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Abstracts tagged "Cell-signalling molecules"

  • Abstract Number: 1655 • ACR Convergence 2025

    Aberrant Noncoding RNAs Are Enriched in Extracellular Vesicles and Implicated in Interferon Activation

    Sandra Williams1, Soyeong Sim2 and Sandra Wolin2, 1National Institute of Arthritis, Musculoskeletal and Skin Diseases; National Cancer Institute, Bethesda, MD, 2National Cancer Institute, Frederick, MD

    Background/Purpose: Extracellular vesicles (EVs) are small structures that enclose a variety of nucleic acids. While much of the published work on EV RNA has focused…
  • Abstract Number: 0926 • ACR Convergence 2025

    Discovery and Characterization of SIM0711: a Potent and Selective IRAK4 PROTAC with Improved Efficacy and Safety

    Minyun Zhou1, Peng Gu2, Mengyu Wang3, Yuxi Yan2, Li Sun3, Yiling Chen3, Xin Wang3, Feng Tang1, Shunwei Zhu2 and Xiaofeng Zhao4, 1State Key Laboratory of Neurology and Oncology Drug Development, Simcere Pharmaceutical group, Nanjing, 2State Key Laboratory of Neurology and Oncology Drug Development, Simcere Pharmaceutical Group, Shanghai, China (People's Republic), 3State Key Laboratory of Neurology and Oncology Drug Development, Simcere Pharmaceutical Group, Nanjing, China (People's Republic), 4State Key Laboratory of Neurology and oncolog Drug Development, Simcere Pharmaceutical Group, Nanjing, China (People's Republic)

    Background/Purpose: IRAK4 plays a pivotal role in the innate immune response by acting downstream of Toll-like receptors (TLRs) and the interleukin-1 receptor (IL-1R), with both…
  • Abstract Number: 0921 • ACR Convergence 2025

    Fibrinogen Co-Modified with Malondialdehyde-Acetaldehyde and Citrulline Promotes Pro-Inflammatory Macrophage Differentiation Through p38 and NF-κB Signaling

    Hannah Johnson1, Wenxian Zhou2, Michael Duryee1, Carlos Hunter1, Geoffrey Thiele1 and Ted Mikuls1, 1University of Nebraska Medical Center, Omaha, NE, 2University of Nebraska Medical Center, Bellevue, NE

    Background/Purpose: Citrulline (CIT) and malondialdehyde-acetaldehyde (MAA) co-adduct native proteins in RA tissues to create a dual pro-inflammatory and pro-fibrotic milieu. Our previous work demonstrated that…
  • Abstract Number: 0916 • ACR Convergence 2025

    UVB-Irradiated Keratinocyte Extracellular Vesicles Trigger Innate Immune Activation via Type I Interferons and STING Pathway

    Ahmed Eldaboush1, Darae Kang2 and Victoria Werth3, 1Department of Dermatology, Perelman Shool of Medicine, University of Pennsylvania, Philadelphia, PA, 2University of Pennsylvania, Potomac, MD, 3University of Pennsylvania, Wynnewood, PA

    Background/Purpose: Extracellular vesicles (EVs) are cell-derived nanoparticles that mediate cell-cell communication. EVs are implicated in photosensitive autoimmune diseases like dermatomyositis (DM) and systemic lupus (SLE),…
  • Abstract Number: 0857 • ACR Convergence 2025

    CD14-dependent MAP kinase signaling is required for pathogenic neutrophil extracellular trap formation in APS

    Thalia Newman1, NaveenKumar Somanathapura1, Chao Liu2, Srilakshmi Yalavarthi1, Pooja Kapoor1, Ajay Tambralli1, Jacqueline Madison1, Yu (Ray) Zuo1 and Jason S. Knight1, 1University of Michigan, Ann Arbor, MI, 2University of Michigan, Superior Charter Twp, MI

    Background/Purpose: Antibodies targeting beta-2-glycoprotein I (anti-β2GPI) promote inflammation and thrombosis in antiphospholipid syndrome (APS). It has been shown that anti-β2GPI activate neutrophils through Toll-like receptor…
  • Abstract Number: 0810 • ACR Convergence 2025

    Spatial Transcriptomic-based Phenotyping of the Fibroblast Niches in Systemic Sclerosis-associated Primary Heart Involvement

    Alexandru Micu1, Alexandru-Emil Matei2, Yi-Nan Li3, Ann-Christin Pecher4, Tim Filla5, Jörg Henes6, Markus Eckstein7, Karin Klingel8, Jörg Distler9 and Andrea-Hermina Györfi10, 1Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University. Hiller Research Center, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University, Düsseldorf, Germany, 2Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University. Hiller Research Center, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University. Fraunhofer Institute for Translational Medicine and Pharmacology ITMP, and Fraunhofer Cluster of Excellence for Immune Mediated Diseases CIMD, Frankfurt am Main, Germany, Düsseldorf, Germany, 3University Hospital of Düsseldorf, Düsseldorf, Germany, 4Department of Internal Medicine II, Hematology, Oncology, Clinical Immunology, and Rheumatology, University Hospital Tübingen, Tübingen, Germany, 5Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University. Hiller Research Center, University Hospital Düsseldorf, Medical Faculty of Heinrich-Heine University., Düsseldorf, Germany, 6Department of Internal Medicine II, Hematology, Oncology, Clinical Immunology, and Rheumatology, University Hospital Tübingen, Tuebingen, Germany, 7Institute of Pathology and Comprehensive Cancer Center EMN, Friedrich-Alexander- Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 8Cardiopathology, Institute for Pathology, Eberhard-Karls-Universität Tübingen, Tübingen, Germany, 9University Hospital Duesseldorf and HHU, Duesseldorf, Germany, 10Department of Rheumatology, University Hospital Düsseldorf, Medical Faculty of Heinrich Heine University., Düsseldorf, Germany

    Background/Purpose: Systemic sclerosis (SSc)-associated primary heart involvement (SSc-pHI) is one of the leading causes of mortality in SSc, yet its underlying cellular and molecular pathomechanisms…
  • Abstract Number: 0808 • ACR Convergence 2025

    Spatial Transcriptomics Show Fibroblast LIF Receptor Drives Fibrosis in Systemic Sclerosis

    Mari Kamiya1, Hung Nguyen1, Miles Tran2, Ce Gao3, Sergio Poli1, Yunju Jeong4, Louis Merriam5, Jinjun Shi6, Rachel Knipe7, Katharine Black8, Lida Hariri9, Carol Feghali-Bostwick10, Rodney Infante11, Janelle Pugashetti12, Justin Oldham12, Ilya Korsunsky13, Kevin Wei14 and Edy Kim1, 1Division of Pulmonary and Critical Care Medicine, Department of Medicine (DOM), Brigham and Women's Hospital (BWH); Harvard Medical School, Boston, MA, 2Brigham and Women's Hospital, Boston, MA, 3Division of Rheumatology, Inflammation and Immunity, DOM, BWH; Harvard Medical School, Boston, MA, 4Division of Pulmonary and Critical Care Medicine, Department of Medicine (DOM), Brigham and Women's Hospital (BWH), Harvard Medical School, Boston, MA, United States; Department of Food and Nutrition, College of Human Ecology, Kyung Hee University, Seoul, Republic of Korea, 5Division of Pulmonary and Critical Care Medicine, Department of Medicine (DOM), Brigham and Women's Hospital (BWH), Boston, MA, 6Center for Nanomedicine and Department of Anesthesiology, Perioperative and Pain Medicine, Brigham and Women's Hospital (BWH); Harvard Medical School, Boston, MA, 7Division of Pulmonary and Critical Care Medicine, DOM, Massachusetts General Hospital; Center for Immunology and Inflammatory Diseases, Massachusetts General Hospital; Harvard Medical School, Boston, MA, 8Division of Pulmonary and Critical Care Medicine, DOM, Massachusetts General Hospital; Harvard Medical School, Boston, MA, 9Department of Pathology, Massachusetts General Hospital; Division of Pulmonary and Critical Care Medicine, DOM, Massachusetts General Hospital; Harvard Medical School, Boston, MA, 10Medical University of South Carolina, Charleston, SC, 11Center for Human Nutrition, Dept. of Molecular Genetics, DOM, University of Texas Southwestern, Dallas, TX, 12Division of Pulmonary and Critical Care Medicine, University of Michigan, Ann Arbor, MI, 13Division of Rheumatology, Inflammation and Immunity, DOM, BWH; Division of Genetics, DOM, BWH; Harvard Medical School, Boston, MA, 14Brigham and Women's Hospital at Harvard Medical School, Boston, MA

    Background/Purpose: Systemic sclerosis (SSc) is an autoimmune, fibroinflammatory disease of skin and visceral organs. Current SSc therapies have limited efficacy for progressive fibrosis. Our prior…
  • Abstract Number: 0797 • ACR Convergence 2025

    Spatial transcriptomics identifies density-sensing fibroblasts in synovial lining

    Sonia Presti1, Kseniia Anufrieva2, Ce Gao3, Sean Prell2, Philip Blazar2, Jeffrey Lange2, Morgan Jones2, Mihir Wechalekar4, Michael Brenner2, Ilya Korsunsky5, Shideh Kazerounian2 and Kevin Wei6, 1Standford University, Stanford, 2Mass General Brigham, Boston, 3Division of Rheumatology, Inflammation and Immunity, DOM, BWH; Harvard Medical School, Boston, MA, 4Flinders Medical Centre, Adelaide, Australia, 5Division of Rheumatology, Inflammation and Immunity, DOM, BWH; Division of Genetics, DOM, BWH; Harvard Medical School, Boston, MA, 6Brigham and Women's Hospital at Harvard Medical School, Boston, MA

    Background/Purpose: The synovial lining is crucial for joint homeostasis, forming a barrier and producing lubricants through specialized fibroblasts. These fibroblasts differ from sublining fibroblasts, which…
  • Abstract Number: 0020 • ACR Convergence 2025

    Bulk RNA-sequencing of Leukocytoclastic Vasculitis Skin Biopsies Show Upregulation of Leukocyte Migration Genes

    Anne Carlton, Lam Tsoi, Joseph Kirma, Jennifer Fox, Paul Harms and Johann Gudjonsson, University of Michigan, Ann Arbor, MI

    Background/Purpose: Vasculitis encompasses multiple conditions united by end-organ damage due to an immune-mediated reaction against the vasculature. Leukocytoclastic vasculitis (LCV) is a subtype of cutaneous…
  • Abstract Number: 0586 • ACR Convergence 2025

    Immune Checkpoint agonists: A New horizon for treatment of psoriatic arthritis

    Siba Raychaudhuri1, Christine Abria2 and Smriti K Raychaudhuri3, 1UC Davis, School of Medicine/ VA Medical Center, Sacramento, Davis, CA, 2Sacramento VA Medical Center, Mather, CA, 3Sacramento VA Medical Center, Davis, CA

    Background/Purpose: Check point inhibitor PD-1 (programmed death protein 1) is upregulated during T lymphocyte activation and is important for limiting the duration of activation. Thus,…
  • Abstract Number: 0932 • ACR Convergence 2024

    IRAK4 Degrader GS-6791 Inhibits TLR and IL-1R-Driven Inflammatory Signaling, and Ameliorates Disease in a Preclinical Arthritis Model

    Grace Teng1, Thomas Fung2, Annamaria Mocciaro2, Ceyda Llapashtica1, Angie Hammond3, Jesse Gurgel4, zhiyu Huang1, Maria Mouchess1, Vanessa Gorney5, Wesley Minto1, Sunish Mohanan1, Adam Schrier1, Wylie Palmer2, Alexandra Borodovsky2 and Gundula Min-oo1, 1Gilead Sciences, Foster City, CA, 2Nurix Therapeutics, San Francisco, CA, 3Gilead Sciences, Inc., Seattle, WA, 4Gilead Sciences, Seattle, CA, 5Alterome Therapeutics, San Diego, CA

    Background/Purpose: Despite advances in treatment, chronic inflammatory diseases such as rheumatoid arthritis (RA) represent areas of high unmet medical need. IRAK4 is a proximal mediator…
  • Abstract Number: 2596 • ACR Convergence 2024

    Clock Gene Bmal1 Contributes to Inflammation via Phosphorylation of NF-κB/p65 in RA-FLS

    Hikari Tsukamoto1, Kenta Kaneshiro1, Kohsuke Yoshida1, Koji Tateishi2, Yasuhiro Terashima2, Nao Shibanuma3, Yoshitada Sakai4 and Akira Hashiramoto1, 1Kobe University Graduate School of Health Sciences, Kobe, Hyogo, Japan, 2Hakuhokai Kakogawa Hospital, Kakogawa, Hyogo, Japan, 3Kobe Kaisei Hospital, Kobe, Hyogo, Japan, 4Kobe University Graduate School of Medicine, Kobe, Hyogo, Japan

    Background/Purpose: Inflammatory cytokines such as TNF-α, IL-6, and IFN-γ show their peaks at midnight in sera of patients with rheumatoid arthritis (RA), which is thought…
  • Abstract Number: 0021 • ACR Convergence 2024

    A Novel Small Molecule Screening Assay Using Normal Human Chondrocytes Toward Osteoarthritis Drug Discovery

    Philip Coryell1, Kenneth Pearce2, Paul Hardy2, Susan Chubinskaya3 and Richard Loeser4, 1University of North Carolina-Chapel Hill, Chapel, NC, 2University of North Carolina-Chapel Hill, Chapel Hill, NC, 3University of Texas Medical Branch, Galveston, TX, 4University of North Carolina, Chapel Hill, NC

    Background/Purpose: A central feature of osteoarthritis (OA) is progressive cartilage degradation driven by increased production of matrix degrading enzymes including MMP-13. There is a critical…
  • Abstract Number: 0023 • ACR Convergence 2024

    Adenosine and Guanosine-based Oligonucleotide Attenuates Catabolic Phenotypes in Chondrocytes and Slows Progression of Surgically Induced Osteoarthritis

    Yoonhee Kim1, Jin Han2 and Seungwoo Han3, 1Kyungpook National University School of Medicine, Buk-gu, Daegu, Republic of Korea, 2Kyungpook National University, Buk-gu, Daegu, Republic of Korea, 3Kyungpook national university hospital, Daegu, South Korea

    Background/Purpose: Adenosine is a potent endogenous modulator of inflammation; however, its clinical application is limited due to its extremely short half-life in blood. In this…
  • Abstract Number: 0038 • ACR Convergence 2024

    The Role of Dual Specificity Phosphatase 22 (DUSP22) in Rheumatoid Arthritis: Mechanism and Genetic Investigations

    Wei-Ting Hung1, Yi-Ming Chen2, Wen-Nan Huang3, Tsai-Hung Yen4, Tse-Hua Tan5 and Huai-Chia Chuang6, 1Taichung Veteran General Hospital, Taichung City, Taiwan (Republic of China), 2Taichung Veterans General Hospital, Taiwan, Taichung, Taiwan (Republic of China), 3Taichung Veterans General Hospital, Taichung, Taiwan, Taichung, Taiwan (Republic of China), 4Taichung Veterans General Hospital, Xitun District, Taichung City, Taiwan (Republic of China), 5National Health Research Institutes, Mao-Li, Taiwan (Republic of China), 6National Health Research Institutes, Zhunan, Taiwan (Republic of China)

    Background/Purpose: Rheumatoid arthritis (RA) is a debilitating autoimmune disorder characterized by chronic inflammation and joint damage. This study investigates the role of Dual Specificity Phosphatase…
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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.).

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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