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

Abstracts tagged "chemokines"

  • Abstract Number: 338 • 2014 ACR/ARHP Annual Meeting

    Bombina Variegate peptide8/Prokineticin 2: A Novel Arthritis-Inducible Chemokine

    Haruyasu Ito, Ken Yoshida, Kentaro Noda and Daitaro Kurosaka, Internal Medicine, Jikei University School of Medicine, Tokyo, Japan

    Background/Purpose Rheumatoid arthritis (RA) is a chronic inflammatory disorder characterized by the joint destruction. Chemokines play important roles as monocyte and neutrophil recruiters in RA.…
  • Abstract Number: 30 • 2014 ACR/ARHP Annual Meeting

    Inhibiting Autocrine Interleukin-6 (IL-6) Trans-Signalling in Human CD14+VE Monocultures Reduces Osteoclast Differentiation

    Lauren A. Jordan1, Fraser L. Collins2, Simon A. Jones1, Ernest H. Choy3, Ann K. Harvey1 and Anwen S. Williams1, 1Cardiff University, Institute of Infection and Immunity, School of Medicine, Cardiff, United Kingdom, 2Michigan State University, Department of Physiology, East Lansing, MI, 3Section of Rheumatology, Cardiff University, Institute of Infection and Immunity, School of Medicine, Cardiff, United Kingdom

    Background/Purpose: Interleukin-6 (IL-6) and the inflammatory CC-chemokine CCL3 are highly expressed in rheumatoid arthritis, juvenile idiopathic arthritis and multiple myeloma. While these mediators contribute to…
  • Abstract Number: 2877 • 2014 ACR/ARHP Annual Meeting

    Novel Function of Tocilizumab As a Modulator of Interleukin-27-Mediated Anti-Inflammatory Responses

    Misato Hashizume1, Jun Kikuchi2, Keiko Yoshimoto2 and Tsutomu Takeuchi2, 1Product Research Department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan, 2Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose The immunological roles of interleukin 27 (IL-27) have been reported in the function of regulatory T cells (Treg), monocytes and osteoclasts, and these cells…
  • Abstract Number: 2880 • 2014 ACR/ARHP Annual Meeting

    Elevated Levels of Soluble Inflammatory Mediators and Lupus-Specific Connective Tissue Disease Questionnaire Scores Discern Unaffected First Degree Relatives of Lupus Patients from Unaffected Individuals Not Related to Lupus Patients

    Melissa E. Munroe1, Kendra A. Young2, Jennifer Fessler3, Dustin Fife3, Diane L. Kamen4, Joel M. Guthridge3, Timothy B. Niewold5, Michael H. Weisman6, Mariko L. Ishimori6, Daniel J. Wallace7, David R. Karp8, John B. Harley9, Gary S. Gilkeson4, Jill M. Norris2 and Judith A. James10,11, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Epidemiology, Colorado School of Public Health, Aurora, CO, 3Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 5Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 6Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 7Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 8Rheumatic Diseases Division, UT Southwestern Medical Center, Dallas, TX, 9Center for Autoimmune Genomics and Etiology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 10Clinical Arthritis and Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 11Rheumatology, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose: Identifying populations at risk of SLE is essential to curtail inflammatory damage and select individuals for prevention trials. First-degree relatives (FDRs) of lupus patients…
  • Abstract Number: 2692 • 2014 ACR/ARHP Annual Meeting

    Up-Regulated Expression of CXCR4 on Circulating B Cells in Patients with Systemic Lupus Erythematosus

    Hironari Hanaoka1, Yuka Okazaki1, Akinori Hashiguchi2, Hidekata Yasuoka3, Tsutomu Takeuchi1 and Masataka Kuwana1, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Department of Pathology, Keio University School of Medicine, Tokyo, Japan, 3Rheumatology, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose It is increasingly appreciated that circulating B cells are functionally altered and are involved in pathogenic process in patients with systemic lupus erythematosus (SLE).…
  • Abstract Number: 1767 • 2013 ACR/ARHP Annual Meeting

    Gender, Race, and Soluble Mediators Distinguish Blood Relatives Who Develop Incomplete Lupus Or Classified SLE In The Lupus Autoimmunity In Relatives (LAUREL) Study

    Melissa E. Munroe1, Kendra A. Young2, Jill M. Norris2, Joel M. Guthridge3, Diane L. Kamen4, Timothy B. Niewold5, Gary S. Gilkeson4, Michael H. Weisman6, Mariko L. Ishimori6, Daniel J. Wallace7, David R. Karp8, John B. Harley9,10 and Judith A. James11,12, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Epidemiology, Colorado School of Public Health, Aurora, CO, 3Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 5Division of Rheumatology and Department of Immunology, Mayo Clinic, Rochester, MN, 6Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 7Cedars-Sinai Medical Center, Los Angeles, CA, 8Rheumatic Diseases Division, UT Southwestern Medical Center, Dallas, TX, 9Division of Rheumatology and The Center for Autoimmune Genomics & Etiology, University of Cincinnati, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 10US Department of Veterans Affairs Medical Center, Cincinnati, OH, 11Oklahoma Medical Research Foundation, Oklahoma City, OK, 12College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose: Identifying populations at risk of SLE is essential to curtail inflammatory damage and identify individuals for prevention trials. Healthy blood relatives (FDRs) of lupus…
  • Abstract Number: 1602 • 2013 ACR/ARHP Annual Meeting

    Autoantibodies, Cytokines and Chemokines In Serum and Cerebrospinal Fluid Of SLE Patients With Cognitive Dysfunction

    Hilda Fragoso-Loyo1, Alí Duarte-García2, Sandra Juárez-Arellano3, Alba Cicero-Casarrubias4, Juanita Romero-Díaz5, Luis LLorente-Peters1 and Jorge Sánchez-Guerrero6, 1Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico, Mexico, 2Department of Medicine, Tufts Medical Center, Boston, MA, 3Department of Neurology, Instituto Nacional de Ciencias Medicas y Nutricion S.Z., Mexico city, Mexico, 4Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 5Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion, Mexico City, Mexico, 6Rheumatology, Mount Sinai Hospital and University Health Network, Toronto Canada, Toronto, ON, Canada

    Background/Purpose: The nature and pathogenesis and cognitive dysfunction (CD) in patients with SLE is unkown.To determine the presence and levels of autoantibodies, cytokines and chemokines…
  • Abstract Number: 949 • 2013 ACR/ARHP Annual Meeting

    Targeting CD1c-Expressing Mdcs To Inhibit Tcell Activation and Thymus and Activation Regulated Chemokine (TARC)-Dependent Chemotaxis In RA

    M.R. Hillen1,2, F.M. Moret1,3, F.P.J.G. Lafeber4, C.E. Hack4, T.R.D.J. Radstake2,5 and J.A.G. van Roon3,6, 1Laboratory for Translational Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 2Department of Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 3Rheumatology & Clinical Immunology, University Medical Center Utrecht, Utrecht, Netherlands, 4Rheumatology & Clinical Immunology, UMC Utrecht, Utrecht, Netherlands, 5Laboratory for Translational Immunology, UMC Utrecht, Utrecht, Netherlands, 6Laboratory for Translational immunology, University Medical Center Utrecht, Utrecht, Netherlands

    Background/Purpose: Recently, we demonstrated strong Th1 and Th17 cytokine induction by CD1c+ myeloid dendritic cells (mDCs) from synovial fluid and identified thymic stromal lympopoeitin (TSLP)…
  • Abstract Number: 940 • 2013 ACR/ARHP Annual Meeting

    Novel Function Of Soluble Interleukin-6 Receptor As An Antagonist Of Interleukin-27-Mediated Anti-Inflammatory Responses

    Misato Hashizume1, Keiko Esaki2, Keiko Yoshimoto3, Hideto Kameda3, Tsutomu Takeuchi3 and Yoshihiro Matsumoto1, 1Product Research Department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan, 2Discovery Research Department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan, 3Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan

    Background/Purpose: The immunological roles of interleukin 27 (IL-27) have been reported in various rheumatic diseases, such as rheumatoid arthritis (RA), lupus, systemic sclerosis and psoriasis.…
  • Abstract Number: 948 • 2013 ACR/ARHP Annual Meeting

    Dual Neutralization Of TNF and IL-17 Provides Greater Efficacy In Collagen Induced Arthritis Through Regulation Of a Gene Transcription Program That Includes CXCL1 and CXCL5

    Carolyn Cuff1, Chung-Ming Hsieh2, Suzanne Mathieu3, Anwar Murtaza4, Margaret Hugunin3, Shaughn Bryant3, Robert O'brien3, Lisa Olson5 and Jeffrey Voss3, 1Immunology, AbbVie, Inc, Worcester, MA, 2Biologics, AbbVie Pharmaceuticals, Worcester, MA, 3Immunology, AbbVie Pharmaceuticals, Worcester, MA, 4Broad Institute, Cambridge, MA, 5AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA

    Background/Purpose: Dual neutralization of TNF and IL-17 is hypothesized to provide greater efficacy in rheumatoid arthritis (RA) and inflammatory diseases compared to either monotherapy as…
  • Abstract Number: 842 • 2013 ACR/ARHP Annual Meeting

    A Cytokine/Chemokine Multiplex Assay That Is Sensitive and Specific For Fibromyalgia Compared To Controls, Systemic Lupus Erythematosus, and Rheumatoid Arthritis

    Daniel J. Wallace1, Igor Gavin2, Oleksiy Karpenko2 and Bruce S. Gillis3, 1Cedars-Sinai Medical Center, Los Angeles, CA, 2University of Illinois College of Medicine at Chicago, Chicago, IL, 3Department of Pathology, University of Illinois College of Medicine at Chicago, Chicago, IL

    Background/Purpose:   Fibromyalgia (FM) is a chronic pain and fatigue syndrome that affects about 6 million adults in the United States.  The clinical diagnosis of…
  • Abstract Number: 774 • 2013 ACR/ARHP Annual Meeting

    Citrullination Of ENA-78/CXCL5 Changes Its Receptor Affinity From CXCR2 To CXCR1 and Induces Monocyte Migration

    Ken Yoshida1, Alisa E. Koch1,2, Ray A. Ohara3, Phillip L. Campbell1, M. Asif Amin1, David A. Fox1 and Jeffrey H. Ruth4, 1Internal Medicine, University of Michigan Medical School, Ann Arbor, MI, 2VA Medical Service, Ann Arbor, MI, 3University of Michigan Medical School, Ann Arbor, MI, 4Internal Medicine, Division of Rheumatology, University of Michigan Medical Center, Ann Arbor, MI

    Background/Purpose: We previously showed that citrullinated epithelial-derived neutrophil-activating peptide 78/CXCL5 (citENA-78/CXCL5) was significantly higher in rheumatoid arthritis (RA) synovial fluids (SFs) compared to osteoarthritis (OA)…
  • Abstract Number: 669 • 2013 ACR/ARHP Annual Meeting

    Up-Regulated Expression Of CXCL5 In Circulating Platelets From Patients With Systemic Sclerosis: A Role In Fibrosis

    Hidekata Yasuoka1, Ken Stern2, Yuka Okazaki3, Tetsuya Nishimoto4, Tsutomu Takeuchi1 and Masataka Kuwana1, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Keio University School of Medicine, Tokyo, Japan, 3Rheumatology, Keio University School of Medicine, Tokyo, Japan, 4Department of Medicine, Medical University of South Carolina, Charleston, SC

    Background/Purpose: Systemic sclerosis (SSc) is a systemic fibroproliferative disease characterized by concomitant occurrence of microvascular injury and autoantibody production. It has long been suggested that…
  • Abstract Number: 642 • 2013 ACR/ARHP Annual Meeting

    Serum Concentrations Of Type I Interferon-Regulated Chemokines Are Associated With Disease Activity In Systemic Lupus Erythematosus

    Eric F. Morand, Kathryn Connelly and Alberta Y. Hoi, Centre for Inflammatory Diseases, Monash University, Melbourne, Australia

    Background/Purpose: Expression array studies suggest the activity of Type I interferon (IFN), as reflected in IFN-induced genes, is associated with phenotypic subsets in SLE. Three…
  • Abstract Number: 635 • 2013 ACR/ARHP Annual Meeting

    Multiple Altered Soluble Inflammatory Mediators Correlate With Disease Activity and Mark Impending Disease Flare In European-American Lupus Patients

    Melissa E. Munroe1, Jourdan R. Anderson2, Krista M. Bean3, Joan T. Merrill4, Joel M. Guthridge3, Virginia C. Roberts3, Linda F. Thompson5,6 and Judith A. James4,7, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Oklahoma Medical Research Foundation, Oklahoma City, OK, 5University of Oklahoma Health Sciences Center, Oklahoma City, OK, 6Immunobiology and Cancer, Oklahoma Medical Research Foundation, Oklahoma City, OK, 7College of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose:  SLE is a waxing and waning disease characterized by immune dysregulation, major organ involvement, and disease flares. Identifying mechanistic mediators of altered disease activity…
  • « Previous Page
  • 1
  • …
  • 7
  • 8
  • 9
  • 10
  • 11
  • 12
  • 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 2026 American College of Rheumatology