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 cell targeting"

  • Abstract Number: 1812 • 2015 ACR/ARHP Annual Meeting

    The First Randomized Control Trial to Evaluate the Effectiveness of Bortezomib for Refractory Systemic Lupus Erythematosus

    Tomonori Ishii1, Yoshiya Tanaka2, Atsushi Kawakami3, Kazuyoshi Saito2, Kunihiro Ichinose4, Yuko Shirota5, Hiroshi Fujii5, Yoko Fujita6, Yukiko Kamogawa5, Tomoaki Machiyama5, Kanae Akita5 and Hideo Harigae5, 1Department of Clinical Trial Implementation, Tohoku University Hospital, Clinical Research, Innovation and Education Center, Sendai, Japan, 2The First Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Japan, 3Department of Immunology and Rheumatology, Nagasaki University, Nagasaki, Japan, 4Department of Immunology and Rheumatology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 5Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan, 6Department of Hematolgy and Rheumatolgy, Tohoku University Graduate School of Medicine, Sendai, Japan

    Background/Purpose: Systemic lupus erythematosus (SLE) is a disease characterized by production and deposition of anti-dsDNA antibody. In recent years, treatment methods targeting antibody-producing B cell…
  • Abstract Number: 2139 • 2015 ACR/ARHP Annual Meeting

    Results of a Phase 1b/2a Study of the Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of XmAb®5871 in Patients with Rheumatoid Arthritis (RA)

    Debra Zack1, Maria Jaraczewska Baumann2, Mariusz Korkosz3, Gabriella Suljok4, Petr Sramek5, Bernadette Rojkovich6, Stafan Daniluk7, Janos Bartalos8 and Paul Foster1, 1Xencor, Inc., San Diego, CA, 2NZOZ Centrum Medyczne HCP, Poznan, Poland, 3Malopolskie Centrum Medyczne, The University Hospital in Krakow, Krakow, Poland, 4Drug Research Center Ltd., Baltonfüred, Hungary, 5PRA CZ, Praha, Czech Republic, 6Polyclinic of the Hospitaller Brothers of St John of God, Budapest, Hungary, 7NZOZ Center of Osteoporosis and Osteoarticular Diseases, Bialystok, Poland, 8PRA Hungary Ltd, Budapest, Hungary

    Background/Purpose: XmAb®5871 is a humanized Fc engineered monoclonal antibody that binds to the B cell restricted surface antigen CD19 and has enhanced Fc binding to…
  • Abstract Number: 2928 • 2014 ACR/ARHP Annual Meeting

    Serum IL-33 Level Is Increased in Rheumatoid Arthritis and Predicts Response to Rituximab in Combination with High Serum IgG Level and Autoantibody Positivity: An Open-Label, Prospective, Multicentre Biological Trial

    Jérémie Sellam1, Houria Chavez2, Stéphanie Rouanet3, Nathalie Vernet3, Bineta Ly4, Sandrine Marion-Thore5, Bernard Combe6, Jean Sibilia7, Jacques Tebib8, Gilles Chiocchia9, Maxime Dougados10, Yassine Taoufik2 and Xavier Mariette11, 1AP-HP, Saint-Antoine Hospital, Rheumatology Department and DHU i2B, Paris, France, 2Biologic Immunology, Hopital Bicetre, Université Paris Sud, AP-HP, Kremlin Bicetre, France, 3Biostatistics, Roche France, Boulogne-Billancourt, France, 4INSERM U1012, Universite Paris-Sud, Kremlin Bicetre, France, 5INSERM U1016, Université Versailles Saint-Quentin, Montigny le Bretonneux, France, 6Immuno-Rhumatologie, Hôpital Lapeyronie, Montpellier, France, 7Division of Rheumatology, University Hospital of Strasbourg, Strasbourg, France, 8Rheumatology, University Hospital Lyon, Lyon, France, 9Université Versailles-Saint Quentin, Montigny le Bretonneux, France, 10INSERM (U1153): Clinical Epidemiology and Biostatistics, PRES Sorbonne Paris-Cité, Paris, France., Paris, France, 11rheumatology, Université Paris-Sud, Le Kremlin Bicêtre, France

    Background/Purpose .  The recent discovered cytokine interleukin-33 (IL33) could be involved in B-cell activation as well as in RA pathophysiology. After a whole-blood transcriptomic analysis…
  • Abstract Number: 2874 • 2014 ACR/ARHP Annual Meeting

    Pro-Inflammatory FcRL4+ Memory B Cells in Joints of RA Patients: Immunoglobulin Gene Characteristics and Antigen Specificity

    Khaled Amara1, Lorraine Yeo2, Natalie Sippl1, Philip Titcombe1, Andrew Filer3, Karim Raza3, Dagmar Scheel-Toellner2 and Vivianne Malmström4, 1Rheumatology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institutet, SE-17176 Solna, Stockholm, Sweden., Stockholm, Sweden, 2Rheumatology Research Group, Centre for Translational Inflammation Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK, Birmingham, United Kingdom, 3Rheumatology Research Group, MRC Centre for Immune Regulation, School of Immunity and Infection, University of Birmingham, Birmingham, United Kingdom, 4Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose:    Our recent findings identified a subset of pro-inflammatory memory B cells in the RA synovium characterized by the expression of the surface protein…
  • Abstract Number: 1955 • 2014 ACR/ARHP Annual Meeting

    Disparity in Internalisation of Monoclonal Antibodies Targeting B Cell Antigens and Regulation By Fc Gamma Receptor IIb: Implications for Targeted Therapy in SLE

    Venkat Reddy1, Geraldine Cambridge2, David A. Isenberg3, Mark Cragg4 and Maria J. Leandro2, 1Centre for Rheumatology Research, Division of Medicine, University College London, London, United Kingdom, 2Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 3Centre for Rheumatology Research, Rayne Building, 4th Floor, Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 4Antibody and Vaccine group, Cancer Sciences Unit, Faculty of Medicine, Southampton University, Southampton, United Kingdom

    Background/Purpose Monoclonal antibodies (mAbs) targeting B cell antigens CD20 and CD22 are used to treat patients with SLE either in the clinic or in clinical…
  • Abstract Number: 1495 • 2014 ACR/ARHP Annual Meeting

    Preclinical and Clinical Phase I Profile of MK-8457, a Selective Spleen Tyrosine Kinase and Zeta-Chain-Associated Protein Kinase 70 Inhibitor, Developed for the Treatment of Rheumatoid Arthritis

    Gene Marcantonio1, Alan Bass2, Gretchen Baltus3, Judith Boice1, Hongmin Chen4, Michael Crackower5, Jeroen Elassaiss-Schaap6, Michael Ellis7, Tomoko Freshwater8, Francois Gervais9, Jane Guo10, Sammy Kim9, Lily Moy5, Alan Northrup7, Jie Zhang-Hoover4, Mathew Maddess11, Richard Miller12, Marcella Ruddy5, Stella Vincent13, Haoling Weng1 and Hani Houshyar14, 1Merck & Co., Whitehouse Station, NJ, 2Safety Assessment, Merck & Co., Boston, MA, 3Immunomodulatory Regulators, Merck & Co., Boston, MA, 4Pharmacology, Merck & Co., Boston, MA, 5Merck & Co., Boston, MA, 6Clinical PK-PD, Merck & Co., Oss, Netherlands, 7Medicinal Chemistry, Merck & Co., Boston, MA, 8PPDM Early Stage, Merck & Co., Rahway, NJ, 9Cell Pathways and Proteins, Merck & Co., Boston, MA, 10Immunology, Merck & Co., Boston, MA, 11Discovery Process Chemistry, Merck & Co., Boston, MA, 12Biochemistry & Biophysics, Merck & Co., Boston, MA, 13PPDM Preclinical ADME, Merck & Co., Boston, MA, 1433 Avenue Louis Pasteur, Merck & Co., Boston, MA

    Background/Purpose: Spleen tyrosine kinase (SYK) is a potential target for treatment of several diseases including rheumatoid arthritis.  SYK is a member of the Zeta-chain-associated protein…
  • Abstract Number: 452 • 2014 ACR/ARHP Annual Meeting

    The Use of Multiplex Bead Array to Follow the Effect of Rituximab on IgG and IgA Serum Autoantibody Responses to Citrullinated Epitopes in Patients with Rheumatoid Arthritis

    Geraldine Cambridge1, Lauren J. Lahey2, Maria J. Leandro1, William H. Robinson2 and Jeremy Sokolove2, 1Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 2VA Palo Alto Healthcare System and Stanford University, Palo Alto, CA

    Background/Purpose The majority of patients with established Rheumatoid arthritis (RA) have autoantibodies against the Fc of IgG (Rheumatoid factors-RhF) and to citrullinated protein antigens (ACPAs).…
  • Abstract Number: 2234 • 2013 ACR/ARHP Annual Meeting

    Targeting Therapy Of Citrullinated Antigen-Specific B Cells Ameliorates Collagen-Induced Arthritis

    Kazuya Michishita1, Kimito Kawahata1, Takeyuki Kanzaki2, Lisa Akahira1, Toshiki Eri1 and Kazuhiko Yamamoto3, 1Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan, 2Internal Medicine, Yamanashi Prefectural Central Hospital, Yamanashi, Japan, 3Department of Allergy and Rhaumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

    Background/Purpose: The clinical benefit of B-cell depletion therapy in rheumatoid arthritis(RA) is a well-known fact, but problems such as relapse of tuberculosis and reactivation of…
  • Abstract Number: 1432 • 2013 ACR/ARHP Annual Meeting

    The Rate Of Serious Infections Remains Stable In Patients With Multiple Retreatments In Real life : Data From The “Auto Immunity and Rituximab” (AIR) Registry

    Jacques-Eric Gottenberg1, Philippe Ravaud2, Patrice Cacoub Sr.3, Thomas Bardin4, Alain G. Cantagrel5, Bernard Combe6, Maxime Dougados7, Rene-Marc Flipo8, Bertrand Godeau9, Loic Guillevin10, Xavier Le Loet11, Eric Hachulla12, Thierry Schaeverbeke13, Jean Sibilia14, Isabelle Pane15, Gabriel Baron16 and Xavier Mariette17, 1Strasbourg University Hospital, Strasbourg, France, 2Epidemiology, Hopital Hotel Dieu, Paris Descartes University, Paris, France, 3Department of Internal Medicine 2., CHU Pitié-Salpêtrière, Paris, France, 4Rhumatology Departement, Hôpital Lariboisière, Paris, France, 5Rheumatology, Purpan University Hospital, Toulouse Cedex 9, France, 6Rheumatology, Lapeyronie Hospital, Montpellier, France, 7Rheumatology B Department, Paris-Descartes University, APHP, Cochin Hospital, Paris, France, 8Rheumatology, Hopital R Salengro CHRU, Lille, France, 9Internal Medicine, University of Paris, AP-HP, Hôpital Mondor Créteil, Creteil, France, 10Department of Internal Medicine,, Referral Center for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, France, 11Rheumatology Department, CHU of ROUEN, Rouen, France, 12Department of Internal Medicine, Claude Huriez University Hospital, Lille, France, 13Rhumatology departement, Groupe Hospitalier Pellegrin, Bordeaux, France, 14Rhumatologie, CHU Hautepierre, Strasbourg, France, 15Hotel Dieu University Hospital Paris, Hotel Dieu University Hospital Paris, Paris, France, 16Epidemiology & Clinical Research, Groupe Hospitalier Bichat-Claude Bernard, Paris, France, 17Rheumatology Departement, Bicêtre University Hospital, Paris, France

    Background/Purpose: Serious infections in patients with rheumatoid arthritis (RA) treated with  rituximab (RTX) are slightly more frequent in common practice than in clinical trials. Morevover,…
  • Abstract Number: 922 • 2013 ACR/ARHP Annual Meeting

    Role Of B Cells and/Or Autoantibodies In Pulmonary Manifestations Of Inflammatory Arthritis

    Lisa K. Peterson1, Jeremy Sokolove2, Paul Jedlicka3, Lauren J. Lahey4, William H. Robinson5 and Leonard L. Dragone6, 1Pediatrics, National Jewish Health, Denver, CO, 2VA Palo Alto Healthcare System and Stanford University, Palo Alto, CA, 3Pathology, University of Colorado Denver, Aurora, CO, 4Medicine, VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 5VA Palo Alto Health Care System and Stanford University, Palo Alto, CA, 6Dept of Pediatrics, National Jewish Health, Denver, CO

    Background/Purpose: RA is a systemic condition affecting approximately 1% of the general population leading to progressive arthritis and extra-articular manifestations (ExRA), including interstitial lung disease…
  • Abstract Number: 38 • 2013 ACR/ARHP Annual Meeting

    Use Of An In Vitro Whole Blood Depletion ASSAY To Compare The Efficacy Of B CELL Depleting Agents In Patients With Systemic LUPUS Erythematosus

    Venkat Reddy1, Geraldine Cambridge2, D.A. Isenberg3, Mark Cragg4 and Maria Leandro5, 1Rheumatology, University College London, London, United Kingdom, 2Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom, 3Centre for Rheumatology Research, University College London, London, United Kingdom, 4Antibody and Vaccine group, Cancer Sciences Unit, Faculty of Medicine, Southampton University, Southampton, United Kingdom, 5Centre for Rheumatology Research, Division of Medicine, University College London, London, United Kingdom

    Background/Purpose: Variability in clinical response to B-cell depletion therapy (BCDT) with the anti-CD20mAb rituximab (RTX) has been well described in Systemic Lupus Erythematosus (SLE). Poor…
  • « Previous Page
  • 1
  • 2
  • 3
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