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  • Abstract Number: 141 • 2018 ACR/ARHP Annual Meeting

    Lymphocyte Activation Gene 3 Plasma Level Is Increased and Associated with Progression in Early Rheumatoid Arthritis

    Janni Maria Pedersen1,2,3, Aida Hansen4, Malene Hvid5, Kim Hørslev-Petersen6, Merete Lund Hetland7, Kristian Stengaard-Pedersen8, Mikkel Østergaard9, Bjarne Kuno Moeller10, Ellen-Margrethe Hauge11, Peter Junker12 and Bent Deleuran1,2, 1Department of Biomedicine, Aarhus University, Aarhus, Denmark, 2Department of Rheumatology, Aarhus University Hospital, Aarhus, Denmark, 3Department of Rheumatology, Aalborg University Hospital, Aalborg, Denmark, 4Biomedicine, Aarhus University, Aarhus, Denmark, 5Department of Clinical Medicine, Aarhus University, Aarhus, Denmark, 6King Christian X Hospital for Rheumatic Diseases, Graasten, Denmark, 7University of Copenhagen, Copenhagen, Denmark, 8Department of Rheumatology, Aarhus University Hospital, Department of Clinical Medicine, Aarhus, Denmark, 9Center for Rheumatology and Spine Diseases, Rigshospitalet Glostrup Copenhagen Center for Arthritis Research, Copenhagen, Denmark, 10Department of Immunology, Aarhus University Hospital, Aarhus, Denmark, 11Department of Rheumatology, Aarhus University Hospital, Aarhus, Aarhus, Denmark, 12Department of Rheumatology C, Odense University Hospital, Odense, Denmark

    Background/Purpose: Lymphocyte activation gene 3 (LAG3) resembles CD4 and is a key checkpoint molecule leading to downregulation of T cell proliferation and antigen presentation via…
  • Abstract Number: LB11 • ACR Convergence 2025

    Efficacy and Safety of Telitacicept in Patients with Sjögren’s Disease: Results from a Multicenter, Randomized, Double-blind, Placebo-controlled, Phase 3 Clinical Study

    Dong Xu1, Shangzhu Zhang1, Lin Qiao1, Li Zhang1, Wenxiang Wang2, Lin Li2, Binghua Xiao2, Jing Zhang2, Qing Zuraw3, Jianmin Fang2 and Xiaofeng Zeng1, 1Department of Rheumatology and Clinical Immunology, Peking Union Medical College Hospital (PUMCH), Chinese Academy of Medical Sciences & Peking Union Medical College; National Clinical Research Center for Dermatologic and Immunologic Diseases (NCRC-DID), Ministry of Science & Technology; State Key Laboratory of Complex Severe and Rare Diseases; Key Laboratory of Rheumatology and Clinical Immunology, Ministry of Education, Beijing, China (People's Republic), 2RemeGen Co., Ltd., Rheumatology, Yantai, China (People's Republic), 3Vor Biopharma Inc., Boston

    Background/Purpose: Sjögren's disease (SjD) is a chronic autoimmune disease whose pathogenesis is associated with aberrant activation of B-lymphocytes. Telitacicept, a novel fusion protein, dually targets and…
  • Abstract Number: 0039 • ACR Convergence 2025

    Hemophagocytic Lymphohistiocytosis Gene Variants in Severe COVID-19 Cytokine Storm Syndrome

    randy Cron1, Abhishek Kamath1, Mingce Zhang1, Devin Abhser2, Lesley Jackson1 and Walter Winn Chatham3, 1University of Alabama at Birmingham, Birmingham, AL, 2Kaiser Permanente Research Bank, Oakland, CA, 3University of Nevada, Las Vegas, Las Vegas, NV

    Background/Purpose: Severe COVID-19 infection resulting in hospitalization shares features with frequently fatal cytokine storm syndromes (CSS), such as hemophagocytic lymphohistiocytosis (HLH) and macrophage activation syndrome…
  • Abstract Number: 0906 • ACR Convergence 2025

    Preclinical Characterization of IBI3034, an TACI and BCMA Chimeric Fc Fusion Protein, that Potently Modulates B Lymphocytes and Serum Immunoglobulin for the Treatment of B cell Related Autoimmune Disease

    Yao Xiong, Shuaixiang Zhou, Zhimin Zhang, Bin Li, Zhihao Ming, Yuyu Wu, Liu Li, Chang Li, Fenggen Fu, Zhihai Wu, Shun Wang, Guogang Yuan, Yuling Song, Jinyang Li, Huizhong Xiong and Bingliang Chen, Innovent Biologics (Suzhou) Co., Ltd., Suzhou, Jiangsu, China (People's Republic)

    Background/Purpose: Dysregulated B-cell activation plays a pivotal role in the pathogenesis of various autoimmune diseases. B-cell activating factor (BAFF) and a proliferation-inducing ligand (APRIL) are…
  • Abstract Number: 0934 • ACR Convergence 2025

    The Use Of Preclinical Models To Understand Drivers Of Lupus Pathogenesis

    Arielle Glatman Zaretsky1, Carley Tasker1, Pablo Abreu1, Ciara Torres2, Li-Hong Ben1, Scott MacDonnell1, Andre Limnander1 and Jamie Orengo1, 1Regeneron, Tarrytown, NY, 2Regeneron, Tarrytown

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is a chronic, multisystem autoimmune disease with a prevalence of 1.4-15.13/100,000 adults globally. SLE is highly heterogenous and can involve…
  • Abstract Number: 1119 • ACR Convergence 2025

    Microbial activation of cytotoxic CD8⁺ T cells promotes skin immune-related adverse events in patients treated with immune checkpoint inhibitors

    Shady Younis1, Suman Acharya1, Gayathri Swaminathan1, Heidi Wong1, Hannah Kim1, Alec Eschholz1, Subramanya Hegde2, Andrew McKnight3, William Robinson4 and Lisa Zaba1, 1Stanford University, Stanford, CA, 2Sanofi US, New Jersey, MA, 3Sanofi US, Cambridge, MA, 4Stanford University, Palo Alto, CA

    Background/Purpose: Immune checkpoint inhibitors (ICIs) have transformed cancer therapy, but their use is often limited by immune-related adverse events (irAEs), particularly in barrier tissues such…
  • Abstract Number: 1723 • ACR Convergence 2025

    Impaired Maintenance of X-Chromosome Inactivation in B Cells, But Not T Cells, Exacerbates Interferon-Driven Systemic Autoimmunity

    Nikhil Jiwrajka1, Claudia Lovell1, Zowie Searcy1, Katherine Forsyth1, Emma Welter1, Natalie Toothacre2, Nuriban Valero-Pacheco1, Katherine Premo1 and Montserrat Anguera1, 1University of Pennsylvania, Philadelphia, PA, 2University of Pennsylvania, Philadelphia

    Background/Purpose: Many systemic autoimmune diseases associated with chronic type 1 interferon (IFN) signaling, including SLE, SjD, and SSc, preferentially afflict females. The biological basis of…
  • Abstract Number: 1759 • ACR Convergence 2025

    Role of a pathogenic bacterial factor produced by a human gut pathobiont in inducing platelet activation and thrombo-inflammation.

    Abhimanyu Amarnani1, Cristobal F. Rivera2, Susan RS Gottesman3, Zakia Azad1, Mingyang Yi4, Joshua Prasad4, Cynthia Loomis4, Andy Lee4, Nimat Ullah4, Bhama Ramkhelawon5 and Gregg J. Silverman1, 1New York University Grossman School of Medicine, New York, NY, 2New York University Grossman Department of Surgery, New York, 3SUNY Downstate Health Sciences University, New York, 4New York University Grossman School of Medicine, New York, 5New York University Department of Surgery, New York

    Background/Purpose: SLE is an autoimmune disease that causes progressive multi-organ damage, leading to renal injury, or lupus nephritis (LN), in half of patients. Despite treatment,…
  • Abstract Number: 1819 • ACR Convergence 2025

    Spatial Transcriptomic Profiling Reveals Interferon Activation and CD8⁺ T Cell Dominance in Systemic Juvenile Idiopathic Arthritis-Macrophage Activation Syndrome Liver Inflammation

    Esraa Eloseily1, Taskin Sabit2, Lara Berklite3, Grant Schulert4 and Alexei Grom4, 1UT Southwestern Children's Medical Center, Dallas, TX, 2Cincinnati Children's Hospital Medical Center, Division of Rheumatology, Cincinnati, OH, 3Cincinnati Children's Hospital, Cincinnati, OH, 4Cincinnati Children's Hospital Medical Center, Cincinnati, OH

    Background/Purpose: Systemic juvenile idiopathic arthritis (SJIA) with macrophage activation syndrome (MAS) involves severe systemic inflammation and hepatocellular injury. Our prior histopathology studies showed increased CD8⁺…
  • Abstract Number: 1829 • ACR Convergence 2025

    Multiomic Investigation of Juvenile Idiopathic Arthritis Synovium Reveals Immune Cell Heterogeneity

    Abigail Thielbar1, Tracy Ting2, Lexi Auld3, Kelly Rogers4, Megan Quinlan-Waters5, Sheila Angeles-Han4, Ekemini Ogbu2, Daniel Lovell2, Jennifer Huggins6, Grant Schulert2, Patricia Vega-Fernandez2 and Yuriy Baglaenko4, 1Cincinnati Children's Hospital, Cincinnati, 2Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3Cincinnati Children's Hospital Medical Center, Division of Rheumatology, Cincinnati, OH, 4Cincinnati Children's Hospital, Cincinnati, OH, 5Cincinnati Children's Hospital Medical Center, CCHMC, 6Cincinnati Children's Medical Center, Cincinnati, OH

    Background/Purpose: Juvenile idiopathic arthritis (JIA) is the most common chronic inflammatory rheumatic disease of childhood, affecting 1:1,000 children worldwide. The hallmark of JIA is immune-mediated…
  • Abstract Number: 2664 • ACR Convergence 2025

    Neutrophil-to-Lymphocyte Ratio (NLR) as a Clinically Accessible Marker for Interferon Signatures in Autoimmune Diseases

    YOSHINOBU KOYAMA1, KENTA SHIDAHARA2, YU NAKAI2, YOSHIHARU SATO3 and YOSHINORI NISHIURA2, 1Japanese Red Cross Okayama Hospital, Okayama, Okayama, Japan, 2Japan Red Cross Okayama Hospital, Okayama-shi, Okayama, Japan, 3DNA Chip Research Inc., Kawasaki-shi, Kanagawa, Japan

    Background/Purpose: Interferons (IFNs) play critical roles in systemic autoimmune diseases, particularly systemic lupus erythematosus (SLE), where heightened type I IFN signaling is a hallmark. Elevated…
  • Abstract Number: 2494 • ACR Convergence 2025

    Abatacept Reduces CD319+ (SLAM-F7) Cytotoxic T Cells and Cytokine Production in Systemic Sclerosis

    Mikel Gurrea-Rubio1, Kohei Maeda2, Qi Wu3, Phillip L Campbell2, Camila I Amarista2, Alexander Stinson4, Ray Ohara5, Laura Cooney6, Michael Whitfield7, Pei-Suen Tsou8, Dinesh Khanna8 and David Fox9, 1University of Michigan - Ann Arbor, Ann Arbor, MI, 2Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA, Ann Arbor, MI, 3Division of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI, USA, Ann Arbor, 4University of Michigan, Department of Internal Medicine, Division of Rheumatology, Ann Arbor, MI, 5University of Michigan, Department of Internal Medicine, Division of Rheumatology, West Bloomfield, MI, 6Immune Tolerance Network, Ann Arbor, MI, 7Geisel School of Medicine, Lebanon, NH, 8University of Michigan, Ann Arbor, MI, 9University of Michigan, Dexter, MI

    Background/Purpose: While the ASSET clinical trial (placebo-controlled blinded trial of abatacept) in patients with diffuse cutaneous systemic sclerosis (dcSSc) did not meet its primary endpoint…
  • Abstract Number: 0389 • ACR Convergence 2024

    Histopathological Features of Liver Tissue Biopsies in SJIA Patients with and Without Clinical Macrophage Activation Syndrome

    Esraa Eloseily1, Lara Berklite2, Jennifer Picarsic1, grant schulert1, Rachel Sheridan1 and Alexei Grom1, 1Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 2Cincinnati Children's Hospital Medical Center, Cincinnti, OH

    Background/Purpose: Systemic Juvenile Idiopathic Arthritis (SJIA) can present with or without Macrophage Activation Syndrome (MAS), a severe, potentially life-threatening complication. Liver tissue injury is commonly…
  • Abstract Number: 1765 • ACR Convergence 2024

    CD8+ T Cells and Monocytes from Children with Macrophage Activation Syndrome Demonstrate Specific Transcriptional Changes Consistent with T Cell Activation and Expansion of Monocytes Shaped by Interferon and TLR Signaling

    Susan Canny1, Hannah DeBerg2, Griffin Gessay2, Ailing Lu3, Mary Eckert4, Andrea La Bella5, Hayley Waterman2, Danish Nadeem2, Susan Shenoi6, Joyce Hui-Yuen7, Daniel Campbell2, Betsy Barnes8 and Jessica Hamerman2, 1University of Washington, Seattle, WA, 2Benaroya Research Institute, Seattle, WA, 3Northwell Health, Manhasset, NY, 4Seattle Children's Hospital, Seattle, WA, 5Cohen Children's Medical Center, Queens, NY, 6Seattle Children's Hospital and Research Center, Mercer Island, WA, WA, 7North Shore LIJ Health System, Great Neck, NY, 8Feinstein Institutes for Medical Science, Manhasset, NY

    Background/Purpose: Macrophage activation syndrome (MAS), a form of secondary hemophagocytic lymphohistiocytosis (sHLH), is a potentially fatal complication of rheumatic diseases. MAS is characterized by a…
  • Abstract Number: 1839 • ACR Convergence 2024

    PPP2R3C Overexpression Suppresses TCR -mediated CD4+ T Cell Abnormal Activation in Systemic Lupus Erythematosus via JNK and AKT-mTOR Pathways

    Xuan Fang, Xiangpei Li and Xiaomei Li, The First Affiliated Hospital of University of Science and Technology of China., He Fei, China (People's Republic)

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is distinguished by immune system dysfunction, leading to heightened activation of T and B cells. This increased activity leads to…
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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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