ACR Meeting Abstracts

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Abstracts tagged "B-Cell Targets"

  • Abstract Number: LB04 • ACR Convergence 2025

    Anti-CD20/BCMA Bispecific CAR-T Cell Therapy Promotes Immune Reset and Sustained Drug Free Remission in Refractory Autoimmune Diseases

    Huihua Ding1, Wensi Li2, Yiwen Shen3, Chunyan Zhang4, Yan Ye3, Ran Wang3, Shaoying Yang3, Chunmei Wu3, Dai Dai3, Chengxiao Zheng2, Yuan Qian2, Xiaobing Luo5, Thule Trinh5, Judy Zhu2, Jiaqi Huang5, Yong Hao3, Xiaoying Yao3, Zhenfen Ling6, Yihong Yao5 and Nan Shen1, 1Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 2Shanghai AbelZeta Ltd., Shanghai, China (People's Republic), 3Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China (People's Republic), 4Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, Shanghai, China, 5AbelZeta Inc., Rockville, 6Shanghai General Hospital, Shanghai, China (People's Republic)

    Background/Purpose: Refractory autoimmune diseases with progressive organ damage remain a major unmet medical need. C-CAR168 is an autologous anti-CD20/BCMA bispecific CAR-T therapy designed to simultaneously…
  • Abstract Number: LB13 • ACR Convergence 2025

    Obinutuzumab Leads to Deep B-Cell Depletion in the Kidney Parenchyma of Patients With Lupus Nephritis: An Exploratory Analysis of the REGENCY Trial

    Brad Rovin1, Elsa Martins2, Cary Austin3, Harini Raghu3, Caleb Chan3, Patrick Chang3, Jay Garg3, Valeria Alberton4, Mittermayer Santiago5, Gustavo Aroca-Martínez6, Fedra Palazuelos7, Teresa Baczkowska8, José Alfaro9, Jorge Ravelo-Hernández10, Richard Furie11, Luís Pinto12, Eduardo Albiero13, Christopher Larsen14, Bongin Yoo3, Jennifer Pulley15, Andrew Thorley3, Thomas Schindler2, Theodore Omachi3, William Pendergraft III3 and Ana Malvar16, 1Department of Internal Medicine, The Ohio State University College of Medicine, Columbus, Ohio, 2F. Hoffmann-La Roche Ltd, Basel, Switzerland, 3Genentech, Inc., South San Francisco, California, 4Pathology Unit, Fernández Hospital, Buenos Aires, Argentina, 5Bahiana School of Medicine and Public Health and UFBA, Federal University of Bahia, and Clínica SER da Bahia, Salvador, Brazil, 6Universidad Simón Bolívar y Clínica de la Costa, Barranquilla, Colombia, 7Centro de Investigación y Tratamiento Reumatológico S.C., Mexico City, Mexico, 8Department of Transplantation Medicine, Nephrology and Internal Medicine, Medical University of Warsaw, Warsaw, Poland, 9Instituto Peruano del Hueso y la Articulación, Lima, Peru, 10Clinica San Juan Bautista, Unidad de Investigacion en Reumatologia e Inmunologia, Lima, Peru, 11Division of Rheumatology, Northwell Health, Great Neck, New York, 12Internal Medicine and Rheumatology, Hospital Pablo Tobón Uribe, Medellín, Colombia, 13Sanatorio Allende, Córdoba, Argentina, 14Arkana Laboratories, Little Rock, Arkansas, 15Roche Products Ltd, Welwyn Garden City, United Kingdom, 16Organización Médica de Investigación, Buenos Aires, Argentina

    Background/Purpose: B cells infiltrate the kidneys in lupus nephritis (LN) and likely contribute to the pathogenesis of kidney injury. The REGENCY trial (NCT04221477) showed that…
  • Abstract Number: LB14 • ACR Convergence 2025

    Promising Early Outcomes With BMS-986353, a CD19-directed Chimeric Antigen Receptor T Cell Therapy in Severe Refractory Idiopathic Inflammatory Myopathies: Safety and Efficacy Findings From the Ongoing Phase 1 Trial

    Rohit Aggarwal1, David Korman2, Margrit Wiesendanger3, Vikas Majithia4, Ellen De Langhe5, Marc Schmalzing6, Melissa Griffith7, Philipp Koehler8, Joanna Schiller8, Dimitrios Mougiakakos9, Mohamad Cherry10, Richard Nash11, Jacques Azzi12, Ernesto Ayala4, Peter Vandenberghe5, Max Topp6, Jonathan Gutman7, Eugen Feist13, Alisha Desai14, Alexis Melton14, Alice Wozniak14, San-San Ou14, Melissa Harnois14, Jerill Thorpe14, Praneeth Jarugula14, Takafumi Ide14, Ashley Koegel14 and Neil Kramer15, 1University of Pittsburgh, Pittsburgh, Pennsylvania, 2Mountain Rheumatology, HCA HealthONE, Denver, Colorado, 3Icahn School of Medicine at Mount Sinai, New York, New York, 4Mayo Clinic Hospital, Jacksonville, Florida, 5University Hospitals Leuven, Leuven, Belgium, 6University Hospital Würzburg, Würzburg, Germany, 7University of Colorado Anschutz Medical Campus, Aurora, Colorado, 8University of Cologne, Faculty of Medicine and University Hospital Cologne, Department I of Internal Medicine, Division of Clinical Immunology and Center for Integrated Oncology (CIO) Aachen Bonn Cologne Duesseldorf, Cologne, Germany, 9University Hospital Magdeburg, Magdeburg, Germany, 10Atlantic Health System, Morristown, New Jersey, 11HealthOne Cares and Colorado Blood Cancer Institute, Denver, Colorado, 12Icahn School of Medicine at Mount Sinai Hospital, New York, New York, 13Helios Vogelsang-Gommern Specialist Clinic, Gommern, Germany, 14Bristol Myers Squibb, Princeton, New Jersey, 15Overlook Medical Center and Atlantic Medical Group, Atlantic Health System, Morristown, New Jersey

    Background/Purpose: Idiopathic inflammatory myopathies (IIMs) are systemic autoimmune diseases affecting muscles, skin, lungs, joints, and several other organs; many patients are refractory to available therapy,…
  • Abstract Number: LB18 • ACR Convergence 2025

    Transcriptomic Signatures of ANA+ and ANA- B Cells Reveal Shifts from Active Disease to Remission in Systemic Lupus Erythematosus

    Rita Pozovskiy1, Yemil Atisha-Fregoso2 and Betty Diamond3, 1Zucker School of Medicine, New York, New York, 2Feinstein Institutes for Medical Research, New York, New York, 3The Feinstein Institutes for Medical Research, Manhasset, New York

    Background/Purpose: In systemic lupus erythematosus (SLE), IgG antibodies that target nuclear antigens (ANA) are pathogenic and part of the diagnostic criteria for SLE. Healthy individuals…
  • Abstract Number: 2458 • ACR Convergence 2025

    Obecabtagene autoleucel (obe-cel), a CD19-targeting Autologous Chimeric Antigen Receptor T-cell Therapy (CAR T) with a fast off-rate binding domain, in Patients (pts) with Severe, Refractory Systemic Lupus Erythematosus (srSLE): Preliminary Results from the Phase I CARLYSLE Study

    Maria Leandro1, Ruth Pepper2, Ben Parker3, Eleni Tholouli4, David Jayne5, Ben Uttenthal6, Josefina Cortés-Hernández7, Pere Barba7, José Andrés Román Ivorra8, Yanqing Hu9, Wolfram Brugger10, Silvia Basilico11, Davide Germano11 and Claire Roddie1, 1University College London and University College London Hospital, London, United Kingdom, 2University College London, University College London Hospital and Royal Free Hospital NHS Trust, London, United Kingdom, 3NIHR Manchester CRF, Manchester Royal Infirmary, Manchester, United Kingdom, 4Manchester Royal Infirmary, Manchester, United Kingdom, 5University of Cambridge, Cambridge, United Kingdom, 6Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom, 7Hospital Universitari Vall d’Hebron-Universitat Autónoma de Barcelona, Barcelona, Spain, 8Hospital Universitari i Politècnic La Fe, Valencia, Spain, 9Autolus Therapeutics, Rockville, MD, 10Autolus Therapeutics, Munich, Germany, 11Autolus Therapeutics, Basel, Switzerland

    Background/Purpose: Pts with srSLE have limited remaining treatment options and represent a population with an unmet need. CD19 CAR Ts have potential for deep depletion…
  • Abstract Number: 1563 • ACR Convergence 2025

    RESET-SSc: Clinical Trial Evaluating Rese-cel (Resecabtagene Autoleucel), A Fully Human, Autologous 4-1BB CD19-CAR T Cell Therapy in Systemic Sclerosis

    Dinesh Khanna1, Monalisa Ghosh1, Ankoor Shah2, Sonali Bracken3, george georges4, Carrie Richardson5, Pei-Suen Tsou1, Charles Ross6, Carleigh Zahn1, Courtney Little7, Carl diCasoli7, Mikaela Raymond7, Adreeja GuhaRay7, Jenell Volkov7, Daniel Nunez7, Thomas Furmanak7, Jason Stadanlick7, Larissa Ishikawa7, Zachary Vorndran7, Alexandra Ellis7, Jazmean Williams7, Steve Flanagan7, Quynh Lam8, Domenick Braccia8, Fatemeh Hadi-Nezhad8, Raj Tummala8, Samik Basu7 and David Chang9, 1University of Michigan, Ann Arbor, MI, 2Duke University, Durham, NC, 3Duke University Medical Center, Durham, NC, USA, Apex, NC, 4Northwestern Medicine, Evanston, IL, 5Northwestern University, Chicago, IL, 6University of Michigan, Ann Arbor, 7Cabaletta Bio, Philadelphia, PA, 8Cabaletta Bio, Philadelphia, 9Cabaletta Bio, Bryn Mawr, PA

    Background/Purpose: The treatment goals for systemic sclerosis (SSc) are to control disease activity, limit progression of organ damage and decrease long-term morbidity and mortality. Therapies…
  • Abstract Number: 0914 • ACR Convergence 2025

    Preclinical Expansion of Autoreactive Naive B cells Drives RA onset in ACPA+ individuals

    Xiaohao Wu1, Mengrui Zhang2, Orr Sharpe3, V. Michael Holers4, Jane Buckner5, Gary Firestein5, Eddie James6, Kevin Deane7 and William H. Robinson8, 1Stanford Uniersity, Stanford, 2Stanford University, Stanford, CA, 3Stanford University, Stanford, 4University of Colorado Anschutz Medical Campus, Aurora, 5Benaroya Research Institute, Seattle, 6Benaroya Research Institute, Benaroya Research Institute, 7University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 8Stanford University, Palo Alto, CA

    Background/Purpose: The cellular and molecular mechanisms underlying the progression from anti-citrullinated protein antibody (ACPA) positivity to clinical rheumatoid arthritis (RA) remain poorly understood. Defining these…
  • Abstract Number: 0279 • ACR Convergence 2025

    Assessment of Baseline IgG4-RD Disease Characteristics and Impact Upon Safety and Efficacy of Inebilizumab: Results from the MITIGATE Study

    Yoshiya Tanaka1, Emma Culver2, Arezou Khosroshahi3, Wen Zhang4, Kazuichi Okazaki5, Matthias Lohr6, nicolas schleinitz7, Xinxin Dong8, melissa rosen9, Sue Cheng8, Daniel Cimbora8 and John Stone10, 1University of Occupational and Environmental Health, Japan, Kitakyushu, Japan, 2John Radcliffe Hospital; University of Oxford, Oxford, United Kingdom, 3Emory University, Atlanta, GA, 4Peking Union Medical College Hospital, Dong Cheng Qu, China (People's Republic), 5Kansai Medical University Kori Hospital, Osaka, Japan, 6Karolinska Institutet, Stockholm, Sweden, 7Aix Marseille university, AP-HM, Marseille, France, 8Amgen, Thousand Oaks, CA, 9Amgen Inc., Thousand Oaks, CA, 10Massachusetts General Hospital , Harvard Medical School, Concord, MA

    Background/Purpose: IgG4-related disease (IgG4-RD) is a progressive, systemic, fibroinflammatory disease characterized by unpredictable and recurring flares, leading to organ damage and decreased quality of life.…
  • Abstract Number: 0006 • ACR Convergence 2025

    QEL-005: CD19 CAR-Regulatory T cell therapy, a novel approach for the treatment of complex immune mediated inflammatory diseases including Rheumatoid Arthritis and Systemic Sclerosis

    Jenny McGovern, Georgios Eleftheriadis, Thomas Grothier, Eva Bugallo Blanco, Anna Koi, Mahsa Nemani, Cameron Allum, Emily Hurley, Daniela Penston, Marc Martinez-Llordella, Luke Devey and Nathalie Belmonte, Quell Therapeutics, London, United Kingdom

    Background/Purpose: Rheumatoid Arthritis (RA) and Systemic Sclerosis (SSc) are immune mediated inflammatory diseases (IMID) where a complex interplay of tissue and immune cell activation drives…
  • Abstract Number: 2448 • ACR Convergence 2025

    Rituximab as the first line treatment in newly diagnosed systemic lupus erythematosus

    Haiting Wang1, Liling Zhao2, Shuang Ye3 and Shaoying Yang2, 1Renji Hospital, Rockville, MD, 2Renji hospital, Shanghai, China (People's Republic), 3Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China, Shanghai, Shanghai, China (People's Republic)

    Background/Purpose: Rituximab (RTX) has been commonly used for the treatment of patients with severe or refractory systemic lupus erythematosus (SLE), yet real-world data concerning RTX…
  • 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 Yaakoub, Diana Alzamareh, Alexander Bae William 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,…
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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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