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: 746 • 2016 ACR/ARHP Annual Meeting

    Discrepancy in Rituximab-Induced B-Cell Depletion in Peripheral Blood and the Kidney and Relationship with Clinical Response in Patients with Lupus Nephritis

    Ruth J. Pepper1, Venkat Reddy2, Scott Henderson3 and Maria J. Leandro4, 1UCL Centre for Nephrology, Royal Free Hospital, London, United Kingdom, 2Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom, 3UCL Centre for Nephrology, University College London, London, United Kingdom, 4Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: Patients with lupus nephritis (LN) achieve variable clinical response following Rituximab (RTX) based B-cell depletion therapy, with rituximab treatment aiming to decrease the use…
  • Abstract Number: 1449 • 2016 ACR/ARHP Annual Meeting

    The Efficiency of the Regulation of Ca2+ Entry through Calcium Release-Activated Calcium Channel in the Treatment of Rheumatoid Arthritis

    Shuang Liu1, Hitoshi Hasegawa2, Takeshi Kiyoi3, Tatsuya Sawasaki4 and Kazutaka Maeyama5, 1Dept. Pharmacology,, Ehime University Graduate School of Medicine, Toon-shi, Japan, 2Department of Bioregulatory Medicine, Ehime University Graduate School of Medicine, Toon, Japan, 3Bioscience, Integrated Center for Sciences, Ehime University, Ehime, Japan, 4Division of Cell-Free Sciences, Proteo-Science Center, Ehime University, Matsuyama, Japan, 5Department of Pharmacology, Informational Biomedicine, Ehime University Graduate School of Medicine, Toon-shi, Ehime, Japan

    Background/Purpose:  The regulation of Ca2+ entry by targeting a store-operated calcium release-activated channel (CRAC), known as ORAI, has shown benefits in the treatment of rheumatoid…
  • Abstract Number: 2117 • 2016 ACR/ARHP Annual Meeting

    B Cell Phenotype and in Vitro Function in Patients with Rheumatoid Arthritis Developing Low Serum Immunoglobulins after Multiple Cycles of Rituximab

    Geraldine Cambridge1, Rita A. Moura2, Venkat Reddy3 and Maria J. Leandro1, 1Centre for Rheumatology, 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, Lisbon, Portugal, 3Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: Repeat treatment with rituximab (RTX) predisposes some patients with rheumatoid arthritis (RA) to develop low levels of serum immunoglobulins (Igs). Understanding B cell function…
  • Abstract Number: 762 • 2016 ACR/ARHP Annual Meeting

    Pragmatic Treatment of Patients with Systemic Lupus Erythematosus with Rituximab: Long-Term Effects on Serum Immunoglobulins

    Venkat Reddy1, Lina Martínez-Estupiñán2, David A. Isenberg3, Maria J. Leandro3 and Geraldine Cambridge3, 1Rheumatology, University College Hospital, London, United Kingdom, 2Rheumatology, Gregorio Marañón Hospital, Madrid, Spain, 3Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: B cell depletion therapy based on rituximab is a therapeutic option for refractory disease in patients with Systemic Lupus Erythematosus (SLE). Hypogammaglobulinemia can be…
  • Abstract Number: 1456 • 2016 ACR/ARHP Annual Meeting

    Identification of a Unique Population of B220hi B-Cells in Inflamed Lymph Nodes (Bin) As a Potential Biomarker of Arthritic Progression in the Tumor Necrosis Factor Transgenic Mouse Model of Rheumatoid Arthritis

    Megan Forney1, Richard Bell2, Edward Schwarz3 and Homaira Rahimi4, 1Orthopedics, University of Rochester, Rochester, NY, 2Pathology, University of Rochester, Rochester, NY, 3Orthopedeatrics, University of Rochester, Rochester, NY, 4Rheumatology, University of Rochester/Golisano Children's Hosp, Rochester, NY

    Background/Purpose: Using the tumor necrosis factor transgenic (TNF-Tg) mouse model of rheumatoid arthritis (RA), we have shown that during progression of knee synovitis, popliteal lymph…
  • Abstract Number: 2430 • 2016 ACR/ARHP Annual Meeting

    Mutations in the Tyrosine-Protein Kinase Lyn Cause an Early-Onset Neutrophilic Vasculitis Syndrome

    Adriana Almeida de Jesus1, Gina A. Montealegre1, Helen Freeman2, Neil Martin3, Ebun Omoyinmi4, Bernadette Marrero1, Katherine R. Calvo5, Chyi-Chia Richard Lee6, April D. Brundidge7, David Kleiner8, Stephen Hewitt8, Dawn C. Chapelle7, Yan Huang1, Nirali Shah8, Stephen Brooks7, Eric Meffre9, Paul Brogan10, Hyesun Kuehn11, Sergio Rosenzweig12, Melinda Merchant8, Zuoming Deng7, Susan Moir13 and Raphaela Goldbach-Mansky14, 1National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD, 2Raigmore Hospital, Inverness, United Kingdom, 3Royal Hospital for Children, Glasgow, United Kingdom, 4University College London Institute of Child Health, London, United Kingdom, 5Department of Laboratory Medicine, Hematology Section, National Institutes of Health Clinical Center, Bethesda, MD, 6Dermatopathology Section, Laboratory of Pathology, National Cancer Institute (NCI), National Institutes of Health (NIH), Bethesda, MD, 7NIAMS/NIH, Bethesda, MD, 8National Cancer Institute, NIH, Bethesda, MD, 9Department of Immunobiology, Yale University School of Medicine, New Haven, CT, 10UCL Institute of Child Health and Great Ormond Street Hospital NHS Foundation Trust, London, United Kingdom, 11Department of Laboratory Medicine, Clinical Center, National Institutes of Health, Bethesda, MD, 12Department of Laboratory Medicine/NIH, Bethesda, MD, 13National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, 14Translational Autoinflammatory Disease Studies, National Institute of Allergy and Infectious Diseases (NIAID), NIH, Bethesda, MD

    Background/Purpose: Tyrosine-protein kinase Lyn is a Src-family tyrosine kinase expressed by hematopoietic and non-hematopoietic cell types. Phosphorylation of a tyrosine residue at position 508 renders…
  • Abstract Number: 781 • 2016 ACR/ARHP Annual Meeting

    The Use of Rituximab in Newly Diagnosed Systemic Lupus Erythematosus Patients: Long Term Steroid Saving Capacity and Clinical Effectiveness

    Borja del Carmelo Gracia Tello Sr.1, David A. Isenberg2 and Amara Ezeonyeji3, 1Internal Medicina, Hospital Clínico Universitario Lozano Blesa, Zaragoza, Zaragoza, Spain, 2Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom, 3Rheumatology, University College of London Hospital, London, London, United Kingdom

    Background/Purpose: To assess the long term steroid saving capacity and clinical effectiveness of B-cell depletion therapy (BCDT) in newly diagnosed SLE patients. Methods: Sixteen female…
  • Abstract Number: 1610 • 2016 ACR/ARHP Annual Meeting

    Safety, Tolerability, and Dose-Dependent Inhibition of T-Cell-Dependent Antibody Response with MEDI4920, a Novel, Engineered CD40L Antagonist: Results of a Single-Ascending Dose Study in Healthy Volunteers

    Marius Albulescu1, Jim Bush2, Firas Almazedi2, Ethan Grant3, Alex Godwood1, Robert Miday4, Krista Arbaugh4, Lisa H. Butler1, Michele Gunsior4, Jing Li5 and David Howe1, 1MedImmune, Cambridge, United Kingdom, 2Covance Clinical Research Unit, Leeds, United Kingdom, 3Translational Medicine, MedImmune, Gaithersburg, MD, 4MedImmune, Gaithersburg, MD, 5MedImmune, Mountain View, CA

    Background/Purpose: The CD40L/CD40 co-stimulatory pathway is important for T-cell-dependent antibody production. Previous clinical programs with intact monoclonal antibodies against CD40L have been discontinued due to…
  • Abstract Number: 2608 • 2016 ACR/ARHP Annual Meeting

    Anti-CCP Antibody Titers Decrease with Altered B-Cell Subpopulation in RA Patients Treated with Tocilizumab

    Atsushi Noguchi1,2, Shinsuke Yasuda1, Ryo Hisada1, Kazumasa Ohmura1, Sanae Shimamura1, Yuka Shimizu1, Masaru Kato1, Kenji Oku1, Toshiyuki Bohgaki1, Olga Amengual1, Tetsuya Horita1, Miho Suzuki3, Yoshihiro Matsumoto4 and Tatsuya Atsumi1, 1Division of Rheumatology, Endocrinology and Nephrology, Hokkaido University Graduate School of Medicine, Sapporo, Japan, 2Division of Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 3Product research department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan, 4Product Research Department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan

    Background/Purpose:  Consecutive RA patients who initiated treatment with TCZ between December 2013 and September 2015 were enrolled in our prospective study. All patients met 2010…
  • Abstract Number: 783 • 2016 ACR/ARHP Annual Meeting

    Review of SLE Cohort to Identify Predictors of Response to B Cell Depletion in Patients with Active SLE

    Pedro Mota1, Ashleigh Hennessey2, Ada Ferenkeh-Koroma2 and David A. Isenberg2, 1Internal Medicine, Hospital da Luz, Lisbon, Portugal, 2Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: The use of Rituximab (RTX) has been documented via published cohort data from over 20 sites worldwide (1,2) demonstrating its useful role in the…
  • Abstract Number: 1650 • 2016 ACR/ARHP Annual Meeting

    Treatment with Tofacitinib Inhibits Human Naive B Lymphocyte Development and Function in Vitro

    Jens Thiel1, Nils Venhoff2, Raquel Lorenzetti3, Bettina Bannert1, Reinhard Voll4, Diego Kyburz5 and Marta Rizzi1, 1Department of Internal Medicine, Clinic for Rheumatology and Clinical Immunology, Freiburg, Germany, 2Department of Internal Medicine, Clinic for Rheumatology and Clincal Immunology, Freiburg, Germany, 3Department of Internal Medicine, Clinic for Rheumatology and Clinical Immunology, 79106, Germany, 4Dpt. Rheumatology & Clinical Immunology and Centre for Chronic Immunodeficiency, University Hospital Freiburg, University Medical Center, University of Freiburg, Freiburg, Germany, 5Department of Biomedicine, Experimental Rheumatology, University of Basel, 4051 Basel, Switzerland

    Background/Purpose:  B cells are pivotal to the pathogenesis of many autoimmune diseases including rheumatoid arthritis (RA). Tofacitinib, a JAK inhibitor, is effective and safe in…
  • Abstract Number: 2701 • 2016 ACR/ARHP Annual Meeting

    Increased Frequency of Regulatory CD19+CD24high Cd38high B Cells in Patients with Ankylosing Spondylitis (AS)

    M. Belén Bautista-Caro1, Eugenio De Miguel1, Diana Peiteado1, Chamaida Plasencia-Rodriguez1, Alejandro Villalba1, Amaya Puig-Kröger2, Paloma Sanchez-Mateos3, Emilio Martín-Mola1 and Maria Eugenia Miranda-Carus1, 1Rheumatology, Hospital La Paz - IdiPaz, Madrid, Spain, 2Immuno-oncology, Hospital Gregorio Marañon, Madrid, Spain, 3Immunology, Hospital Gregorio Marañon, Madrid, Spain

    Background/Purpose: CD19+CD24highCD38high B cells have been described to have a regulatory capacity and their frequency is altered in the peripheral blood of patients with various…
  • Abstract Number: 811 • 2016 ACR/ARHP Annual Meeting

    Basophils Are Activated and Stimulate Both B Cells and Fibroblasts in Systemic Sclerosis

    Benjamin Chaigne1, Nicolas Dumoitier2, Alexis Regent1, Benjamin Terrier3, Jonathan London2, Matthieu Groh1, Nathalie Thieblemont4 and Luc Mouthon5, 1National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, 2INSERM U1016, Institut Cochin, Equipe Neutrophiles et Vascularites, Paris, France, 3Internal Medicine, Cochin Hospital, Paris, France, 4Inserm U1016, Paris, France, 5Department of Internal Medicine, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, Paris, France

    Background/Purpose: Systemic sclerosis (SSc) is a rare multisystem connective tissue disease characterized by skin and internal organs fibrosis and vascular abnormalities, along with the presence…
  • Abstract Number: 1826 • 2016 ACR/ARHP Annual Meeting

    STAT3 Phosphorylation Mediates the Stimulatory Effects of Interferon Alpha on B Cell Differentiation and Activation in SLE

    Julie Ducreux1, Floor Aleva2, Aurelie Degroof3, Alina Ferster4, Andre van der Ven2, Frank van de Veerdonk2, Frédéric A. Houssiau1 and Bernard R. Lauwerys1, 1Pôle de pathologies rhumatismales inflammatoires et systémiques, Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium, 2Department of General Internal Medicine, Radboud University, Nijmegen, Netherlands, 3Pôle de Maladies Rhumatismales, Institut de Recherche Expérimentale et Clinique, Université catholique de Louvain, Brussels, Belgium, 4Service d'Onco-Hématologie, Hôpital Reine Fabiola, Brussels, Belgium

    Background/Purpose:  In our previous work, we reported a link between interferon alpha inhibition and decreased expression of B cell activation genes in ex vivo whole…
  • Abstract Number: 2712 • 2016 ACR/ARHP Annual Meeting

    Inverse Correlation Between IL-10-Producing Bregs and IFN-Gamma-Producing NK Cells in Psoriatic Arthritis and Psoriasis

    Athanasios Mavropoulos1, Areti Varna1, Christos Liaskos1, Efterpi Zafiriou2, Marianna Vlychou3, Christina Katsiari4, Dimitrios Bogdanos5 and Lazaros I. Sakkas6, 1Department of Rheumatology, School of Health Sciences, University of Thessaly, Larissa, Greece, 2Dermatology, University of Thessaly, Larissa, Greece, 3Radiology, University of Thessaly, Larissa, Greece, 4Department of Rheumatology, University of Thessaly, Larrisa, Thessaly, Greece, 5Department of Rheumatology, University of Thessaly, Larissa, Greece, 6University, Athens, Greece

    Background/Purpose:  A recent study from our group has shown functional impairment and numerical decrease of transitional and memory IL-10-producing regulatory B cells (Bregs) in patients…
  • « Previous Page
  • 1
  • …
  • 7
  • 8
  • 9
  • 10
  • 11
  • …
  • 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].

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].

Copyright Policy

View ACR Policies.

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology