ACR Meeting Abstracts

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Abstracts tagged "B-Lymphocyte"

  • 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: 0644 • ACR Convergence 2022

    Long-lived Plasma Cells in the Lupus Bone Marrow Are Imprinted by Interferon

    Jennifer Barnas1, Diana Alzamareh2, Neha Nandedkar-Kulkarni2, Jennifer Albrecht2, Nida Meednu2, Cameron Baker2, Andrew McDavid1 and Jennifer Anolik2, 1University of Rochester, Rochester, NY, 2University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Systemic lupus erythematous (SLE) is a complex autoimmune disorder with heterogeneous disease presentation and a multi-pronged pathogenesis. Although autoreactive plasma cells (PC) play a…
  • Abstract Number: 1651 • ACR Convergence 2022

    CAR T Cell Treatment of Refractory Systemic Lupus Erythematosus

    Georg Schett1, Sebastian Böltz2, Fabian Müller2, Arnd Kleyer3, Simon Völkl2, Michael Aigner2, Regina Gary2, Sascha Kretschmann2, David Simon3, Soraya Kharboutli2, Dimitrios mougiakakos4, Gerhard Kroenke3 and Andreas Mackensen2, 1Universitätsklinikum Erlangen, Erlangen, Germany, 2FAU Erlangen-Nürnberg, Erlangen, Germany, 3Department of Internal Medicine 3 – Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg and Universitätsklinikum Erlangen, 91054 Erlangen, Germany; Deutsches Zentrum Immuntherapie, Friedrich-Alexander-UniversityErlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, 4University of Magdeburg, Magdeburg, Germany

    Background/Purpose: Chimeric antigen receptor (CAR) T cells have been used to treat refractory forms of B cell and plasma cell malignancies. B cells are also…
  • Abstract Number: 0006 • ACR Convergence 2022

    Oral Administration of a Novel Pyrrolopyrimidine Derivative That Inhibits BAFF Signaling Suppresses B Cell Differentiation and Production of Autoantibody in Autoimmune Model Mice

    Keiko Yoshimoto1, Katsuya Suzuki2, Yumi Ikeda1, Tsutomu Takeuchi3 and Yuko Kaneko4, 1Div. of Rheumatology, Keio University School of Medicine, Tokyo, Japan, 2Div. of Rheumatology, Keio University School of Medicine, Shinjuku, Japan, 3Keio University and Saitama Medical University, Tokyo, Japan, 4Keio University, Tokyo, Japan

    Background/Purpose: We reported that the expression level of a BAFF receptor (BR3) was upregulated in peripheral monocytes of patients with primary Sjogren's syndrome (pSS) and…
  • Abstract Number: 0754 • ACR Convergence 2022

    Persistent but Disturbed Germinal Center Reaction Among 3rd SARS-CoV-2 Vaccination After Rituximab Exposure

    Ana-Luisa Stefanski1, Hector Rincon-Arevalo1, Eva Schrezenmeier2, Franziska Szelinski1, Jacob Ritter3, Yidan Chen1, Christian Meisel4, Hubert Schrezenmeier5, Andreia C. Lino6 and Thomas Dörner1, 1Department of Rheumatology and Clinical Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany, 2Department of Nephrology and Medical Intensive Care, Charité Universitätsmedizin Berlin; DRFZ Berlin; Berlin Institute of Health Charité Universitätsmedizin Berlin, Berlin, Germany, 3Department of Rheumatology and Clinical Immunology, Berlin Institute of Health Charité Universitätsmedizin Berlin, Berlin, Germany, 4Department of Medical Immunology, Charité University Medicine and Labor Berlin-Charité Vivantes, Berlin, Germany, 5Institute of Transfusion Medicine, Ulm University, Ulm, Germany and Institute for Clinical Transfusion Medicine and Immunogenetics, German Red Cross Blood Transfusion Service Baden-Württemberg – Hessen and University Hospital Ulm, Ulm, Germany, 6Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany

    Background/Purpose: Durable vaccine-mediated immunity relies on the generation of long-lived plasma cells and memory B cells (MBCs), differentiating upon germinal center (GC) reactions. SARS-CoV-2 mRNA…
  • Abstract Number: 1700 • ACR Convergence 2022

    IL-21/STAT3 Pathway Mediated Th2-like Vδ2 T Cells Promote Plasmablasts Differentiation in IgG4-Related Disease

    Jieqiong Li1 and Wen Zhang2, 1Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing, China, 2Peking Union Medical College Hospital, Beijing, China

    Background/Purpose: To explore the phenotype and role of gamma delta (γδ) T cells in the pathogenesis of IgG4-related disease (IgG4-RD), focusing on the effect on…
  • Abstract Number: 0008 • ACR Convergence 2022

    CD11c+ T-Bet+ B Cells Traffic to Human Bone Marrow

    Jennifer Barnas1, Diana Alzamareh2, Nida Meednu2 and Jennifer Anolik2, 1University of Rochester, Rochester, NY, 2University of Rochester Medical Center, Rochester, NY

    Background/Purpose: CD11c+ age/autoimmunity-associated B cells (ABC) are associated with autoantibody producing cells and disease flare in systemic lupus erythematosus. ABC were initially identified in aged…
  • Abstract Number: 0775 • ACR Convergence 2022

    The Distribution and Frequency of Autoreactive B Cells Are Altered in Autoimmune Patients After TNF Inhibitor Treatment

    Tam Quach1, Meggan Mackay2, Cynthia Aranow2 and Anne Davidson2, 1Feinstein Institute for Medical Research, Manhasset, NY, 2Feinstein Institutes for Medical Research, Manhasset, NY

    Background/Purpose: The development of new autoantibodies and secondary autoimmunity is a common and significant side effect of TNF inhibitors (TNFi) which are widely used to…
  • Abstract Number: 1713 • ACR Convergence 2022

    Bank1 Signaling Shapes the Gut Microbiota Composition by Controlling the Gut Mucosal B-cell Response in Lupus

    Georgina Galicia-Rosas, María Botía Sánchez, Daniel Toro-Domínguez, Lorena Albadalejo and Marta Alarcon-Riquelme, Center for Genomics and Oncological Research (GENYO), Granada, Spain

    Background/Purpose: Mucosa-associated commensal bacteria have been shown to be involved in the pathogenesis of systemic lupus erythematosus (SLE). However, its exact role remains to be…
  • Abstract Number: 0011 • ACR Convergence 2022

    B Cell Subsets Contributing to the Autoreactive Plasma Cell Pool in Lyn-/- Mice

    Kristina Ottens, Jalyn Schneider and Anne Satterthwaite, UT Southwestern Medical Center, Dallas, TX

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is characterized by autoantibodies (autoAbs) against nucleic acid containing antigens. These antibodies form immune complexes that promote inflammation and cause organ…
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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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