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Abstracts tagged "chemokines"

  • Abstract Number: 1139 • 2015 ACR/ARHP Annual Meeting

    Differential Inflammatory Profile in Experimental Models of Arthritis

    Ana C. Ortiz1, Anne Crilly1, Lynette Dunning1, Carmen Huesa1, C. S. Goodyear2, John C. Lockhart1, William R. Ferrell2 and Iain B. McInnes2, 1Institute of Biomedical and Environmental Health Research, University of the West of Scotland, Paisley, United Kingdom, 2Institute of Infection, Immunity and Inflammation, College of Medicine, Veterinary Medicine and Life Sciences, University of Glasgow, Glasgow, United Kingdom

    Background/Purpose: While osteoarthritis (OA) in humans is characterized by cartilage degradation, osteophyte formation and joint remodeling, inflammation and synovitis are now recognized to contribute to…
  • Abstract Number: 1148 • 2015 ACR/ARHP Annual Meeting

    The Role of TRPC6 in CXCR2-Mediated Chondrocyte Phenotypic Stability

    Joanna Sherwood1, Jessica Bertrand1, Francesco Dell'Accio2 and Thomas Pap3, 1Institute for Experimental Musculoskeletal Medicine, University Hospital Münster, Münster, Germany, 2EMR, Queen Mary's School of Medicine and Dentistry, London, United Kingdom, 3Institute of Experimental Musculoskeletal Medicine, University Hospital Münster, Münster, Germany

    Background/Purpose: We have recently demonstrated that ELR+ CXC chemokines signaling via the CXCR2 receptor, are produced by healthy chondrocytes and are retained within the cartilage…
  • Abstract Number: 1361 • 2015 ACR/ARHP Annual Meeting

    Synovial Macrophages Promote TGF-β Signaling but Protect Against Influx of S100A8/S100A9-Producing Cells after Intra-Articular Injections of Oxidized Low-Density Lipoproteins

    Wouter de Munter1, Martijn H. van den Bosch1, Arjen Blom1, Birgitte Walgreen2, Monique Helsen1, Leo Joosten3, Johannes Roth4, Thomas Vogl5, Fons van de Loo1, Marije Koenders1, Wim van den Berg1, Peter van der Kraan1 and Peter van Lent1, 1Experimental Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 2Experimentel Rheumatology, Radboud university medical center, Nijmegen, Netherlands, 3Internal Medicine, Radboud university medical center, Nijmegen, Netherlands, 4Institute of Immunology, University of Münster, Münster, Germany, 5University of Muenster, Muenster, Germany

    Background/Purpose:  In previous studies we found that synovial macrophages regulate joint pathology during experimental osteoarthritis (OA). Recently, we found that high systemic levels of LDL…
  • Abstract Number: 1911 • 2015 ACR/ARHP Annual Meeting

    Monocyte Chemoattractant Protein-1 (MCP-1, CCL2) Is a Potential Local Marker of Renal Involvement in Scleroderma

    Edward Stern1,2, Cassandra Hong2, Voon H. Ong2, Aine Burns1, Robert Unwin3 and Christopher P. Denton4, 1Nephrology, Royal Free Hospital, London, United Kingdom, 2Rheumatology, UCL Division of Medicine, London, United Kingdom, 3Nephrology, UCL Division of Medicine, London, United Kingdom, 4Rheumatology and Connective Tissue Diseases, University College London, London, United Kingdom

    Background/Purpose: Renal disease in scleroderma (SSc), including scleroderma renal crisis (SRC), remains a major clinical challenge. Previous studies showed up to 50% of SSc patients…
  • Abstract Number: 1964 • 2015 ACR/ARHP Annual Meeting

    Biomarkers in Temporal Artery Biopsies and Sera of Patients with Giant Cell Arteritis

    Katja Lakota1, Tadeja Kuret2, Polona Žigon1, Ziga Rotar1, Matija Tomsic1, Saša Čučnik1,2, Snezna Sodin Semrl1,3 and Alojzija Hocevar1, 1Department of Rheumatology, University Medical Centre Ljubljana, Ljubljana, Slovenia, 2Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia, 3Faculty of Mathematics, Natural Science and Information Technology, University of Primorska, Koper, Slovenia

    Background/Purpose: Giant cell arteritis (GCA) is a large- and medium- vessel arteritis characterized by a range of histological patterns of vascular wall injury. The temporal…
  • Abstract Number: 2013 • 2015 ACR/ARHP Annual Meeting

    TIARP Attenuates Autoantibody-Mediated Arthritis Via the Suppression of Neutrophil Infiltration into the Joint

    Asuka Inoue1, Isao Matsumoto1, Yuki Tanaka2, Naoto Umeda1, Hoshimi Kawaguchi1, Hiroshi Ebe1, Yoshihiro Matsumoto3 and Takayuki Sumida1, 1Department of Internal Medicine, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan, 2Department of Internal Medicine, University of Tsukuba, Tsukuba, Japan, 3Product Research Department, Chugai Pharmaceutical Co., Ltd., Gotemba, Japan

    Background/Purpose: TIARP (TNFα-induced adipose-related protein) is dominantly expressed in macrophages (Mφ), neutrophils (PMN) and fibroblast-like synoviocytes (FLS). Recently, we found that TIARP functions as a…
  • Abstract Number: 2086 • 2015 ACR/ARHP Annual Meeting

    Inhibition of Macrophage Inflammatory Protein 1-Alpha (CCL3) Significantly Reduced Bone Resorption in Vitro and the Development of Erosive Joint Pathology in Collagen-Induced Arthritis

    Lauren A. Jordan1, Ruth Davies1, Alastair J. D. Robertson2, Ann K. Harvey1, Ernest H. Choy1, Malin Erlandsson3, Maria I. Bokarewa4, Rachel J. Errington1 and Anwen S. Williams1, 1Cardiff University, Institute of Infection and Immunity, Tenovus Building, University Hospital of Wales, Cardiff, United Kingdom, 2William Harvey Hospital, Willesborough, Ashford, United Kingdom, 3University of Goteborg, Goteborg, Sweden, 4Guldhedsgatan 10, University of Goteborg, Goteborg, Sweden

    Background/Purpose: The destruction of bone is a common feature of diseases like rheumatoid arthritis (RA) and multiple myeloma (MM).  CCL3 is significantly elevated in the…
  • Abstract Number: 2834 • 2015 ACR/ARHP Annual Meeting

    CXCL10 Expression Is Elevated in Synovial Fluid of Psoriatic Arthritis Patients

    Anastasiya Muntyanu1, Fatima Abji2, Kun Liang3, Vinod Chandran4 and Dafna Gladman4, 1Toronto Western Hospital, University of Toronto, Toronto, ON, Canada, 2Rheumatology, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 3Department of Statistics and Actuarial Science, University of Waterloo, Waterloo, ON, Canada, 4Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

    Background/Purpose: Psoriatic arthritis (PsA), an inflammatory musculoskeletal disease, develops in approximately 30% of patients with psoriasis. We previously identified C-X-C motif chemokine 10 (CXCL10) as…
  • Abstract Number: 2993 • 2015 ACR/ARHP Annual Meeting

    Serum CXCL4 Increase in Patients with Undifferentiated Connective Tissue Disease at Risk for Systemic Sclerosis Is Associated with Anti-Scl70 Antibodies and ICAM-1, a Marker of Endothelial Activation

    Serena Vettori1, Rosaria Irace2, Veronica Giacco2, Antonella Riccardi2, Lucia Vicedomini2, Luciana Pellecchia2 and Gabriele Valentini2, 1Department of Internal and Experimental Medicine, Rheumatology Unit, Second University of Naples, Naples, Italy, 2Internal and Experimental Medicine, Rheumatology Unit, Second University of Naples, Naples, Italy

    Background/Purpose: CXCL4 is a pleiotropic antiangiogenic and immunomodulatory chemokine, that has been shown to be increased in the sera of patients with systemic sclerosis (SSc)…
  • Abstract Number: 922 • 2014 ACR/ARHP Annual Meeting

    A Potential Role for TLR4 Activation in Osteoarthritis Associated Pain

    Rachel E. Miller1, Shingo Ishihara2, Phuong Tran3, Richard J. Miller4 and Anne-Marie Malfait5, 1Rheumatology/Biochemistry, Rush University Medical Center, Chicago, IL, 2Internal Medicine, Rush University Medical Center, Chicago, IL, 3Rheumatology, Rush University Medical Center, Chicago, IL, 4Molecular Biochemistry and Pharmacology, Northwestern University, Chicago, IL, 5Internal Medicine/Biochemistry, Rush University Medical Center, Chicago, IL

    Background/Purpose - Damage associated molecular patterns (DAMPs) result from cellular stress and extracellular matrix breakdown. They may contribute to osteoarthritis (OA) pathogenesis by promoting synovitis…
  • Abstract Number: 760 • 2014 ACR/ARHP Annual Meeting

    Use of Multiplex Cytokine Analysis of Dermal Blister Fluid to Assess Local Inflammatory and Immune Activity in Systemic Sclerosis

    Kristina E.N. Clark1, Henry Lopez2, Xu Shiwen1, Bahja Ahmed Abdi1, George Martin3, Korsa Khan4, David J. Abraham1, Christopher P. Denton5 and Richard J. Stratton1, 1Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School, London, United Kingdom, 2Murigenics, Vallejo, CA, 3Aero Dap, Vallejo, CA, 4Centre for Rheumatology and Connective Tissue Diseases, UCL medical School, London, United Kingdom, 5Centre for Rheumatology and Connective Tissue Diseases, UCL Medical School Royal Free Campus, London, United Kingdom

    Background/Purpose Clinical diversity in systemic sclerosis (SSc) suggests complex multifaceted pathogenesis involving interplay of growth factors or cytokines within the lesional microenvironment.  We analysed dermal…
  • 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…
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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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