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Abstracts tagged "T cells"

  • Abstract Number: 139 • 2017 Pediatric Rheumatology Symposium

    Dysregulation of miRNA in mononuclear cells of patients with enthesitis related arthritis

    Amita Aggarwal1 and Sushma Singh2, 1Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, 2Department of Clinical Immunology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India

    Background/Purpose:  Enthesitis related arthritis (ERA) is the most common category of JIA in Asia. Identifying dysregulated microRNA may help in understanding the pathogenesis of ERA.…
  • Abstract Number: 2 • 2017 Pediatric Rheumatology Symposium

    Murine Model of Arthritis Flare Identifies CD8+ Tissue Resident Memory T Cells in Recurrent Synovitis

    Margaret H Chang1, Anais Levescot2, Allyn Morris2, Nathan Nelson-Maney3, Robert Fuhlbrigge4 and Peter A. Nigrovic2, 1Immunology, Boston Children's Hospital, Boston, MA, 2Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 3Division of Rheumatology, Immunology, and Allergy, Brigham and Women’s Hospital, Boston, MA, 4Children's Hospital Colorado, Aurora, CO

    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: 35 • 2017 Pediatric Rheumatology Symposium

    Kv1.3 Expression on Urinary Leukocytes in Lupus Nephritis:  Potential for Targeted Immunotherapy

    Anne Stevens1, Andrew Hinkle2, Megan Yuasa3, David Peckham4, Chelsea Olsen5, Craig Philips5, Shawn P. Iadonato4 and Peter Probst6, 1University of Washington, Pediatrics, Seattle, WA, 2Center for Immunity and Immunotherapies, Seattle Children's Research Institute, Seattle, WA, 3Seattle Children’s Research Institute, Seattle, WA, 4Kineta Inc, Seattle, WA, 5KPI Therapeutics, Inc., Seattle, WA, 6Kineta, Inc, Seattle, WA

    Background/Purpose: Lymphocyte activation depends upon a calcium signaling cascade that is regulated by voltage-gated potassium channels. Effector memory T cells (TEM), which are implicated in…
  • Abstract Number: 147 • 2017 Pediatric Rheumatology Symposium

    Epigenetic and Transcriptomic Profiling of Primary Juvenile Idiopathic Arthritis Patient Cells: Better Understanding of Disease Pathogenesis

    Lucas Picavet1, Janneke Peeters2, Sandra Coenen3, Arjan Boltjes4, Femke van Wijk5, Paul Coffer2, Bas Vastert6 and Jorg van Loosdregt7, 1Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, Netherlands, 2Center for Molecular Medicine and Regenerative Medicine Center Utrecht, University Medical Center Utrecht, Utrecht, Netherlands, 3University Medical Center Utrecht, Utrecht, Netherlands, 4Laboratory of Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 5Laboratory for Translational Immunity, University Medical Center Utrecht, Utrecht, Netherlands, 6Division of Pediatric Rheumatology, University Medical Center Utrecht, Utrecht, Netherlands, 7Division of Pediatrics, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: For many autoimmune diseases, including Juvenile Idiopathic Arthritis (JIA), the molecular mechanisms remain elusive. JIA can be used as a model to study autoimmune…
  • Abstract Number: 15L • 2016 ACR/ARHP Annual Meeting

    Selective Oral ROCK2 Inhibitor Reduces Clinical Scores in Patients with Psoriasis vulgaris and Normalizes Skin Pathology Via Concurrent Regulation of IL-17 and IL-10 Levels

    Alexandra Zanin-Zhorov1, Jonathan Weiss1, Alissa Trzeciak1, Carmen Arencibia1, Seetharam Polimera1, Wei Chen1, Jingya Zhang1, Melanie Nyuydzefe1, Judilyn Fuentes-Duculan2, Kathleen Bonifacio2, Norma Kunjravia2, Inna Cueto2, Mark Berger1, James Krueger2, Samuel Waksal1 and John Ryan1, 1Kadmon, New York, NY, 2Rockefeller University, New York, NY

    Background/Purpose: Rho-associated kinase 2 (ROCK2) was shown to be implicated in regulation of autoimmunity in mice and humans1. Previous findings demonstrated that oral administration of…
  • Abstract Number: 183 • 2016 ACR/ARHP Annual Meeting

    Protective Role of Mucosal-Associated Invariant T (MAIT) Cells in an Imiquimod-Induced Psoriasis Model

    Goh Murayama1, Asako Chiba2, Hitomi Toda2, Ken Yamaji1, Naoto Tamura3 and Sachiko Miyake4, 1Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 2Juntendo Univ Sch of Med, Juntendo University School of Medicine, Tokyo, Japan, 3Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 4Immunology, Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Psoriasis is a chronic inflammatory disease of the skin and is often accompanied by arthritis. The underlying pathogenesis of psoriasis is still unclear, but…
  • Abstract Number: 1612 • 2016 ACR/ARHP Annual Meeting

    Abatacept Targets T Follicular Helper Cells in Patients with Rheumatoid Arthritis

    Shingo Nakayamada1, Satoshi Kubo2, Maiko Yoshikawa2, Yusuke Miyazaki2, Ippei Miyagawa3, Shigeru Iwata4, Kazuhisa Nakano5, Kazuyoshi Saito6,7 and Yoshiya Tanaka8, 1First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 3University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 4First Department of Internal Medicine, School of Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 5The First department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 6The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 7First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, KItakyushu, Japan, 8University of Occupational and Environmental Health, Kitakyushu, Japan

    Background/Purpose:  In the pathogenesis of rheumatoid arthritis (RA), T cells can differentiate into functionally distinct subsets, leading to the persistent inflammation and immune abnormality associated…
  • Abstract Number: 1919 • 2016 ACR/ARHP Annual Meeting

    Analysis of T Cell Repertoire Diversity of CD4+ Memory and NaïVe T Cells By Next Generation Sequencing and Its Association with Rheumatoid Arthritis Disease Parameters

    Keiichi Sakurai1, Hirofumi Shoda1, Kazuyoshi Ishigaki2, Yumi Tsuchida1, Yasuo Nagafuchi1, Shuji Sumitomo1, Akari Suzuki2, Keishi Fujio1 and Kazuhiko Yamamoto1, 1Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 2Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan

    Background/Purpose:  Rheumatoid arthritis (RA) is an autoimmune disease characterized by peripheral polyarthritis. The importance of CD4+ T cell in the pathophysiology of RA is well-known…
  • Abstract Number: 2708 • 2016 ACR/ARHP Annual Meeting

    Type 17 Immunity in Spondyloarthritis Is Expanded Across Multiple Lymphocyte Subsets

    Davide Simone1, Hussein Al Mossawi1, Anna Ridley2, Jelle De Wit1, Takuya Sekine1, Nuha Ansar1, Karen Doig1 and Paul Bowness1, 1Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, United Kingdom, 2Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Science, University of Oxford, Oxford, United Kingdom

    Background/Purpose: The spondyloarthritides (SpA) are a group of chronic inflammatory disorders involving the axial spine and the peripheral joints. Genetic, functional and clinical trial evidences…
  • Abstract Number: 3036 • 2016 ACR/ARHP Annual Meeting

    IL-22 Is Dysregulated in Psoriatic Arthritis and Acts to Limit IFN-γ Driven Inflammatory Chemokine Production

    Amara Ezeonyeji1, Helen Baldwin2, Milica Vukmanovic-Stejic3 and Michael R. Ehrenstein4, 1Rheumatology, Medicine, University College London, London, United Kingdom, 2Rheumatology, Centre for Rheumatology Research, University College London, london, United Kingdom, 3Infection & Immunity, University College London, london, United Kingdom, 4Medicine, University College London, London, United Kingdom

    Background/Purpose: IL-22 is an IL-10 family cytokine with both pro-inflammatory and anti-inflammatory effects and its dysregulation is associated with the development of autoimmune disease including…
  • Abstract Number: 268 • 2016 ACR/ARHP Annual Meeting

    Effect of Abatacept Treatment on T Cells in Muscle Tissue and Peripheral Blood in Polymyositis and Dermatomyositis Patients

    Quan Tang1, Daniel Ramsköld2, Olga Krystufkova3, Herman F Mann4, Cecilia Wick5, Maryam Dastmalchi6, Peter Brodin7, Vivianne Malmström8, Jiri Vencovsky9 and Ingrid E. Lundberg6, 1Department of Medicine, Rheumatology Unit, Department of Medicine, Karolinska University Hospital, Solna, Karolinska Institutet, Stockholm, Sweden, 2Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, Stockholm, Sweden, 3Institute of Rheumatology, Department of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 41st Faculty of Medicine, Charles University, Prague, Prague, Czech Republic, 5Rheumatology Unit, Department of Medicine, Solna, Karolinska Institutet, Stockholm, Sweden, 6Department of Medicine, Rheumatology Unit, Karolinska University Hospital, Karolinska Institutet, Stockholm, Sweden, 7Science for Life Laboratory, Department of Medicine Solna, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, 8Department of Medicine, Rheumatology Unit, Department of Medicine, Karolinska Institute, Karolinska University Hospital, Stockholm, Sweden, 9Pediatria II, Reumatologia, PRINTO, Istituto Giannina Gaslini, Genoa, Italy

    Background/Purpose:  Abatacept (CTLA4-Ig), a blocking agent for T cell co-stimulation, has been proven beneficial in several autoimmune diseases. The aim of the study was to…
  • Abstract Number: 1749 • 2016 ACR/ARHP Annual Meeting

    The Role of Mucosal-Associated Invariant T (MAIT) Cells in Lupus Dermatitis

    Goh Murayama1, Asako Chiba2, Hirofumi Amano3, Ken Yamaji1, Naoto Tamura1 and Sachiko Miyake4, 1Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 2Juntendo Univ Sch of Med, Juntendo University School of Medicine, Tokyo, Japan, 3Department of Rheumatology and Internal Medicine, Juntendo University School of Medicine, Tokyo, Japan, 4Immunology, Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Mucosal-associated invariant T (MAIT) cells are innate T cells that are restricted by MHC-related molecule-1 (MR1) and express a semi-invariant TCRa chain: Va7.2-Ja33 in…
  • Abstract Number: 1920 • 2016 ACR/ARHP Annual Meeting

    Vitamin D Induces a Type 1 Regulatory T Cell (Tr1)-like Phenotype in Human C-C Chemokine Receptor Type 6 (Ccr6)+ th Cells and Promotes Their Migration to an Inflammatory Environment

    Wendy Dankers1, Jan Piet van Hamburg1, Nadine Davelaar1, Patrick Asmawidjaja1, Hoyan Wen1, Johannes van Leeuwen2, Edgar Colin3 and Erik Lubberts1, 1Rheumatology and Immunology, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 2Internal Medicine, Erasmus MC, University Medical Center, Rotterdam, Netherlands, 3Rheumatology, ZGT, Almelo, Netherlands

    Background/Purpose: The active vitamin D metabolite 1,25(OH)2D3 suppresses various experimental autoimmune diseases. In addition, serum vitamin D levels, vitamin D intake and polymorphisms in the…
  • Abstract Number: 2710 • 2016 ACR/ARHP Annual Meeting

    Bacterial Dysbiosis Associates with Functional Intraepithelial Lymphocyte Changes in Inflammatory Bowel Disease and Spondyloarthritis

    Neha Ohri1,2,3, Mark Gerich3,4, Blair Fennimore3,5, Diana Ir6, Charles Robertson6, Daniel Frank6, Liron Caplan7, Brandie Wagner8 and Kristine Kuhn9,10, 1Division of Rheumatology, Mount Sinai West, New York City, NY, 2Division of Rheumatology, University of Colorado, Aurora, CO, 3Mucosal Inflammation Program, University of Colorado, Aurora, CO, 4Division of Gastroenterology, University of Colorado, Aurora, CO, 5Department of Gastroenterology, University of Colorado, Aurora, CO, 6Division of Infectious Disease, University of Colorado, Aurora, CO, 7Denver Veterans Affairs Medical Center and UC Denver SOM, Denver, CO, 8Department of Biostatistics and Informatics, University of Colorado, Aurora, CO, 9Division of Rheumatology, University of Colorado School of Medicine, Aurora, CO, 10Mucosal Inflammation Program, University of Colorado School of Medicine, Aurora, CO

    Background/Purpose:  The microbiome is hypothesized to influence human health and disease. Changes in resident bacteria, termed dysbiosis, occur in spondyloarthritis (SpA) and inflammatory bowel disease…
  • Abstract Number: 3040 • 2016 ACR/ARHP Annual Meeting

    Th17 Migration into the Synovial Fluid of Patients with Active Psoriatic Arthritis Is Enhanced By Regulatory T Cells

    Helen Baldwin1, Amara Ezeonyeji2, Mohammed Rohan Butt2 and Michael R. Ehrenstein3, 1Rheumatology, University College London, London, United Kingdom, 2Rheumatology, Medicine, University College London, London, United Kingdom, 3Medicine, University College London, London, United Kingdom

    Background/Purpose: Uncontrolled migration of Th17 cells into the skin and joints is a major driver in the pathogenesis of psoriatic arthritis (PsA). Modulation of T…
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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.).

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].

ACR Abstract Embargo Policy

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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