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Abstracts tagged "B cells"

  • Abstract Number: 814 • 2016 ACR/ARHP Annual Meeting

    The Regulatory B Cells Ameliorate Skin Sclerosis, Lung Fibrosis, and Autoimmunity Via an Anti-Oxidative Effect in Systemic Sclerosis Model Mice

    Ayumi Yoshizaki, Takemichi Fukasawa, Satoshi Ebata, Kouki Nakamura, Takashi Yamashita, Ryosuke Saigusa, Yohei Ichimura, Takehiro Takahashi, Takashi Taniguchi, Asano Yoshihide and Shinichi Sato, Dermatology, The University of Tokyo Graduate School of Medicine, Tokyo, Japan

    Background/Purpose: Systemic sclerosis (SSc) is a connective tissue disease characterized by vascular damage, excessive deposition of extracellular matrix, and fibrosis in the several organs, including…
  • Abstract Number: 1840 • 2016 ACR/ARHP Annual Meeting

    A Dichotomy of Regulatory Immunome Is Related to Disease Activity in Juvenile Systemic Lupus Erythematosus

    Joo Guan Yeo1,2, Thaschawee Arkachaisri1,3, Justin Hung Tiong Tan1, Jing Yao Leong4, Lena Das1, Loshinidevi D/O Thana Bathi2, Phyllis Chen2 and Salvatore Albani3,4, 1Rheumatology and Immunology, KK Women's and Children's Hospital, Singapore, Singapore, 2Singhealth Translational Immunology and Inflammation Centre, Singapore Health Services Pte Ltd, Singapore, Singapore, 3Duke-National University of Singapore Medical School, Singapore, Singapore, 4SingHealth Translational Immunology and Inflammation Centre, Singapore Health Services Pte Ltd, Singapore, Singapore

    Background/Purpose: The pathogenesis of SLE involves disturbances to the homeostatic balance between the immune effector and regulatory system. The conventional mono-dimensional mechanistic interrogation of one…
  • Abstract Number: 2785 • 2016 ACR/ARHP Annual Meeting

    Translatable in Vitro Immunocyte Functional Measures of CC-292 and CC-90008 Inhibitors of the Bruton’s Tyrosine Kinase (Btk)/Tec Family and the Pathology Observed in the MLR/Lpr Mouse Model of Systemic Lupus Erythematosus (SLE)

    Garth Ringheim1, Jolanta Kosek2, Lori Capone3, Mary Adams4,5, Eun Mi Hur4 and Peter H. Schafer5, 186 Morris Avenue, Celgene Corporation, Summit, NJ, 2Translational Development, Celgene Corporation, Summit, NJ, 3Celgene Corporation, Summit, NJ, 4Inflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ, 5Department of Translational Development, Celgene Corporation, Summit, NJ

    Background/Purpose:  CC-292 and CC-90008 are covalent Btk/Tec family kinase inhibitors that block Btk activity by binding with high affinity to the adenosine triphosphate (ATP) binding…
  • Abstract Number: 4L • 2015 ACR/ARHP Annual Meeting

    Efficacy and Safety of Epratuzumab in Patients with Moderate-to-Severe Systemic Lupus Erythematosus: Results from Two Phase 3 Randomized, Placebo-Controlled Trials

    Megan E. B. Clowse1, Daniel J Wallace2, Richard Furie3, Michelle Petri4, Marilyn Pike5, Piotr Leszczynski6, C Michael Neuwelt7, Kathryn Hobbs8, Mauro Keiserman9, Liliana Duca10, Kenneth Kalunian11, Sabine Bongardt12, Christian Stach12, Carolyn Beaudot13, Brian Kilgallen13, Catrinel Galateanu14 and Caroline Gordon15,16, 1Rheumatology, Duke University, Durham, NC, 2Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 3North Shore LIJ Health System, Manhasset, NY, 4Division of Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD, 5Med Pharm Consulting Inc, Cambridge, MA, 6Dept. of Rheumatology and Clinical Immunology, J. Strus Poznan Municipal Hospital, Poznan University of Medical Sciences, Poznan, Poland, 7Division of Rheumatology, Alameda County Medical Center, Oakland, CA, 8Denver Arthritis Clinic, Denver, CO, 9School of Medicine, Pontifical Catholic University, Porto Alegre, Brazil, 10Clinica Neomed, Brasov, Romania, 11UCSD School of Medicine, La Jolla, CA, 12UCB Pharma, Monheim, Germany, 13UCB Pharma, Raleigh, NC, 14UCB Pharma, Brussels, Belgium, 15Rheumatology Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom, 16NIHR/Wellcome Trust Clinical Research Facility, University Hospital Birmingham NHS Foundation Trust, Birmingham, United Kingdom

    Background/Purpose: In phase 2b trials, epratuzumab, a humanized anti-CD22 mAb that modulates B cell signaling without total B cell depletion, significantly improved disease activity in…
  • Abstract Number: 1103 • 2015 ACR/ARHP Annual Meeting

    Phosphatidylserine Outer Layer Translocation Is Implicated in IL-10 Secretion By Human Regulatory B Cells

    Charlotte Hua1, Rachel Audo2, Michael Hahne2, Bernard Combe3, Jacques Morel3 and Claire I. Daien3, 1Department of Rheumatology, Lapeyronie Hospital and Montpellier University, Montpellier, France, 2IGMM-CNRS UMR5535, Montpellier, France, 3Department of rheumatology, Lapeyronie Hospital and Montpellier University, Montpellier, France

    Background/Purpose: B cells can have a negative regulatory role, mainly mediated by interleukin 10 (IL-10) and we recently showed that IL-10 producing B cells (B10…
  • Abstract Number: 1641 • 2015 ACR/ARHP Annual Meeting

    B Cell Depletion with Rituximab in Patients with Rheumatoid Arthritis: Multiplex Bead Array Reveals Kinetics of IgG and IgA Autoantibodies to Citrullinated Antigens

    Geraldine Cambridge1, Lauren J. Lahey2, Maria J. Leandro1, William H. Robinson3 and Jeremy Sokolove4, 1Rheumatology, University College London, London, United Kingdom, 2Medicine, VA Palo Alto HealthCare System and Stanford University, Palo Alto, CA, 3VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 4Medicine, VA Palo Alto Health Care System and Stanford University, Palo Alto, CA

    Background/Purpose: Seropositivity for rheumatoid factors and anti-citrullinated (Cit) protein antibodies (ACPA) are the strongest predictor for clinical response to rituximab (RTX) in rheumatoid arthritis (RA).…
  • Abstract Number: 3157 • 2015 ACR/ARHP Annual Meeting

    B Cell Profile As a Biomarker of Disease Segmentation and Flare Prognosis in SLE

    Chungwen Wei1, Bridget Neary2, Jamie Biear3, Jennifer Barnard3,4, Michelle Petri5, Alex Rosenberg6, Jennifer H. Anolik7 and Ignacio Sanz1, 1Rheumatology, Emory University, Atlanta, GA, 2Emory University, Atlanta, GA, 3Rheumatology, University of Rochester, Rochester, NY, 4Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 5Rheumatology, Johns Hopkins University Hospital, Baltimore, MD, 6University of Rochester, Rochester, NY, 7University of Rochester Medical Center, Rochester, NY

    Background/Purpose: B cell abnormalities in SLE are well-established contributors to disease pathogenesis. Perturbation of B cell homeostasis in SLE is often described separately for each…
  • Abstract Number: 1104 • 2015 ACR/ARHP Annual Meeting

    Mouse B Cells Require Glucose and Free Fatty Acids As Carbon Sources for Cytokine and Chemokine Secretion

    Doujiao Wu1, Dongyue Huang2, Edward Pearce1 and Alfred Kim2, 1Pathology & Immunology, Washington University School of Medicine, Saint Louis, MO, 2Rheumatology, Washington University School of Medicine, Saint Louis, MO

    Background/Purpose: B cells contribute to disease pathophysiology through several mechanisms, including cytokine and chemokine secretion. A wide variety of stimuli can activate B cells including…
  • Abstract Number: 1667 • 2015 ACR/ARHP Annual Meeting

    Clinical Parameters and B Cell Subsets As Biomarkers of Response to Tocilizumab in Rheumatoid Arthritis

    Anna Laura Fedele, Barbara Tolusso, Elisa Gremese, Silvia Canestri, Clara Di Mario, Marcin Nowik and Gianfranco Ferraccioli, Division of Rheumatology, Institute of Rheumatology, Catholic University of the Sacred Heart, Rome, Italy

    Background/Purpose: Tocilizumab (TCZ) is an effective treatment for Rheumatoid Arthritis (RA) and it is a modifier of B cell subsets in vivo, inducing changes in…
  • Abstract Number: 1105 • 2015 ACR/ARHP Annual Meeting

    The IgG/IgG4 mRNA Ratio By Quantitative PCR Accurately Diagnoses IgG4-Related Disease and Predicts Treatment Response

    Lowiek Hubers1, Marieke Doorenspleet2, Paulus Klarenbeek3, Emma Culver4, Lucas Maillette de Buy Wenniger5, Roger Chapman4, Stan Van de Graaf6, Joanne Verheij7, Thomas Van Gulik8, Frank Baas9, Ellie Barnes4, Ulrich Beuers1 and Niek De Vries3, 1Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research, Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 2Dept. of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and immunology Center | Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 3Dept. of Clinical Immunology & Rheumatology, Amsterdam Rheumatology and immunology Center, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 4Translational Gastroenterology Unit and NDM Oxford University, Translational Gastroenterology Unit and NDM Oxford University, John Radcliffe Hospital/Oxford University, Oxford, United Kingdom, 51Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research, Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 6Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research,, Dept. of Gastroenterology & Hepatology and Tytgat Institute of Liver and Intestinal Research, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 7Dept. of Pathology, Dept. of Pathology, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 8Dept. of Surgery, Dept. of Surgery, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands, 9Dept. of Genome Analysis, Academic Medical Center/University of Amsterdam, Amsterdam, Netherlands

    Background/Purpose : IgG4-associated cholangitis (IAC) and autoimmune pancreatitis (AIP) are major manifestations of IgG4-related disease (IRD). Misdiagnosis and inadequate treatment are common since IAC and…
  • Abstract Number: 1668 • 2015 ACR/ARHP Annual Meeting

    Patterns of Relapse in the Rheumatoid Arthritis Cohort Treated with Rituximab at University College London

    Elena Becerra, Geraldine Cambridge, Inmaculada de la Torre and Maria J. Leandro, Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom

    Patterns of relapse in the Rheumatoid Arthritis cohort treated with Rituximab at University College LondonBackground/Purpose: Two patterns of relapse were defined in the first studies…
  • Abstract Number: 1107 • 2015 ACR/ARHP Annual Meeting

    Inhibition of B Cell Activation and Plasma Cell Differentiation By Epratuzumab, a Humanized Monoclonal Antibody Targeting CD22

    Natalia V. Giltiay1, Geraldine L. Shu2, Anthony Shock3 and Edward A. Clark1,2, 1Division of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, 2Department of Immunology, University of Washington, Seattle, WA, 3UCB Pharma, Slough, United Kingdom

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by B cell hyperactivity and production of autoantibodies. Treatment of patients with moderate-to-severe SLE with epratuzumab, a humanized…
  • Abstract Number: 1754 • 2015 ACR/ARHP Annual Meeting

    BANK1 Controls the Development of SLE By Modulating TLR7 Signaling and Type I IFN-Induced Translation Initiation Pathway in B Cells

    Ying-Yu Wu1, Ramesh Kumar2, Harini Bagavant1 and Marta E. Alarcon Riquelme3, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Oklahoma Medical Research Foundation, Oklahoma Cty, OK, 3Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Center for Genomics and Oncological Research Pfizer-University of Granada-Junta de Andalucia, Oklahoma City, OK

    Background/Purpose: BANK1 is a susceptibility gene for SLE, and we have shown that stimulation of TLR9 agonist leads to a reduction in the activation of…
  • Abstract Number: 1 • 2015 ACR/ARHP Annual Meeting

    The Integrin Very Late Antigen-4 Plays a Key Role in the Recruitment of B Cells at the Inflammatory Foci

    Estefanía Armas-González1, Ana Díaz-Martín2, María Jesús Domínguez-Luis3, María Teresa Arce-Franco2 and Federico Díaz-González4, 1Universidad de La Laguna, Pharmacology Department, Tenerife, Spain, 2Hospital Universitario de Canarias, Rheumatology Service, Tenerife, Spain, 3CIBICAN, Center of Biomedical Research of the Canary Islands, University of La Laguna, Tenerife, Spain, 4Investigation Unit, Sociedad Española de Reumatológía, Madrid, Spain

    Background/Purpose: Experimental data suggest that B cells must migrate and accumulate into the synovial membrane to exert their pathogenic role in rheumatoid arthritis (RA). Leukocyte…
  • Abstract Number: 1108 • 2015 ACR/ARHP Annual Meeting

    Epratuzumab, a Monoclonal Antibody Targeting CD22 on B Cells, Stimulates the Phosphorylation of Upstream Inhibitory Signals of the B Cell Receptor

    Simon Lumb1, Sarah J. Fleischer2, Capucine Daridon2, Alison Maloney1, Anthony Shock1 and Thomas Dorner2, 1UCB Pharma, Slough, United Kingdom, 2Charité University Medicine Berlin, CC12, Dept. Medicine/Rheumatology and Clinical Immunology and German Rheumatism Research Center Berlin (DRFZ), a Leibniz Institute, Berlin, Germany

    Background/Purpose: Epratuzumab, a humanized monoclonal antibody targeting CD22, is currently in phase 3 clinical trials in patients with systemic lupus erythematosus (SLE). Previous work suggests…
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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 CT on October 25. 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].

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