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

Abstracts tagged "T-Lymphocyte"

  • Abstract Number: 2476 • ACR Convergence 2025

    Blinatumomab in rapid progressive systemic sclerosis

    Christina Gebhardt1, Franziska Szelinski2, Hector Rincon-Arevalo2, Giulia Magno3, Veit Buecklein3, Gerulf Haenel4, Gerhard Zugmaier5, Michael von Bergwelt3, Marion Subklewe3, Thomas Dörner6, Alla Skapenko7 and Hendrik Schulze-Koops7, 1LMU Hospital, Division for Rheumatology and Clinical Immunology, München, Germany, 2Charite Universitétsmedizin Berlin, Germany, Berlin, Germany, 3LMU Klinikum, Med. Klinik und Poliklinik III, Munich, Germany, 4LMU Gene Center, Munich, Germany, 5Amgen, Munich, Germany, 6Charite Universitétsmedizin Berlin, Germany and DRFZ, Berlin, Berlin, Germany, 7LMU Hospital, Division for Rheumatology and Clinical Immunology, Munich, Bayern, Germany

    Background/Purpose: Systemic sclerosis is a severe, potentially fatal disease, characterized by progressive fibrosis of skin and internal organs. Blinatumomab is a bispecific CD3/CD19-T-cell engager (BiTe)…
  • Abstract Number: 1758 • ACR Convergence 2025

    Treg need a MAIT: Investigating the contribution of MAIT cells to impaired UV-induced Treg expansion in lupus photosensitive reactions

    Grace Crossland1, Lindsay Mendyka1, Vianey Chavez1, Kaitlyn Dowling1, Michael Constantinides2 and Sladjana Skopelja-Gardner1, 1Dartmouth College, Lebanon, NH, 2Scripps, La Jolla

    Background/Purpose: Most systemic lupus erythematosus (SLE) patients experience sensitivity to ultraviolet (UV) light, which can trigger disfiguring skin lesions or systemic flares. In healthy skin,…
  • Abstract Number: 1755 • ACR Convergence 2025

    Multi-Omic Profiling Of CD8+ T Cells In Axial Spondyloarthritis (axSpA) And Reactive Arthritis (ReA) Implicates Common Pathways

    Zoya Qaiyum1, Michael Tang2, Shirin Soleimani3, Addison Pacheco2, Melissa Lim4, Fataneh Tavasolian4, Trevor Pugh3 and Robert Inman2, 1Schroeder Arthritis Institute, University Health Network, Toronto, ON, Canada, 2University Health Network, Toronto, ON, Canada, 3Princess Margaret Cancer Centre, University Health Network, Toronto, Canada, 4University of Toronto, Toronto, ON, Canada

    Background/Purpose: The strong clinical and genetic associations between axial spondyloarthritis (axSpA) and inflammatory bowel disease (IBD) underscore the pathogenic role of the gut-joint axis. We…
  • Abstract Number: 1003 • ACR Convergence 2025

    Potent Engineering of Polyfunctional CD8+ T Cells by a Novel In Vivo CAR mRNA Product Candidate (CPTX2309) in a Targeted Lipid Nanoparticle (tLNP) Utilizing CellSeekerTM Technology 

    Yan Zhang1, Brittany Ross1, Aditi Upadhye1, Diana Galvan1, Shaun E Grosskurth1, Yanjie Bao1, Romina Riener1, Annabel Wang1, Aric Frantz1, Gregor B Adams1, Michael Rosenzweig1, Ramin Farzaneh-Far1, Priya Karmali1, Adrian I Bot1, Carl June2 and Haig Aghajanian1, 1Capstan Therapeutics, San Diego, CA, 2University of Pennsylvania, Philadelphia, PA

    Background/Purpose: A major objective in autoimmunity is immune reset, requiring autoreactive B cell depletion in tissues. We designed an in vivo CAR product candidate (CPTX2309)…
  • 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: 0999 • ACR Convergence 2025

    Myositis Induced by Histidyl-Transfer tRNA Synthetase is Exacerbated by Membranopathy and Suppressed by Regulatory T Cells

    Samantha Coss1, Nicholas Young2, Shane Bruckner3, Braden Zeno4, Gianni Giarrano5, Hannah Bulgart6, Paula Clemens7, Jisna Paul2, Chester V. Oddis8, noah weisleder9, Dana Ascherman8 and Wael Jarjour10, 1Nationwide Children's Hospital, Columbus, OH, 2Division of Rheumatology and Immunology, Department of Internal Medicine, The Ohio State University Wexner Medical Center, Columbus, OH, Columbus, OH, 3OSU, Columbus, OH, 4Ohio State University, upper arlington, OH, 5Division of Rheumatology, Nationwide Children's Hospital, Columbus, OH, 6Department of Molecular and Cellular Biochemistry, University of Kentucky College of Medicine, Lexington, KY, 7Department of Medicine, University of Pittsburgh School of Medicine, Pittsburgh, PA, 8University of Pittsburgh, Pittsburgh, PA, 9University of Kentucky, Lexington, KY, 10The Ohio State University, Columbus, OH

    Background/Purpose: Idiopathic inflammatory myopathies (IIMs) are a heterogeneous group of autoimmune disorders targeting muscle as well as extra-muscular organs. Among the most common autoantibodies associated…
  • 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: 0982 • ACR Convergence 2025

    Impact of Immunosuppressive Therapies on Shingrix Vaccine Response in Immune-Mediated Inflammatory Diseases

    cristiana Sieiro1, Juan García Herrero2, Jose Ordas Martínez3, Carolina Álvarez Castro3, Alejandra López Robles3, Ronald Colindres3, Ana María Sahagún4 and Jose María Ruiz de Morales3, 1Univrsity of Manchester, Manchester, United Kingdom, 2complejo asistencial universitario de leon, León, Spain, 3Complejo Asistencial Universitario de León, León, Spain, 4University of Leon, León, Spain

    Background/Purpose: Herpes zoster (HZ) is a common infection, particularly in older adults and women, and can lead to complications like neuropathic pain. The risk is…
  • Abstract Number: 0514 • ACR Convergence 2025

    Transitional Monocytes and Innate T Cell Populations Help Distinguish Ro Seropositive vs Ro Seronegative Sjögren’s Disease Using Whole Blood Immunophenotyping

    Nicholas Bauer1, Rufei Lu1, Carla Guthridge1, Tayte Stephens2, Benjamin Jones3, Wade DeJager4, Susan Macwana1, Caroline Shiboski5, Alan Baer6, Christopher Lessard1, Astrid Rasmussen1, Stephen Shiboski5, Judith James1, Linda F. Thompson1, Blake M. Warner7, A. Darise Farris1 and Joel Guthridge1, 1Oklahoma Medical Research Foundation, Oklahoma City, OK, 2University of Oklahoma Health Science Center, Oklahoma City, OK, 3Oklahoma State University, Oklahoma City, OK, 4Oklahoma Medical Research Foundation, Oklahoma City, 5University of California San Francisco, San Francisco, CA, 6Johns Hopkins University School of Medicine, Baltimore, MD, 7National Institutes of Health, Bethesda, MD

    Background/Purpose: Blood immunophenotyping reveals systemic immune alterations and therapeutically actionable molecular endotypes in Sjögren’s Disease (SjD). Reported changes include reduced memory B cells, plasmacytoid dendritic…
  • Abstract Number: 0089 • ACR Convergence 2025

    Expansion of PD-1hi Tfh and Tph cells in the peripheral blood of seropositive clinically suspect arthralgia patients: association with progression to rheumatoid arthritis

    Maria-Eugenia Miranda-Carus1, Mariana Gutierrez-Riart2, Beatriz Nieto-Carvalhal3, Laura Nuño2, Alejandro Villalba1, Diana Peiteado1, Irene Monjo Henry1, Marta Novella-Navarro1 and Eugenio de Miguel1, 1Hospital Universitario La Paz, Madrid, Spain, 2Hospital Universitario La Paz, Madrid, 3Hospital Universitario La Paz, Mdrid

    Background/Purpose: Subjects with clinically suspect arthralgia (CSA) are at risk for developing rheumatoid arthritis (RA) and therapeutic interventions may prevent or delay progression. Still, a…
  • Abstract Number: 1139 • ACR Convergence 2024

    Comprehensive Single-cell Profiling of Diverse Circulating Immune Cells in Idiopathic Inflammatory Myopathies Identifies a Novel Pathogenic Subset of Monocytes

    Shinji Izuka1, Toshihiko Komai2, Hayato Yuuki2, Ikuko Ueda3, Manabu Fujimoto4, Hiroyuki Fukui5, Masaru Takeshita6, Natsuka Umezawa7, Shinsuke Yasuda7, Mitsutaka Yasuda8, Yuichiro Fujieda9, Tatsuya Atsumi9, Takeshi Iwasaki10, Akio Morinobu10, Yuya Kondo11, Isao Matsumoto11, Toshio Kawamoto12, Masakazu Matsushita12, Naoto Tamura13, Taro Iwamoto14, Hiroshi Nakajima14, Ken Yoshida15, Takeo Isozaki16, Nobuyuki Yajima16, Keiichi Sakurai17, Kimito Kawahata17, Yasuyuki Kamata18, Kojiro Sato18, Yoshiya Tanaka19, Akari Suzuki20, Kazuhiko Yamamoto21, Tomohisa Okamura22 and Keishi Fujio2, 1Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan., Tokyo, Japan, 2Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan., Bunkyo, Tokyo, Japan, 3Department of Dermatology, Osaka University Graduate School of Medicine, Suita, Japan., Suita, Japan, 4Department of Dermatology, Osaka University Graduate School of Medicine, Suita, Japan., Suita, Osaka, Japan, 5Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan., Tokyo, Japan, 6Keio University School of Medicine, Shinjuku-ku, Tokyo, Japan, 7Department of Rheumatology, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan., Tokyo, Japan, 8Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan., Sapporo, Japan, 9Department of Rheumatology, Endocrinology and Nephrology, Faculty of Medicine and Graduate School of Medicine, Hokkaido University, Sapporo, Japan, Sapporo, Japan, 10Department of Rheumatology and Clinical Immunology, Graduate School of Medicine, Kyoto University, Kyoto, Japan., Kyoto, Japan, 11Department of Rheumatology, Faculty of Medicine, University of Tsukuba, Ibaraki, Japan., Tsukuba, Japan, 12Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan., Tokyo, Japan, 13Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 14Department of Allergy and Clinical Immunology, Chiba University Hospital, Chiba, Japan., Chiba, Japan, 15Division of Rheumatology, Department of Internal Medicine, The Jikei University School of Medicine, Tokyo, Japan., Tokyo, Japan, 16Division of Rheumatology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan., Tokyo, Japan, 17Division of Rheumatology and Allergology, Department of Internal Medicine, St. Marianna University School of Medicine, Kawasaki, Kanagawa, Japan., Kawasaki, Japan, 18Division of Rheumatology and Clinical Immunology, Department of Medicine, Jichi Medical University, Tochigi, Japan., Tochigi, Japan, 19Department of Internal Medicine, University of Occupational and Environmental Health, Kitakyushu, Fukuoka, Japan, 20Laboratory for Autoimmune Diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan., Kanagawa, Japan, 21Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan., Laboratory for Autoimmune Diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Kanagawa, Japan., Kawasaki, Japan, 22Department of Allergy and Rheumatology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan., Department of Functional Genomics and Immunological Diseases, Graduate School of Medicine, The University of Tokyo, Japan., Bunkyo, Tokyo, Japan

    Background/Purpose: Idiopathic inflammatory myopathies (IIMs) are heterogeneous diseases, making it crucial to identify distinct pathological processes to improve a treatment strategy. Transcriptomic analyses have revealed…
  • Abstract Number: 2677 • ACR Convergence 2024

    N-Acetylcysteine Blocks the Mechanistic Target of Rapamycin in Pro-Inflammatory Effector-Memory CD4 and CD8 T Cells Re-Expressing CD45RA in Patients with Active Systemic Lupus Erythematosus

    Joy Park1, Lanlan Ji1, Jorge Cabezas1, Xiaojing Wang2, Bryan Blaker1, Dilip Rao1, Aparna Godavarthy1, Lucero Blaker1, FNU Ruchi1, Ioana Coman1, Nancy Olsen3, Joshua Lewis2, Mariko Ishimori4, Kyriakos Kirou5, Christina Donath1, Sara Kahlown6, Damira Sereda1, Marlene Marte Furment1, Sandy Nasr7, Sravani Lokineni1, rosalind Ramsey-Goldman8, Michael Weisman9, Arthur Weinstein10, Cynthia Aranow11, Banki Katalin12, Michael McDermott13, Daniel Wallace14 and Andras Perl1, 1SUNY, Syracuse, NY, 2SUNY Upstate Medical University, Syracuse, NY, 3Penn State University/Milton S Hershey, Hershey, PA, 4Cedars-Sinai Health System, Los Angeles, CA, 5Hospital for Special Surgery, New York, NY, 6SUNY Upstate University Hospital, Department of Medicine, Rheumatology Fellowship Program, Syracuse, NY, 7SUNY Upstate University Hospital, syracuse, NY, 8Northwestern University, Chicago, IL, 9Stanford University, Los Angeles, CA, 10Georgetown University, Pasadena, CA, 11Feinstein Institutes for Medical Research, New York, NY, 12SUNY Upstate University Hospital, Department of Pathology, Syracuse, NY, 13University of Rochester, Rochester, NY, 14Cedars Sinai, Los Angeles, CA

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease of unknown etiology with significant mortality attributed to infections due to toxicity of immunosuppressant medications. Our…
  • Abstract Number: 1514 • ACR Convergence 2024

    Immunosenescent and Exhausted T Cells in Patients with Systemic Lupus Erythematosus and Cognitive Impairment

    Erik Cimé-Aké1, Guadalupe Lima2, Emilio G. Lazarini1, Sandra Juárez3, Luis Llorente2 and Hilda Fragoso-Loyo1, 1Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán. Immunology and Rheumatology Department, Mexico City, Mexico, 2Instituto Nacional de Ciencias Médicas y Nutrición. Salvador Zubirán. Immunology and Rheumatology Department, Mexico City, Mexico, 3Instituto Nacional de Ciencias Médicas y Nutrición. Salvador Zubirán. Neurology and Psychiatry Department, Mexico City, Mexico

    Background/Purpose: Cognitive impairment (CI) in systemic lupus erythematosus (SLE) may result from a chronic pro-inflammatory state in which immunosenescent and exhausted T-lymphocytes could be involved.…
  • Abstract Number: 2691 • ACR Convergence 2024

    Transcriptomic Changes in CD4+ T Lymphocytes in Eosinophilic Granulomatosis with Polyangiitis

    Roberto Ríos-Garcés1, Núria Farran1, Salvador Naranjo-Suarez2, Roser Alba-Rovira1, Sergio Prieto-González3, Itziar Tavera-Bahillo1, Roser Solans-Laqué4, Ebymar Arismendi5, Marc Corbera-Bellalta1, Javi Marco-Hernández1, Farah Kamberovic1, Nina Visocnik1, Maria Cid6 and Georgina Espígol-Frigolé1, 1Vasculitis Research Group, Autoimmune Diseases Department, IDIBAPS, Hospital Clinic, University of Barcelona, Barcelona, Spain, 2Angiogenesis in Liver Disease Research Group, IDIBAPS, Hospital Clinic, University of Barcelona, Barcelona, Spain, 3Vasculitis Research Group, Autoimmune Diseases Department, IDIBAPS, Hospital Clinic, University of Barcelona, bar, Spain, 4Internal Medicine Service, Vall d'Hebron Hospital University and Campus, Barcelona, Spain, 5Pneumology Department, Hospital Clinic, IDIBAPS, University of Barcelona, CIBERES, Barcelona, Spain, 6Hospital Clinic Barcelona. University of Barcelona, Barcelona, Spain

    Background/Purpose: Eosinophilic Granulomatosis with polyangiitis (EGPA) is a rare systemic autoimmune disorder, included within the ANCA-associated vasculitis. It is characterized by a diverse clinical profile,…
  • Abstract Number: 1660 • ACR Convergence 2024

    Systemic Inflammation and Transcriptional Reprogramming Contribute to Progression to Active Rheumatoid Arthritis in ACPA+ Individuals

    Mark Gillespie1, Ziyuan He1, Adam Savage1, Pravina Venkatesan1, Marla Glass1, Lauren Okada2, Nhung Tran2, Yudong He2, Samir Rachid Zaim1, Padmapriyadarshini Ravisankar2, Christy Bennett1, Julian Reading2, Jessica Garber2, Palak Genge2, Veronica Hernandez2, Alexander Heubeck2, Erin Kawelo2, Upaasana Krishnan2, Kevin Lee2, Regina Mettey2, Blessing Musgrove2, Vaishnavi Parthasarathy2, Cole Phalen2, Charles Roll2, Tyanna Stuckey2, Morgan Weiss1, Claire Gustafson2, Qiuyu Gong2, Emma Kuan2, Tao Peng2, Lucas Graybuck2, Kristen Demoruelle3, Kristine Kuhn4, David Boyle5, Fan Zhang4, Thomas Bumol6, Ananda Goldrath2, Xiaojun Li1, V. Michael Holers7, Peter Skene1, Gary Firestein8, Kevin Deane9 and Troy Torgerson10, 1Allen Institute for Immunology, Seattle, WA, 2Allen Institute for Immunology, Seattle, 3University of Colorado Anschutz Medical Campus, Golden, CO, 4University of Colorado, Aurora, CO, 5UCSD, La Jolla, CA, 6Allen Institute for Immunology, San Diego, CA, 7University of Colorado, Denver, CO, 8University of California, San Diego, San Diego, CA, 9University of Colorado Denver Anschutz Medical Campus, Aurora, CO, 10Allen Institute for Immunology, Enumclaw, WA

    Background/Purpose: Elevated levels of RA-associated autoantibodies (ACPA, RF) prior to the clinical onset of inflammatory arthritis (IA) define a state of risk for future development…
  • 1
  • 2
  • 3
  • …
  • 6
  • 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