto, ON, Canada, 2Genetics and Development, Krembil Research Institute, University Health Network, Toronto, ON, Canada, 3Genetics and Development, Krembil Research Institute, Toronto, ON, Canada, 4Krembil Research Institute, University Health Network, Toronto, ON, Canada

    Background/Purpose:  Anergic autoreactive B cells are thought to play a critical role in systemic lupus erythematosus (SLE), a chronic autoimmune disease where breach of tolerance…
  • Abstract Number: 1909 • 2016 ACR/ARHP Annual Meeting

    The Transcription Factor Fra2 Is Playing a Key Role in Treg Development and Autoimmunity

    Florian Renoux1, Mara Stellato2, Daniela Impellizzieri3, Riyun Huang4, Arun Subramaniam5, Clara Dees6, Jeorg HW Distler6, Gabriela Kania2, Onur Boyman3 and Oliver Distler2, 1Depertment of Rheumatology, University Hospital Zurich, Schlieren, Switzerland, 2Department of Rheumatology, University Hospital Zurich, Zurich, Switzerland, 3Division of Clinical Immunology, University Hospital Zurich, Zurich, Switzerland, 4Immune Mediated Diseases, Sanofi-Genzyme, Framingham, MA, 5Sanofi-Genzyme, Framingham, MA, 6Department of Internal Medicine 3, University of Erlangen-Nuremberg, Erlangen, Germany

    Background/Purpose:   Decreased numbers or altered functions of regulatory T cells (Tregs) have been reported in many inflammatory rheumatic diseases, and Tregs are considered promising…
  • Abstract Number: 2058 • 2016 ACR/ARHP Annual Meeting

    Ectonucleotidase-Mediated Protection of Lupus Mice from Exaggerated Immune Responses and Arterial Vasculopathy

    Jason S Knight1, Levi F Mazza1, Srilakshmi Yalavarthi1, Yogen Kanthi2 and David J Pinsky2, 1Division of Rheumatology, University of Michigan, Ann Arbor, MI, 2Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, MI

    Background/Purpose: CD39 and CD73 are so-called ectonucleotidases, surface enzymes expressed by leukocytes and endothelial cells that jut into the extracellular space. There, they mediate the…
  • Abstract Number: 2928 • 2016 ACR/ARHP Annual Meeting

    Hypomethylation of an Intragenic Alternative Promoter Contributes to Impaired Treg Function in Rheumatoid Arthritis By Transcriptional Interference with Expression of the Treg-Specific Protein, Glycoprotein a Repetitions Predominant (GARP)

    Alla Skapenko, Jan Leipe and Hendrik Schulze-Koops, Division of Rheumatology and Clinical Immunology, University of Munich, Munich, Germany

    Background/Purpose:  The expression of Treg specific genes, such as the master transcription factor of Tregs, FoxP3 or the Treg specific surface molecule, glycoprotein A repetitions…
  • Abstract Number: 922 • 2016 ACR/ARHP Annual Meeting

    Negative Regulation of IL-17 Receptor Signaling By Regnase-1 Limits Immunopathology in a Mouse Model of Psoriatic Skin Disease

    Sarah L. Gaffen1, Leticia Monin2, Nicole Ward3, Johann Gudjonsson4, Abhishek Garg5, Alicia Mathers2 and Pappachan Kolattukudy6, 1Division of Rheumatology and Clinical Immunology, Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, 2University of Pittsburgh, Pittsburgh, PA, 3Case Western Reserve University, Cleveland, OH, 4Dermatology, University of Michigan, Ann Arbor, MI, 5Rheumatology/Clinical Immun, University of Pittsburgh, Pittsburgh, PA, 6University of Central Florida, Orlando, FL

    Background/Purpose: IL-17 cytokines have emerged as drivers of autoimmunity. Indeed, the IL-17A-targeting antibody secukinumab (Cosentyx) was recently approved for treatment of plaque psoriasis, and shows…
  • Abstract Number: 1911 • 2016 ACR/ARHP Annual Meeting

    Potent and Selective Tyk2 Inhibitor Highly Efficacious in Rodent Models of Inflammatory Bowel Disease and Psoriasis

    Wenyan Miao1, Craig Masse1, Jeremy Greenwood2, Rosana Kapeller1 and William Westlin1, 1Nimbus Therapeutics, Cambridge, MA, 2Schrodinger Inc., New York, NY

    Background/Purpose:  Tyk2 is a member of the JAK family kinases and is a key mediator of IL-12, IL-23, and type I interferon signaling. These cytokines…
  • « Previous Page
  • 1
  • …
  • 11
  • 12
  • 13
  • 14
  • 15
  • …
  • 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