ACR Meeting Abstracts

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Abstracts tagged "T Cell"

  • Abstract Number: 1726 • ACR Convergence 2025

    Inflammatory arthritis immune related adverse events represent a unique autoimmune disease entity primarily driven by T cells, but likely not autoantibodies

    Xingxing Zhu1, yue Yu1, Yangfen Li1, Panwen wang2, ying li2, Chantal McCabe2, shiju chen2, Brenna Sharp2, Amber Wolzen2, Hannah Langenfeld1, Andrew C. Hanson1, Cynthia Crowson3, svetomir Markovic2, John Davis1, Haidong Dong2, Uma Thanarajasingam1 and Hu Zeng1, 1Mayo Clinic, Rochester, MN, 2Mayo Clinic, Rochester, 3Mayo Clinic, Stewartvillle, MN

    Background/Purpose: The immunological basis of inflammatory arthritis (IA) immune related adverse event (irAE) following anti-PD-1/PD-L1 immune checkpoint inhibition (ICI) therapy is incompletely understood. The relationship…
  • Abstract Number: 0101 • ACR Convergence 2025

    Enrichment of putative bacteria-reactive gut-derived IL-17+ tissue resident memory helper T cells in arthritic ankles in the SKG mouse model of spondyloarthritis

    Benjamin Cai1, Megan Soon2, Zewen Kelvin Tuong2, Mark Morrison2, Anne-Sophie Bergot3 and Ranjeny Thomas4, 1Frazer Institute, The University of Queensland, Brisbane, Queensland, Australia, 2Frazer Institute, The University of Queensland, Brisbane, Australia, 3Frazer Institute, The University of Queensland, Woolloongabba, Queensland, Australia, 4Frazer Institute, University of Queensland, Brisbane, Queensland, Australia

    Background/Purpose: In spondyloarthropathy (SpA), arthritis is often associated with gut inflammation. The strong genetic association with HLA-B27 implicates involvement of T cells, but how gut…
  • Abstract Number: 0920 • ACR Convergence 2025

    Functional Characterization of NEMO-NDAS Causing Variants in Patients’ PBMCs and in Wildtype and Mutant U937 Cells

    Elizabeth Morgan1, Bin Lin2, Sara alehashemi1, Adriana de Jesus1, Keith Kauffman3, Christopher Friend1, Farzana Bhuyan1, Kader Gedik1, Kat Uss1, Lauren Krausfeldt4, Jason Brenchley5, Zoran Gucev6, Kathryn Cook7, Vafa Mammadova8, Gulnara Nasrullayeva8, Mariana Correia Marques9, Abigail Bosk10, Brian Nolan11, Scott Canna12, Maude Tusseau13, Andrea Bohrer14, Katrin Mayer-Barber15, Timothy Moran16, Andrew Oler4, Daniel Barber3 and Raphaela Goldbach-Mansky1, 1Translational Autoinflammatory Diseases Section (TADS), Laboratory of Clinical Immunology and Microbiology (LCIM), NIAID, NIH, Bethesda, MD, 2NIH, Bethesda, MD, 3T-Lymphocyte Biology Section, Laboratory of Parasitic Diseases, NIAID, NIH, Bethesda, MD, 4Bioinformatics and Computational Biosciences Branch, Office of Cyber Infrastructure and Computational Biology, NIAID, NIH, Bethesda, MD, 5Barrier Immunity Section, Laboratory of Viral Diseases, NIAID, NIH, Bethesda, MD, 6University Children's Hospital, Medical Faculty Skopje, Skopje, Macedonia, 7Akron Children’s Hospital, Akron, OH, 8Azerbaijan Medical University, Baku, Azerbaijan, 9Translational Genetics and Genomics Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 10Children’s National Hospital, Washington DC, 11Lurie Children’s Hospital, Chicago, 12Children's Hospital of Philadelphia, Philadelphia, PA, 13Hôpital Femme-Mère-Enfant, Bron, France, 14Inflammation and Innate Immunity Unit, Laboratory of Clinical Immunology and Microbiology (LCIM), NIAID, NIH, Bethesda, MD, 15Inflammation and Innate Immunity Unit, Laboratory of Clinical Immunology and Microbiology (LCIM), Bethesda, MD, 16University of North Carolina School of Medicine, Chapel Hill, NC

    Background/Purpose: NEMO-deleted 5 autoinflammatory syndrome (NEMO-NDAS) is an inflammatory disease caused by mosaic splice-site variants that lead to exon 5 skipping in IKBKG, encoding NEMO.…
  • Abstract Number: 0997 • ACR Convergence 2025

    Identification of Novel HLA Class II–Restricted Autoantigens in Scleroderma and Ulcerative Colitis Using TargetScan 

    Olivia Pryor1, Catalina Burbano2, Nathaniel Bagge2, Rutuja Kulkarni2, Heather F. Jones2, Livio Dukaj2, Shoshana M.K. Bloom2, Jackson Lirette2, Rachel Lent2, Prachi Dhanania2, Nicole A. Ladd2, Ryan Kritzer2, Hana Husic2, Shobitha Jillella2, Candace R. Perullo2, Jinyu Zhu2, Teagan J. Parsons2, Ira Jain2, Rakshika Balasubramaniyam2, Kenneth L. Jahan2, Vivin Karthik2, Alexander Cristofaro1, Chandan K. Pavuluri2, Jenna LaBelle2, Laurie Barefoot2, Shrikanta Chattopadhyay2, Kim M. Cirelli2, Mollie M. Jurewicz2, Andrew P. Ferretti2 and Cagan Gurer2, 1TScan Therapeutics, Waltham, 2TScan Therapeutics, Waltham, MA

    Background/Purpose: Selective modulation of autoimmune responses through antigen-specific therapies represents a promising direction for improving treatment specificity and safety. Genetic associations with HLA class II…
  • Abstract Number: 1789 • ACR Convergence 2025

    Spatial Analysis of Advanced Osteoarthritis Synovial Tissue

    jacob Dickman1, Stephanie Ruzicka1, Holub Meaghan2, Jutras Brandon3, Adam Edelstein3 and Robert Lochhead4, 1Medical College of Wisconsin, Milwaukee, WI, 2Central Michigan University College of Medicine, Mount Pleasant, MI, 3Northwestern University, Chicago, IL, 4Medical College of Wisconsin, GERMANTOWN, WI

    Background/Purpose: Osteoarthritis (OA) is a joint pathology involving joint cartilage destruction and synovial inflammation. Severe knee OA is often surgically treated with total knee arthroplasty…
  • Abstract Number: 0110 • ACR Convergence 2025

    SKG Mice Develop CD4⁺ T Cell–Driven Psoriasis and Enable Study of Endogenous Antigen-Specific Responses

    Yuka Nakao1, Astha Patel1, Bahram Razani2, Steven yu1, Steven Lazarevsky2, Marlys Fassett2 and Judith Ashouri1, 1University of California, San Francisco, San Francisco, CA, 2UCSF Department of Dermatology, San Francisco, CA

    Background/Purpose: Psoriasis (Pso) and psoriatic arthritis (PsA) are chronic immune-mediated diseases affecting millions, yet early immunologic triggers remain poorly defined. Therapies targeting TNFα, IL-17, and…
  • Abstract Number: 0948 • ACR Convergence 2025

    Presentation of Apoptotic Cell-Derived Autoantigens in Systemic Autoimmune Disease

    Lance Peterson1, Hannah KL De Cleene2, Cheryl Lichti2, David Bending3 and Kodi Ravichandran2, 1Rheumatology and Immunology, Pediatrics, Washington University School of Medicine, St. Louis, MO, 2Department of Pathology and Immunology, Washington University School of Medicine, St. Louis, MO, 3Institute of Immunology and Immunotherapy, University of Birmingham, Birmingham, England, United Kingdom

    Background/Purpose: Systemic lupus erythematosus is a chronic, multisystem autoimmune disease characterized by the dysregulated clearance of dying cells, which results in the release of damage-associated…
  • Abstract Number: 1000 • ACR Convergence 2025

    A Deep-Learning Based Approach Uncovers Novel Mediators of Micro-RNA Restraint of Type-2 Immunity

    Shaan Sekhon1, Robin Kageyama2, Neil Sprenkle3, Hannah Happ2, Eric Wigton2, Heather Pua3 and Mark Ansel2, 1University of California, San Francisco, Berkeley, 2University of California, San Francisco, San Francisco, 3Vanderbilt University, Nashville

    Background/Purpose: MicroRNAs, such as miR-24 and miR-27, co-expressed within the Mirc11 and Mirc22 clusters, orchestrate a regulatory network critical to Th2 cell differentiation and cytokine…
  • Abstract Number: 2140 • ACR Convergence 2025

    Identification of immune phenotypes in systemic juvenile idiopathic arthritis associated lung disease (SJIA-LD) using high parameter flow cytometry

    Haeja Kessler1, Noel Gibson1, Alyssa Sproles2, Celine Lages1, Paul Dascani3, Sherry Thornton4 and Grant Schulert4, 1Cincinnati Children's Hospital Medical Center, Cincinnati, 2Cincinnati Children's Hospital, Cincinnati, OH, 3Cytek Biosciences, Pittsburgh, 4Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose: Systemic Juvenile Idiopathic Arthritis (sJIA) is a unique subtype of juvenile idiopathic arthritis with life threatening complications including macrophage activation syndrome and chronic lung…
  • Abstract Number: 0273 • ACR Convergence 2025

    Effector CD8+ T cells and PD-1hi CXCL13hi CD4+ T cells contribute to recurrent immune checkpoint inhibitor mediated inflammatory arthritis

    Synat Keam1, Yuanteng Li2, Yanshuo Chu1, Jean Tayar3, Huifang Lu4, Michael Wu5, Sandeep Agarwal6, Nitin Jain7, Pavlos Msaouel1, Adi Diab2, Cara Haymaker1, Linghua Wang1, Roza Nurieva8 and Sang Kim9, 1The University of Texas MD Anderson Cancer Center, houston, 2MD Anderson Cancer Center, Houston, TX, 3The University of Texas, MD Anderson Cancer Center, Houston, TX, 4UT MD Anderson Cancer Center, Houston, TX, 5Baylor College of Medicine, Houston, 6Baylor College of Medicine, Houston, TX, 7The Universty of Texas MD Anderson Cancer Center, Houston, 8University of Texas MD Anderson, Houston, TX, 9Yale University, Branford, CT

    Background/Purpose: Immune checkpoint inhibitor (ICI) therapy is associated with life- and/or organ-threatening immune-related adverse events, including inflammatory arthritis (ICI-IA). However, the mechanisms behind ICI-IA, especially…
  • Abstract Number: 0950 • ACR Convergence 2025

    Ep300-Catalyzed Rad50 Lactylation Compromises Genomic Stability and Drives CD4+T cells Cell Senescence in SLE

    mingyang zhang1, huanzi dai2, cun lan3 and mingyang sun3, 1Daping Hospital, Army Medical University, chongqing, Chongqing, China (People's Republic), 2Daping Hospital & Research Institute of Surgery, Army Medical University, Chongqing, PR China., Chongqing, China (People's Republic), 3Daping Hospital, Army Medical University, chongqing, China (People's Republic)

    Background/Purpose: Senescent CD4+ T cells are increasingly implicated in systemic lupus erythematosus (SLE) pathogenesis. While metabolic reprogramming in lupus T cells enhances glycolysis and lactate…
  • Abstract Number: 1001 • ACR Convergence 2025

    LBL-057, a Novel ADCC Enhanced PD-1 Agonist VHH-Fc Antibody

    Hongyan Shang1, Xiao Huang2, Duqing Jiang1, Jianming Sun2, Yurong Qin2, Guojin Wu2, Chengze Ni1, Jing Guan2, Jordan Zhu3, Xiaoqiang Kang2 and Hong Ling2, 1Nanjing Leads Biolabs Co., Ltd., nanjing, China (People's Republic), 2Nanjing Leads Biolabs Co., Ltd., Nan Jing, China (People's Republic), 3Nanjing Leads Biolabs Co., Ltd., Nan Jing

    Background/Purpose: Programmed cell death protein 1 (PD-1) is expressed on activated T cells and serves as a key co-inhibitory checkpoint molecule in immune regulation. Aberrant…
  • Abstract Number: 2277 • ACR Convergence 2025

    Immunophenotyping of peripheral blood mononuclear cells reveals potential cellular biomarkers of disease in rheumatoid arthritis

    John Bui1, Jason Dubovsky2, Jennifer Abrams3, Sara Charmsaz4, Michelle Blake1, Joshua Beilke4, Anne-Renee van der Vuurst de Vries1, Joseph Arron5, Jonathan Graf6 and Jeffrey Bluestone7, 1Sonoma Biotherapeutics, Seattle, WA, 2Sonoma Biotherapeutics, South San Francisco, 3Sonomabio, San Francisco, CA, 4Sonoma Biotherapeutics, Seattle, 5Sonoma Biotherapeutics, San Francisco, CA, 6UCSF, San Francisco, CA, 7Sonoma Biotherapeutics, South San Francisco, CA

    Background/Purpose: Emerging cell-based therapies for rheumatoid arthritis (RA) target the underlying immunologic activity of disease. Objective biomarkers to-date are downstream sequelae of RA immunologic drivers.…
  • Abstract Number: 0471 • ACR Convergence 2025

    An Open-label, Randomized, Controlled Phase 1/2 Study to Assess the Safety and Efficacy of KYV-101 Anti-CD19 CAR-T Cell Therapy in Active and Difficult-to-treat ACPA positive Rheumatoid Arthritis: Preliminary Results of the COMPARE Trial

    Fredrik Albach1, Ioanna Minopoulou1, Artur Wilhelm2, Robert Biesen1, Arnd Kleyer1, Norman Drzeniek3, Edgar Wiebe4, Anja Fleischmann3, Dominic Borie5, Vincent Casteleyn3, Tobias Alexander3, Christian Furth6, Jan Zernicke3, Burkhard Muche7, Sandra Hermann4, Pfeil Alexander8, Veronika Scholz3, Elpida Phithak3, Olaf Penack9, Kamran Movassaghi9, Eva Vanessa Schrezenmeier10, Udo Schneider3, Antonia Busse11, Georg Schett12, Ulrich Keller11, Lars Bullinger9, Gerhard Krönke13, Marie Luise Hütter-Krönke14 and David Simon15, 1Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, Berlin, Germany, 2Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany, Berlin, 3Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, Berlin, 4Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany, Berlin, Berlin, Germany, 5Kyverna Therapeutics, Emeryville, CA, 6Department of Nuclear Medicine, Charité-Universitätsmedizin Berlin, Berlin, Germany, Berlin, 7Charité – Universitätsmedizin Berlin, corporate member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany, 8Department of Internal Medicine III, Jena University Hospital - Friedrich Schiller University Jena, Jena, Germany, 9Department of Hematology, Oncology and Tumor Immunology, Charité - Universitätsmedizin Berlin, Campus Virchow Klinikum, Berlin, Germany, Berlin, 10Department of Nephrology, Charité - Universitätsmedizin Berlin, Berlin, Germany, Berlin, 11Department of Hematology, Oncology and Cancer Immunology, Charité - Universitätsmedizin Berlin, Campus Steglitz, Berlin, Germany; Max-Delbrück-Center for Molecular Medicine, Berlin, Germany; German Cancer Consortium (DKTK) partner site Charité Berlin and German Cancer Research Center (DKFZ), Heidelberg, Germany, Berlin, 12Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 13Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany, Berlin, Berlin, Germany, 14Department of Hematology, Oncology and Cancer Immunology, Charité - Universitätsmedizin Berlin, Campus Steglitz, Berlin, Germany, Berlin, 15Department of Rheumatology and Clinical Immunology, Charité - Universitätsmedizin Berlin, Berlin, Germany; Deutsches Rheuma-Forschungszentrum Berlin, Berlin, Germany, Berlin, Germany

    Background/Purpose: Rheumatoid Arthritis (RA) is a chronic autoimmune disease characterized by autoreactive B cells that produce anti-citrullinated protein antibodies (ACPA), contributing to sustained synovial inflammation…
  • Abstract Number: 0979 • ACR Convergence 2025

    IL-23 upregulates IFN-γ secretion in Th17.1, but not in Th17 or classical Th1 cells

    Bennie van Heeswijk1, Wida Razawy2, Anne-Marie Mus-Otten3, Patrick Asmawidjaja2, Pieter Leenen2 and Erik Lubberts4, 1Erasmus MC, University Medical Center Rotterdam, Hoofddorp, Netherlands, 2Erasmus University Medical Center, Rotterdam, the Netherlands, Rotterdam, Netherlands, 3Erasmus medical center, Rotterdam, Netherlands, 4Erasmus MC, University Medical Center Rotterdam, Rotterdam, Netherlands

    Background/Purpose: Interleukin-23 (IL-23) is a key cytokine in the pathogenesis of psoriatic diseases, as demonstrated by the clinical success of IL-23-targeted therapies. Monocytes are a…
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All abstracts accepted to PRYSM 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.

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