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Abstracts tagged "T Cell"

  • Abstract Number: 0993 • ACR Convergence 2025

    NOD2 mutations mediate IL-17 predisposition in patients with Blau syndrome

    Leah Huey1, Emily Vance2, Bryce Binstadt3 and Ruth Napier2, 1Oregon Health & Science University, Denver, CO, 2University of Colorado Anschutz, Aurora, CO, 3University of Minnesota, Minneapolis, MN

    Background/Purpose: Blau syndrome is a pediatric rheumatic disease characterized by dermatitis, arthritis, and uveitis. Blau syndrome is caused by inborn or de novo mutations in…
  • Abstract Number: 0889 • ACR Convergence 2025

    Potentially pathogenic memory CD4 T cells with a B cell helper phenotype expand in ACPA+ individuals during progression to rheumatoid arthritis

    Ziyuan He1, Marla Glass1, Pravina Venkatesan2, Alexandra Ferrannini3, Marie Feser4, Christy Bennett1, David Boyle5, Kristen Demoruelle6, Kristine Kuhn7, Fan Zhang8, Thomas Bumol9, Ananda Goldrath3, Peter Skene3, V. Michael Holers10, Xiaojun Li1, Adam Savage1, Gary Firestein11, Kevin Deane12, Troy Torgerson13 and Mark Gillespie1, 1Allen Institute for Immunology, Seattle, WA, 2Allen Insitute, Seattle, WA, 3Allen Institute for Immunology, Seattle, 4University of Colorado Anschutz Medical Campus, Aurora, CO, 5UCSD, La Jolla, CA, 6University of Colorado Anschutz Medical Campus, Golden, CO, 72022 - 2023 / Adult/ University of Colorado, Aurora, CO, 8The University of Colorado, Aurora, CO, 9Allen Institute for Immunology, San Diego, CA, 10University of Colorado, Denver, CO, 11University of California, San Diego, San Diego, CA, 12University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 13Allen Institute for Immunology, Enumclaw, WA

    Background/Purpose: Prior to the onset of clinically apparent inflammatory arthritis (IA)/synovitis (clinical RA), ACPA+ ‘at-risk’ individuals (ARI) show alterations in the abundance of effector T…
  • Abstract Number: 0054 • ACR Convergence 2025

    Microbial Cues Promote Arthritis and Alter T Cell Selection in SKG Mice

    Astha Patel1, Steven yu1, Yuka Nakao1, Mohana Mukherjee1, Diego Orellana2, Jose Scher3, Peter Turnbaugh1, Renuka Nayak4 and Judith Ashouri1, 1University of California, San Francisco, San Francisco, CA, 2University of California San Francisco, San Francisco, CA, 3New York University School of Medicine, New York, NY, 4University of California, San Francisco (UCSF), San Francisco, CA

    Background/Purpose: Dysbiosis of the gut microbiota has been linked to rheumatoid arthritis (RA), but it remains unclear whether these microbial alterations are causal or secondary…
  • Abstract Number: 1697 • ACR Convergence 2025

    Dynamic Effects of T cell Engager Therapy on B and T cells in Autoimmune Disease.

    Laura Bucci1, Tobias Rothe2, Ann-Kathrin Goetz3, Kirill Anoshkin1, Danae-Mona Nöthling1, Melanie Hagen1, Sebastian Böltz1, Andreas Wirsching1, Georg Schett4 and Ricardo Grieshaber-Bouyer5, 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 (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, 4Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 5University Hospital Erlangen, Erlangen, Germany

    Background/Purpose: Treatment of autoimmune disease with T cell engagers (TCEs) leads to profound peripheral B cell depletion, followed by their reconstitution. However, the dynamics of…
  • Abstract Number: 0991 • ACR Convergence 2025

    MTHFD2 is a Novel Metabolic Target in Autoimmune Disease

    Laura McMillan, Celia Evans, Marina Makrecka-Kuka, Niamh Richmond, Gareth Davies, Hamel Patel, Michael Herdman, Mark Whitmarsh, Alessandro Mazzacani, Peter Bunyard, Madduri Ravin Rao and Iain Kilty, Sitryx Therapeutics, Oxford, United Kingdom

    Background/Purpose: Aberrant activation and persistence of adaptive immune responses play a central role in autoimmune pathogenesis. Where traditional immunosuppressive therapies offer a broad targeting approach,…
  • Abstract Number: 0887 • ACR Convergence 2025

    Dynamics of cytotoxic and regulatory CD8 T cells underlies outcome in ICI-myotoxicity

    Runci Wang1, Chunyan Xiang2, Adrien Procureur3, Julian Sanchez-Dal Cin3, Qing Wang4, Xinyue Lian5, Michelle Rosenzwajg3, Yves Allenbach6, Deepak Rao7, Qiong Fu8, Nan Shen9, Joe-Elie Salem3 and Shuang Ye10, 1Department of Rheumatology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China (People's Republic), 2Shanghai Institute of Rheumatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University (SJTUSM), shanghai, China (People's Republic), 3Sorbonne Université, Paris, France, 4Zhongshan Hospital, Shanghai, China (People's Republic), 5Renji Hospital, Shanghai, China (People's Republic), 6SORBONNE UNIVERSITE, Paris, France, 7Brigham and Women's Hospital, Boston, MA, 8Renji Hospital, Shanghai, Shanghai, China, 9Shanghai Jiang Tong University School of Medicine, Shanghai, China (People's Republic), 10Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China, Shanghai, Shanghai, China (People's Republic)

    Background/Purpose: Immune checkpoint inhibitor (ICI) therapies for cancer can induce immune-related adverse events (irAEs) involving musculoskeletal (MSK) systems. ICI myotoxicity (ICI-M) can present as a…
  • Abstract Number: 0015 • ACR Convergence 2025

    CDR111 is a novel CD19 and BCMA dual-targeting T cell engager (TCE) for the treatment of severe and refractory autoimmune diseases

    Philipp Richle, Stephanie Jungmichel, Alessio Vantellini, André Fonseca, Anna Howald, Fabian Scheifele, Loredana iuliano, Ariadna Vilarrasa, Romina Doerig, Hannes Merten, Philip Knobel, Daniel Lenherr-Frey, Christian Leisner and Leonardo Borras, CDR-Life, Horgen, Zurich, Switzerland

    Background/Purpose: B cells and plasma cells are central to the pathogenesis of many autoimmune diseases. While B cell depletion therapies (BCDTs), such as anti-CD20 monoclonal…
  • Abstract Number: L03 • ACR Convergence 2024

    CD9 Expressing T Follicular Helper Cells Are a Highly Functional Subset Expanded in Systemic Lupus Erythematosus

    Kyleigh Brimmer1, Olivia Antao1, Daniel Mayer1, Gina Sanchez1, Rebecca Francis1, Htay Htay Kyi2, Mary Salim2, Boyan Xia2, Eugenio Capitle2 and Jason Weinstein1, 1Center for Immunity and Inflammation, Rutgers New Jersey Medical School, Newark, NJ, 2Division of Allergy, Immunology and Rheumatology, University Hospital, Newark, NJ

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is characterized by the generation of autoantibodies that promote tissue injury. The development of pathogenic autoantibody-secreting B cells in lupus…
  • Abstract Number: L16 • ACR Convergence 2024

    Dapirolizumab Pegol Demonstrated Significant Improvement in Systemic Lupus Erythematosus Disease Activity: Efficacy and Safety Results of a Phase 3 Trial

    Megan Clowse1, David Isenberg2, Joan Merrill3, Thomas Dörner4, Michelle Petri5, Edward Vital6, Eric Morand7, Teri Jimenez8, Stephen Brookes9, Janine Gaiha-Rohrbach10, Christophe Martin11, Annette Nelde12 and Christian Stach13, 1Division of Rheumatology and Immunology, Duke University, Durham, NC, 2Department of Ageing, Rheumatology and Regenerative Medicine, Division of Medicine, University College London, London, United Kingdom, 3Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Department of Medicine/Rheumatology and Clinical Immunology, Charité Universitätsmedizin Berlin, Berlin, Germany, 5Johns Hopkins University School of Medicine, Baltimore, MD, 6Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds and NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 7Centre for Inflammatory Diseases, Monash University, Melbourne, Australia, 8UCB, Raleigh, NC, 9Biogen, Maidenhead, United Kingdom, 10Biogen, Cambridge, MA, 11UCB, Slough, United Kingdom, 12Biogen, Baar, Switzerland, 13UCB, Monheim am Rhein, Germany

    Background/Purpose: Dapirolizumab pegol (DZP) is a novel, polyethylene glycol (PEG)-conjugated antigen-binding (Fab') fragment, lacking an Fc domain, that inhibits CD40L signaling. By binding to CD40L,…
  • Abstract Number: 0096 • ACR Convergence 2024

    Simultaneous Contribution of Brain-Intrinsic and Peripheral Disease Mechanisms to Neuropsychiatric Symptoms of Systemic Lupus Erythematosus (NPSLE)

    Hadijat Makinde1, Mohammad Khan1, Cecilia Stumpf2, Yidan Wang3, Tyler Therron2, Margaret Goldman2, Deborah Winter4 and Carla Cuda1, 1Northwestern University, Chicago, IL, 2Northwestern University, Chicago, 3Northwestern University, Hanover Park, IL, 4Northwestern University, Skokie, IL

    Background/Purpose: While NPSLE are among the least understood complications, increasing evidence points to microglia, a brain-resident innate immune cell population, as a driver of disease.…
  • Abstract Number: 0922 • ACR Convergence 2024

    Generation and Pathophysiological Analysis of M694I Variant Knock-in Mice of Human MEFV Gene: Insights from Single-Cell RNA Sequencing

    Tomohiro Koga, Yoshika Tsuji and Atsushi Kawakami, Nagasaki University, Nagasaki, Japan

    Background/Purpose: The primary objective of this study was to generate knock-in mice with the M694I variant of the human MEFV gene, a critical variant in…
  • Abstract Number: 1768 • ACR Convergence 2024

    A Potential Role of Longstanding IL-18 Stimulation in the Susceptibility for Macrophage Activation Syndrome in Patients with Systemic Juvenile Idiopathic Arthritis

    Greta Rogani1, Remco Erkens1, Marein Putmans1, Rianne Scholman1, Jorg van Loosdregt2 and Sebastiaan Vastert1, 1University Medical Center Utrecht, Utrecht, Netherlands, 2University Medical Center Utrecht, La Jolla, CA

    Background/Purpose: Macrophage Activation Syndrome (MAS) is a pathologic condition of immune hyperactivation, which occurs in 10-30% of cases of Still’s Disease (SD), the spectrum of…
  • Abstract Number: 1845 • ACR Convergence 2024

    Treg Expansion and IL-6 Induced STAT3 Phosphorylation in CD4+ T Cells Is a Biomarker of Disease Flare in Rheumatoid Arthritis

    Amy Anderson1, Luke Jones2, Fiona Rayner3, Jessica Swift1, Daniel Maunder1, Henrique de Paula Lemos1, David Swan4, Abbie Degnan1, Imogen Wilson1, Julie Diboll1, Gary Reynolds1, Jasmine Sim1, Andrew Melville5, Stefan Siebert5, Iain McInnes6, Carl Goodyear5, Catharien Hilkens1, Karim Raza7, Christopher Buckley8, Kenneth Baker1, Arthur Pratt3, Andrew Filer7 and John Isaacs1, 1Translational and Clinical Research Institute, NIHR Newcastle Biomedical Research Centre, Newcastle University and The Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom, 2Rheumatology Research Group, Institute for Inflammation and Ageing, NIHR Birmingham Biomedical Research Center and Clinical Research Facility, Birmingham, United Kingdom, 3Translational and Clinical Research Institute, NIHR Newcastle Biomedical Research Centre, Newcastle University and The Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, England, United Kingdom, 4Translational and Clinical Research Institute, NIHR Newcastle Biomedical Research Centre, Newcastle University and The Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, 5School of Infection and Immunity, College of Medical, Veterinary and Life Sciences, University of Glasgow, Glasgow, United Kingdom, 6University of Glasgow, College of Medical Veterinary and Life Sciences, Glasgow, United Kingdom, 7Rheumatology Research Group, Institute for Inflammation and Ageing, NIHR Birmingham Biomedical Research Center and Clinical Research Facility, University of Birmingham, Birmingham, United Kingdom, 8Kennedy Institute of Rheumatology, University of Oxford, Oxford, United Kingdom

    Background/Purpose: Understanding the mechanisms that drive disease flares in patients with rheumatoid arthritis (RA) may aid in the development of biomarkers to facilitate targeted treatment…
  • Abstract Number: 1864 • ACR Convergence 2024

    S-4321, a Novel Dual-cell Bidirectional PD-1:FcγRIIb Selective Agonist Antibody for the Treatment of Autoimmune Disease

    Julia Manasson1, Marisella Panduro2, Michael Cianci2, Minasri Borah2, Stephanie Grebinoski2, Joshua Vitlip2, Stephen Lutz2, Ishan Sharma2, Elliott Wittenberg2, Allison Colthart2, Samuel Perry2, Maria Cecilia Ramello2, Chelsea R. Parker Harp2, Jyothsna Visweswaraiah2, Ryan Peckner2, Alex Pellerin2, Heather Vital3, John Sundy4, Nathan Higginson-Scott2, Kevin L. Otipoby2 and Daniela Cipolletta2, 1Seismic Therapeutic, New York, NY, 2Seismic Therapeutic, Watertown, MA, 3Seismic Therapeutic, Lexington, MA, 4Seismic Therapeutic, Chapel Hill, NC

    Background/Purpose: The dysregulation of immune checkpoint receptors on T cells and antigen presenting cells (APCs) drives autoimmunity while receptor agonism is expected to restore immune…
  • Abstract Number: 2632 • ACR Convergence 2024

    Genetically-engineered Ro-specific Regulatory T Cells to Treat Primary Sjögren’s Disease

    Zhi Feng sherman Lim1, Yi Tian Ting1, Fabien Vincent2, Maureen Rischmueller3, Eric Morand4 and Joshua Ooi1, 1Monash University-T Cell Therapies Research Group, Clayton, Victoria, Australia, 2Monash University, Clayton, Victoria, Australia, 3RheumatologySA, Adelaide, Australia, 4School of Clinical Sciences, Monash University, Melbourne, Victoria, Australia

    Background/Purpose: Autoantigen-specific regulatory T cells (Tregs) are potent, and specific, suppressors of pathogenic autoimmunity, and can be harnessed to treat autoimmune disease. In primary Sjögren’s…
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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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