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Abstracts tagged "Fibroblasts, Synovial"

  • Abstract Number: 1928 • ACR Convergence 2026

    Spatial and Functional Characterization of SPP1+ Macrophages in Pre-RA and RA Synovium

    Megan Hanlon1, Raghav Sharma1, Ursula Fearon2, Kevin Wei3 and Ellen Gravallese4 Affiliations: 1Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 2Trinity College Dublin, Dublin, Dublin, Ireland, 3Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 4Brigham and Women's Hospital, Harvard Medical School, Chestnut Hill, MA

    Background/Purpose: We have reported an enrichment of secreted phosphoprotein-1 synovial tissue macrophages (SPP1+ STM) in rheumatoid arthritis (RA) synovium compared to control, correlating significantly with…
  • Abstract Number: 2016 • ACR Convergence 2026

    Celastrol-Loaded Synthetic High-Density Lipoprotein Nanoparticles Preferentially Target Inflamed Synovial Macrophages and Attenuate Zymosan-Induced Arthritis

    Daniel McDougle1, April Kim1, Anna Schwendeman1, David Fox2 and James Moon1 Affiliations: 1University of Michigan, Ann Arbor, MI, 2University of Michigan, Dexter, MI

    Background/Purpose: Effective joint-targeted delivery remains a critical unmet need in inflammatory arthritis. Synthetic high-density lipoprotein (sHDL) nanodiscs are nanoparticles that solubilize hydrophobic therapeutics while exploiting…
  • Abstract Number: 2018 • ACR Convergence 2026

    Development of a Patient-Derived 3D Synovial Organoid Platform for Personalized Drug Testing in Rheumatoid Arthritis

    Amber Dassen1, Eva Philippon2, Aziza Elmesmari3, Domenico Somma4, Lisanne van Rooijen1, Aldo jongejan1, Anne-Marieke van Stalborch1, Jaap van Buul1, Stefano Alivernini5, Jan Piet van Hamburg2, Mariola Kurowska-Stolarska6 and Sander Tas2 Affiliations: 1Amsterdam University Medical Center, Amsterdam, Netherlands, 2Amsterdam UMC, Amsterdam, Netherlands, 3University of Glasgow, Glasgow, United Kingdom, 4School of infection and immunity, Glasgow, United Kingdom, 5Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Rome, Italy, 6Research into Inflammatory Arthritis Centre Versus Arthritis (RACE), University of Glasgow, Glasgow, United Kingdom

    Background/Purpose: To evaluate the utility of 3D synovial organoids (SOs) for therapeutic profiling in rheumatoid arthritis (RA) and advance their development toward a scalable, fully…
  • Abstract Number: 2023 • ACR Convergence 2026

    Patient-derived synovial organoids as an inflammatory driver of cartilage degeneration in in-vitro engineered human joint disease models

    André N. Tiaden1, Simone Haener-Massimi1, Atharva Damle1, Yasmina Bauer1, Ulrich A. Walker2, Petros Ismailidis3, Florian B. Imhoff3, Diego Kyburz3, Andrea Barbero1 and Stavros Giaglis1 Affiliations: 1University of Basel / University Hospital Basel, Basel, Switzerland, 2Basel University Hospital, Basel, Switzerland, 3University Hospital Basel, Basel, Switzerland

    Background/Purpose: Chronic synovial inflammation drives progressive joint destruction in degenerative and inflammatory arthropathies, with activated fibroblast-like synoviocytes (FLS) and infiltrating immune cells creating a pathogenic…
  • Abstract Number: 0078 • ACR Convergence 2026

    3D Patient-Derived Synovial Organoids (Synovioids): From Biopsy to Personalized Drug Selection in Rheumatoid Arthritis

    Katerina Apostolopoulou1, Harold Gomez2, Celina Geiss3, Marine LeChelch4, Marija Lugar3, Alexandra Khmelevskaya5, Barbora Lavickova6, Lauriane Cabon6 and Caroline Ospelt7 Affiliations: 1Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, University of Zurich and Institute of Human Biology (IHB), Roche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland, 2360 Labs, Roche Pharma Research and Early Development, Basel, Basel-Stadt, Switzerland, 3Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, University of Zurich, Schlieren, Zurich, Switzerland, 4Roche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Zurich, Switzerland, 5Center of Experimental Rheumatology, Department of Rheumatology, University Hospital Zurich, University of Zurich, Zurich, Zurich, Switzerland, 6Institute of Human Biology (IHB), Roche Pharma Research and Early Development, Roche Innovation Center Basel,, Basel, Basel-Stadt, Switzerland, 7University Hospital Zurich, Zurich, Zurich, Switzerland

    Background/Purpose: RA exhibits significant heterogeneity in disease mechanisms and therapeutic responses, with 30-40% treatment failure rates. Traditional 2D models lack cellular complexity and fail to accurately predict individual…
  • Abstract Number: 2027 • ACR Convergence 2026

    Spatial transcriptomics of B cell targeting T-cell engager therapy reveals extrafollicular niche collapse and a pretreatment fibrogenic-stromal signature in multidrug-resistant RA

    Futoshi Iwata1, Laura Bucci2, Maria Del Mar Muñiz Moreno3, Melanie Hagen2, Andreas Wirsching2, Carlo Tur2, Sebastian Boeltz4, Danae-Mona Noethling5, Jochen Wacker1, Aline Bozec2, Maria G. Raimondo6, Markus Eckstein7, Georg Schett6 and Ricardo Grieshaber-Bouyer4 Affiliations: 1Department of Internal Medicine 3, Rheumatology & Immunology, Friedrich-Alexander-University (FAU) Erlangen-Nurnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Bayern, Germany, 2Department of Internal Medicine 3, Rheumatology & Immunology, Friedrich-Alexander-University (FAU) Erlangen-Nurnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 3Department of Pathology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Bayern, Germany, 4Department of Internal Medicine 3, Rheumatology & Immunology, Friedrich-Alexander-University (FAU) Erlangen-Nurnberg and Universitätsklinikum Erlangen, Erlangen, Germany; Deutsches Zentrum Immuntherapie, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 5Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 6Department of Medicine 3-Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany Deutsches Zentrum Immuntherapie (DZI), Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 7Department of Pathology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany

    Background/Purpose: Deep B cell depletion via T-cell engagers (TCE) is being evaluated as a potential treatment for refractory rheumatoid arthritis (RA) and other autoimmune diseases.…
  • Abstract Number: 0090 • ACR Convergence 2026

    Vascular Inflammation Drives Synovial Fibroblast Expansion and Remodelling In Rheumatoid Arthritis

    Sandra Mills1, Jennifer Anolik2 and Hani Awad1 Affiliations: 1University of Rochester, Rochester, NY, 2University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Background: Rheumatoid arthritis (RA) is a chronic autoimmune disease driven by pathogenic crosstalk among immune, vascular, and stromal cells within the synovium. Currently, RA…
  • Abstract Number: 2035 • ACR Convergence 2026

    FBXW11 inhibition reprograms activated rheumatoid arthritis (RA) fibroblast-like synoviocytes (FLS) to a non-inflammatory phenotype and suppresses inflammatory arthritis

    Camilla Machado1, Sho Sendo2, Yosuke Ono3, Takaichi Okano4, Xiaofu Wei1, David Gemperline5, Michael Chalmers5, Junpeng Xiao5, Robert Benschop5, Wei Wang1, David Boyle6 and Gary Firestein7 Affiliations: 1UCSD, San Diego, CA, 2Kobe University Hospital, Kobe city, Hyogo, Japan, 3UCSD, Chuo City, Japan, 4kobe university hospital, Kobe, Japan, 5Eli Lilly and Company, Indianapolis, IN, 6UCSD, La Jolla, CA, 7University of California, San Diego, San Diego, CA

    Background/Purpose: Neddylation is a key cellular regulatory mechanism that targets proteins for degradation. This process is aberrant in RA FLS due to deficient expression of…
  • Abstract Number: 0091 • ACR Convergence 2026

    Vascularized Synovium-on-a-Chip – a Patient-Derived Rheumatoid Arthritis Model that Mimics Disease, Biological Heterogeneity, and Actual Treatment Response

    Theresa Wampler Muskardin1, Ruiqi Chen2, Yeji Lee3, Carolyn Harris3, Andrra Nimoni3, Christele Felix3, Hattie Heiland3, Romy Kallas3, Daniel Ramirez4, David Mayman3, Timothy Niewold3 and Weiqiang Chen5 Affiliations: 1Hospital for Special Surgery and Weill Cornell Medicine, New York, NY, 2New York University, New York City, 3Hospital for Special Surgery, New York, NY, 4Hospital for Special Surgery, New York, 5New York University, New York

    Background/Purpose: In rheumatoid arthritis (RA), reasons for treatment resistance and strategies that would be more effective in treatment-resistant patients remain unknown.  Accurate models to study…
  • Abstract Number: 2050 • ACR Convergence 2026

    Distinct lining fibroblast states define healthy and osteoarthritic human synovium

    Alexandra Damerau1, Marika Berntien1, Max Cowan2, Stephan Oehme3, Tazio Maleitzke4, Tobias Winkler5, Timo Gaber6, Mark Coles2, Christopher Buckley2 and Frank Buttgereit7 Affiliations: 1Charité - Universitätsmedizin Berlin, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 2Kennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom, 3Charité - Universitätsmedizin Berlin, Center for Musculoskeletal Surgery, Berlin, Germany, 4Copenhagen University Hospital, Trauma Orthopaedic Research Copenhagen Hvidovre, Copenhagen, Denmark, 5Medical University Vienna, Department of Orthopedics and Trauma Surgery, Vienna, Austria, 6Charité - Universitätsmedizin Berlin, Department of Rheumatology and Clinical Immunology, Berlin, Germany, 7Charite - Universitaetsmedizin Berlin, Dept. of Rheumatology and Clinical Immunology, Berlin, Berlin, Germany

    Background/Purpose: Osteoarthritis (OA) is a whole-joint disease in which the synovium contributes to inflammation, pain, and structural joint remodeling. Synovial fibroblasts are central regulators of…
  • Abstract Number: 0092 • ACR Convergence 2026

    β-Dominant Type I Interferon Stimulation Produces Coordinated TYK2/MX1/STAT2/PKR/MCSF Signaling in Rheumatoid Arthritis Fibroblast-Like Synoviocyte and Macrophage Cocultures, Implicating Distinct Chronic Inflammation in Patients with High Circulating IFN-β/α Activity

    Jod Prado1, Carolyn Harris2, Timothy Niewold2 and Theresa Wampler Muskardin3 Affiliations: 1Rutgers Robert Wood Johnson Medical School, New Brunswick, NJ, 2Hospital for Special Surgery, New York, NY, 3Hospital for Special Surgery and Weill Cornell Medicine, New York, NY

    Background/Purpose: Despite advances in therapy including biologic and targeted synthetic treatments, up to 40% of rheumatoid arthritis (RA) patients fail to achieve adequate response to…
  • Abstract Number: 2055 • ACR Convergence 2026

    Targeting the Progesterone Receptor as a Regulator of ECM Remodeling and Fibrosis in Osteoarthritis.

    Paramvir Kaur1, Nabangshu Das1, Evan Pollock-Tahiri1, Behdad Ravarian1, Kabriya Thavaratnam1, Shabana Vohra1, Keemo Delos Santos1, Katrina Hueniken2, Tatjana Pejic3, Jason S. Rockel1, Roman Krawetz3, Rajiv Gandhi4 and Mohit Kapoor1 Affiliations: 1UHN, Toronto, Canada, 2Schroeder Arthritis Institute, Toronto, ON, Canada, 3University of Calgary, Calgary, Canada, 4University of Calgary, Toronto, Canada

    Background/Purpose: Synovial inflammation and fibrosis contribute to joint pain and degeneration in osteoarthritis (OA). Our previous studies suggest that the progesterone receptor (PGR) in synovial…
  • Abstract Number: 0097 • ACR Convergence 2026

    Fibrin deposits and SPP1hi macrophages mark active tissue remodeling niches from early to established RA

    Ian Mantel1, Annabelle Small2, Yakir Reshef3, Melanie Smith1, Edward Dicarlo4, Brendan Boyce5, Michael Clay6, Lakshay Sood7, Philip Blazar8, David Boyle9, Mary Buchanan10, Yoshimi Endo4, Melissa Griffith11, Paul Hsu12, Laith Jazrawi13, Susan Lee9, Ogonna Nwawka14, Meghan Sahr1, Darren Tabechian15, Nida Meednu5, Tyler Cavin16, Angelica Cornelison16, Caleb Marlin17, Accelerating Medicines Partnership: Autoimmune & Immune Mediated Diseases consortium18, Joan Bathon19, Rebecca Blank13, S. Louis Bridges, Jr.20, Andrew Filer21, Gary Firestein22, Ellen Gravallese23, Michael Holers24, Katherine Liao25, Kenneth Saag26, Susan Goodman1, Michael Brenner27, Ranjeny Thomas28, Kevin Wei29, Soumya Raychaduhuri3, Larry Moreland30, Jennifer Anolik31, Mihir Wechalekar32 and Laura Donlin1 Affiliations: 1Hospital for Special Surgery, New York, NY, 2Flinders University, Bedford Park, South Australia, Australia, 3Brigham and Women's Hospital, Boston, 4Hospital for Special Surgery, New York, 5University of Rochester, Rochester, NY, 6Department of Pathology, University of Colorado Anschutz Medical Campus, Aurora, 7Brigham and Women's Hospital, Boston, MA, 8Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 9University of California San Diego, San Diego, CA, 10University of Colorado Denver, Aurora, 11University of Colorado, Aurora, CO, 12University of California San Diego, San Diego, 13NYU Grossman School of Medicine, New York, NY, 14Hospital for Special Surgery, Weill Cornell Medicine, New York, NY, 15University of Rochester Medicine, Rochester, 16University of Rochester, Rochester, 17Oklahoma Medical Research Foundation, Oklahoma City, OK, 18University of Colorado and Oklahoma Medical Research Foundation, Aurora, CO, 19Columbia University Medical Center, New York, NY, 20Self, Birmingham, AL, 21The University of Birmingham, Birmingham, United Kingdom, 22University of California, San Diego, San Diego, CA, 23Brigham and Women's Hospital, Harvard Medical School, Chestnut Hill, MA, 24University of Colorado School of Medicine, Aurora, CO, 25Mass General Brigham/Harvard Medical School, Boston, MA, 26The University of Alabama at Birmingham, Birmingham, AL, 27Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 28University of Queensland, Brisbane, Queensland, Australia, 29Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, 30University of Colorado, Denver, CO, 31University of Rochester Medical Center, Rochester, NY, 32Rheumatology Synovial Tissue Translational Research Group, Flinders University, and Rheumatology Unit, Flinders Medical Centre, Adelaide, Australia

    Background/Purpose: Chronic inflammation frequently drives tissue remodeling, where fibrin accumulation is common. In rheumatoid arthritis (RA), excessive fibrin deposits in synovial tissue associate with clinical…
  • Abstract Number: 2399 • ACR Convergence 2026

    Extracellular matrix biomarkers reveal differential effects of anti-inflammatory therapies on tissue destruction and fibrogenesis across immune-mediated disease

    Anne-Christine Bay-Jensen1, Dovile Sinkeviciute1, Signe Holm Nielsen1, Morten Karsdal1, Joachim Mortensen1 and Christian Thudium2 Affiliations: 1Nordic Bioscience, Herlev, Denmark, 2Nordic Bioscience, Herlev, Hovedstaden, Denmark

    Background/Purpose: A substantial proportion of patients with autoimmune rheumatic diseases exhibit a pronounced fibrotic pathotype, which may limit optimal response to currently available anti-inflammatory therapies…
  • Abstract Number: 0113 • ACR Convergence 2026

    Interferon-γ Activates the GBP5-TSG6 Axis and Modulates Interleukin-1β-Induced Inflammatory Signaling Responses in Osteoarthritis Synovial Fibroblasts

    Yiyu Xiao1, Mahamudul Haque2 and Salahuddin Ahmed3 Affiliations: 1Washington State University, Spokane, WA, 2Department of Pharmaceutical Sciences, Washington State University, Spokane, WA, Spokane, WA, 3Department of Pharmaceutical Sciences, Washington State University, Spokane, WA

    Background/Purpose: Osteoarthritis (OA) is a degenerative joint disease characterized by progressive cartilage destruction with limited disease-modifying treatment options. OA synovial fibroblasts (OASFs) contribute to disease…
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