ACR Meeting Abstracts

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Abstracts tagged "T Cell"

  • Abstract Number: 0985 • ACR Convergence 2025

    Lupus Skin Shapes a Distinct Inflammatory Milieu that Drives the Skewing of Treg and inflammatory T cells

    Hiroshi Kato1, Lin Zhang1, Mehrnaz Gharaee-Kermani2, Amy Hurst1, Rachael Bogle3, Alex Tsoi3, Johann Gudjonsson2 and J. Michelle Kahlenberg2, 1Michigan Medicine, Ann Arbor, MI, 2University of Michigan, Ann Arbor, MI, 3University of Michigan, Holland, OH

    Background/Purpose: Cutaneous lupus erythematosus (CLE) is a frequent manifestation of systemic lupus erythematosus (SLE) and remains an important contributor to morbidity in lupus patients. Despite…
  • Abstract Number: 1482 • ACR Convergence 2025

    Evaluation of T Cell Subpopulations, CD4/CD8 Ratio and p16INK4a in Patients with Systemic Lupus Erythematosus and Cognitive Impairment

    Erik Cimé-Aké1, Guadalupe Lima1, Emilio Godinez-Lazarini1, Sandra Juárez1, Hilda Marín-López1, Amairani Gómez-Rodríguez1, Daniela Flores-Hernández1, Ileana Flores-Hernández1, Diego F. Hernández-Ramírez1, Luis Llorente1 and Hilda Fragoso-Loyo2, 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, Mexico City, Mexico, Mexico City, Mexico

    Background/Purpose: Cognitive impairment (CI) in systemic lupus erythematosus (SLE) may be associated with different T cell subpopulations distribution and chronic pro-inflammatory state in which immunosenescence…
  • Abstract Number: 2641 • ACR Convergence 2025

    Cizutamig, a BCMA T-cell engager: preclinical to clinical translation of design optimization for the treatment of autoimmune diseases

    Ricardo Grieshaber-Bouyer1, Jamie Haddon2, Maria Gabriella Raimondo3, Carlo Tur3, Sebastian Böltz3, Tobias Dashi4, Melanie Hagen5, Andreas Wirsching3, Tobias Rathe4, Xuan Wu6, Peter Wung2, Francis Kim2, Yonghong Zhu6, Ken Song2, Timothy Lu7 and Georg Schett8, 1University Hospital Erlangen, Erlangen, Germany, 2Candid Therapeutics, San Diego, CA, 3Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 4Department of Internal Medicine 3- Rheumatology and Immunology, Friedrich-Alexander-Universität Erlangen-Nürnberg and Universitätsklinikum Erlangen, Erlangen, Germany, Erlangen, Germany, 5Friedrich-Alexander-University Erlangen-Nuremberg, Department of Internal Medicine 3 - Rheumatology and Immunology, Erlangen, Germany, 6EpimAb Biotherapeutics, Shanghai, China (People's Republic), 7Candid Therapeutics, San Diego, 8Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany

    Background/Purpose: Emerging data show the potential of T-cell engagers (TCEs) for deep B cell depletion to treat autoimmune diseases. Cizutamig is a purposefully designed BCMAxCD3…
  • Abstract Number: 0869 • ACR Convergence 2025

    PD-1 inhibitor unleashes pathogenic CD8+ T cells and induce arthritis in collagen-primed mice

    Clement Adedeji1, Muhammad Hamdan1, Hong-Jai Park2, Kelsey Wang1 and Sang Kim3, 1Yale University, New Haven, 2Yale University, New Haven, CT, 3Yale University, Branford, CT

    Background/Purpose: Background/Purpose: Immune checkpoint inhibitors (ICIs) are associated with immune-related adverse events, including inflammatory arthritis (ICI-arthritis). The pathophysiology of ICI-arthritis, particularly the role of T…
  • Abstract Number: 0986 • ACR Convergence 2025

    LBL-053, A Novel Anti-TL1A/p40 Bispecific Antibody for the Treatment of Autoimmune Disorders.

    Shuijun Hu1, Fengxia Li1, Aixia Liu1, Hailin Wang1, Xiaoxiao Liu1, Jianming Sun1, Yurong Qin1, Guojin Wu1, Jing Guan1, Hui Yuwen1, Jordan Zhu2, Xiaoqiang Kang1, Xiao Huang1 and Hong Ling1, 1Nanjing Leads Biolabs Co., Ltd., Nan Jing, China (People's Republic), 2Nanjing Leads Biolabs Co., Ltd., Nan Jing

    Background/Purpose: Inflammatory bowel disease (IBD) is a chronic, immune-mediated, inflammatory disease of the digestive tract. Several biological agents have greatly improved clinical course, remission, and…
  • Abstract Number: 1508 • ACR Convergence 2025

    Dissecting the Role of T Cell Subsets and Complements in Lupus Pathogenesis in Systemic Lupus Erythematosus Patients with Obesity

    Sheila Serin1, Megan Schluentz1, Chandana Keshavamurthy1, Alexandra Reese1, Sneha Centala1, Bettina Boone1, Samantha Ahrens2, William Davis3, Robert Quinet1, Jerald Zakem4, Samina Hayat5, Sarwat Umer6, Teresa leeth7, Daniyal Nadeem7 and Xin Zhang8, 1Department of Rheumatology, Ochsner Health, New Orleans, LA, 2Multi-specialty Clinical Research, Ochsner Health, New Orleans, LA, 3Ochsner Health System, New Orleans, LA, 4Ochsner Health Systems, Metairie, LA, 5Louisiana state university Shreveport, Shreveport, LA, 6LSUHSC Shreveport, Shreveport, LA, 7Louisiana State University Health Science, Shreveport, LA, 8Ochsner Medical Center, New Orleans, LA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease characterized by systemic inflammation, autoantibody production, and multiorgan involvement. Although genetic, hormonal, and environmental factors…
  • Abstract Number: 2693 • ACR Convergence 2025

    CAR T-cell Therapy in SLE: A Systematic Review

    Alberto Nordmann-Gomes1, Leila Khalili2, Wei Tang3, Laura Geraldino-Pardilla4, Yevgeniya Gartshteyn5, Robert Clancy4, Stephen Suh6, Maya Souvignier6, Michel Sadelain6 and Anca Askanase2, 1Columbia University Irving Medical Center, New York, NY, 2Columbia University Medical Center, New York, NY, 3Westchester Medical Center, Valhalla, NY, 4Columbia University, New York, NY, 5Columbia University Medical Center, Glen Rock, NJ, 6Columbia University Irving Medical Center, New York City, NY

    Background/Purpose: CAR T-cell therapy is poised to revolutionize the treatment of systemic lupus erythematosus (SLE). Recently, several authors have reported their experience using CAR T-cell…
  • 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: 0003 • ACR Convergence 2024

    CLN-978, a CD19-directed T Cell Engager (TCE), Leads to Rapid and Deep B Cell Depletion and Has Broad Potential for Development in Autoimmune Diseases

    Máire F. Quigley1, Jennifer S. Michaelson1, Jeffrey Jones1, Farrukh T. Awan2, Geoffrey P. Shouse3, Yue Zhang1, Todd Shearer1, Judy Inumerable1, Irina M. Shapiro1, Patrick A. Baeuerle1 and Stephen Wax1, 1Cullinan Therapeutics, Inc., Cambridge, 2UT Southwestern Medical Center, Dallas, 3City of Hope Comprehensive Cancer Center, Duarte

    Background/Purpose: CD19-directed CAR T cell therapy has been reported to induce profound B cell depletion and deep clinical responses, including drug-free remission, in patients with…
  • Abstract Number: 0499 • ACR Convergence 2024

    PD-1hiCXCR5-CD4+T Peripheral Helper Cells Enrich in Rheumatoid Arthritis and Predict Clinical Response to Anti-TNF Treatment

    Wanki Ho1, Huaqun Zhu1, Hua Ye1, Dongdong Fu2 and Xi Xu1, 1Peking University People's Hospital, Beijing, China, 2Xinxiang Central Hospital, Xinxiang, Henan, China (People's Republic)

    Background/Purpose: PD-1hiCXCR5-CD4+T peripheral helper cells (Tph) are newly identified pathogenic CD4+T helper cells and participate in rheumatoid arthritis (RA) pathogenesis. However, the clinical significance of…
  • Abstract Number: 1134 • ACR Convergence 2024

    First-in-Human Evaluation of the Safety, Tolerability and Pharmacokinetics of the T Cell Receptor Signal Modulator AX-158

    Christopher VanDeusen1, Andres Gagete1, Annelize Koch2 and D Scott Batty Jr1, 1Artax Biopharma, Inc, Cambridge, MA, 2Simbec-Orion, Merthyr Tydfil, Wales, United Kingdom

    Background/Purpose: Nck is a cytosolic protein that binds a domain of the T cell receptor (TCR) following TCR interaction to amplify responses from low affinity…
  • Abstract Number: 1785 • ACR Convergence 2024

    Comparative Immuno-Metabolomics Shows Singular Changes in Systemic Lupus Erythematosus Metabolic Phenotype Induced by T-Cell Activation

    Martin Stradner1, Fernanda Monedeiro2, Elmar Zuegner2, Barbara Prietl3, Monika Oberhuber4, Michael Khalil5, Christoph Magnes2, Hans-Peter Brezinsek1, Angela Libiseller3 and Thomas Pieber3, 1Div. of Rheumatology and Immunology, Medical University of Graz, Graz, Austria, 2Joanneum Research, Graz, Austria, 3Div. of Endocrinology, Medical University of Graz, Graz, Austria, 4CBmed, Graz, Austria, 5Dept. of Neurology, Medical University of Graz, Graz, Austria

    Background/Purpose: Metabolic processes have a critical role in regulating immune cell function, therefore being relevant to understanding the pathogenesis and progression of autoimmune diseases.  Here…
  • Abstract Number: 1850 • ACR Convergence 2024

    Exhausted T-cells Are Increased in Autoimmune Diseases and Predict Response to Anti-TNF in RA and SPA Patients

    Samuel Bitoun1, Marie Naigeon2, Matthieu Roulleaux- Dugage2, Caroline De Oliveira2, Caroline Berthot2, Xavier Mariette3, Gaetane Nocturne3 and Nathalie Chaput-Gras2, 1Service de Rhumatologie, Hôpital Bicêtre, AP-HP, Le Kremlin-Bicetre, France, 2Laboratoire d'immunomonitoring en Oncologie, INSERM US23, CNRS UMS 3655, Gustave Roussy,, Villejuif, France, 3Service de Rhumatologie, Hôpital Bicêtre, AP-HP, Le Kremlin Bicetre, France

    Background/Purpose: Exhaustion can occur after prolonged activation of T cells limiting their immunosurveillance function leading to cancer emergence. Among the exhaustion markers expressed on T…
  • Abstract Number: 1988 • ACR Convergence 2024

    A Randomized, Open-Label Study on the Effect of Nipocalimab on Vaccine Responses in Healthy Participants

    Marta Cossu1, Carolina Bobadilla Mendez2, Amanda Jackson3, Eugene Myshkin4, Grace Liu5, Edwin Lam6, Ulf H. Beier2, Kathleen Weisel2, Brittney Scott2, Jocelyn H. Leu6, Sheng Gao2 and Dessislava Dimitrova2, 1Janssen Pharmaceutical Research and Development, a Johnson & Johnson company, Leiden, Netherlands, 2Janssen Research & Development, LLC, a Johnson & Johnson company, Spring House, PA, 3Janssen Research & Development, LLC, La Jolla, CA, 4Janssen Research & Development, LLC, a Johnson & Johnson company, Cambridge, MA, 5Janssen Research & Development, LLC, a Johnson & Johnson company, Raritan, NJ, 6Janssen Research & Development, LLC, a Johnson & Johnson company, Spring House, PA, PA

    Background/Purpose: Nipocalimab is a human IgG1 monoclonal antibody targeting the neonatal Fc receptor (FcRn) that selectively reduces IgG levels without impacting antigen presentation, T- and…
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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.

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 6:00 PM CT on March 18. 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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