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
  • Abstract Number: 793 • 2015 ACR/ARHP Annual Meeting

    Mesenchymal Stem Cells Promote the Generation of CD206+ Macrophage and Increase Its Phagocytic Activity in Systemic Lupus Erythematosus

    Wei Deng, Weiwei Chen, Zhuoya Zhang, Saisai Huang, Wei Kong, Yue Sun, Xuebing Feng, Xiaojun Tang, Genhong Yao and Lingyun Sun, Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China

    Background/Purpose: Umbilical cord (UC)-derived mesenchymal stem cells (MSCs) have been confirmed to exert therapeutic effects on systemic lupus erythematosus (SLE). Deficiency in SLE macrophages exhibits…
  • Abstract Number: 794 • 2015 ACR/ARHP Annual Meeting

    CD163+ Macrophages Display Mixed Polarizations in Discoid Lupus Skin

    Benjamin Chong1, Lin-chiang Tseng1, Gregory Hosler2, Noelle Teske1, Song Zhang3, David R. Karp4, Nancy J. Olsen5 and Chandra Mohan6, 1Dermatology, University of Texas Southwestern Medical Center, Dallas, TX, 2Propath, Dallas, TX, 3Clinical Sciences, University of Texas Southwestern Medical Center, Dallas, TX, 4UT Southwestern Medical Center, Dallas, TX, 5Divsion of Rheumatology, Department of Medicine, Penn State MS Hershey Medical Center, Hershey, PA, 6Biomedical Engineering, University of Houston, Houston, TX

    Background/Purpose: Discoid lupus erythematosus (DLE) is the most common form of chronic cutaneous lupus. Lesional skin of DLE patients contains macrophages that may transition from…
  • Abstract Number: 795 • 2015 ACR/ARHP Annual Meeting

    High Mobility Group Box-1 (HMGB1) Affects Macrophage Polarization and Phagocytosis in Systemic Lupus Erythematosus Patients

    Fleur Schaper1, Gerda Horst1, Karina de Leeuw1, Hendrika Bootsma1, Pieter C Limburg2, Peter Heeringa3, Marc Bijl4 and Johanna Westra5, 1Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands, 2Laboratory Medicine, University Medical Center Groningen, University of Groningen, Groningen, Netherlands, 3Pathology and Medical Biology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands, 4Internal Medicine and Rheumatology, Martini Hospital, Groningen, Netherlands, 5Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands

    High mobility group box-1 (HMGB1) affects macrophage polarization and phagocytosis in systemic lupus erythematosus patients. F Schaper, G Horst, K de Leeuw, H Bootsma, PC…
  • Abstract Number: 796 • 2015 ACR/ARHP Annual Meeting

    Single Cell Gene Expression Studies in Lupus Patient Monocytes Reveal a Unique Anti-Inflammatory Population of Non-Classical  Monocytes Associated with Clinical Quiescence

    Zhongbo Jin1, Wei Fan2,3, Mark A. Jensen4, Jessica M. Dorschner1, Danielle Vsetecka1, Shreyasee Amin5, Ashima Makol6, Floranne C. Ernste7, Thomas Osborn7, Kevin G. Moder5, Vaidehi Chowdhary5 and Timothy B. Niewold1, 1Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 2Department of Rheumatology, Ren Ji Hospital, School of Medicine, Shanghai Jiao Tong University, China, Shanghai, China, 3Mayo Clinic, Rochester, MN, 4Divsion of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 5Rheumatology, Mayo Clinic, Rochester, MN, 6Division of Rheumatology, Department of Internal Medicine, Mayo Clinic, Rochester, MN, 7Division of Rheumatology, Mayo Clinic, Rochester, MN

    Background/Purpose: Our previous gene expression studies in sorted immune cell populations in SLE has shown that different cell types from the same blood sample demonstrate…
  • Abstract Number: 797 • 2015 ACR/ARHP Annual Meeting

    Divergent Phenotypic Patterns Between Systemic Lupus Erythematosus and Healthy Anti-Nuclear Antibody Positive Individuals Reveal Distinct Differences in B Cell and Myeloid Populations Among Ethnicities

    Samantha Slight-Webb1, Rufei Lu2, Holden T. Maecker3, Paul J. Utz4, Joel M. Guthridge1 and Judith A. James5, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Division of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 4Medicine, Stanford University School of Medicine, Stanford, CA, 5Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disorder that arises from genetic and environmental factors. Thus, patients with different ancestral backgrounds display differences in…
  • Abstract Number: 798 • 2015 ACR/ARHP Annual Meeting

    Keratinocyte-Associated IL-6 Is Elevated in Cutaneous Lupus Rashes and Production of IL-6 By Keratinocytes Is Enhanced in Non-Involved Lupus Skin

    Jasmine Stannard1, Emily Myers2, Tamra J. Reed3, Lori Lowe4 and J. Michelle Kahlenberg5, 1Int. Medicine/Rheumatology, University of Michigan, Ann Arbor, MI, 2Georgetown University, Washington, DC, 3Internal Medicine, Rheumatology, University of Michigan, Ann Arbor, MI, 4Dermatology, University of Michigan, Ann Arbor, MI, 5Internal Medicine, Division of Rheumatology, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: Systemic lupus erythematosus (SLE) is a devastating autoimmune disease with severe complications such as immune-complex mediated nephritis and scarring skin lesions.  Treatment modalities for…
  • Abstract Number: 799 • 2015 ACR/ARHP Annual Meeting

    Transcriptional Profiling of Cutaneous Lupus Reveals Pronounced Changes in Keratinocyte and Myeloid Lineage Expressed Genes and Demonstrates Uniquely Regulated Interferon Pathways Between Rash Subtypes

    Celine C. Berthier1, Jasmine Stannard2, Emily Myers3, William Swindell4, Lori Lowe4, Tamra J. Reed5, Johann Gudjonsson4 and J. Michelle Kahlenberg6, 1Nephrology, Division of Nephrology, University of Michigan Medical Center, Ann Arbor, MI, 2Int. Medicine/Rheumatology, University of Michigan, Ann Arbor, MI, 3Internal Medicine, Rheumatology, Georgetown University, Washington, DC, 4Dermatology, University of Michigan, Ann Arbor, MI, 5Internal Medicine, Rheumatology, University of Michigan, Ann Arbor, MI, 6Internal Medicine, Division of Rheumatology, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: Cutaneous lupus rashes can be substantial, disfiguring, and often refractory to usual lupus therapies.  Phenotypic presentation and risk of systemic lupus manifestations differs by…
  • Abstract Number: 800 • 2015 ACR/ARHP Annual Meeting

    A High-Throughput System for Quantification of in Vitro Neutrophil Extracellular Trap Formation with Fluorescence Immunocytochemistry

    Tineke Kraaij1, Sylvia Kamerling1, Ton Rabelink1, René E. M. Toes2, Cees van Kooten1 and Onno Teng1, 1Nephrology, LUMC, Leiden, Netherlands, 2Rheumatology, Leiden University Medical Center, Leiden, Netherlands

    Background/Purpose: Neutrophil extracellular traps (NETs) consist of decondensed chromatin and antimicrobial peptides and are able to trap and kill pathogens. Several studies suggest a pathogenic…
  • Abstract Number: 801 • 2015 ACR/ARHP Annual Meeting

    Artesunate Modulates Atherosclerosis Related Factors through the Inhibition of STAT1

    Xuebing Feng1, Weiwei Chen2, Lihui Xiao1 and Lingyun Sun2, 1Department of Rheumatology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China, 2Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China

    Background/Purpose: While type I interferon (IFN) has been linked to atherosclerosis progression in systemic lupus erythematosus (SLE), little is known about its regulation and intervention.…
  • Abstract Number: 802 • 2015 ACR/ARHP Annual Meeting

    Identification of Cyclin-Dependent Kinase 1 As a Novel Regulator for Controlling Type I Interferon Signaling in Systemic Lupus Erythematosus

    Lingling Wu1, Bo Qu1, Yuting Qin1 and Nan Shen1,2, 1Shanghai Institute of Rheumatology,Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, 2The Center for Autoimmune Genomics and Etiology (CAGE),Cincinnati Children’s Hospital Medical Center,Cincinnati, Ohio, United States of America, Cincinnati, OH

    Background/Purpose: Type I interferon (IFN) signaling has been  a central pathogenic pathway in systemic lupus erythematosus (SLE). The application of specific inhibitors of IFN  pathway has emerged…
  • Abstract Number: 803 • 2015 ACR/ARHP Annual Meeting

    Interferon-Alpha Mediated Lowering of Pentraxin-3 Levels in Systemic Lupus Erythematosus?

    Lina Wirestam1, Helena Enocsson2, Christopher Sjöwall2, Thomas Skogh2, Maija-Leena Eloranta3, Lars Rönnblom3 and Jonas Wetterö2, 1Department of Clinical & Experimental Medicine, Rheumatology/AIR, Linkoping, Sweden, 2Department of Clinical and Experimental Medicine, Rheumatology/AIR, Linköping, Sweden, 3Medical Sciences, Rheumatology clinic, Uppsala, Sweden

    Background/Purpose: The type I interferon (IFN) system is important in the pathogenesis of systemic lupus erythematosus (SLE). We have previously shown an inhibitory effect of…
  • Abstract Number: 804 • 2015 ACR/ARHP Annual Meeting

    Prolactin Induces Interferon Regulatory Factor 1 Activation and Histone H4 Hyperacetylation in Primary Monocytes Comparable to Changes Seen in Monocytes from Systemic Lupus Erythematosus Patients

    Yiu Tak Leung1, Kathleen E. Sullivan2, Kelly Maurer3, Li Song4 and Lihua Shi3, 1Medicine/Rheumatology, University of Pennsylvania, Philadelphia, PA, 2Allergy Immunology, The Children's Hospital of Philadelphia, Philadelphia, PA, 3Immunology ARC 1216, The Children's Hospital of Philadelphia, Philadelphia, PA, 4Allergy Immunology, Children's Hospital of Philadelphia, Philadelphia, PA

    Background/Purpose: : Epigenetic changes have been described in systemic lupus erythematosus (SLE) and offer a potential explanation for the chronicity of disease. We previously found…
  • Abstract Number: 805 • 2015 ACR/ARHP Annual Meeting

    Interferon Activity in Early and Established SLE: Interferon Score Is Lower in Early Disease and Not Seen without Antibodies to Extractable Nuclear Antigens

    Alaa A A Mohamed1,2,3, Md Yuzaiful Md Yusof1,4, Yasser El-Sherbiny5, Paul Emery5,6 and Edward M. Vital2,5, 1Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom, 2NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom, 3Rheumatology and Rhabilitation, Assiut University, Assiut, Egypt, 4NIHR Leeds Musculoskeletal Biomedical Research Unit,Leeds Teaching Hospital NHS Trust, Leeds University, Leeds, United Kingdom, 5Leeds Institute of Rheumatic and Musculoskeletal Medicine, Leeds University, Leeds, United Kingdom, 63. NIHR Leeds Musculoskeletal Biomedical Research Unit, Leeds Teaching Hospital NHS Trust, Leeds University, Leeds, United Kingdom

    Background/Purpose: SLE patients have increased expression of interferon-stimulated genes (ISG) and multiple autoantibodies.  Some patients initially present with early incomplete SLE (E-ILE) with ANA but…
  • Abstract Number: 806 • 2015 ACR/ARHP Annual Meeting

    STAT1 Activation Promotes TLR8 Overexpression and Facilitates Mirokine Signaling Via Exosomes Containing a Mir-21 Endogenous Ligand: A Novel Innate Inflammatory Pathway in Systemic Lupus Erythematosus

    Giancarlo R. Valiente1,2, Nicholas A. Young2, Lai-Chu Wu3,4, Jeffrey Hampton5, Mary Severin6, Amy Lovett-Racke6 and Wael N. Jarjour7, 1Medical Scientist Training Program, The Ohio State University College of Medicine, Columbus, OH, 2Rheumatology & Immunology, The Ohio State University Wexner Medical Center, Columbus, OH, 3Immunology and Rheumatology, The Ohio State University Wexner Medical Center, Columbus, OH, 4Biological Chemistry and Pharmacology, The Ohio State University College of Medicine, Columbus, OH, 5Immunology and Rheumatoloty, The Ohio State University Wexner Medical Center, Columbus, OH, 6Microbial Infection and Immunity, The Ohio State University College of Medicine, Columbus, OH, 7Dept of Rheumatology/Medicine, The Ohio State University Wexner Medical Center, Columbus, OH

    Background/Purpose: The adaptive arm of the immune system plays a significant role in the pathophysiology of Systemic Lupus Erythematosus (SLE). However, recent studies suggest that…
  • Abstract Number: 807 • 2015 ACR/ARHP Annual Meeting

    High Levels of Serum IFN-Alpha Mark a Subgroup of SLE Patients with Distinct Immunophenotypic Features and Hyperresponsiveness to Toll-like Receptor Stimulation

    Uma Thanarajasingam1, Mark A. Jensen2, Jessica M. Dorschner3 and Timothy B. Niewold3, 1Division of Rheumatology, Mayo Clinic, Rochester, MN, 2Divsion of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 3Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN

    Background/Purpose: IFN-alpha is a pathogenic factor in SLE.  High serum interferon activity (IFN-high) marks a subgroup of SLE patients strongly associated with increased disease severity…
  • « Previous Page
  • 1
  • …
  • 1922
  • 1923
  • 1924
  • 1925
  • 1926
  • …
  • 2607
  • 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