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Abstracts tagged "Tumor necrosis factor (TNF)"

  • Abstract Number: 1624 • ACR Convergence 2025

    Disease activity status in Takayasu’s arteritis influences the angiogenic potential of patient-derived endothelial cells

    Luciana Yamamoto de Almeida1, Kaitlin Quinn2, James Simone2, Lily Dai2, Benjamin Turturice2, Urvashi Kaundal2, Chloe Palmer2, Karyssa Stonick3, davide Randazzo4, Carmelo Carmona-Rivera5 and Peter Grayson6, 1National Institutes of Health, Bethesda, MD, 2National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), Bethesda, MD, 3National Insitute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, 4Light Imaging Section, Office of Science and Technology, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, Bethesda, 5Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, Bethesda, MD, 6National Institutes of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), Chevy Chase, MD

    Background/Purpose: Takayasu's arteritis (TAK) is a rare, systemic, chronic large vessel vasculitis of unknown etiology primarily affecting the aorta and its branches. Arterial damage, with…
  • Abstract Number: 1367 • ACR Convergence 2025

    Molecular Signature Response Classifier Identifies Contribution of GLP-1 Therapy to TNF Inhibitor Response in Rheumatoid Arthritis Patients

    Lixia Zhang1, Angus Wong2, Alex Jones2, Sherry Guardiano2, Reginald Seeto2 and Ryan T, Phan3, 1Scipher Medicine, Plainsboro, NJ, 2Scipher Medicine, Waltham, 3Scipher Medicine, Los Gatos

    Background/Purpose: Tumor necrosis factor-α inhibitors (TNFi) are extensively utilized in the management of rheumatoid arthritis (RA). Therapeutic responses remain highly heterogeneous. Emerging evidence suggests glucagon-like…
  • Abstract Number: 1181 • ACR Convergence 2025

    Clinical Relevance of Tumor Necrosis Factor Superfamily Cytokines

    Robert Corty1, Gul Karakoc1, Ahmad Jawdat2, Hui Yu3, Jonathan Mosley4, Michael Stein1 and Vivian Kawai5, 1Vanderbilt University Medical Center, Nashville, TN, 2University of Alabama at Birmingham, Birmingham, 3University of Miami, Miami, 4UT Southwestern Medical Center, Dallas, 5University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: The tumor necrosis factor superfamily (TNFSF) includes 48 proteins involved in immune activation, inflammation, and cell death and represent an area of intense focus…
  • Abstract Number: 1165 • ACR Convergence 2025

    Real-World On-Label Treatment Persistence Through 24 Months in Biologic-Naïve and Biologic-Experienced Patients with Psoriatic Arthritis: Comparison of Guselkumab versus Subcutaneous Tumor Necrosis Factor Inhibitors

    Philip J. Mease1, Jessica A. Walsh2, Timothy P. Fitzgerald3, Soumya Chakravarty4, Elizabeth Adamson5, Bruno Emond6, Carmine Rossi7, Samuel Schwartzbein7, Kana Yokoji7, Yuxi Wang7, Patrick Lefebvre7, Dominic Pilon7, Shikha Singla8 and Joseph F Merola9, 1Department of Rheumatology, Providence-Swedish Medical Center and University of Washington, Seattle, WA, 2Division of Rheumatology, Salt Lake City Veterans Affairs Health and University of Utah Health, Salt Lake City, UT, 3Johnson & Johnson, Horsham, PA, USA, PA, 4Johnson & Johnson, Horsham, PA, USA; Drexel University College of Medicine, Philadelphia, PA, USA, Villanova, PA, 5Johnson & Johnson, Horsham, PA, USA, Horsham, PA, 6Analysis Group, Inc., Montreal, QC, Canada, QC, 7Analysis Group, Inc., Montreal, QC, Canada, QC, Canada, 8Medical College of Wisconsin, Milwaukee, WI, 9Department of Dermatology and Department of Medicine, UT Southwestern Medical Center, Dallas, TX

    Background/Purpose: A prior analysis found that patients (pts) with psoriatic arthritis (PsA) treated with guselkumab (GUS), an IL-23p19 subunit inhibitor, were approximately 2× more likely…
  • Abstract Number: 0872 • ACR Convergence 2025

    Silencing of Schnurri-3 protects from TNF-induced bone loss and is accompanied by upregulation of type I Interferon-Stimulated Genes (ISGs) in osteoblasts.

    Priyanka Kushwaha1, Albert Tai2, Catherine Manning3, Yeon Suk Yang4, Jae-Hyuck Shim4 and Ellen M. Gravallese5, 1Division of Rheumatology, Inflammation and Immunity, Brigham and Women’s Hospital, Boston, MA, 2Department of Immunology, Tufts University School of Medicine, Boston, MA, 3Brigham and Women's Hospital at Harvard Medical School, Boston, MA, 42Department of Medicine/Division of Rheumatology, University of Massachusetts Chan Medical School, Worcester, MA, 5Brigham and Women's Hospital, Harvard Medical School, Chestnut Hill, MA

    Background/Purpose: Schnurri-3 (SHN3) is an adaptor protein and a negative regulator of osteoblast (OB) function. Its inhibition prevents bone loss and joint erosion in models…
  • Abstract Number: 0398 • ACR Convergence 2025

    Efficacy of Tumor Necrosis Factor Inhibitors in Children Diagnosed With Non-Systemic Juvenile Idiopathic Arthritis ≤ 2 Years Old Using The Childhood Arthritis and Rheumatology Research Alliance Registry

    Christina Gulla1, Tara Lozy2 and Ginger Janow3, 1Hackensack University Medical Center, Hackensack, NJ, 2Joseph M. Sanzari Children's Hospital, Center for Discovery and Innovation, Hackensack Meridian School of Medicine, Nutley, 3Joseph M. Sanzari Children's Hospital at Hackensack Meridian Health, Hackensack, NJ

    Background/Purpose: Juvenile Idiopathic Arthritis (JIA) is the most common pediatric rheumatic disease. Tumor necrosis factor inhibitors (TNFi) are key treatments in non-systemic JIA (sJIA), but…
  • Abstract Number: 0086 • ACR Convergence 2025

    Androgen Upregulates Interferon Signaling in Osteoclast Differentiation During Inflammatory State

    Kiana Chen1, Chia-Lung Wu2, Gulzada Kulzhanova2 and Homaira Rahimi3, 1University of Rochester School of Medicine and Dentistry, Bronx, NY, 2University of Rochester Medical Center, Rochester, 3University of Rochester, Rochester, NY

    Background/Purpose: Rheumatoid arthritis (RA) is characterized by chronic inflammatory erosions and female predominant disease. Androgen, the dominant sex hormone in males, is protective against bone…
  • Abstract Number: 0085 • ACR Convergence 2025

    Single Cell RNA-seq Revealed Immune/epithelial Cell Abnormalities Underlying the Pathogenesis of Rheumatoid Arthritis-related Interstitial Lung Disease

    Kensuke Suga1, Amara Seng2, Changfu Yao3, Tanyalak Parimon3, Youn Jung Choi2, Justyna Fert-Bober4, Barry Stripp3, Jon Giles5, Peter Chen3 and Nunzio Bottini6, 1Kao Autoimmunity Institute, Cedars-Sinai Medical Center, Beverly Hills, CA, 2Kao Autoimmunity Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 3Women's Guild Lung Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 4Smidt Heart Institute, Cedars-Sinai Medical Center, Los Angeles, CA, 5Cedars Sinai Medical Center, Los Angeles, CA, 6Cedars Sinai Medical Center, Beverly Hills, CA

    Background/Purpose: Interstitial lung disease (ILD) is one of the extra-articular manifestations of rheumatoid arthritis (RA) characterized by inflammation and/or fibrosis. Clinically relevant RA-ILD occurs in…
  • Abstract Number: 2689 • ACR Convergence 2025

    Comparison of Incidence of Psoriatic Arthritis in Patients With Psoriasis Treated With Interleukin-17 Inhibitors vs Interleukin-23 Inhibitors, Interleukin-12/23 Inhibitors, and Tumor Necrosis Factor Inhibitors in Real-World Practice: A Retrospective Study

    April Armstrong1, Joseph Merola2, Gang Wang3, Ariane Faucher4, Riley Taiji4, Francis Vekeman4, Alexis Shew5, Tim Nguyen5 and Laura Coates6, 1University of California Los Angeles, Los Angeles, CA, USA, Los Angeles, CA, 2UT Southwestern Medical Center, Dallas, TX, 3Department of Dermatology, Xijing Hospital, The Fourth Military Medical University, Xi'an, China (People's Republic), 4STATLOG, Inc, Montreal, QC, Canada, 5Novartis Pharmaceuticals Corporation, East Hanover, NJ, 6Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, England, United Kingdom

    Background/Purpose: Biologic therapies for moderate to severe psoriasis (PsO) include inhibitors of IL-17 (IL-17i), IL-23i, IL-12/23i, and tumor necrosis factor (TNFi). Previous studies that assessed…
  • Abstract Number: 2677 • ACR Convergence 2025

    Quantified Imaging Response at the Sacroiliac Joints to TNF-Inhibitor Therapy in Youth with Axial Disease

    Timothy Brandon1, Rui Xiao2, Daniel Lovell3, Edward Oberle4, Matthew Stoll5, Nancy A. Chauvin6, Michael Francavilla7, Walter P. Maksymowych8 and Pamela Weiss9, 1Children's Hospital of Philadelphia, Philadelphia, PA, 2University of Pennsylvania, Philadelphia, PA, 3Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 4Nationwide Children's Hospital, Columbus, OH, 5University of Alabama at Birmingham, Birmingham, AL, 6The Cleveland Clinic, Hummelstown, PA, 7Department of Pediatric Radiology, Children’s Hospital Philadelphia, Philadelphia, PA, 8Department of Medicine, University of Alberta, 568 Heritage Building, Edmonton, AB, Canada, 9Childrens Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: This study assessed the timeline for the resolution of inflammation, changes in structural lesions at the sacroiliac joints (SIJ), and their correlation with patient-reported…
  • Abstract Number: 2644 • ACR Convergence 2025

    Single Cell RNA-seq Profiling Reveals a Blood Monocyte Phenotype Associated with Response to TNF Inhibitor Therapy in RA Patients

    Kathryne Marks1, Alice Horisberger2, Ifeoluwakiisi Adejoorin1, Leah Santacroce1, Mehreen Elahee3, Joan Bathon4, Kevin Wei5, Daniel Solomon6 and Deepak Rao1, 1Brigham and Women's Hospital, Boston, MA, 2Lausanne University Hospital (CHUV), Lausanne, Switzerland, 3Brigham and Women's Hospital, Wexford, PA, 4Columbia University, NEW YORK, NY, 5Brigham and Women's Hospital at Harvard Medical School, Boston, MA, 6Division of Rheumatology, Inflammation, and Immunity, Brigham and Women's Hospital, Boston, MA

    Background/Purpose: TNF inhibitors (TNFi) are the most common biologic DMARD used to treat RA; however, no robust biomarkers have been established to predict likelihood of…
  • Abstract Number: 2391 • ACR Convergence 2025

    Antinuclear Antibody Positivity in Patients with Psoriasis and Psoriatic Arthritis and the Risk of Developing Clinical Symptoms of SLE Following TNF Inhibitor Therapy

    Damira Sereda1, Leilani Leechalad1 and Andras Perl2, 1SUNY Upstate Medical University, Syracuse, NY, 2SUNY, Syracuse, NY

    Background/Purpose: It has been reported that the presence of positive ANA in patients treated with TNF inhibitors (TNFi) could be associated with the development of…
  • Abstract Number: 2236 • ACR Convergence 2025

    Treatment-induced autoantibodies in Rheumatoid Arthritis patients receiving anti-TNF inhibitors or JAK inhibitors

    EVRIPIDIS KALTSONOUDIS1, Nikolaos Kougkas2, Panagiota Karagianni3, Tereza Memi4, Nikolaos Koletsos5 and Eleftherios Pelechas6, 1Rheumatology Clinic, University of Ioannina, IOANNINA, Ioannina, Greece, 24th Department of Internal Medicine, Aristotle University, Thessaloniki, Thessaloniki, Greece, 3BioAcuHealth.gr, Ioannina, Ioannina, Greece, 4University Hospital of Ioannina, Ioannina, Ioannina, Greece, 5School of Health Sciences, Faculty of Medicine, University of Ioannina, Department of Rheumatology, Ioannina, Greece, Ioannina, Ioannina, Greece, 6Hatzikosta General Hospital of Ioannina, Ioannina, Ioannina, Greece

    Background/Purpose: Rheumatoid arthritis (RA) can coexist with other autoimmune disorders such as Sjögren’s syndrome and systemic lupus erythematosus (SLE). In these cases, the terms secondary…
  • Abstract Number: 1926 • ACR Convergence 2025

    Real World  Rate of Efficacy of Adalimumab Biosimilars Following a Mandated Switch in an Academic Medical Center

    Katharine McCarthy, viktoriya avlasevich and Darren Tabechian, URMC, Rochester, NY

    Background/Purpose: The proliferation of similar biotherapeutic products (biosimilars) has helped to reduce the cost burden of biologic therapies for health care systems1. Multiple studies have…
  • Abstract Number: 0585 • ACR Convergence 2024

    Cycling to TNFi vs. Switching to IL-17Ai After a First TNFi Discontinuation Among Patients with PsA and axSpA: The CorEvitas PsA/SpA Registry

    Alexis Ogdie1, Nicole Middaugh2, Maya Marchese2, Jessica A Walsh3, Natalia Bello4, Jeffrey Lisse4, Andris Kronbergs5, Elsie Grace6, Marcus Ngantcha4 and Philip Mease7, 1Department of Medicine, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, 2CorEvitas, LLC, Waltham, MA, 3Division of Rheumatology, Salt Lake City Veterans Affairs Health and University of Utah Health, Salt Lake City, UT, 4Eli Lilly and Company, Indianapolis, IN, 5Eli Lilly, Indianapolis, IN, 6Eli Lilly and Company, Indianapolis, 7Swedish Medical Center/Providence St. Joseph Health; University of Washington School of Medicine, Seattle, WA

    Background/Purpose: Treatment guidelines recommend tumor necrosis factor inhibitors (TNFi) and interleukin-17A inhibitors (IL-17Ai) as options for patients with PsA or axSpA with persistent disease activity…
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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].

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