ACR Meeting Abstracts

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Abstracts tagged "B cells"

  • Abstract Number: 986 • 2014 ACR/ARHP Annual Meeting

    Integrated Comprehensive Analysis of Immune Cell Subsets and Serum Protein Profile Identifies the Role of Pre-Germinal Center B Cells in Sjogren’s Syndrome Pathogenesis

    Yoshiaki Kassai1, Katsuya Suzuki2, Rimpei Morita3, Maiko Takiguchi1, Rina Kurisu1, Takahiro Miyazaki1, Akihiko Yoshimura3 and Tsutomu Takeuchi2, 1Inflammation Drug Discovery Unit, Takeda Pharmaceutical Company Limited, Kanagawa, Japan, 2Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 3Department of Microbiology and Immunology, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose Whole blood flow cytometric analysis and serum protein profiling were commonly utilized to characterize disease-specific alterations in a wide variety of autoimmune diseases. However,…
  • Abstract Number: L3 • 2014 ACR/ARHP Annual Meeting

    Low Protein A20 Expression in Minor Salivary Glands Is Associated with Lymphoma Development in Primary Sjögren’s Syndrome

    Svein Joar A. Johnsen1, Einar Gudlaugsson2, Ivar Skaland2, Emiel Janssen2, Malin V. Jonsson3, Lars Helgeland4, Ellen Berget5, Roland Jonsson6 and Roald Omdal1, 1Clinical Immunology Unit, Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway, 2Stavanger University Hospital, Stavanger, Norway, 3Department of Clinical Dentistry - Section for Oral and Maxillofacial Radiology, University of Bergen, Bergen, Norway, 4Haukeland University Hospital, Bergen, Norway, 5University of Bergen, Bergen, Norway, 6Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, Bergen, Norway

    Background/Purpose: Patients with primary Sjogrens syndrome (pSS) have an increased risk of developing lymphomas, especially of the subtype mucosa-associated lymphoid tissue (MALT) lymphoma. Chronic antigen…
  • Abstract Number: 2870 • 2014 ACR/ARHP Annual Meeting

    B Cell-Intrinsic Deletion of the Type 1 Interferon Receptor Does Not Impact the Development of Murine Lupus

    Shaun W. Jackson1,2, Nicole Scharping1, Socheath Khim1 and David Rawlings1,2, 1Seattle Children's Research Institute, Seattle, WA, 2Pediatrics, University of Washington, Seattle, WA

    Background/Purpose Type 1 interferon (IFN) is strongly implicated in lupus pathogenesis, and patients with SLE frequently express a “type 1 IFN gene signature”. Type 1…
  • Abstract Number: 1947 • 2014 ACR/ARHP Annual Meeting

    Prolactin Promotes Survival of Immature B Cells from MRL/Lpr Mice

    Karina Chavez-Rueda1, Rocio Flores-Fernández1, Francisco Blanco-Favela1, María Legorreta-Haquet2, Luis Chávez-Sánchez2, Rafael Hernández-González3 and Emiliano Tesoro-Cruz3, 1UIM en Inmunologia, IMSS, Mexico DF, Mexico, 2IMSS, Mexico DF, Mexico, 3Departamento de Investigación Experimental y Bioterio, Instituto Nacional de Ciencias Médicas y Nutrición, Mexico DF, Mexico

    Background/Purpose Prolactin (PRL) plays an important role in modulating the immune response. PRL is secreted by the pituitary gland as well as many other organs…
  • Abstract Number: 1000 • 2014 ACR/ARHP Annual Meeting

    Pathogenic Role of CXC Chemokine receptor 3-Positive B Cells in Bone Destruction of Rheumatoid Arthritis

    Yuri Hirosaki, Hiroaki Niiro, Shun-ichiro Ota, Naoko Ueki, Hirofumi Tsuzuki, Kumiko Noda, Siamak Jabbarzadeh-Tabrizi, Hiroki Mitoma, Yojiro Arinobu, Mitsuteru Akahoshi, Hiroshi Tsukamoto and Koichi Akashi, Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan

    Background/Purpose :B cells can function as potent effector cells by production of autoantibody, immune complex formation and inflammatory cytokines. Clinical efficacy of B-cell depletion therapy…
  • Abstract Number: 2872 • 2014 ACR/ARHP Annual Meeting

    B-Cell Autoepitope and Tetramer Analysis Reveals Expansion of Apoptotic Autoantigen La and snRNP Reactive B Cells in BXD2 Mice

    Jennie Hamilton1, Jun Li2, Qi Wu3, PingAr Yang3, Bao Luo3, Hao Li4, Troy Randall5, John Edwin Bradley5, Justin J. Taylor6, John D. Mountz7,8 and Hui-Chen Hsu3,4, 1University of Alabama at Birmingham, Birmingham, AL, 2Med - Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 5Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 6Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 7Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL, 8Birmingham VA Medical Center, Birmingham, AL

    Background/Purpose Systemic lupus erythematous (SLE) is characterized by production of highly pathogenic IgG autoantibodies (autoAbs).  While serum autoAb profiling is standard, it remains challenging to…
  • Abstract Number: 1946 • 2014 ACR/ARHP Annual Meeting

    CD22 Is Required for Formation of Memory B Cell Precursors within Germinal Centers

    Craig Chappell, Kevin Draves and Edward Clark, Immunology, University of Washington, Seattle, WA

    Background/Purpose CD22 is a sialic-acid binding co-receptor expressed primarily on B cells that has a number of functions including adhesion, regulation of B cell homeostasis and…
  • Abstract Number: 999 • 2014 ACR/ARHP Annual Meeting

    Microrna-155 As an Epigenetic Regulator of B-Cell Activation in Rheumatoid Arthritis: In Vivo and in Vitro Evidences

    Stefano Alivernini1, Barbara Tolusso1, Silvia Canestri1, Luca Petricca1, Clara Di Mario2, Elisa Gremese1 and Gianfranco Ferraccioli1, 1Division of Rheumatology, Institute of Rheumatology and Affine Sciences, Catholic University of the Sacred Heart, Rome, Italy, 2Division of Pathology, Catholic University of the Sacred Heart, Rome, Italy

    Background/Purpose: MicroRNAs (miRs) are a novel class of post-transcriptional regulators. miR-155 was shown to be a regulator of B cell biology in haematological diseases as…
  • Abstract Number: 2873 • 2014 ACR/ARHP Annual Meeting

    Epratuzumab Induces Broad Inhibition of B Cell Receptor Proximal Signaling but Has Opposing Effects on Distal Signaling in B Cell Subsets: A Profile of Effects on Functional Immune Signaling By Single Cell Network Profiling

    Alison Maloney1, Drew Hotson2, Stephen Rapecki1, Gianluca Fossati1, Simon Lumb1, David Rosen2, Santosh Putta2, Nikil Wale2, David Spellmeyer2, Alessandra Cesano2, Rachael Hawtin2 and Anthony Shock1, 1UCB Pharma, Slough, United Kingdom, 2Nodality Inc., South San Francisco, CA

    Background/Purpose Epratuzumab is a humanized monoclonal antibody targeting the B cell-specific protein CD22 and is in Phase 3 clinical trials in patients with systemic lupus…
  • Abstract Number: 1945 • 2014 ACR/ARHP Annual Meeting

    Pharmacodynamic Effects of the CD22-Targeted Monoclonal Antibody Epratuzumab on B Cells in Patients with Systemic Lupus Erythematosus

    Anthony Shock1, Brian Kilgallen2, Willem Koetse2, Christian Stach3, Sabine Bongardt3 and Catrinel Galateanu4, 1UCB Pharma, Slough, United Kingdom, 2UCB Pharma, Raleigh, NC, 3UCB Pharma, Monheim, Germany, 4UCB Pharma, Brussels, Belgium

    Background/Purpose Epratuzumab is a humanized monoclonal antibody (mAb) that targets the B cell-specific protein CD22 and is currently in Phase 3 clinical trials in patients…
  • Abstract Number: 998 • 2014 ACR/ARHP Annual Meeting

    β2 Adrenoceptor Signal Is Augmented in B Cells in the Course of Arthritis to Increase IL-10

    Georg Pongratz1, Clemens Wiest2, Madlen Melzer2 and Rainer Straub3, 1Internal Medicine I, University Hospital Regensburg, Regensburg, Germany, 2University Hospital Regensburg, Regensburg, Germany, 3Internal Medicine, University Hospital Regensburg, Regensburg, Germany

    Background/Purpose Splenic B cells from collagen-induced arthritis (CIA) mice react to a β2-adrenoceptor (AR) stimulus with increased IL-10 production and adoptive transfer of these cells…
  • Abstract Number: 2836 • 2014 ACR/ARHP Annual Meeting

    Effects of Blisibimod, an Inhibitor of B Cell Activating Factor, on Patient Reported Outcomes and Disease Activity in Patients with Systemic Lupus Erythematosus

    Michelle Petri1, Renee S. Martin2, Colin Hislop2, Morton A. Scheinberg3 and Richard Furie4, 1Johns Hopkins University School of Medicine, Baltimore, MD, 2Anthera Pharmaceuticals Inc, Hayward, CA, 3Rheumatology Hospital Abreu Sodre Pesquisa Clínica, São Paulo, Brazil, 4Division of Rheumatology and Allergy-Clinical Immunology, North Shore - Long Island Jewish Health System, Great Neck, NY

    Background/Purpose: To conduct secondary endpoint analyses of the effects of subcutaneously-administered blisibimod (A-623, AMG 623), an inhibitor of B-cell activating factor (BAFF), on patient-reported outcomes and…
  • Abstract Number: 1944 • 2014 ACR/ARHP Annual Meeting

    Targeting CD22 with Epratuzumab Impacts Cytokine Production By B Cells

    Vanessa Fleischer1,2, Julia Sieber1,2, Sarah J. Fleischer3,4, Anthony Shock5, Guido Heine6, Capucine Daridon1,2 and Thomas Dörner1,2, 1CC12, Dept. Medicine/Rheumatology and Clinical Immunology, Charité University Medicine Berlin, Berlin, Germany, 2German Rheumatism Research Centre Berlin, Berlin, Germany, 3Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 4Department of Medicine/Rheumatology and Clinical Immunology, Charité University Medicine Berlin, Berlin, Germany, 5UCB Pharma, Slough, United Kingdom, 6Department of Dermatology, Venerology and Allergology, Charité University Medicine Berlin, Berlin, Germany

    Background/Purpose CD22 is a negative co-receptor of the B-cell receptor (BCR) and, when targeted by epratuzumab, partially inhibits BCR signaling, for example by reducing Syk…
  • Abstract Number: 995 • 2014 ACR/ARHP Annual Meeting

    Rheumatoid Arthritis Patients Have Alterations in Inherently Autoreactive 9G4+ B-Cell Subpopulations in Peripheral Blood

    Rita A. Moura1,2, Maria J. Leandro3, Venkat Reddy1, João E. Fonseca2,4 and Geraldine Cambridge3, 1Centre for Rheumatology Research, Division of Medicine, University College London, London, United Kingdom, 2Rheumatology Research Unit, Instituto de Medicina Molecular, Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal, 3Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 4Rheumatology Department, Centro Hospitalar de Lisboa Norte, EPE, Hospital de Santa Maria, Lisbon, Portugal

    Background/Purpose B-cells utilizing the VH-region immunoglobulin gene VH4-34 produce natural autoreactive antibodies. The rat monoclonal antibody 9G4 recognizes B-cells with VH4-34-encoded B-cell receptors (9G4+ B-cells)…
  • Abstract Number: 2820 • 2014 ACR/ARHP Annual Meeting

    Dual Role for B Cells in Promoting Bone Erosion in Rheumatoid Arthritis Via Effects on Osteoclast and Osteoblast Differentiation

    Nida Meednu1, Hengwei Zhang2, Teresa Owen3, Lianping Xing4 and Jennifer H. Anolik5, 1Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 2Pathology and Laboratory Medicine, University of Rochester, Rochester, NY, 3Rheumatology, University of Rochester, Rochester, NY, 4Pathology & Lab Medicine, University of Rochester, Rochester, NY, 5Medicine- Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY

    Background/Purpose Rheumatoid arthritis (RA) is a systemic autoimmune disease that often leads to joint damage, a process mediated by an imbalance between bone resorption and…
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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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