ACR Meeting Abstracts

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Abstracts tagged "B-Lymphocyte"

  • Abstract Number: 0003 • ACR Convergence 2023

    Expanded Extrafollicular B Cells Were Improved by RTX in IgG4-related Disease

    Yusho Ishii1, Aakriti Alisha Arora1, Scott Jenks1, Iñaki Sanz2 and Arezou Khosroshahi1, 1Emory University, Atlanta, GA, 2Emory University School of Medicine, Atlanta, GA

    Background/Purpose: IgG4-related disease (IgG4-RD) is an immune-mediated disease characterized by fibrotic masses with expansion of IgG4-producing plasma cell in multiple organs such as pancreas, lacrimal…
  • Abstract Number: 0924 • ACR Convergence 2023

    Distinct Cell-Bound Complement Activation Products Associate with Disease Activity and Immune Transcriptional Signatures in SLE

    Gabriel Arguelles, Lynne Mitchell, Dennis Hourcade, John Atkinson, Elisha Roberson and Alfred Kim, Washington University School of Medicine, St. Louis, MO

    Background/Purpose: Complement plays a central role in SLE, generating an array of bioactive soluble and cell-bound complement activation products (CB-CAPs) during disease activity. Data are…
  • Abstract Number: 2582 • ACR Convergence 2023

    Expansion of Circulating HLA-DR+ Peripheral Helper T Cells and CXCR5−CD38+ Mature Naïve B Cells in ACPA-positive Individuals At-risk for and with Classified RA

    Hideto Takada1, Kristen Demoruelle1, Kevin Deane1, Shohei Nakamura2, Yasuhiro Katsumata3, Katsunori Ikari2, Jane Buckner4, William H. Robinson5, Jennifer Seifert1, Marie Feser1, LauraKay Moss1, Jill Norri6, Masayoshi Harigai3, Elena Hsieh1, Michael Holer1 and Yuko Okamoto2, 1University of Colorado Anschutz Medical Campus, Aurora, CO, 2Tokyo Women's Medical University School of Medicine, Tokyo, Japan, 3Tokyo Women's Medical University, Division of Rheumatology, Department of Internal Medicine, Tokyo, Japan, 4Benaroya Research Institute at Virginia Mason, Seattle, WA, 5Stanford University, Palo Alto, CA, 6Colorado School of Public Health, Denver, CO

    Background/Purpose: Production of ACPA following T and B cell interactions is a hallmark of ACPA+ RA. Recently identified peripheral helper T (Tph) cells have B…
  • Abstract Number: 0004 • ACR Convergence 2023

    CD22 X CD79b Bispecific Ab Potently Inhibits B Cell Activation and Plasmablast Accumulation

    Timothy Burwell1, Jeffrey Hall1, Suzanne Cole2, Sarah Tursi1, Isabelle Baribaud3, Kyle Bednar1, Naresh Kumar1, Julie Carman1, Navin Rao2 and Edith Janssen2, 1Janssen Research and Development, LLC, Spring House, PA, 2Janssen Research & Development, LLC, Spring House, PA, 3IGM Biosciences, Inc., Doylestown, PA

    Background/Purpose: B cells contribute to the development and progression of autoimmune diseases through multiple mechanisms. Consequently, modulating B cell activation, B cell effector function, and…
  • Abstract Number: 0925 • ACR Convergence 2023

    IL-4 Acts Through Aryl Hydrocarbon Receptor to Antagonize TLR7-induced Double Negative 2 B Cells in Lupus

    Changming Lu, Hui-chen Hsu, Min Gao, Jose Rubio, Winn Chatham and John Mountz, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: We recently showed that in SLE, IL-4 suppressed the development of interferon-beta (IFNβ) and TLR7-stimulated T-bet+ double negative 2 (DN2) B cells. Here we…
  • Abstract Number: 2583 • ACR Convergence 2023

    A Predictive Model for Progression to Clinical Arthritis Based on Lymphocyte Subsets and ACPA in At-risk Individuals with Arthralgia

    Klára Prajzlerová1, Olga Kryštůfková2, Nikola Kaspříková3, Nora Růžičková2, Hana Hulejová1, Petra Hánová1, Jiri Vencovsky4, Ladislav Senolt5 and Maria Filkova2, 1Institute of Rheumatology, Prague, Czech Republic, 2Institute of Rheumatology and Department of Rheumatology, First Faculty of Medicine, Charles University, Prague, Czech Republic, 3Faculty of Informatics and Statistics, Prague University of Economics and Business, Prague, Czech Republic, 4Institute of Rheumatology, Prague, Czech Republic, Department of Rheumatology, 1st Faculty of Medicine, Charles University, Prague, Czech Republic, 5Institute of Rheumatology and Department of Rheumatology, First Faculty of Medicine, Praha, Czech Republic

    Background/Purpose: The positivity of antibodies against citrullinated proteins (ACPA) substantially increases the risk of developing rheumatoid arthritis (RA). The definition of individuals with arthralgia at…
  • Abstract Number: 0007 • ACR Convergence 2023

    Targeting NF-κB Signalling in B Cells from ANCA-associated Vasculitis Impairs B Cell Biology as a Potential Novel Target

    Ana Merino-Vico1, Jan Piet van Hamburg1, Paul Tuijnenburg1, Aram Al-Soudi1, Carlo Bonasia2, Boy Helder1, Abraham Rutgers2, Wayel H. Abdulahad2, Coen A. Stegeman2, Jan-Stephan Sanders2, Laura Bergamaschi3, Paul A. Lyons3, Theo Bijma2, Laura Van Keep1, Kirsten wesenhagen1, Aldo Jongejan1, Henric Olsson4, Niek De Vries1, Taco W. Kuijpers1, Peter Heeringa2 and Sander Tas5, 1Amsterdam University Medical Centers, Amsterdam, Netherlands, 2University Medical Center Groningen, Groningen, Netherlands, 3University of Cambridge, Cambridge, United Kingdom, 4AstraZeneca, Gothenburg, Sweden, 5Amsterdam UMC, locatie AMC, Utrecht, Netherlands

    Background/Purpose: B cells have gained increased interest in ANCA-associated vasculitis (AAV) research, as the treatment of this autoimmune disease with rituximab (an anti-CD20 B cell…
  • Abstract Number: 0928 • ACR Convergence 2023

    Skewing of B Cell Receptor Repertoire in Unswitched Memory B Cells Is Associated with Disease Activity of Systemic Lupus Erythematosus and Targeted by Belimumab

    Keishi Fujio1, Mineto Ota1, Masahiro Nakano2, Yasuo Nagafuchi3, Satomi Kobayashi1, Hiroaki Hatano2, Ryochi Yoshida1, Yuko Akutsu1, Takahiro Itamiya1, Nobuhiro Ban4, Yumi Tsuchida1, Hirofumi Shoda1, Kazuhiko Yamamoto5, Kazuyoshi Ishigaki6 and Tomohisa Okamura7, 1Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 2Laboratory for Autoimmune Diseases, RIKEN Center for Integrative Medical Sciences, Tokyo, Japan, 3Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, Department of Functional Genomics and Immunological Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 4Research Division, Chugai Pharmaceutical Co., Ltd., Yokohama, Japan, 5Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo and Laboratory for Autoimmune Diseases, Center for Integrative Medical Sciences, RIKEN, Yokohama, Japan, 6RIKEN, Tokyo, Japan, 7Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo and Department of Functional Genomics and Immunological Diseases, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

    Background/Purpose: Despite the involvement of B cells in the pathogenesis of immune-mediated diseases, the biological mechanisms underlying their function are poorly understood. To address this…
  • Abstract Number: 2602 • ACR Convergence 2023

    Spatially Resolved Cellular Signatures Predict Corticosteroid Treatment Response in Giant Cell Arteritis

    Cecilia Ansalone1, Sam McAllister2, Ethan Pickerill3, Lin Zhang3, Annie Peacock2, Dominic McGovern4, Holly Leslie5, Victoria Kellior2, Evelyn Qian2, David Gemperline3, Aysin Tulunay Virlan2, Sylvia Wright6, Paul Cauchi6, Timothy Beckman6, Lisa Hutton6, John Cole1, Isabella Wulur3, Robert Benschop3, Nigel Jamieson5, Carl Goodyear1 and Neil Basu1, 1University of Glasgow, Glasgow, United Kingdom, 2University of Glasgow - School of Infection & Immunity, Glasgow, United Kingdom, 3Eli Lilly and Company, Indianapolis, IN, 4University of Glasgow - School of Medicine, Glasgow, United Kingdom, 5University of Glasgow - School of Cancer Sciences, Glasgow, United Kingdom, 6NHS Greater Glasgow and Clyde, Glasgow, United Kingdom

    Background/Purpose: Corticosteroids (CS) remain the mainstay of giant cell arteritis (GCA) therapy. Between ~30-70% patients relapse following CS taper and are consequently at risk of…
  • Abstract Number: 0014 • ACR Convergence 2023

    The 330 Genetic Risk Loci of Systemic Lupus Erythematosus (SLE) Now Known Are Consonant with Multiple Causal Mechanisms Involving Epstein-Barr Virus (EBV)-Encoded Transcription Co-factors (TFs) in EBV-Infected B Cells

    Viktoryia Laurynenka1, Xiaoting Chen2, sreeja Parameswaran2, Leah Kottyan2, Matthew Weirauch2, Iouri Chepelev3, Kenneth Kaufman3 and John Harley3, 1Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3US Department of Veterans Affairs Medical Center, Cincinnati, OH

    Background/Purpose: Association of EBV infection with SLE, data suggesting an anti-EBNA1 molecular mimicry fostering SLE autoimmunity, and mechanisms in EBV infected B cells support a…
  • Abstract Number: 0932 • ACR Convergence 2023

    The Landscape of Immune Cells in Systematic Lupus Erythematosus Patients with Epstein-Barr Virus Infection by Single-cell Sequencing

    Lingzhen Hu1, Jianxin Tu1, Jiajun Gui2, Mengyuan Fang2, Xiaowei Chen1 and Li Sun1, 1The First Affliated Hospital of Wenzhou Medical University, Wenzhou, China, 2The First Clinical College, Wenzhou Medical University, Wenzhou, China

    Background/Purpose: This study aimed to analyze the immune cell profiles, especially B cells and B-cell receptor (BCR) of systematic lupus erythematosus (SLE) patients with or…
  • Abstract Number: 0082 • ACR Convergence 2023

    A VAV1-Directed Molecular Glue Degrader, MRT-6160, Reduces Joint Inflammation in a Collagen-Induced Arthritis Autoimmune Disease Model

    Adam Cartwright1, Foram Desai2, Sophia Nguyen2, Alexandra Trouilloud2, Elisa Liardo1, Daric Wible2, Ilaria Lamberto2, Bradley Demarco2, Chris King2, Debora Bonenfant1, Sharon Townson2, Owen Wallace2, Filip Janku2, Laura McAllister1, Alison Paterson2 and Marisa Peluso2, 1Monte Rosa Therapeutics, Basel, Switzerland, 2Monte Rosa Therapeutics, Boston, MA

    Background/Purpose: VAV1 is a member of the VAV family of guanine nucleotide exchange factors (GEFs) and plays a critical role in mediating T- and B-cell…
  • Abstract Number: 0951 • ACR Convergence 2023

    Single Cell Analysis of Transitional B Cells in Systemic Sclerosis Highlights Defective Peripheral Tolerance

    Claire Beesley1, Nina Goldman1, David Abraham1, Christopher Denton1, Rizgar Mageed2 and Voon Ong3, 1University College London, London, United Kingdom, 2Queen Mary University of London, London, United Kingdom, 3UCL Medical School Royal Free Campus, London, United Kingdom

    Background/Purpose: Transitional B cells comprise a distinct population of B cells that have recently migrated to the periphery from the bone marrow. In systemic sclerosis…
  • Abstract Number: 0105 • ACR Convergence 2023

    Characterization of B-Cell Subsets in Antiphospholipid Syndrome Patients: Implications for Disease Phenotype and Pathogenesis

    Yin Long1, Jiuliang zhao2, Mengtao Li2 and Xiaofeng Zeng2, 1Peking Union Medical College Hospital Department of Rheumatology and Clinical Immunology, Beijing, China, 2Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Beijing, China

    Background/Purpose: Primary antiphospholipid syndrome (PAPS) is an autoimmune disorder characterized by the presence of pathogenic autoantibodies. The key immune cell subsets change in PAPS patients…
  • Abstract Number: 1227 • ACR Convergence 2023

    Serious Infections Following Rituximab Administration in Children with Systemic Lupus Erythematosus

    Jordan Roberts1, Anna Faino2, Mersine Bryan1, Jonathan Cogen1 and Esi Morgan1, 1Seattle Children's Hospital, Seattle, WA, 2Seattle Children’s Research Institute, Seattle, WA

    Background/Purpose: Rituximab has been associated with high rates of infection among adults with systemic lupus erythematosus. However, studies of infection risk following rituximab among children…
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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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