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Abstracts tagged "B-Cell Targets"

  • Abstract Number: 1537 • ACR Convergence 2025

    Local Immune effector Cell-Associated Toxicity Syndrome (LICATS) in CAR T-cell treated patients with Autoimmune Disease

    Melanie Hagen1, Fabian Müller2, Andreas Wirsching1, Soraya Kharboutli3, Silvia Spoerl3, Christina Duesing4, Tobias Krickau5, Markus Metzler5, Simon Völkl3, Michael Aigner3, Sascha Kretschmann3, Ingrid Vasova3, Marc Saake5, Stefan Schliep5, Torsten Kubacki6, Nicolas Hunzelmann6, Laura Bucci1, Jule Taubmann7, Christina Bergmann1, Andrea-Hermina Györfi8, Sascha Dietrich9, Jörg Distler10, Ricardo Grieshaber-Bouyer11, Andreas Mackensen12 and Georg Schett13, 1Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 2University Hospital of Erlangen, Erlangen, Germany, 3Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 4Klinik für Rheumatologie, Düsseldorf, Germany, 5Friedrich-Alexander-Universität Erlangen-Nürnberg, University Hospital Erlangen, Erlangen, Germany, 6University and University Hospital Cologne, Cologne, Germany, Cologne, Germany, 7Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 8Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University., Düsseldorf, Germany, 9Heinrich Heine University Duesseldorf, University Hospital Duesseldorf, Duesseldorf, Germany, 10University Hospital Duesseldorf and HHU, Duesseldorf, Germany, 11University Hospital Erlangen, Erlangen, Germany, 12Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Germany, 13Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany

    Background/Purpose: CD19-targeting chimeric antigen receptor (CAR) T-cell therapy has revolutionized treatment strategies for severe B-cell driven autoimmune diseases (AID) like Systemic Lupus erythematosus (SLE), Systemic…
  • Abstract Number: 0912 • ACR Convergence 2025

    CD11c⁺CD21⁻ Autoimmune-Associated B Cells Derived from Double-Negative IgD⁻CD27⁻ Subsets Exhibit Enhanced IFNLR1 Expression in Systemic Lupus Erythematosus

    Roukaya Yaakoubi, Diana Alzamareh, Alexander William Bae and Jennifer Barnas, university of rochester, rochester, NY

    Background/Purpose: Autoimmune-associated B cells (ABCs) are increasingly recognized for their role in the pathogenesis of systemic lupus erythematosus (SLE), yet their developmental origins and specific…
  • Abstract Number: 0263 • ACR Convergence 2025

    A Multicenter Retrospective Case Series of Patients with Susac Syndrome treated with Rituximab

    Michelle Benjamin1, Mattia Wruble Clark2, Shamik Bhattacharyya3, Audra Horomanski1 and Kristin Galetta4, 1Stanford University, Palo Alto, CA, 2Mass General Brigham, Somerville, MA, 3Brigham and Women's Hospital, Malden, MA, 4Stanford Medical Center, Palo Alto

    Background/Purpose: Susac Syndrome (SuS) is a rare immune-mediated vasculo-occlusive disease characterized by a triad of encephalopathy, hearing loss, and branched retinal artery occlusions. Deficits can…
  • Abstract Number: 0005 • ACR Convergence 2025

    LBL-047, A First-In-Class Anti-BDCA2/TACI Fusion Protein, Inhibits the Function of Both pDCs and B cells

    Fengxia Li1, Jianming Sun1, Hailin Wang1, Yan Zhu1, Xiaoxiao Liu1, Jing Li1, Yurong Qin1, Guojin Wu1, Jing Guan1, Min Chen1, Jordan Zhu2, Xiaoqiang Kang1, Xiao Huang1 and Hong Ling1, 1Nanjing Leads Biolabs Co., Ltd., Nan Jing, China (People's Republic), 2Nanjing Leads Biolabs Co., Ltd., Nan Jing

    Background/Purpose: Blood dendritic cell antigen 2 (BDCA2) is specifically expressed on pDCs whose uncontrolled production of type I IFN play a crucial role in the…
  • Abstract Number: 2442 • ACR Convergence 2025

    Reduction in Extrafollicular B Cell Responses in SLE Patients after CAR T Cell Therapy

    Danae-Mona Nöthling1, Kirill Anoshkin1, Panagiotis Garantziotis1, Laura Bucci1, Tobias Rothe2, Jule Taubmann3, Futoshi Iwata1, Melanie Hagen1, Andreas Wirsching1, Simon Völkl4, Fabian Müller5, Aline Bozec1, Andreas Mackensen6, Georg Schett7 and Ricardo Grieshaber-Bouyer8, 1Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 2Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlagen, Germany, 3Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 4Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 5University Hospital of Erlangen, Erlangen, Germany, 6Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Germany, 7Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 8University Hospital Erlangen, Erlangen, Germany

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by aberrant B cell activation and autoantibody production. CD19-targeted chimeric antigen receptor (CAR) T-cell therapy induces a short,…
  • Abstract Number: 1532 • ACR Convergence 2025

    Preliminary Safety, Efficacy, and Cellular Kinetics of CTA313, a CD19/BCMA Dual-Targeted Universal CAR-T Therapy, for Active Systemic Lupus Erythematosus

    Hanwei Wang1, Yue Xie2, Guojiao Yang3, Lu Han3, Jiangtao Ren4, Yali Zhou4, Wengang Ge3, Jan Davidson-Moncada4 and Huan Zhou5, 1The Third People’s Hospital of Bengbu, Beng bu, China (People's Republic), 2Bioheng Therapeutics Limited, Nan Jing Shi, China (People's Republic), 3Bioheng Therapeutics Co., Limited, Nanjing, China (People's Republic), 4Bioheng Therapeutics Co., Limited, Nan Jing, China (People's Republic), 5Clinical Research Hospital of the First Affiliated Hospital of Anhui Medical University, Hefei, China (People's Republic)

    Background/Purpose: SLE is characterized by B cell activation, autoantibody production and autoreactivity. Recently, CAR-T therapy has emerged as a promising strategy to deplete autoreactive B…
  • Abstract Number: 0913 • ACR Convergence 2025

    Potent and Selective Oral IRF5 Degrader, KT-579, Demonstrates In Vitro and In Vivo Activity Comparable or Superior to Approved or Clinically Active Agents in Human Cellular Assays and Lupus Efficacy Models

    Veronica Campbell1, Yi Zhang1, Virginia Massa1, Jordan Leedberg1, Erik Corcoran1, Emily Lurier1, Ryan Camire2, Chris Carroll1, Chris Ho1, Dapeng Chen1, Bradley Enerson1, Revonda Mehovic1, Ziyan Zhao1, Lincoln Howarth1, Susanne Breitkopf1, Sarah Martinez1, Melissa Ford1, Xue Fei1, Murugappan Sathappa1, Juliet Williams3, Matthew Weiss3, Arsalan Shabbir3 and Nello Mainolfi4, 1Kymera Therapeutics, Watertown, MA 02472, 2Kymera Therapeutics, Watertown, MA 02472, MA, 3Kymera Therapeutics, Watertown, 4Kymera Therapeutics, Watertown, MA

    Background/Purpose: IRF5 is a transcription factor and regulator of immune responses activated downstream of pattern recognition receptors, in particular endosomal toll-like receptors (TLR), TLR7, TLR8…
  • Abstract Number: 0262 • ACR Convergence 2025

    Preclinical Characterization of ABB071 – a Humanized anti-CD180 Antibody that Modulates Multiple Pro-inflammatory Immune Pathways for the Treatment of Autoimmune and Inflammatory Disorders

    Margaret McDaniel, Brenda Stevens, Socheath Khim, Alan Wahl, Che-Leung Law and Edward Clark, Abacus Bioscience, Seattle, WA

    Background/Purpose: CD180 is a Toll-like receptor (TLR) homolog expressed on antigen-presenting cells (APCs): B cells, dendritic cells, monocytes, and macrophages. While the extracellular domain of…
  • Abstract Number: 0003 • ACR Convergence 2025

    In Vivo Generation of anti-CD19 CAR T Cells Utilizing Circular RNA Encapsulated in Targeted Lipid Nanoparticles

    Xiaoyu Pan1, Xiaoning Wang1, Zhihao Chen1, Xiaowen Zou1, Siqi Li1, Jian Ye1, Fei Lin1, Yang He1, Edo Kon2, Peng Zhu1, Mengyun Chen1 and Weiyi Zhang1, 1RiboX Therapeutics, Shanghai, China (People's Republic), 2RiboX Therapeutics, Cambridge, MA

    Background/Purpose: Chimeric Antigen Receptor (CAR) T-cell therapy has revolutionized cancer treatment and shown promise in addressing autoimmune diseases. However, current ex vivo CAR T-cell therapies…
  • Abstract Number: 2695 • ACR Convergence 2025

    B-cell depletion and lymphoid follicle disruption upon different B-cell depleting agents

    Carlo Tur1, Markus Eckstein2, Laura Bucci1, Janina Auth3, Christina Bergmann1, Simon Rauber4, Melanie Hagen1, Danae-Mona Nöthling1, Sebastian Böltz1, Andreas Wirsching1, Filippo Fagni5, Giulia Corte6, Panagiotis Garantziotis1, Jule Taubmann7, jochen wacker1, Andreas Ramming8, Maria Antonietta D'Agostino9, Arndt Hartmann10, Fabian Müller11, Andreas Mackensen12, Ricardo Grieshaber-Bouyer13, Georg Schett14, Aline Bozec1 and Maria Gabriella Raimondo1, 1Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 2Institute of Pathology and Comprehensive Cancer Center EMN, Friedrich-Alexander- Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 3Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Bayern, Germany, 4Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Bayern, Germany, 5Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Bayern, Germany, 6- Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 7Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and University Hospital Erlangen, Erlangen, Germany, 8Department of Internal Medicine 3, Rheumatology & Immunology, Friedrich-Alexander-University (FAU) & Universitätsklinikum Erlangen, Erlangen, Germany, 9Division of Rheumatology and Clinical Immunology - Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, 10Institute of Pathology and Comprehensive Cancer Center EMN, Friedrich-Alexander- Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Bayern, Germany, 11University Hospital of Erlangen, Erlangen, Germany, 12Department of Medicine 5 - Hematology and Oncology, Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU) and Uniklinikum Erlangen, Erlangen, Germany, 13University Hospital Erlangen, Erlangen, Germany, 14Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany

    Background/Purpose: Advanced protein-based therapies targeting B-cells, including glycoengineered CD20 monoclonal antibody obinutuzumab (OBI) and the CD19/CD3 T-cell engager blinatumumab (BLI), show promise for managing severe…
  • Abstract Number: 2425 • ACR Convergence 2025

    Neutrophil Transcriptomics in SLE: Exploring Intrinsic, Ex Vivo Adaptation, and CAR-T Cell Therapy-Induced Changes

    Ehsan Dehdashtian1, Stefania Gallucci2, Guangnan Hu3, Dominic Borie4 and Roberto Caricchio5, 1UMass Chan Medical School, Worcester, MA, 2Temple University School of Medicine, Worcester, MA, 3UMass Chan School of Medicine, Worcester, MA, 4Kyverna Therapeutics, Emeryville, CA, 5University of Massachusetts Chan Medical School, Worcester, MA

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by dysregulation of the adaptive and innate immune systems. Neutrophils, key players in innate immunity,…
  • Abstract Number: 1529 • ACR Convergence 2025

    Updated Phase 1 Trial Data Assessing the Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of BMS-986353 (CC-97540), a CD19-directed Chimeric Antigen Receptor T Cell Therapy Using a Next-Generation Process for Severe, Refractory SLE

    Georg Schett1, David Simon2, Margrit Wiesendanger3, Anca Askanase4, Vikas Majithia5, Neil Kramer6, Jacques Morel7, Philip J. Mease8, Ellen De Langhe9, Amit Saxena10, dominique Farge11, Alain Lescoat12, Alisha Desai13, Griff McTume14, Whitney Handy14, Sharmila Das13, Jerill Thorpe14, Alexis Melton14, Ashley Koegel14 and Emily Littlejohn15, 1Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 2Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany, Berlin, Germany, 3Icahn School of Medicine at Mount Sinai, New York, NY, 4Columbia University Medical Center, New York, NY, 5Mayo Clinic Hospital, Jacksonville, FL, 6Overlook Medical Center; Atlantic Medical Group, Atlantic Health System, Summit, NJ, 7CHU and University of Montpellier, Montpellier, France, 8Department of Rheumatology, Providence-Swedish Medical Center and University of Washington, Seattle, WA, 9University Hospitals Leuven, Leuven, Belgium, 10Division of Rheumatology, Department of Medicine, NYU Grossman School of Medicine, New York, NY, 11Hôpital Saint-Louis, Paris, France, 12CHU Rennes University Hospital, Rennes, France, 13Bristol Myers Squibb, Princeton, NJ, 14Bristol Myers Squibb, Princeton, 15Cleveland Clinic, Cleveland, OH

    Background/Purpose: BMS-986353 (CC-97540; CD19 NEX-T) is a CD19-directed chimeric antigen receptor (CAR) T cell therapy that expresses the same CAR as lisocabtagene maraleucel (liso-cel); it…
  • Abstract Number: 0910 • ACR Convergence 2025

    Development of Four Distinct Human IgG4-Producing Mouse Models Recapitulating IgG4-Related Disease

    MIN GANG KIM1, JINA YEO2, HEA RIM KANG3, JAE HYUN MOON3, Seon Uk Kim4, SeoYoon Ban5, MI HYEON KIM6 and Eun Young Lee7, 1Seoul National University College of Medicine, Seoul, Republic of Korea, 2Division of Rheumatology, Department of Internal Medicine, Gachon University Gil Medical Center, Incheon, Republic of Korea, 3Seoul National University College of Medicine, Jongno-gu, Seoul, Republic of Korea, 4Seoul National University, Jongno-gu, Seoul, Republic of Korea, 5Department of Cancer biology, Graduate School of College of Medicine, Seoul National University, Korea, Seoul, Republic of Korea, 6Hallym university dongtan sacred heart hospital, Seocho-gu, Seoul, Republic of Korea, 7Seoul National University College of Medicine, Seoul, South Korea

    Background/Purpose: IgG4-related disease (IgG4RD) is an immune-mediated fibroinflammatory condition characterized by multi-organ involvement, elevated serum IgG4, and IgG4-positive plasma cell infiltrates that form tumor-like lesions…
  • Abstract Number: 0239 • ACR Convergence 2025

    Safety of Rilzabrutinib, a BTK Inhibitor, in Adult Patients with IgG4-related disease (IgG4-RD) in a 52-week Phase 2 Open-label Study

    Alireza Meysami1, Mollie Carruthers2, John Stone3, Fernando Martinez-Valle4, nicolas schleinitz5, Daniela Ghetie6, Robert Spiera7, Jeea Choi8, Leda Mannent9 and Owen Hagino8, 1Henry Ford Health, Detroit, MI, 2Vancouver General Hospital, Vancouver, BC, Canada, 3Massachusetts General Hospital , Harvard Medical School, Concord, MA, 4Vall d’Hebron Hospital, Barcelona, Spain, 5Aix Marseille university, AP-HM, Marseille, France, 6Oregon Health and Science University, Portland, OR, 7Scleroderma, Vasculitis, and Myositis Center, Hospital for Special Surgery, Weill Cornell Medical College, New York, NY, 8Sanofi, Morristown, NJ, 9Sanofi, Gentilly, France

    Background/Purpose: IgG4- related disease (IgG4-RD) is a chronic, progressive, immune-mediated fibrotic disease with limited treatment options. Rilzabrutinib is an orally available, reversible, inhibitor of Bruton's…
  • Abstract Number: 0002 • ACR Convergence 2025

    KITE-363: An Autologous Anti-CD19/CD20 CAR-T Product for the Treatment of Autoimmune Rheumatic Diseases

    Brian Kim, Christine Lowe, Francisco Flores, Jeremy Margaitis, Alessandro Calo, Stacey Valny, Anna Konecny, Eva Jaghatspanyan, Sean Yoder, Kenneth Ertel, Simone Filosto, Jodi Murakami and David Barrett, Kite, a Gilead Company, Santa Monica, CA

    Background/Purpose: B-cell dysregulation is a key factor in the development and progression of autoimmune diseases, and B-cell inhibition has been a cornerstone of treatment for…
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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.).

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