ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2025
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • 2020-2009 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 Targets"

  • Abstract Number: 0011 • ACR Convergence 2025

    KT502, a novel CD19-directed TCE (T-cell engager), leads to rapid and deep B-cell depletion with low cytokine release

    Min Bao, John Wang, Jay Zhao and Weihao Xu, Kali Therapeutics, San Mateo, CA

    Background/Purpose: Chimeric antigen receptor T-cell (CAR-T) therapies targeting CD19 have shown unprecedented effects in treatment-resistant autoimmune diseases such as systemic lupus erythematosus (SLE), rheumatoid arthritis…
  • Abstract Number: 2464 • ACR Convergence 2025

    IMC-002 (IMM0306), a First-in-Class Bi-specific Fusion Protein, Demonstrates Improvements in Systemic Lupus Erythematosus (SLE) Disease Activity Measures and Biomarkers in Patients with Moderate to Severe Active SLE in the Open-label Phase 1b/2 Study

    Haihong Yao1, Wenzhi Tian2, Qian Zheng2, Min Chen2, Guoping Jiang3, Zhichun Liu4, Yingkun Nie5, Rui Wu6, Zhaohui Zheng7 and Zhanguo Li1, 1Peking University People's Hospital, Beijing, China (People's Republic), 2ImmuneCare Biopharmaceuticals (Shanghai) Co.,Ltd, Shanghai, China (People's Republic), 3Jilin Province People's Hospital, Changchun, China (People's Republic), 4The Second Affiliated Hospital of Soochow, Suzhou, China (People's Republic), 5The Second Affiliated Hospital of Harbin Medical University, Haerbin, China (People's Republic), 6The First Affiliated Hospital of Nanchang University, Nanchang, China (People's Republic), 7The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China (People's Republic)

    Background/Purpose: Deep B cell depletion has been confirmed to be the main mechanism for complete clinical response of SLE patients. We analyzed the peripheral blood…
  • Abstract Number: 1593 • ACR Convergence 2025

    Comparison of rituximab induction and maintenance regimens in ANCA-associated vasculitis: PK/PD modelling approach in real-world patients

    Blaise Pasquiers1, Benoit Blanchet2, Xavier Puéchal3, Xavier Declèves1, Pascal Cohen4, Claire Goulvestre1, Marion Casadevall1, Ines Benhabiles1, Michel Vidal1, David Ternant1, Benjamin Terrier5 and Alicja Puszkiel6, 1Hopital Cochin, Paris, France, 2National Referral Centre for Rare Autoimmune and Systemic Diseases, Hôpital Cochin, Paris, France, 3Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, and Université Paris Cité, Paris ( 75014 ), Ile-de-France, France, 4Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, Paris, France, 5Cochin Hospital, Paris, France, 6Cochin Hospital, Paris

    Background/Purpose: For the treatment of antineutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), rituximab (RTX) may be given as a 4-dose regimen (375 mg/m2 weekly for 4…
  • Abstract Number: 0946 • ACR Convergence 2025

    A Novel Preclinical Tool for Evaluating CD20 Antibody Efficacy Based on BAFF/CD20 Dual-target Humanized Mice

    Juan Liang1 and Ting Wang2, 1Gempharmatech, Nanjing, Jiangsu, China, 2GemPharmatech, Nanjing, China (People's Republic)

    Background/Purpose: CD20, a well characterized B-cell surface marker involved in B-cell activation and differentiation, plays a critical role in the pathogenesis of B-cell mediated diseases…
  • Abstract Number: 0843 • ACR Convergence 2025

    Efficacy and Safety of BMS-986353, a CD19-Directed Chimeric Antigen Receptor T Cell Therapy Manufactured Using a Next-Generation Process: Updated Data From a Phase 1 Trial in Patients With Systemic Sclerosis

    Dinesh Khanna1, David Korman2, Elana Bernstein3, Neil Kramer4, Vikas Majithia5, Philip J. Mease6, Georg Schett7, Jacques Azzi8, Richard Nash9, Ran Reshef3, Mohammad Cherry10, Ernesto Ayala5, Matthew Schwede11, Monalisa Ghosh12, Fabian Müller13, Alisha Desai14, San-San Ou15, Sharmila Das14, Jerill Thorpe16, Melissa Harnois14, Alexis Melton16, Ashley Koegel16 and Margrit Wiesendanger8, 1University of Michigan, Ann Arbor, MI, 2Mountain Rheumatology, Denver, CO, 3Columbia University Irving Medical Center, New York, NY, 4Overlook Medical Center; Atlantic Medical Group, Atlantic Health System, Summit, NJ, 5Mayo Clinic Hospital, Jacksonville, FL, 6Department of Rheumatology, Providence-Swedish Medical Center and University of Washington, Seattle, WA, 7Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 8Icahn School of Medicine at Mount Sinai, New York, NY, 9Health One Cares, Denver, CO, 10Atlantic Health System, Morristown, NJ, 11Swedish Cancer Institute, Seattle, WA, 12C. S. Mott Children's Hospital University of Michigan Health, Ann Arbor, MI, 13University Hospital of Erlangen, Erlangen, Germany, 14Bristol Myers Squibb, Princeton, NJ, 15Bristol Myers Squibb, Seattle, WA, 16Bristol Myers Squibb, Princeton

    Background/Purpose: BMS-986353 (CC-97540) is an investigational CD19-directed T-cell therapy expressing the chimeric antigen receptor (CAR) used in globally-approved lisocabtagene maraleucel; it is manufactured via the…
  • Abstract Number: 0009 • ACR Convergence 2025

    MRT-6160, a VAV1-Directed Molecular Glue Degrader, Attenuates T and B Cell Effector Functions and Inhibits Disease Progression in a Spontaneous MRL-Faslpr Mouse Model

    Adam Cartwright1, Lucas Gyger1, Foram Desai2, Shailee Vora2, Anna Kostikova1, Xudong Wang2, Peter Trenh2, Katie May2, Sophia Nguyen2, Chris King2, Daniel Lam2, Xavi Lucas1, Mary Zlotosch2, Elisa Liardo1, Daric Wible2, Ilaria Lamberto2, Bradley Demarco2, Debora Bonenfant1, Sharon Townson2, Eswar Krishnan2, Filip Janku2, John Castle1, Laura McAllister1, Alison Paterson2 and Marisa Peluso2, 1Monte Rosa Therapeutics, Basel, Switzerland, 2Monte Rosa Therapeutics, Boston, MA

    Background/Purpose: VAV1, an immune cell restricted guanine nucleotide exchange factor (GEF) and scaffolding protein, plays a critical role in mediating T- and B-cell receptor activity.…
  • Abstract Number: 2463 • ACR Convergence 2025

    Allogenic anti- CD19 CAR-T cells induce remission in refractory systemic lupus erythematosus

    Chunnei Yang1, Chuanyin Sun2, Binghe Tan3, Chao Hu1, Liyan Wan2, Changling Xie3, Qian Tan3, Mingyao Liu3, Jin Lin2, Bing Du3 and Hongyan Tong1, 1Department of Hematology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China (People's Republic), 2Department of Rheumatology, The First Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang, China (People's Republic), 3BRL Medicine Inc., Shanghai, Shanghai, China (People's Republic)

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease associated with significant morbidity and mortality. The treatment approach for SLE primarily involves immunomodulation and…
  • Abstract Number: 1578 • ACR Convergence 2025

    Use of the CD19/CD3 T cell engager blinatumomab in refractory diffuse systemic sclerosis : a case series

    Marc Scherlinger1, Yannick dieudonne2, Anna Molto3, Emmanuel Chatelus4, aurelien Guffroy5, Thierry Martin2, Jacques-eric GOTTENBERG6, Celestine Simand7, Anne El Aatmani8, Justine Decroocq9, Eden Sebbag1, Jean Sibilia10 and Jérôme AVOUAC11, 1Rheumatology Department, National Center for Rare autoimmune disease RESO,Strasbourg University Hospital, Strasbourg, France, 2Immunology Department, National Center for Rare autoimmune disease RESO,Strasbourg University Hospital, Strasbourg, France, 3Assistance Publique Hôpitauxde Paris, Paris, France, 4Department of Rheumatology, University Hospital Strasbourg, France, Strasbourg, France, 5CHU de Strasbourg, Strasbourg, 6Hautepierre Hospital, STRASBOURG, Alsace, France, 7ICANS, Strasbourg, France, 8CHU de Strasbourg, Strasbourg, France, 9APHP, Paris, France, 10Rheumatology Department, National Center for Rare autoimmune disease RESO,Strasbourg University Hospital, Strasbourg, Alsace, France, 11Rheumatology department, Cochin hospital, Paris, France

    Background/Purpose: Systemic sclerosis (SSc) is a severe autoimmune disease with limited treatments. While anti-CD19 CAR T-cell therapy shows promise, its use is limited by cost…
  • Abstract Number: 0943 • ACR Convergence 2025

    Type I and Type II IFNs have both independent and overlapping effects on SLE disease severity

    Haylee Cosgrove1, Xiaoyan Gong1, Aidan Matunis1 and Jeremy Tilstra2, 1University of Pittsburgh, Pittsburgh, 2University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: The pathogenesis of systemic lupus erythematosus (SLE) is thought to be strongly influenced by the interferon (IFN) signaling pathway, particularly type I IFNs (IFNα/β).…
  • Abstract Number: 0804 • ACR Convergence 2025

    Comparative Risk of All-Cause Mortality with Belimumab versus Oral Immunosuppressant Use in Patients with Non-Renal Systemic Lupus Erythematosus

    Grace Haeun Lee1, Sara Barmettler2, Lingxiao Zhang3 and April Jorge2, 1Division of Rheumatology, Allergy, and Immunology, Department of Medicine, Massachusetts General Hospital, Boston, MA, 2Massachusetts General Hospital, Boston, MA, 3Massachusetts General Hospital, Boston

    Background/Purpose: Belimumab is a monoclonal antibody targeting B-lymphocyte stimulator (BLyS) used in the treatment of active systemic lupus erythematosus (SLE). Our objective was to investigate…
  • Abstract Number: 0008 • ACR Convergence 2025

    Characterization of S-1117, a novel pan-IgG protease engineered for reduced immunogenicity using the IMPACT platform

    Julia Manasson1, Liliana Sanmarco2, Alex Pellerin2, Maria Cecilia Ramello2, Agustin Plasencia2, Jordan Anderson2, Tobias Green2, Andita Newton2, Ryan Peckner2, Yi Xing2, Heather Vital3, Nathan Higginson-Scott2, John Sundy4, Kevin L. Otipoby2 and Ivan Mascanfroni2, 1Seismic Therapeutic, New York, NY, 2Seismic Therapeutic, Watertown, MA, 3Seismic Therapeutic, Lexington, MA, 4Seismic Therapeutic, Durham, NC

    Background/Purpose: Pathogenic autoantibodies are key effectors of inflammation, promoting tissue damage in autoantibody-mediated diseases such as inflammatory myopathies, lupus nephritis, Sjogren’s syndrome, antiphospholipid syndrome, and…
  • Abstract Number: L17 • ACR Convergence 2024

    Allogenic CD19 CAR NK Cells Therapy in Refractory Systemic Lupus Erythematosus: An Open-label, Single Arm, Prospective and Interventional Clinical Trial

    Yiyi Yu1, Ruina Kong1, Xia Xu1, Suxuan Liu1, Qian Chen1, Xiaofang Li2, Ming Sun2, Jianmin Yang1, Dongbao Zhao1 and Jie Gao1, 1Changhai Hospital, Shanghai, China, 2Rui Therapeutics, Nanjing, China

    Background/Purpose: Treatment of systemic lupus erythematosus (SLE) typically necessitates long-term immunosuppression with hormones, immunosuppressants and biologics. CD19-targeting chimeric antigen receptor (CAR) T cells have shown excellent…
  • Abstract Number: 0011 • ACR Convergence 2024

    Preclinical Manufacturability and Activity of KYV-102 from Patients with Systemic Lupus Erythematosus Using Ingenui-T: A Rapid, Autologous Chimeric Antigen Receptor T-Cell Manufacturing Solution Utilizing Whole Blood

    Brandon Kwong1, Daniel Anaya1, Soo Park2, Sunetra Biswas2, Jeevitha Jeevan2, Jesus Banuelos2, Madison Strobach2, Nicole Khoshnoodi1, Timothy Klasson1, Santiago Foos-Russ1, Jennifer Zeng1, Candice Gibson3, Jazmin Bravo2, Simone Sandoval1, Shouvonik Sengupta1, Shairaz Shah1, Tom Van Blarcom2 and Karen Walker2, 1Kyverna Therapeutics, Inc., Emeryville, CA, 2Kyverna Therapeutics, Inc., Emeryville, 3Kyverna Therapeutics, Inc., Emerybille

    Background/Purpose: Apheresis in conventional chimeric antigen receptor (CAR) T-cell therapy can be burdensome, and conventional manufacturing cultures apheresis-derived cells for 7-14 days, leading to a…
  • Abstract Number: 0778 • ACR Convergence 2024

    Comprehensive Immune Profiling of Anti-CD19 Chimeric Antigen Receptor T-Cell Therapy in Patients with Autoimmune Disease

    Justin Chou1, Ricardo Grieshaber-Bouyer2, Michelle J Wu3, Christina Bergmann2, Jule Taubmann4, Fabian Müller5, Aline Bozec4, Tobias Rothe2, Andreas MAckensen6, Amber Podoll7, Jonathan Gutman7, Aiden Haghikia8, Dimitrios Mougiakakos9, Gary Tong3, Pouya Kheradpour3, Francis Kim10, Prameela Ramesan10, Brandon Kwong10, Kunbin Qu10, Bishwa Ganguly10, Dominic Borie10, James Chung10 and Georg Schett11, 1Kyverna Therapeutics, Emeryville, CA, 2Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 3Verily Life Sciences, South San Francisco, CA, 4Friedrich-Alexander Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, 5Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Germany, 6Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Bayern, Germany, 7University of Colorado Anschutz Medical Campus, Aurora, CO, 8Otto-von-Guericke University, Magdeburg, Germany, 9Otto-von-Guericke University, Magdeburg, Germany, Magdeburg, Germany, 10Kyverna Therapeutics, Inc., Emeryville, CA, 11Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany

    Background/Purpose: Anti-CD19 chimeric antigen receptor (CAR) T-cell therapy represents a promising advancement in the treatment of autoimmune diseases, including systemic sclerosis (SSc), idiopathic inflammatory myopathy…
  • Abstract Number: 1749 • ACR Convergence 2024

    Safety and Long-term Efficacy of CD19-CAR T-cell Therapy in 30 Patients with Autoimmune Disease

    Melanie Hagen1, Fabian Müller2, Andreas Wirsching1, Carlo Tur1, Tobias Krickau3, Markus Metzler4, Laura Bucci1, Christina Bergmann5, Janina Auth1, Jule Taubmann6, Panagiotis Garantziotis7, Sebastian Boeltz8, Soraya Kharboutli9, Silvia Spoerl9, Simon Völkl10, Michael Aigner9, Sascha Kretschmann9, Ingrid Vasova9, Andreas MAckensen11, Ricardo Grieshaber-Bouyer8 and Georg Schett12, 1Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Bayern, Germany, 2Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Germany, 3Department of Pediatrics and Adolscent Medicine, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Bayern, Germany, 4Department of Pediatrics and Adolscent Medicine, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 5Department Internal Medicine III, Friedrich-Alexander-University (FAU) Erlangen-Nurnber, Frankfurt, Germany, 6Friedrich-Alexander Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, 7Department of Internal Medicine 3-Rheumatology and Immunology, Friedrich Alexander University Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 8Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 9Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 10Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Bayern, Germany, 11Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Bayern, Germany, 12Friedrich-Alexander-Universität Erlangen-Nürnberg, Erlangen, Germany

    Background/Purpose: Treating autoimmune diseases like Systemic Lupus erythematosus (SLE), Idiopathic Inflammatory Myositis (IIM) or Systemic Sclerosis (SSc) is challenging and often requires life-long immunosuppressive therapy.…
  • « Previous Page
  • 1
  • …
  • 4
  • 5
  • 6
  • 7
  • 8
  • …
  • 17
  • 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 »

Embargo Policy

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].

Wiley

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

© Copyright 2025 American College of Rheumatology