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
  • Abstract Number: LB22 • ACR Convergence 2025

    Early Evidence of Proof-of-Concept of an Albumin-DNASE1L3 Fusion Protein (NTR-441) for the Rapid Enzymatic Inactivation of NETs in SLE with DNASE1L3-Deficiency

    Andreas Reiff1, Tadej Avcin2, Bernd Jilma3, Peter Korosec4, Matthias Weiss-Tessbach3, Christian Schoergenhofer3, Masa Bizjak5, Barbara Jenko Bizjan6, Barbara Cugalj Kern5, Kim Simpfendorfer7, Christian Lood8, Tyler Artner9, Angelene Prasanna1, Ken Olivier1, Ghazaleh Gouya1, Ralph Lambalot9, Abdul Hakkim1 and Tobias Fuchs1, 1Neutrolis, Cambridge, Massachusetts, 2University Medical Centre Ljubljana, Ljubljana, Slovenia, 3Medical University of Vienna, Vienna, Austria, 4University Clinic of Respiratory and Allergic Diseases, Golnik, Slovenia, 5University Medical Center Ljubljana, Ljubljana, Slovenia, 6University of Ljubljana, Ljubljana, Slovenia, 7Feinstein Institutes for Medical Research, Manhasset, New York, 8University of Washington, Seattle, Washington, 9Neutrolis, Cambridge

    Background/Purpose: Excessive formation and impaired clearance of Neutrophil Extracellular Traps (NETs) have been linked to autoimmune and inflammatory diseases, notably systemic lupus erythematosus (SLE). DNASE1-like…
  • Abstract Number: LB19 • ACR Convergence 2025

    Rosnilimab, a Selective and Potent Depleter of Pathogenic T Cells, Demonstrates Efficacy, Safety, and Translational Proof of Mechanism in a Rheumatoid Arthritis Phase 2B Trial

    Jonathan Graf1, Amy Archer2, Sergiy Kovalenko3, Katarzyna Kolossa4, John Serpa5, Tamta Kobakhidze6, Daniela Cepoi7, Andrea Everding8, Costantino Pitzalis9, Catherine Aversa2, Martin Dahl2, May Hafez2, Paul Lizzul2, Priya Raina2, Bruce Randazzo2, Yangsu Ren2, Khalil Saikali2, Cailin Sibley10, Gerd Burmester11, Jacques-eric GOTTENBERG12, Iain McInnes13, Eduardo Mysler14, Lee Simon15, Josef Smolen16, Jeffrey Sparks17, Ronald van Vollenhoven18, Michael Weinblatt19 and Paul Emery20, 1UCSF, San Francisco, California, 2AnaptysBio Inc, San Diego, California, 3Arensia Exploratory Medicine, Kyiv, Ukraine, 4MICS Centrum Medyczne, Bydgoszcz, Poland, 5Allied Biomedical Research Institute, Miami, Florida, 6Research Institute of Clinical Medicine Todua Clinic, Tbilisa, Georgia, 7Nicolae Testemitanu State University of Medicine & Pharmacy, Chisinau, Moldova, 8MVZ Rheumatologie & Autoimmunmedzin Hamburg GmbH, Hamburg, Germany, 9QMUL, Bromley Kent, United Kingdom, 10AnaptysBio Inc, San Diego, 11Charité - Universitétsmedizin Berlin, Berlin, Germany, 12Hautepierre Hospital, STRASBOURG, France, 13University of Glasgow, Glasgow, United Kingdom, 14OMI, Buenos Aires, Argentina, 15SDG LLC, West Newton, Massachusetts, 16Medical University of Vienna, Vienna, Austria, 17Brigham and Women's Hospital, Boston, Massachusetts, 18Amsterdam UMC, Amsterdam, Netherlands, 19Brigham and Women's Hospital/ Harvard Medical School, Waban, Massachusetts, 20University of Leeds, Leeds, United Kingdom

    Background/Purpose: Over 50% of RA patients require multiple b/tsDMARD classes due to inadequate or lost response. Rosnilimab, an investigational monoclonal antibody that selectively targets and…
  • 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: LB09 • ACR Convergence 2025

    Rotation or Change of Biologic After TNF blocker treatment failure for axial Spondyloarthritis

    Elisa Dalix1, Philippe Goupille2, Daniel Wendling3, Christian Roux4, Jean-Hughes Samon5, Olivier Brocq6, Anne Tournadre7, Arnaud Constantin8, Maxime Breban9, Gregoire Cormier10, Tristan Pascart11, Thierry Lequerre12, Pascal Claudepierre13, Eric Lespessailles14, Benoit Legoff15, Jeremie Sellam16, Athan Baillet17, Thierry Schaeverbeke18, Stephan Pavy19, Valerie Devauchelle-Pensec20, Elisabeth Gervais21, Laure Gossec22, Corinne Miceli23, Yves-Marie Pers24, Cedric Lukas25, Renaud Felten26, Beatrice Bouvard27, Amelie Denis28, Emmanuelle Dernis28, Emilie Presles29, Florence Rancon29 and Hubert Marotte30, 1Université Jean Monnet, CHU Saint-Etienne, Mines Saint-Etienne, INSERM, Saint-Etienne, France, 2Department of Rheumatology and INSERM-CIC1415, University Hospital of Tours, EA 7501 GICC, University of Tours, Tours, France, 3Rhumatologie, CHU de Besançon, Besancon, France, 4Service de rhumatologie, CHU de Nice, IbV, Université Cote d'Azur, Nice, France, 5Service de Rhumatologie, Hôpital Maison Blanche, Centre Hospitalier Universitaire de Reims, Reims, France; Université de Reims Champagne-Ardenne, Faculté de Médicine, EA 3797, Reims, France, 6Rheumatology Department, CHPG Monaco, Monaco, Monaco, 7Rheumatology Department, CHU Clermont-Ferrand, Clermont-Ferrand, France, 8Rheumatology Center, Toulouse University Hospital, Toulouse, France, 9INSERM UMR1173, INFLAMEX, Laboratoire d'Excellence, Rheumatology Division, Ambroise Paré Hospital (AP-HP), Paris, France, 10Rheumatology, Centre Hospitalier Departemental Vendee, La Roche-sur-Yon, France, 11Department of Rheumatology, Université Catholique de Lille Hôpital Saint Philibert, Lomme, France, 12Department of Rheumatology & CIC-CRB 1404, Inserm, PANTHER UMR 1234, University of Rouen Normandie, Normandie University, CHU Rouen, Rouen, France, 13AP-HP, Henri-Mondor Hospital, Department of Rheumatology, EpiDermE, Université Paris Est Créteil, Créteil, France, 14Translational Medicine Research Platform, PRIMMO, University Hospital Centre of Orleans, Orleans, France, 15Nantes Université, ONIRIS, Univ Angers, CHU Nantes, INSERM, Regenerative Medicine and Skeleton, RMeS, UMR 1229, Nantes, France, 16Rheumatology Department, Sorbonne Université, Saint-Antoine Hospital Assistance Publique Hôpitaux de Paris (AP-HP), Centre de Recherche Saint-Antoine (CRSA) Inserm UMRS-938,, Paris, France, 17Université Grenoble Alpes, 4UMR5525, Grenoble, France, 18Department of Rheumatology, Hôpital Pellegrin, Bordeaux, France, 19Department of Rheumatology, Hôpital Bicêtre, Assistance Publique - Hôpitaux de Paris, Le Kremlin-Bicetre, 20Department of Rheumatology, Université de Bretagne Occidentale, CHU Brest, INSERM (U1227), LabEx IGO, Brest, France, 21LITEC, Université de Poitiers, CHU Poitiers, Poitiers, France, 22Sorbonne Université, AP-HP & EULAR, Paris, France, 23Immunoregulation Unit, Institut Pasteur, Cochin AP-HP, Paris, France, 24IRMB, University of Montpellier, Inserm U1183, CHU Montpellier, Montpellier, France, 25Rheumatology department, CHU and University of Montpellier, Montpellier, France; UMR UA11 Inserm (IDESP), University of Montpellier, Montpellier, France, 26Service de Rhumatologie, CHU de Strasbourg - Hôpital de Hautepierre, Strasbourg, France, 27Rhumatologie, Centre Hospitalier Universitaire, Angers, France, 28CH Le Mans, Le Mans, France, 29CHU Saint-Etienne, CIC 1408, Saint-Etienne, France, 30Université Jean Monnet, CHU de Saint-Etienne, CIC 1408, Mines Saint-Etienne, INSERM, SSINBIOSE 1059, Saint-Etienne, France

    Background/Purpose: Axial spondyloarthritis (axSpA) is initially treated with non-steroidal anti-inflammatory drugs. In case of inadequate response, ACR/EULAR recommend biological disease-modifying antirheumatic drugs (bDMARDs). Up to…
  • Abstract Number: LB12 • ACR Convergence 2025

    Randomized, Double-Blind, Placebo-Controlled Phase IIa Trial of an Innovative Intra-Articular Apoptotic Cell Therapy in Knee Osteoarthritis (OA): 3-Month Positive Outcomes and Identification of Responder Population (NCT06233474)

    Philip Conaghan1, Bernt Husøy2, Cecilie Rovsing3, Sidsel L Boll4, Liliana Groppa5, Amir Oron6, Asger Bihlet7, Ali Mobasheri8, Tobias Winkler9, Dror Mevorach10, Einat Galamidi11, Lital Weinfeld-Bergman12, Lior Binder12 and Oren Hershkovitz11, 1University of Leeds, Leeds, United Kingdom, 2Sanos Clinic, Herlev, Denmark, 3Sanos Clinic, Gandrup, Denmark, 4Sanos Clinic, Vejle, Denmark, 5T. Mosneaga Republican Clinical Hospital, Chisinau, Moldova, 6Kaplan MC, Rehovot, Israel, 7NBCD A/S, Soeborg, Denmark, 8University of Oulu, Oulu, Finland, 9Charité - Universitätsmedizin Berlin, Berlin, Germany, 10Hadassah-University Hospital, Jerusalem, Israel, 11Enlivex Therapeutics, Ness Ziona, Israel, 12Enlivex Therapeutics, Nes Ziona, Israel

    Background/Purpose: OA is a prevalent disabling disease growing globally due to aging populations and rising obesity. In primary OA, the effects of joint tissue damage accumulate with age,…
  • Abstract Number: LB17 • ACR Convergence 2025

    Circulating biomarkers for organ involvement in systemic lupus erythematosus: a series of systematic reviews and meta-analyses

    Sitian Zang1, Ranran Yao1, Yan Wang1, Danxue Zhu1, Jing He1 and Zhanguo Li2, 1Peking University People's Hospital, Beijing, China (People's Republic), 2Peking Univeristy People's Hospital, Beijing, China (People's Republic)

    Background/Purpose: Systemic lupus erythematosus (SLE) features heterogeneous clinical manifestations. The identification of biomarkers that facilitate initial disease recognition is a cornerstone of optimized clinical management.…
  • 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: 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: LB05 • ACR Convergence 2025

    ER Stress-Induced ATP2A3 Drives Rheumatoid Arthritis via Activation of STING Signaling

    yujie cai, Nanfang hospital, Guangzhou, China (People's Republic)

    Background/Purpose: Rheumatoid arthritis (RA) is an autoimmune disease characterized by persistent synovial inflammation and joint bone destruction. Endoplasmic reticulum (ER) stress plays an important role…
  • 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: 0010 • ACR Convergence 2025

    XmAb657, a CD19 x CD3 T-Cell Engaging Bispecific Antibody for Autoimmune Disease

    Matthew Bernett1, Gregory Moore2, Katrina Bykova2, Viralkumar Davra2, Seung Chu2, Michael Sheard2, Ruschelle Love2, Norman Barlow2, Engie Salama2, Jitendra Kanodia2, Panida Lertkiatmongkol2, Dipankar Chaudhuri2, Kendra Avery2, Hanh Nguyen2, Rumana Rashid2, Ke Liu2, Jing Qi2, Araz Eivazi2, Thuy Truong2, Sher Karki2, James Ernst2, Rena Bahjat2 and John Desjarlais2, 1Xencor, Inc., Pasadena, CA, 2Xencor, Inc., Pasadena

    Background/Purpose: B cell depletion is a validated therapeutic strategy in autoimmune disease, but current approaches targeting CD20 may only partially eliminate disease-driving subsets such as…
  • 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: 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: 0007 • ACR Convergence 2025

    WITHDRAWN

  • 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…
  • « Previous Page
  • 1
  • 2
  • 3
  • 4
  • …
  • 2607
  • 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