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Abstracts tagged "B-Cell Targets"

  • Abstract Number: 2425 • ACR Convergence 2024

    Ianalumab Induced Durable Depletion of Circulating B Cell Subsets and Associated Changes in B Cell and Neutrophil Transcriptomic and Proteomic Profiles in Patients with Systemic Lupus Erythematosus: 52-Week Treatment Results from a Phase 2 Trial

    Marianna Rowlands1, Thomas Dörner2, Diego Saldana Miranda3, Justin McMullen3, Aida Santos da Costa3, Ulrike Sommer3, Rainer Hillenbrand3, Andre Nogueira da Costa3, Claire Bonal3, Isabelle Isnardi3, Edward Khokhlovich1 and Stephen J Oliver3, 1Biomedical Research, Novartis, Cambridge, MA, 2Department of Medicine, Rheumatology and Clinical Immunology,Charite Universitätsmedizin Berlin, Germany and DRFZ, Berlin, Berlin, Germany, 3Novartis Pharma AG, Basel, Switzerland

    Background/Purpose: Ianalumab (VAY736), a B cell activating factor receptor (BAFFR) targeting mAb, depletes B cells via both antibody dependent cellular cytotoxicity and blockade of BAFF:BAFFR…
  • Abstract Number: 0006 • ACR Convergence 2024

    NX-5948, a Clinical-Stage BTK Degrader, Achieves Deep Suppression of BCR, TLR, and FcR Signaling in Immune Cells and Demonstrates Efficacy in Preclinical Models of Arthritis and Other Inflammatory Diseases

    Mark Noviski1, Jun Ma1, Nivetha Brathaban1, Aishwarya Kumar1, Dhwani Haria1, Jenny McKinnell1, Robert Cass1, Frederick Cohen1, Davorka Messmer2, Gwenn Hansen1 and Ryan Rountree1, 1Nurix Therapeutics, San Francisco, CA, 2Nurix Therapeutics, San Diego, CA

    Background/Purpose: Bruton’s tyrosine kinase (BTK) mediates signaling downstream of the B cell receptor (BCR), toll-like receptors (TLRs), and Fc receptors (FcRs). This makes BTK an…
  • Abstract Number: 0536 • ACR Convergence 2024

    A Population Modeling and Simulation of the Effect of Obexelimab Exposure on the QTc Interval in Healthy Volunteers and Patients with Rheumatoid Arthritis or IgG4-Related Disease

    Claire Mukashyaka1, Xiaodong Wang1, Sujata Arora1, Mason Yamashita1, Allen Poma1 and Tanya Fischer2, 1Zenas BioPharma, Waltham, MA, 2Zenas BioPharma, Waltham, CA

    Background/Purpose: Obexelimab is a novel bifunctional antibody that inhibits B cells, CD19-expressing plasma cells, and plasmablast activity and has the potential to provide clinical benefit…
  • Abstract Number: 1551 • ACR Convergence 2024

    Efficacy of Belimumab on Different Phenotypes of Joint and Skin Manifestations of Systemic Lupus Erythematosus: Preliminary Data from a Multicenter, Nationwide, Cohort of Patients: The BElimumab in Real Life Setting Study-New Joint and Skin (BeRLISS-NeJS)

    Luca Iaccarino1, Marisol Bracalenti2, Alberto Cauli3, Lorenzo Cavagna4, Rossella De Angelis5, Roberto Depascale2, Giacomo Emmi6, Roberto Gerli7, Marcello Govoni8, Alberto Lo Gullo9, Simone Negrini10, Luca Quartuccio11, Maurizio Rossini12, Carlo Salvarani13, Paola Tomietto14, Angelo Vacca15, Margherita Zen16 and doria Andrea2, 1University of Padua, PADOVA, Italy, 2University of Padova, Padova, Italy, 3University of Cagliari, Cagliari, Italy, 4University of Pavia and Fondazione IRCCS Policlinico San Matteo Hospital of Pavia, Pavia, Pavia, Italy, 5Università Politecnica delle Marche, Ancona, Italy, 6University of Trieste, Trieste, Italy, 7University of Perugia, Perugia, Italy, 8Rheumatology Unit, Department of Medical Sciences, University of Ferrara and Azienda Ospedaliero-Universitaria S.Anna, Ferrara, Italy, Ferrara, Italy, 9Rheumatology Unit, Papardo Hospital, Messina, Italy, 10University of Genova, Genova, Italy, 11Division of Rheumatology, Department of Medicine (DMED), University of Udine, Udine, Italy, Udine, Italy, 12Rheumatology Unit, University of Verona, Verona, Italy, 13Azienda USL-IRCCS di Reggio Emilia and University of Modena and Reggio Emilia, Reggio Emilia, Italy, Reggio Emilia, Italy, 14Azienda Sanitaria Universitaria Giuliano Isontina, trieste, Italy, 15University of Bari, Bari, Italy, 16University of Padova, Padova, Padua, Italy

    Background/Purpose: To evaluate the efficacy of belimumab on different skin and joint manifestations of the disease in a multicenter, nationwide, cohort (BeRLISS-NeJS) of patients with…
  • Abstract Number: 2436 • ACR Convergence 2024

    Characterization of RO7507062, a CD19-Targeting T-Cell Bispecific Antibody (CD19TCB), and Design of Its Ongoing Phase 1 Trial in Systemic Lupus Erythematosus

    Florian Kollert1, Sarah Robertson2, Veit Erpenbeck2, Franziska Regenass-Lechner3, Remy Hallet3, Jason Neale2, Cary M. Looney2, Nicolas Frances2, Celine Marban-Doran2, Sophia Fredrika Soehrman Brossard2, Laurie Millar4, Beki Finch5, Johannes Sam6, Benjamin A. Fisher7, Maria Leandro8, Thomas Dörner9, Christian Klein10 and Franz Schuler2, 1University Hospital Basel, Basel, Switzerland, 2F. Hoffmann-La Roche Ltd., Basel, Switzerland, 3F. Hoffmann-La Roche Ltd, Basel, Switzerland, 4F. Hoffmann-La Roche Ltd., Welwyn Garden City, England, United Kingdom, 5F. Hoffmann-La Roche Ltd., Welwyn Garden City, United Kingdom, 6F. Hoffmann-La Roche Ltd, Schlieren, Zurich, Switzerland, 7University of Birmingham, Birmingham, United Kingdom, 8University College London, London, United Kingdom, 9Department of Medicine, Rheumatology and Clinical Immunology,Charite Universitätsmedizin Berlin, Germany and DRFZ, Berlin, Berlin, Germany, 10F. Hoffman-La Roche Ltd., Schlieren, Zurich, Switzerland

    Background/Purpose: CD20-directed B-cell depletion therapy shows efficacy in hematological malignancies and in multiple autoimmune indications. More recently, promising data for the use of CD19-targeted B-cell…
  • Abstract Number: 0008 • ACR Convergence 2024

    Preclinical Development and Manufacturability of KYV-201, an Investigational Allogeneic Anti-CD19 Chimeric Antigen Receptor T Cell for the Treatment of Autoimmune Disease

    Ashley Mahne1, Ryan Rodriguez2, Jessica Wang1, Daniel Anaya1, Joseph K. Cheng1, Brandon Kwong1, Jesus Banuelos3, Peter Starokadomskyy3, Soo Park3, Candice Gibson4, Shouvonik Sengupta1, Simone Sandoval1, Jazmin Bravo3, Jeanne Flandez1, Shairaz Shah1, Amanda Goodsell1, Nicole Khoshnoodi1, Jennifer Zeng1, Santiago Foos-Russ1, Mario Lorente1, Jennifer Adrian1, Timothy Klasson1, Yong Zhang5, Jessica Seitzer6, Birgit Schultes5 and Tom Van Blarcom3, 1Kyverna Therapeutics, Inc., Emeryville, CA, 2Kyverna Therapeutics, Inc., Emerville, CA, 3Kyverna Therapeutics, Inc., Emeryville, 4Kyverna Therapeutics, Inc., Emerybille, 5Intellia Therapeutics, Inc., Cambridge, MA, 6Intellia Therapeutics, Inc., Cambridge

    Background/Purpose: Autologous anti-CD19 chimeric antigen receptor (CAR) T cells show early clinical evidence of safety and efficacy for treating several autoimmune diseases (Müller F. N Engl…
  • Abstract Number: 0666 • ACR Convergence 2024

    Interferon-stimulated Genes on Peripheral CD8+ T Cells of SLE Patients Were the Keys for Early Response to BAFF/APRIL-targeted Therapy

    Cuiling Fan1, Shixian Chen2 and Juan Li1, 1Department of Rheumatology and Immunology, Nanfang Hospital, Southern Medical University, Guangzhou, China, Guangzhou, China (People's Republic), 2Nanfang Hospital, Southern Medical University, guangzhou, China (People's Republic)

    Background/Purpose: Systemic lupus erythematosus (SLE) is a heterogeneous autoimmune disease. BAFF/APRIL-targeted therapy exert therapeutic effects through the inhibition of B-cell activating factor (BAFF) and a…
  • Abstract Number: 1646 • ACR Convergence 2024

    A Novel E3 Ligase of GILZ: Validation of a Steroid-sparing Therapeutic Target in SLE

    Iolanda Miceli1, Rochelle Sherlock2, Pamela Hall2, IanIan Cheang2, Akshay D'Cruz3, Taylah Bennett2, Terry Lim Kam Sian2, Rangi Kandane-Rathnayake4, Eric Morand5 and Sarah Jones2, 1Monash University, Glen Iris, Victoria, Australia, 2Monash University, Melbourne, Australia, 3Monash University, Me, Australia, 4Monash University, Clayton, Victoria, Australia, 5School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia

    Background/Purpose: SLE is primarily mediated by B cell dysregulation on a background of type I interferon (IFN) activation. This multi-faceted nature of immune defects in…
  • Abstract Number: 2437 • ACR Convergence 2024

    Aryl Hydrocarbon Receptor as an Intrinsic Novel Checkpoint That Inhibits TLR7-induced B-cell Activation in SLE

    Changming Lu1, Jose Rubio2, Hui-Chen Hsu1 and John D. Mountz3, 1University of Alabama at Birmingham, Birmingham, AL, 2University of Alabama at Birmingham, Hoover, AL, 3University Alabama Birmingham, Birmingham, AL

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by an increase in T-bet+ IgD−CD27− double negative 2 (DN2) B cells, attributed to heightened TLR7 signaling. Identifying…
  • Abstract Number: 0222 • ACR Convergence 2023

    Predictors of Adverse Prognosis Following Hospitalization for COVID-19 Infection in Patients with Immune Mediated Inflammatory Diseases Treated with Rituximab

    Pei-hsinq Lai1, Ting-wei Chang2, Shih-hsun Lan2, Chiao-Feng Cheng2, Cheng-Hsun Lu2 and Song-Chou Hsieh2, 1Taipei City Hospital, Zhongxiao Branch, Taipei, Taiwan, 2National Taiwan University Hospital, Taipei, Taiwan

    Background/Purpose: Rituximab (RTX) is widely used in immune mediated inflammatory disease (IMID) patients refractory to conventional treatment. Previous studies have indicated that RTX in IMID…
  • Abstract Number: 0926 • ACR Convergence 2023

    Single-cell Multi-Omic Evaluation of Differences in Immune Cell Populations in Progression Toward Systemic Lupus Erythematosus

    Aleksandra Bylinska, Miles Smith, Samantha Slight-Webb, Carla Guthridge, Caleb Marlin, Kevin Thomas, Christian Wright, Marci Beel, Susan Macwana, Wade DeJager, Judith James and Joel Guthridge, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Several groups of individuals are at higher risk for SLE, including those with African American ancestry (AA), lupus-associated autoantibodies (ANA+), or some clinical symptoms…
  • Abstract Number: 2191 • ACR Convergence 2023

    Efficacy of anti-CD38 Treatment with Daratumumab in Two Cases of Refractory and Severe Sjogren Disease

    Gaetane Nocturne1, Mathilde di Filippo2, Oriane Marmontel2, Pascale Chretien1, Roman Krzysiek1, François Lifermann3, Nawal Rahal1, Rakiba Belkhir4, Philippe Moulin2 and Xavier Mariette5, 1APHP, Le Kremlin-Bicêtre, France, 2Hospices Civils de Lyon, Lyon, France, 3Department of Internal Medicine, Centre Hospitalier de Dax, Dax, France, 4Rheumatology Department, Université Paris-Saclay, INSERM U1184, Hôpital Bicêtre, APHP, FHU CARE, Le Kremlin-Bicêtre, France, 5Université Paris-Saclay, Le Kremlin-Bicêtre, France

    Background/Purpose: Sjögren's disease (Sjo) is a systemic autoimmune disease. In 80% of the patients, Sjo is responsible for dryness, fatigue, and joint pain. In 10%…
  • Abstract Number: 0425 • ACR Convergence 2023

    Long-term Safety of Rituximab in Rheumatoid Arthritis: A Systematic Review and Meta-analysis

    Ioasaf Karafotias, Joshua Rothwell, Maryam Adas, Bechman Katie, Mark Russell, Sam Norton and James Galloway, King's College London, London, United Kingdom

    Background/Purpose: Rituximab targets CD20-bearing B cells and is used to treat Rheumatoid Arthritis (RA). Common Variable Immune Deficiency (CVID) is a primary immune deficiency syndrome…
  • Abstract Number: 0956 • ACR Convergence 2023

    Effects of B Cell Depletion by CD19-targeted CAR-T Cells in a Murine Model of Systemic Sclerosis

    Jérôme Avouac1, Anne Cauvet2, Cindy Orvain3, Morgane boulch4, Philippe Bousso4 and Yannick ALLANORE5, 1Service de Rhumatologie, Hôpital Cochin, AP-HP.Centre – Université Paris Cité, Paris, France, 2INSERM U1016, Paris, France, 3INSERM U1016, Paris, 4Institut Pasteur, Paris, France, 5Université Paris Cité, Paris, France

    Background/Purpose: Chimeric antigen receptor (CAR)-T cells represent a potentially curative strategy for B cell malignancies. A first successful clinical experience has been recently reported in…
  • Abstract Number: 2310 • ACR Convergence 2023

    Machine Learning Approaches for Prediction of Renal Flares in Systemic Lupus Erythematosus: Knowledge-Driven Models Outperformed Data-Driven Models

    Nursen Cetrez1, Julius Lindblom1, Raffaele Da Mutten2, Dionysis Nikolopoulos2 and Ioannis Parodis1, 1Karolinska Institutet, Stockholm, Sweden, 2Karolinska Institutet and Karolinska University Hospital, Division of Rheumatology, Department of Medicine Solna, Stockholm, Sweden

    Background/Purpose: Renal flares in patients with SLE result in significant nephron loss. Thus, identification of reliable early signals of impending renal flares is anticipated to…
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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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