ACR Meeting Abstracts

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Abstracts tagged "chemokines"

  • Abstract Number: 1764 • 2019 ACR/ARP Annual Meeting

    CCL25, a Novel Fibroblast and Macrophage Chemoattractant That Potentiates RA Bone Erosion

    Sadiq Umar1, Katrien Raemdonck 1, Karol Palasiewicz 1, Michael Volin 2, Shiva Arami 1, Suncica Volkov 1, Nadera Sweiss 1, M Amin 3 and Shiva shahrara 1, 1University of Illinois at chicago, Chicago, IL, 2Department of Microbiology & Immunology, Midwestern University, Downer Grove, IL, 3University of Michigan, Ann Arbor, MI

    Background/Purpose: Background/Purpose: CCL25 and its receptor CCR9 have been detected in the inflamed joint; however their role is undefined in rheumatoid arthritis (RA). Hence studies…
  • Abstract Number: 9 • 2019 ACR/ARP Annual Meeting

    Chemokine CXCL 10 Gene Expression as a Potential Activity Biomarker of Systemic Lupus Erythematosus

    Julian Torres Vazquez1, Alejandro Corzo Cruz 2, David Alberto Comoto Santacruz 2 and Omar Eloy Muñoz Monroy 1, 1Universidad del Ejército y Fuerza Aérea/ Esc. Mil. Gdos. Snd., SEDENA, Mexico City, Distrito Federal, Mexico, 2Universidad del Ejército y Fuerza Aérea/ Esc. Mil. Gdos. Snd., SEDENA, Mexico City, Mexico

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by a wide range of systemic dysfunctions as well as an elevated erythrocyte sedimentation rate. Chemokine CXCL 10…
  • Abstract Number: 17 • 2019 ACR/ARP Annual Meeting

    Transcription Factor Fli-1 Impacts Lupus Nephritis by Orchestrating CXCL10/CXCR3 Axis

    Xuan Wang1, Mara Lennard Richard 1, Tomika Caldwell 2, Brittany Henry 2, Tammy Nowling 2, Jim Oates 3, Gary Gilkeson 4 and Xian Zhang 1, 1Medical University of South Carolina, Charleston, SC, 2Medical University of South Carolina, Charleston, 3Division of Rheumatology & Immunology/Medical University of South Carolina, Charleston, SC, 4Division of Rheumatology & Immunology/Ralph H. Johnson VA Medical Center/Medical University of South Carolina, Charleston, SC

    Background/Purpose:  Lupus nephritis is a major cause of death in both animal models and human patients.  Expression of Fli-1, a member of the Ets family…
  • Abstract Number: 21 • 2019 ACR/ARP Annual Meeting

    Immuno-Phenotypic Analysis of Peripheral Blood Mononuclear Cells in Rheumatoid Arthritis Patients Treated with E6011, a Humanized Anti-Fractalkine Monoclonal Antibody

    Tomohiro Yamada1, Jungo Kakuta 1, Eri Fusaoka-Nishioka 1, Jun-ichi Ito 2, Nobuyuki Yasuda 3, Tetsu Kawano 3 and Toshio Imai 3, 1KAN Research Institute Inc., Kobe, Japan, 2EISAI Co. Ltd., Tsukuba, Japan, 3KAN Research Institute, Inc., Kobe, Japan

    Background/Purpose: Fractalkine (FKN) and its solo receptor CX3CR1 are deeply involved in the pathogenesis of rheumatoid arthritis (RA). FKN is expressed on vascular endothelium, while…
  • Abstract Number: 92 • 2018 ACR/ARHP Annual Meeting

    Lupus Nephritis Serum Induces Neutrophil Chemotaxis Towards Glomerular Endothelial Cells in Vitro

    Dayvia Russell1, Margaret Markiewicz2, Xian Zhang2 and Jim C. Oates3, 1Research Service, Ralph H. Johnson VA Medical Center, Charleston, SC, 2Division of Rheumatology & Immunology, Department of Medicine, Medical University of South Carolina, Charleston, SC, 3Medical Service, Ralph H. Johnson VA Medical Center, Charleston, SC

    Title: Lupus Nephritis Serum Induces Neutrophil Chemotaxis towards Glomerular Endothelial Cells In Vitro Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic inflammatory disease associated with…
  • Abstract Number: 840 • 2018 ACR/ARHP Annual Meeting

    The CCL21/CCR7 Axis Drives Vascular, Inflammatory and Destructive Remodeling in Rheumatoid Arthritis

    Katrien Van Raemdonck1,2, Karol Palasiewicz1,2, Sadiq Umar1,2 and Shiva Shahrara2, 1Jesse Brown VA Medical Center, Chicago, IL, 2Medicine, Division of Rheumatology, University of Illinois at Chicago, Chicago, IL

    Background/Purpose: The synovial tissue of rheumatoid arthritis (RA) patients exhibits abundant expression of CCL21, produced excessively by RA fibroblasts and macrophages. While CCR7 mediates CCL21-driven…
  • Abstract Number: 983 • 2018 ACR/ARHP Annual Meeting

    A MAPK Activated Kinase 2 Inhibitor Attenuates Inflammatory and Destructive Arthritis in Human Ex Vivo Models

    Tue Wenzel Kragstrup1,2, Anders Mellemkjær3, Morten Aagaard Nielsen4, Line Dam Heftdal2, Marie Iversen3, Peter Schafer5 and Bent Deleuran2, 1Randers Regional Hospital, Randers, Denmark, 2Department of Biomedicine, Aarhus University, Aarhus, Denmark, 3Aarhus University, Aarhus, Denmark, 4Of Biomedicine, Aarhus University, Aarhus, Denmark, 5Celgene Corporation, Summit, NJ

    Background/Purpose: Targeting intracellular pathways with oral small molecules is an attractive therapeutic approach for treating immune mediated inflammatory diseases. The mitogen-activated protein kinase (MAPK) pathway…
  • Abstract Number: 987 • 2018 ACR/ARHP Annual Meeting

    CCL11 Is Involved in Cell Migration in Rheumatoid Arthritis

    Kuninobu Wakabayashi, Takeo Isozaki, Shinichiro Nishimi and Tsuyoshi Kasama, Div of Rheumatology, Showa University School of Med, Shinagawa-ku Tokyo, Japan

    Background/Purpose: Chemokine C-C motif ligand 11 (CCL11) also known as eotaxin-1 is produced by a variety of cell types. By interacting with C-C chemokine receptor…
  • Abstract Number: 995 • 2018 ACR/ARHP Annual Meeting

    Anti-Fractalkine Monoclonal Antibody Inhibits Joint Destruction through Suppression of Osteoclast Precursor Migration and Induces Synovial Cell Death in Collagen-Induced Arthritis Model Mice

    Kana Hoshino-Negishi1, Masayoshi Ohkuro2, Tomoya Nakatani1, Wataru Ikeda1, Yoshikazu Kuboi1, Naoto Ishii1, Nobuyuki Yasuda1 and Toshio Imai3, 1KAN Research Institute, Inc., Kobe, Japan, 2Research Project Promotion Group, EA Pharma Co., Ltd., Kawasaki, Japan, 3President & CEO, Chief Scientific Officer, KAN Research Institute, Inc., Kobe, Japan

    Background/Purpose: In the Phase 1/2 clinical study, E6011, a novel humanized anti-fractalkine (FKN) mAb demonstrated a promising efficacy in active RA patients who were inadequately…
  • Abstract Number: 1001 • 2018 ACR/ARHP Annual Meeting

    Anti-Fractalkine Monoclonal Antibody Dislodges Intravascular Monocytes Involved in Exacerbation of Synovial Inflammation in Collagen-Induced Arthritis Model

    Wataru Ikeda1, Kana Hoshino-Negishi1, Eri Fusaoka-Nishioka1, Tomoya Nakatani1, Yoshikazu Kuboi1, Naoto Ishii1, Nobuyuki Yasuda1 and Toshio Imai2, 1KAN Research Institute, Inc., Kobe, Japan, 2President & CEO, Chief Scientific Officer, KAN Research Institute, Inc., Kobe, Japan

    Background/Purpose: In the Phase 1/2 clinical study, E6011, a novel humanized anti-fractalkine (FKN) mAb demonstrated a promising efficacy in active RA patients who were inadequately…
  • Abstract Number: 1417 • 2018 ACR/ARHP Annual Meeting

    Hemophagocytic Lymphohistiocytosis (HLH) Mimickers: CXCL9 As a Potential Biomarker Distinguishing HLH from Other Hyperferritinemic Syndromes

    Giulia Marucci1, Ivan Caiello2, Manuela Pardeo1, Virginia Messia1, Giusi Prencipe1, Antonia Pascarella1, Fabrizio De Benedetti3 and Claudia Bracaglia1, 1Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy, 2Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy, 3IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy

    Background/Purpose: Increased ferritin is considered biomarker highly suggestive of primary and secondary HLH and it is one of the HLH-2004 diagnostic and MAS guidelines (1,2),…
  • Abstract Number: 1473 • 2018 ACR/ARHP Annual Meeting

    Performance of the Meso Scale Multiplex Platform in the Assessment of Serum Cytokines / Chemokines in Rheumatoid Arthritis

    Peter M. Maloley1, Bryant R. England2, Harlan Sayles1, Geoffrey M. Thiele1, Michael J. Duryee3, Jeffrey Payne4 and Ted R. Mikuls5, 1University of Nebraska Medical Center, Omaha, NE, 2Rheumatology, VA Nebraska-Western Iowa Health Care System & University of Nebraska Medical Center, Omaha, NE, 3Internal Medicine Division of Rheumatology, University of Nebraska Medical Center, Omaha, NE, 4College of Dentistry, University of Nebraska Medical Center, Lincoln, NE, 5Internal Medicine, Division of Rheumatology, VA Nebraska-Western Iowa Health Care System and University of Nebraska Medical Center, Omaha, NE

     Background/Purpose:  Cytokines and chemokines (CK) are central to RA pathogenesis, a fact underscored by the emergence of multiplex immunoassays for quantifying CK values in both…
  • Abstract Number: 2920 • 2018 ACR/ARHP Annual Meeting

    Correlations of Type I Interferon Score and Interferon Induced Chemokines CXCL10 and CXCL9 with Cutaneous and Muscular Disease Activity in Juvenile Dermatomyositis

    Gian Marco Moneta1, Ivan Caiello1, Lucilla Rava'2, Silvia Rosina3, Luisa Bracci Laudiero1,4, Angelo Ravelli3,5, Fabrizio De Benedetti6 and Rebecca Nicolai7, 1Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy, 2Epidemiology Unit, IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy, 3University of Genova, Genova, Italy, 4Institute of Translational Pharmacology, CNR, Roma, Italy, 5Rheumatology, Giannina Gaslini Institute, Genova, Italy, 6IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy, 7Division of Rheumatology, IRCCS Ospedale Pediatrico Bambino Gesù, Rome, Italy

    Background/Purpose: Interferons (IFNs) seem to play an important role in the pathogenesis of juvenile dermatomyositis (JDM). We previously reported that expression of both type I…
  • Abstract Number: 2135 • 2017 ACR/ARHP Annual Meeting

    ADAM-17 Is Expressed in the Inflammatory Myopathy, and Is Involved with Interstitial Lung Disease

    Airi Nishimi, Takeo Isozaki, Shinichiro Nishimi, Sho Ishii, Takahiro Tokunaga, Hidekazu Furuya, Kuninobu Wakabayashi and Tsuyoshi Kasama, Div of Rheumatology, Showa University School of Med, Shinagawa-ku Tokyo, Japan

    Background/Purpose: A disintegrin and metalloprotesase (ADAM) family is protease that is thought to have an important role in tissue destruction and inflammatory reaction. ADAMs are…
  • Abstract Number: 2145 • 2017 ACR/ARHP Annual Meeting

    Anti-CXCR3 Antibody Suppresses Inflammation in C Protein-Induced Myositis Model

    Ji Yong Choi1, Joo Youn Lee2, Ji Soo Park3, Sehui Shon3, Kathleen Phillips4, Eun Young Lee1, Eun Bong Lee1 and Yeong Wook Song3,5, 1Division of Rheumatology, Department of Internal Medicine, Seoul National University, Seoul, Korea, Republic of (South), 2Department of Molecular medicine and biopharmaceutical science, Seoul National University, seoul, Korea, Republic of (South), 3Department of Molecular medicine and biopharmaceutical science, Seoul National University, Seoul, Korea, Republic of (South), 4Pfizer Inc. Cambridge, MA. USA, Cambridge, MA, 5Division of Rheumatology, Department of Internal Medicine, Seoul National University Hospital, Seoul, Korea, Republic of (South)

    Background/Purpose: CXCR3 is a chemokine receptor that plays an important role in T cell chemotaxis in human autoimmune diseases. CXCR3, which is activated by ligand…
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Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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