ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • 2026 ACR/ARP PRSYM
    • 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 "Monocytes/macrophages"

  • Abstract Number: 1651 • ACR Convergence 2025

    Compound Heterozygosity for the Ile692del and Val726Ala Pathogenic MEFV Variants and Elevated IL-18 (CHIVE-18 syndrome) Is Distinct from Familial Mediterranean Fever (FMF) and Includes a Pronounced Response to Interferon Stimulation in Myeloid Cell Populations

    Mary Maclean1, Sabrina Helmold Hait2, Cindy Phung3, Deborah Stone4, Sophie georgin-Lavialle5, Scott Canna6, Carl Esperanzate7, Amanda Ombrello8, Daniel Kastner9, Ivona Aksentijevich10 and Massimo Gadina11, 1NIH-NIAMS, Rockville, MD, 2NIAMS/NIH, Bethesda, MD, 3National Institute of Arthritis, Musculoskeletal, and Skin Diseases (NIAMS), Bethesda, MD, 4NIH, Bethesda, MD, 5Sorbonne university, Tenon hospital, DMU3ID, CEREMAIA, ERN RITA, Paris, France, 6Children's Hospital of Philadelphia, Philadelphia, PA, 7National Human Genome research Institute (NHGRI), National Institutes of Health (NIH), Bethesda, MD, 8National Institutes of Health, Rockville, MD, 9National Human Genome Research Institute, Bethesda, MD, 10100, Bethesda, MD, 11National Institute of Arthritis Musculoskeletal and Skin diseases, Bethesda, MD

    Background/Purpose: Familial Mediterranean fever (FMF) is an autoinflammatory disease associated with biallelic pathogenic variants in the MEFV gene encoding the myeloid-restricted inflammasome sensor pyrin. The…
  • Abstract Number: 1682 • ACR Convergence 2025

    Sjögren’s Disease Salivary Gland Fibroblast Subsets are Proinflammatory and Aberrantly Promote Pain

    Sara McCoy1, Rachael Bogle2, michele larsen3, Li Chen4, thomas pranzatelli5, Paola Perez6, john chiorini7, Alan Baer8, A. Darise Farris9, Christopher Lessard9, Astrid Rasmussen9, Caroline Shiboski10, Stephen Shiboski10, Alexander Mikesell3, Zachary Campbell3, Alex Tsoi2, Johann Gudjonsson11 and Blake M. Warner12, 1University of Wisconsin–Madison, Madison, WI, 2University of Michigan, Holland, OH, 3University of Wisconsin, Madison, 4University of Michigan, Ann Arbor, 5NIH, Bethesda, 6NIDCR, Bethesda, MD, 7NIH, bethesda, MD, 8Johns Hopkins University School of Medicine, Baltimore, MD, 9Oklahoma Medical Research Foundation, Oklahoma City, OK, 10University of California San Francisco, San Francisco, CA, 11University of Michigan, Ann Arbor, MI, 12National Institutes of Health, Bethesda, MD

    Background/Purpose: Fibroblasts (fb) are increasingly recognized as dynamic signaling hubs in rheumatic disease, yet their contribution to Sjögren Disease (SjD) remains poorly defined. We dissect…
  • Abstract Number: 1757 • ACR Convergence 2025

    Skin-to-Joint Immune Cell Migration and Synovial Reprogramming in Psoriatic Arthritis Onset

    Maria Gabriella Raimondo1, Hashem Mohammadian2, Mario Angeli2, Vladyslav Fedorchenko2, Kaiyue Huang3, Yi-Nan Li4, Raphael Micheroli5, Jörg Distler6, Ursula Fearon7, Juergen Rech2, Francesco Ciccia8, Juan Cañete9, Adam Croft10, Mariola Kurowska-Stolarska11, Stefano Alivernini12, Maria Antonietta D'Agostino13, Georg Schett2, Simon Rauber14 and Andreas Ramming15, 1Department of Medicine 3 - Rheumatology and Immunology, Friedrich-Alexander-Universität (FAU) Erlangen-Nürnberg and Uniklinikum Erlangen, Erlangen, Germany, 2Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Germany, 3Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, 4University Hospital of Düsseldorf, Düsseldorf, Germany, 5University Hospital Zurich, Zurich, Switzerland, 6University Hospital Duesseldorf and HHU, Duesseldorf, Germany, 7Trinity College Dublin, Dublin, Dublin, Ireland, 8Rheumatology Section, University of Campania L. Vanvitelli, Naples, Italy, Naples, Italy, 9Rheumatology Department, Hospital Clínic and IDIBAPS, Barcelona, Spain, Barcelona, Spain, 10University of Birmingham, Hagley, Stourbridge, United Kingdom, 11University of Glasgow, Glasgow, 12Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, 13Division of Rheumatology and Clinical Immunology - Università Cattolica del Sacro Cuore, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy, 14Uniklinikum Erlangen, Friedrich-Alexander-Universität Erlangen-Nürnberg, Germany, Erlangen, Bayern, Germany, 15Department of Internal Medicine 3, Rheumatology & Immunology, Friedrich-Alexander-University (FAU) & Universitätsklinikum Erlangen, Erlangen, Germany

    Background/Purpose: Psoriatic arthritis (PsA) develops in about 30% of individuals with psoriasis (PsO), highlighting a critical connection between skin and joint inflammation. However, the mechanisms…
  • Abstract Number: 0025 • ACR Convergence 2025

    Expansion and Transcriptional Reprogramming of CD14⁺ and CD16⁺ Monocytes in Behçet’s Disease

    Elio Carmona1, Rabia Deniz2, Cemal Bes3, Haner Direskeneli4, Ahmet Gul5 and Amr Sawalha6, 1Division of Pediatric Rheumatology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA, Pittsburgh, 2University of Health Sciences Basaksehir Çam and Sakura City Hospital, Istanbul, Turkey, 3University of Health Sciences, Basaksehir Çam and Sakura City Hospital, Istanbul, Turkey, 4Marmara University, ISTANBUL, Turkey, 5Istanbul University, Istanbul, Turkey, 6University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Behçet’s disease (BD) is a chronic, relapsing inflammatory disease characterized by complex immunopathogenesis and limited treatment options. Monocytes are known to play a significant…
  • Abstract Number: 1768 • ACR Convergence 2025

    TREM-1 and TREM-2 Define Inflammatory and Protective Axes in ANCA-Associated Glomerulonephritis

    Lea Dionet1, Alexandre Lanau2, Paul Breillat3, Quentin Delcros4, Federica Pallotti5, Margot Poux6, Pierre Isnard1, Arthur Lavigne4, Xavier Puéchal7, alexandre karras8, Jean-Paul Duong9, Olivia Lenoir10, Pierre-Louis Tharaux11 and Benjamin Terrier12, 1INSERM, Paris, France, 2Institut Curie, Paris, France, 3INSERM, PARIS 17, Ile-de-France, France, 4AP-HP, Paris, France, 5Internal Medicine and Clinical Immunology, Rennes, France, 6Université de Paris, PARIS 04EME, France, 7Department of Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hospital Cochin, and Université Paris Cité, Paris ( 75014 ), Ile-de-France, France, 8HEGP - assistance publique hopitaux de paris, paris, France, 9INSERM, Paris, 10Paris Cardiovascular Research Center, Université Paris Cité, INSERM U970, Paris, France, PARIS, Ile-de-France, France, 11Paris Cardiovascular Research Center, Université Paris Cité, INSERM U970, Paris, France, PARIS, France, 12Cochin Hospital, Paris, France

    Background/Purpose: ANCA-associated vasculitis (AAV) is a small-vessel vasculitis that can lead to life-threatening renal injury. Neutrophils, monocytes and macrophages play a pivotal role not only…
  • Abstract Number: 0047 • ACR Convergence 2025

    Monocyte Transcriptomic Signatures Uncover Potential Pathogenic Mechanisms of the APOL1 High Risk Genotype (HRG)

    Vishnuprabu Pandian1, Adebola Agboola1, Sivasubramanian ramani2, Christele Felix3, Andrra Nimoni3, Jasmin Divers4, Timothy Niewold5 and Ashira Blazer2, 1University of Maryland, Baltimore, Baltimore, Maryland, 2University of Maryland Baltimore, Baltimore, Maryland, 3Hospital for Special Surgery, New York, NY, 4NYU Grossman Long Island School of Medicine, New York, New York, 5Hospital for Special Surgery, New York, New York

    Background/Purpose: Compared to the low-risk genotype (LRG) the APOL1 high-risk genotype (HRG) confers an increased risk of end stage kidney disease among individuals with systemic…
  • Abstract Number: 1812 • ACR Convergence 2025

    Inflammasome and UPR activation in monocytes of HLA B27 positive children with Enthesitis related arthritis category of JIA

    Shivika Guleria1 and Amita Aggarwal2, 1SGPGIMS, Lucknow, Lucknow, Uttar Pradesh, India, 2Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India, Lucknow, Uttar Pradesh, India

    Background/Purpose: Enthesitis related arthritis (ERA) is a chronic immune-inflammatory disease with unknown etiology. HLA-B27 is the strongest risk factor predisposing to ERA like Spondyloarthritis (SpA).…
  • Abstract Number: 0066 • ACR Convergence 2025

    RA-required synovial tissue-resident monocyte lineage cells are comprised of three distinct subpopulations.

    Yidan Wang1, Samuel Dowling2, Jessica Maciuch2, Vanessa Manada De Lobos2, Meghan Mayer2, Kainat Mian1, Tyler Therron3, Hadijat Makinde1, Carla Marie Cuda1, Deborah Rachelle Winter4 and Harris R Perlman1, 1Northwestern University, Chicago, IL, 2Northwestern University, Chicago, 3Northwestern Feinberg School of Medicine, Chicago, IL, 4Northwestern University, Skokie, IL

    Background/Purpose: Tissue-resident monocyte-lineage cell (TRMC) are an extravascular population distinct from circulating monocytes and synovial macrophages and are critical for the development of inflammatory arthritis.…
  • Abstract Number: 1828 • ACR Convergence 2025

    CD14+CXCL10+Monocytes Remodel the Peripheral Immune Network in sJIA via UBE2D1-Driven Inflammatory Programming

    Xuemei Tang1, Qiang Luo2, Jun Yang3, Haiguo Yu4, Xinglin Wu1, Xiwen Luo5, Xi Yang5, Zhiyong Zhang5, Yunfei An5, Xiaodong Zhao1 and Hongmei Song6, 1Department of Rheumatology and Immunology, Children's Hospital of Chongqing Medical University, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, Chongqing, China, Chongqing, China (People's Republic), 2Department of Rheumatology and Immunology, Children’s Hospital of Chongqing Medical University, Chongqing Key Laboratory of Child Rare Diseases in Infection and Immunity, National Clinical Research Center for Child Health and Disorders, Ministry of Education Key Laboratory of Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing, China (People's Republic), 3Rheumatology and Immunology Department of Shenzhen Children's Hospital, Shenzhen, 518100, China., Shenzhen, China (People's Republic), 4Department of Rheumatology and Immunology, Nanjing Children's Hospital, Nanjing, 210000, China., Nanjing, China (People's Republic), 5Department of Rheumatology & Immunology, Children’s Hospital of Chongqing Medical University, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, National Clinical Research Center for Child Health and Disorders (Chongqing), Ministry of Education Key Laboratory of Child Development and Disorders, Chongqing Key Laboratory of Child Infection and Immunity, Chongqing, China., Chongqing, China (People's Republic), 6Pediatric Department of Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, 100000, China., Beijing, China (People's Republic)

    Background/Purpose: Systemic juvenile idiopathic arthritis (sJIA) is an autoinflammatory disorder characterized by systemic immune dysregulation. However, reliable biomarkers to predict its unpredictable disease course are…
  • Abstract Number: 0098 • ACR Convergence 2025

    The Deubiquitinase TRABID is a Regulator of Osteogenesis and Inflammation in Spondyloarthritis:

    Archita Srinath1, Sungsin Jo2, Daniele Mauro3, Mariia Korshko4, Mansi Aparnathi5, Shaghayegh Foroozan Boroojeni6, Tae-Hwan Kim7, Francesco Ciccia8 and Nigil Haroon9, 1University of Toronto, Toronto, ON, Canada, 2Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea, 3University of Campania, Italy, Naples, Italy, 4UHN, Toronto, ON, Canada, 5Schroeder Arthritis Institute, University Health Network, Toronto, ON, Canada, 6University Health Network/University of Toronto, Toronto, ON, Canada, 7Department of Rheumatology, Hanyang University Hospital for Rheumatic Diseases, Seoul, Republic of Korea, 8University of Campania, Naples, Italy, 9Department of Medicine/Rheumatology, University Health Network, Schroeder Arthritis Institute, University of Toronto, Toronto, ON, Canada

    Background/Purpose: Axial Spondyloarthritis (AxSpA) is characterized by both inflammation and new bone formation. Current therapeutic targets aim to control inflammation, however over 40% of patients…
  • Abstract Number: 1831 • ACR Convergence 2025

    Distinct Proteomic Signature Predicts Post-MMF Withdrawal Flares in Systemic Lupus Erythematosus Patients

    Christian Wright1, Miles Smith2, Rufei Lu2, Catriona Wagner3, Aleksandra Bylinska2, Carla Guthridge2, Nicholas Domingez2, Susan Macwana2, Wade DeJager4, Marci Beel5, Joan Merrill6, Eliza Chakravarty2, Ellen Goldmuntz7, Study Team ALE06 Clinical8, Judith James2 and Joel Guthridge2, 1University of Oklahoma Health Sciences Center, Oklahoma City, OK, 2Oklahoma Medical Research Foundation, Oklahoma city, OK, 3Oklahoma Medical Research Foundation, Santa Cruz, CA, 4Oklahoma Medical Research Foundation, Oklahoma City, 5Oklahoma Medical Research Foun, Oklahoma City, OK, 6Oklahoma Medical Research Foundation, Oklahoma City 73104, OK, 7NIAID/ NIH, Washington, DC, 8Autoimmunity Center of Excellence, Oklahoma City, OK

    Background/Purpose: : Systemic Lupus Erythematosus (SLE) follows a characteristic relapsing-remitting course with unpredictable flares interspersed with periods of relative quiescence. Mycophenolate mofetil (MMF) has emerged…
  • 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: 1421 • ACR Convergence 2024

    Differential Impact of B-cell Targeted Monotherapy and Combination Regimen on the Peripheral Blood Transcriptome of Adults with Active Sjögren Disease

    Coziana Ciurtin1, Lucia Martin-Gutierrez1, John Casement2, Kyle Thompson3, Fai Ng4, Andre van Maurik5 and Elizabeth Jury1, 1University College London, London, United Kingdom, 2Newcastle University, Newcastle, United Kingdom, 3Newcastle University, Newcastle, England, United Kingdom, 4Newcastle University, Newcastle upon Tyne, England, United Kingdom, 5Precision Medicine, GlaxoSmithKline, Stevenage, United Kingdom

    Background/Purpose: Sjögren disease (SD) is characterised by B-cell hyperactivity associated with increased levels of B-lymphocyte stimulator (BlyS), but there are no effective biologic treatments for…
  • Abstract Number: 1656 • ACR Convergence 2024

    Loss of Nr4a1 Expression Protects Cartilage During Post-traumatic Osteoarthritis

    Katherine Escalera-Rivera, Jennifer Jonason and Jennifer Anolik, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Osteoarthritis (OA) is a complex disease involving pathological processes in joint tissues such as the cartilage and synovium. Cartilage is degraded by matrix metalloproteinases…
  • Abstract Number: 1712 • ACR Convergence 2024

    Transcriptome Analysis Characterizes the Role of Monocytes in Ankylosing Spondylitis with TNF-blocker Treatment

    Yulong Tang1, Jiangnan Xie2, Dachun Zhuo1, Qi ZHU3, Jiucun Wang1 and Jing Liu2, 1Fudan University, Shanghai, China (People's Republic), 2Fudan University, Shanghai, Shanghai, China (People's Republic), 3Shanghai Guanghua Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai, China (People's Republic)

    Background/Purpose: Ankylosing spondylitis (AS) is an autoimmune and auto-inflammatory disease characterized by chronic inflammation of the spine, sacroiliac joint, and occasionally peripheral joints. TNF-α inhibitor…
  • « Previous Page
  • 1
  • 2
  • 3
  • 4
  • …
  • 8
  • 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 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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2026 American College of Rheumatology