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 "B cells"

  • Abstract Number: 860 • 2014 ACR/ARHP Annual Meeting

    Inhibition of G Protein βγ Signaling Inhibits Nephritis in Lupus Prone Mice

    Teresa Owen1, Javier Rangel-Moreno2, Jesi To3, Bruce Goldman4, Alan Smrcka3 and Jennifer H. Anolik5, 1Rheumatology, University of Rochester, Rochester, NY, 2Medicine- Allergy, Immunology, and Rheumatology, University of Rochester, Rochester, NY, 3Pharmacology & Physiology, University of Rochester, Rochester, NY, 4Pathology, University of Rochester, Rochester, NY, 5Medicine- Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY

    Background/Purpose G protein-coupled receptors (GPCRs), including chemokine receptors on leukocytes, signal through G protein Gβγ subunits. An important target of Gβγ is phosphoinositide 3 kinase γ…
  • Abstract Number: 2693 • 2014 ACR/ARHP Annual Meeting

    Hyporesponsiveness to TLR9 in Term of Cytokines Production By B Cells in SLE-Patients

    Julia Sieber1, Capucine Daridon1, Sarah J. Fleischer1, Vanessa Fleischer1, Falk Hiepe1, Tobias Alexander2, Guido Heine3, Gerd Burmester4, Simon Fillatreau5 and Thomas Dörner1, 1Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 2Dept. Medicine/Rheumatology and Clinical Immunology, Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 3Charité University Medicine, Dept. Dermatology, Venerology and Allergology, Berlin, Germany, 4Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology, Berlin, Germany, 5German Rheumatism Research Center (DRFZ), Berlin, Germany

    Background/Purpose The role of B cells in immunity has been mainly related to the generation of antibodies and formation of immune complexes. However, B cells…
  • Abstract Number: 1938 • 2014 ACR/ARHP Annual Meeting

    Effects of Mesenchymal Stem Cells on Human B Cell Proliferation

    Erin Collins1, Maosong Qi2 and Gary S. Gilkeson3, 1Medicine/Rheumatology, Medical University of South Carolina, Charleston, SC, 2Medicine/ Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 3Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC

    Background/Purpose: Human mesenchymal stem cells (MSC) are progenitor cells that have immunomodulatory properties.  MSCs have been used to treat a variety of autoimmune diseases, including…
  • Abstract Number: 859 • 2014 ACR/ARHP Annual Meeting

    TGF-β3-Producing CD4+CD25–LAG3+ Regulatory T Cells Control B Cell Responses

    Tomohisa Okamura1, Kaoru Morita1, Mariko Inoue1, Toshihiko Komai1, Yukiko Iwasaki1, Shuji Sumitomo1, Shinichiro Nakachi1, Hirofumi Shoda2, Keishi Fujio2 and Kazuhiko Yamamoto1, 1Department of Allergy and Rheumatology, Graduate School of Medicine, the University of Tokyo, Tokyo, Japan, 2Department of Allergy and Rheumatology, The University of Tokyo, Tokyo, Japan

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibody production and associated with a wide range of clinical manifestations. Recent case-control association…
  • Abstract Number: 2691 • 2014 ACR/ARHP Annual Meeting

    A Novel CD123–CD11c– Dendritic Cell Subset Increased in Relation to Disease Activity in Patients with Systemic Lupus Erythematosus

    Satoshi Kubo1, Shingo Nakayamada1, Naoki Yunoue1, Maiko Yoshikawa1, Kunihiro Yamaoka1 and Yoshiya Tanaka2, 1The First Department of Internal Medicine, University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2University of Occupational and Environmental Health, Japan, Kitakyushu, Japan

    Background/Purpose Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by overproduction of autoantibodies by B cells and breaking self-tolerance of T cells and dendritic…
  • Abstract Number: 1754 • 2014 ACR/ARHP Annual Meeting

    Peripheral CD5+ b-Cells in ANCA-Associated Vasculitis

    Sebastian Unizony1, Noha Lim2, Vincent Carey3, Deborah J. Phippard2, Nadia Tchao2, Eli M. Miloslavsky4, Peter A. Merkel5, Paul Monach6, William St. Clair7, Robert F. Spiera8, Adam Asare2, Philip Seo9, Carol A. Langford10, Gary S. Hoffman11, Cees Kallenberg12, Ulrich Specks13 and John H. Stone4, 1Rheumatology, Allergy and Immunology, Massachusetts General Hospital, Boston, MA, 2Immune Tolerance Network, Bethesda, MD, 3Channing Division of Network Medicine, Brigham and Women's Hospital, Boston, MA, 4Rheumatology, Massachusetts General Hospital, Boston, MA, 5Vasculitis Center, Division of Rheumatology, University of Pennsylvania, Philadelphia, PA, 6Rheumatology, Boston University, Boston, MA, 7Rheumatology and Immunology, Duke University, Durham, NC, 8Rheumatology, Hospital for Special Surgery, New York, NY, 9Rheumatology Division, Johns Hopkins Vasculitis Center, Johns Hopkins University, Baltimore, MD, 10Center for Vasculitis Care and Research, Cleveland Clinic, Cleveland, OH, 11Rheumatic & Immunologic Dis, Cleveland Clinic Foundation, Cleveland, OH, 12Rheumatology and Clinical Immunology, University of Groningen, Groningen, Netherlands, 13Frederichs Dr NW, Mayo Clinic, Rochester, MN

    Background/Purpose We explored the utility of peripheral CD19+ CD5+ B-cells (CD5+ B-cells) as biomarkers in ANCA-associated vasculitis (AAV)   Methods CD5+ B-cells were measured longitudinally by…
  • Abstract Number: 858 • 2014 ACR/ARHP Annual Meeting

    ABT-199, a Potent and Selective BCL-2 Inhibitor, Prevents Lupus Nephritis in the Spontaneous NZB/W F1 Mouse Model By Depleting Selective Lymphocyte Populations While Sparing Platelets

    Li Chun Wang1, Stuart Perper1, Annette Schwartz2, Christian Goess3, Liz O'connor4, Dawna Hartman2, Candace Graff2, Andrew Souers5, Joel Leverson5, Steven Elmore5 and Lisa Olson2, 1Immunology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 2AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 3Pharmacology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 4Toxicology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 5AbbVie Inc, North Chicago, IL

    Background/Purpose Proteins in the BCL-2 family are key regulators of apoptosis, or programmed cell death. Navitoclax, a selective inhibitor of both BCL-2 and BCL-X(L) demonstrated…
  • Abstract Number: 2185 • 2014 ACR/ARHP Annual Meeting

    Alterations in B Cell Complement Processing Related to a Lupus-Associated Variant in Complement Receptor 2

    Brendan M. Giles1 and Susan A. Boackle2, 1University of Colorado School of Medicine, Aurora, CO, 2Medicine/Rheumatology, University of Colorado School of Medicine, Aurora, CO

    Background/Purpose: We have recently identified a variant in intron 1 of complement receptor 2 (CR2/CD21) that is associated with decreased risk of lupus (rs1876453; Pmeta=4.2×10-4,…
  • Abstract Number: 1718 • 2014 ACR/ARHP Annual Meeting

    B Cell Subsets Homeostasis and Functional Properties Are Altered in a Murine Model of Systemic Sclerosis

    Sébastien Sanges1,2,3, Niloufar Kavian4, Carine Hauspie1,3,5, Carole Nicco4, Thomas Guerrier1,3, Virginie Dutoit-Lefèvre1,3, Guillaume Lefèvre1,2,5,6, Alexandra Forestier1,2,3, Vincent Sobanski1,2,6, Christelle Faveeuw7, Myriam Labalette1,3,5, Frédéric Batteux4, David Launay1,2,3 and Sylvain Dubucquoi1,3,5, 1Université Lille Nord de France, Faculté de Médecine Henri Warembourg, Lille, Lille, France, 2Service de médecine interne, Centre National de Référence de la Sclérodermie Systémique, Hôpital Claude Huriez, CHRU Lille, Lille, France, 3EA 2686, Lille, Lille, France, 4Université Paris Descartes, EA 1833, Hôpital Cochin, AP-HP, Paris, Paris, France, 5Institut d’Immunologie, Centre de Biologie-Pathologie-Génétique, CHRU Lille, Lille, France, 6EA 2686, Lille, LILLE, France, 7Institut National de la Santé et de la Recherche Médicale Unité 547, Institut Pasteur de Lille, Institut Fédératif de Recherche 142, Université de Lille Nord de France, Lille, France

    Background/Purpose Systemic sclerosis (SSc) is a multi-organ fibrotic disease associated with auto-immune abnormalities. Several clinical and experimental observations suggest that B cells are involved in…
  • Abstract Number: 756 • 2014 ACR/ARHP Annual Meeting

    Nucleosome, a Basic Repeating Unit of Chromatin, in Patients with Systemic Sclerosis: Possible Association with Immunological Abnormalities Via Abnormal Activation of T and B Cells

    Ayumi Yoshizaki1, Yoshihide Asano2, Takashi Taniguchi1, Ryosuke Saigusa1, Kouki Nakamura1, Takashi Yamashita1, Takehiro Takahashi1, Tetsuo Toyama1, Yohei Ichimura1, Zenshiro Tamaki1, Miki Miyazaki1 and Shinichi Sato1, 1Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2University of Tokyo Graduate School of Medicine, Tokyo, Japan

    Background/Purpose Nucleosome is the basic repeating units of chromatin. Each nucleosome is composed of an inner core of histones H3 and H4 and an outer…
  • Abstract Number: 1951 • 2014 ACR/ARHP Annual Meeting

    A Novel CD27(-) Spleen Tyrosine Kinase (Syk) Bright Memory B-Cell Subset Is Expanded in SLE

    Sarah Fleischer1, Claudia Giesecke1, Henrik Mei1, Peter E. Lipsky2, Capucine Daridon3 and Thomas Dörner3, 1Charité University Medicine Berlin, CC12, Dept. Medicine/Rheumatology and Clinical Immunology and German Rheumatism Research Center Berlin (DRFZ), Berlin, Germany, Berlin, Germany, 2Peking Union Medical College Hospital, Beijing, China, 3CC12, Dept. Medicine/Rheumatology and Clinical Immunology, Charité University Medicine Berlin, Berlin, Germany

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease known to be associated with a breakdown of self-tolerance, B-cell hyperactivity and disturbed B-cell homeostasis of…
  • Abstract Number: 1623 • 2014 ACR/ARHP Annual Meeting

    Increased CD95 (Fas) Expression on Naive B Cells Is Associated with a Switch to Double Negative and Plasma Cells in the Peripheral Blood, and Correlates with Disease Activity in Systemic Lupus Erythematosus

    Julie Ducreux1, Séverine Nieuwland2, Frédéric A. Houssiau1 and Bernard R. Lauwerys1, 1Institut de Recherche Expérimentale et Clinique, Pôle de Maladies Rhumatismales, Université catholique de Louvain, Brussels, Belgium, 2Institut de Recherche Expérimentale et Clinique, Pôle de pathologies rhumatismales, Université catholique de Louvain, Brussels, Belgium

    Background/Purpose: systemic lupus erythematosus (SLE) is characterized by a break of tolerance to autoantigens, and polyclonal activation of B cells. We performed multicolor flow cytometry…
  • Abstract Number: 662 • 2014 ACR/ARHP Annual Meeting

    Interferon Regulatory Factor-5 Promotes Disease in the MRL/Lpr Mouse Model of Lupus

    Amanda Watkins1, Ramon Bonegio2, Guneet Kochar1, Gabriella Wilson1, Bari Laskow1, Christophe Richez1, Ian Rifkin1 and Kei Yasuda3, 1Boston University School of Medicine, Boston, MA, 2Renal, Boston University School of Medicine, Boston, MA, 3Medicine, Boston University School of Medicine, Boston, MA

    Background/Purpose Interferon regulatory factor 5 (IRF5) polymorphisms are strongly associated with an increased risk of developing Systemic Lupus Erythematosus (SLE).  SLE is caused, in part,…
  • Abstract Number: 1950 • 2014 ACR/ARHP Annual Meeting

    Circulating CD19+CD38+CD43+  B Cell Subset in SLE Patients Have More Cell Cycle Related Genes Than Healthy Controls

    Hiroshi Fujii1, Tomoaki Machiyama1, Kanae Akita2, Yukiko Kamogawa1, Ryu Watanabe1, Yoko Fujita3, Yuko Shirota4, Shinichiro Saito5, Tomonori Ishii6 and Hideo Harigae1, 1Department of Hematology and Rheumatology, Tohoku University, Sendai, Japan, 2Department of Heatology and Rheumatology, Tohoku University, Sendai, Japan, 3Department of Hematolgy and rheumatolgy, Tohoku University, Sendai, Japan, 4Department of Hematology and Rheumatolgy, Tohoku University, Sendai, Japan, 5Department of hematology and rheumatology, Tohoku University, Sendai, Japan, 6Seiryouchou Aobaku, Tohoku University, Sendai, Japan

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic inflammatory disease associated with deposition of autoantibodies such as anti DNA antibody. After activation of B cells…
  • Abstract Number: 1640 • 2014 ACR/ARHP Annual Meeting

    Cyclophosphamide Diminishes Plasmablasts and Transitional B Cells and Suppresses Autocrine Production of B Cell Activating Factor of Tumor Necrosis Factor Family (BAFF) in These Cells in Patients with Systemic Lupus Erythematosus

    Yuko Okamoto1, Yasuhiro Katsumata1, Yasushi Kawaguchi1, Manabu Kawamoto1, Takahisa Gono1, Masanori Hanaoka1, Tomoaki Higuchi1, Hidenaga Kawasumi1 and Hisashi Yamanaka2, 1Institute of Rheumatology, Tokyo Women's Medical University, Tokyo, Japan, 2Institute of Rheumatology, Tokyo Women’s Medical University, Tokyo, Japan

    Background/Purpose . B cell activating factor of tumor necrosis factor family (BAFF) is a positive regulator of B cell function and expressed in dendritic cells,…
  • « Previous Page
  • 1
  • …
  • 14
  • 15
  • 16
  • 17
  • 18
  • …
  • 25
  • 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