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  • Abstract Number: 2779 • 2016 ACR/ARHP Annual Meeting

    Better Health-Related Quality of Life and Work Capacity in Patients Achieving Inactive Disease and Clinical Response in Patients with Non-Radiographic Axial Spondyloarthritis

    Maxime Dougados1, Desiree van der Heijde2, Wen-Chan Tsai3, Diego Saaibi4, Randi Bonin5, Lisa Marshall6, Heather Jones7, Ronald Pedersen8, Bonnie Vlahos9 and Miriam Tarallo10, 1Rheumatology, Paris Descartes University, Paris, France, 2Leiden University Medical Center, Leiden, Netherlands, 3Kaohsiung Medical University, Kaohsiung City, Taiwan, 4MEDICITY S.A.S, Bucaramanga, Colombia, 5Clinical Affairs, Pfizer, Collegeville, PA, 6Inflammation Global Medical Affairs, Pfizer, Collegeville, PA, 7Inflammation & Immunology, Pfizer, Collegeville, PA, 8Department of Biostatistics, Pfizer, Collegeville, PA, 9GIPB - Clinical Sciences, Pfizer, Collegeville, PA, 10GHV, Pfizer, Rome, Italy

    Background/Purpose: Few studies have evaluated the relationship between disease activity/clinical response and patient-reported outcomes (PROs) of pain, fatigue, health-related quality of life (HRQoL), and work…
  • Abstract Number: 2780 • 2016 ACR/ARHP Annual Meeting

    A Modification of the Psoriatic Arthritis Disease Activity Score (mPASDAS) Using SF-12 As a Measure of Quality of Life

    Matthew Got1, Suzanne Li2, Anthony V. Perruccio3,4, Dafna D Gladman1 and Vinod Chandran5, 1University of Toronto, Toronto, ON, Canada, 2University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 3Krembil Research Institute, Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 4Arthritis Program, Toronto Western Hospital, University Health Network, Toronto, ON, Canada, 5Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada

    Background/Purpose: The Psoriatic Arthritis Disease Activity Score (PASDAS) is a newly developed composite disease activity measure that summarizes psoriatic arthritis (PsA) disease activity with a…
  • Abstract Number: 2781 • 2016 ACR/ARHP Annual Meeting

    Immunization with ApoB100 Peptide Vaccine Reduces Atherosclerosis Development in a Mouse Model of Systemic Lupus Erythematosus

    Ingrid Yao-Mattisson, Maria Wigren, Gunilla Nordin Fredrikson and Jan Nilsson, Lund University, Malmö, Sweden

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by impaired self-tolerance causing damage to multiple organs including the cardiovascular system. Current therapies do…
  • Abstract Number: 2782 • 2016 ACR/ARHP Annual Meeting

    Bortezomib Treatment Prevents Glomerulosclerosis Associated with Lupus Nephritis in a Murine Model through Suppressive Effects on the Immune and Renin-Angiotensin Systems

    Kazuhisa Nozawa1, Yuko Matsuki2, Ken Yamaji3, Naoto Tamura4 and Yoshinari Takasaki3, 12-1-1 Hongo Bunkyo-ku, Juntendo University, Tokyo, Japan, 2Department of Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 3Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 4Rheumatology, Juntendo University, Tokyo, Japan

    Background/Purpose:   Lupus nephritis (LN) is one of the main causes of morbidity and mortality in SLE. Although a combination therapy using steroids and immunosuppressant…
  • Abstract Number: 2783 • 2016 ACR/ARHP Annual Meeting

    Human Mesenchymal Stem Cells from Different Tissues Exert Distinct Therapeutic Effect on Systemic Lupus Erythematosus

    Xiaojun Tang1, Zhuoya Zhang2 and Lingyun Sun1, 1Department of Rheumatology and Immunology, The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China, 2The Affiliated Drum Tower Hospital of Nanjing University Medical School, Nanjing, China

    Background/Purpose:  Previous clinical data has shown that transplantation of umbilical cord mesenchymal stem cells (UC-MSCs) could effectively alleviate the disease symptoms in both patients with…
  • Abstract Number: 2784 • 2016 ACR/ARHP Annual Meeting

    Mesenchymal Stem Cells Ameliorate Lupus By Promoting T Cell Apoptosis Via Bcl-2/Bim Independent Pathway in MRL/Lpr Mice

    Saisai Huang1, Dandan Wang2 and Lingyun Sun1, 1Department of Rheumatology and Immunology, 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: Systemic lupus erythematosus (SLE) is an inflammatory autoimmune disease, involving in dysfunction of many organs. The abnormality of apoptosis plays an important role in…
  • Abstract Number: 2785 • 2016 ACR/ARHP Annual Meeting

    Translatable in Vitro Immunocyte Functional Measures of CC-292 and CC-90008 Inhibitors of the Bruton’s Tyrosine Kinase (Btk)/Tec Family and the Pathology Observed in the MLR/Lpr Mouse Model of Systemic Lupus Erythematosus (SLE)

    Garth Ringheim1, Jolanta Kosek2, Lori Capone3, Mary Adams4,5, Eun Mi Hur4 and Peter H. Schafer5, 186 Morris Avenue, Celgene Corporation, Summit, NJ, 2Translational Development, Celgene Corporation, Summit, NJ, 3Celgene Corporation, Summit, NJ, 4Inflammation and Immunology Translational Development, Celgene Corporation, Summit, NJ, 5Department of Translational Development, Celgene Corporation, Summit, NJ

    Background/Purpose:  CC-292 and CC-90008 are covalent Btk/Tec family kinase inhibitors that block Btk activity by binding with high affinity to the adenosine triphosphate (ATP) binding…
  • Abstract Number: 2786 • 2016 ACR/ARHP Annual Meeting

    The Janus Kinase Inhibitor Tofacitinib Ameliorates Murine Lupus and Its Associated Vascular Dysfunction

    Yasuko Furumoto1, Carolyne K. Smith2, Luz P. Blanco3, Wanxia L. Tsai4, Wenpu Zhao5, Victoria Hoffmann6, Seth Thacker7, Giuseppe Sciumè8, Leti Nuñez1, Alan Remaley9, John J O'Shea10, Mariana Kaplan11 and Massimo G. Gadina12, 1NIAMS NIH, Translational Immunology Section, Office of Science and Technology, Bethesda, MD, 2Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 3Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 4National Institute of Arthritis and Musculoskeletal and Skin Diseases, Bethesda, MD, 5NIAMS NIH, Systemic Autoimmunity Branch, Bethesda, MD, 6Division of Veterinary Resources, National Institutes of Health, Bethesda, MD, 7NHLBI NIH, Lipoprotein Metabolism Section, Bethesda, MD, 8NIAMS NIH, Molecular Immunology and Inflammation Branch, Bethesda, MD, 9NHLBI, National Institutes of Health, Bethesda, MD, 10NIAMS NIH, National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD, 11NIAMS/NIH, Bethesda, MD, 12Translational Immunology Section, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD

    Background/Purpose: Dysregulation of innate and adaptive immune responses contributes to the pathogenesis of systemic lupus erythematosus (SLE) and its associated premature vascular damage. To date,…
  • Abstract Number: 2787 • 2016 ACR/ARHP Annual Meeting

    Bortezomib Treatment Induces Higher Mortality Rate in Lupus Model Mice with High Disease Activity

    Hiroshi Fujii1, Tomoko Ikeda1, Masato Nose2, Tomoyuki Muto3, Kanae Akita1, Yukiko Kamogawa1, Tsuyoshi Shirai1, Yuko Shirota1, Tomonori Ishii4 and Hideo Harigae1, 1Department of Hematology and Rheumatology, Tohoku University Graduate School of Medicine, Sendai, Japan, 2Institute for Promotion of Advanced Science and Technology, Ehime University, Matsuyama, Japan, 3Tohoku University Graduate School of Medicine, Sendai, Japan, 4Tohoku University Hospital, Senndai, Japan

    Background/Purpose: SLE is a chronic inflammatory disease triggered by the deposition of autoantibodies. One of the goals for SLE therapy is to suppress the production…
  • Abstract Number: 2788 • 2016 ACR/ARHP Annual Meeting

    Suppression of IL-1 Signaling Ameliorates Dermatitis in a Murine Model of Systemic Lupus Erythematosus

    Jeremy Tilstra1, Sheldon Bastacky2 and Mark Shlomchik3, 1Rheumatology, Univ of Pittsburgh Medical Center, Pittsburgh, PA, 2Pathology, University of Pittsburgh Medical Center, Pittsburgh, PA, 3Immunology, University of Pittsburgh, Pittsburgh, PA

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is a prototypical autoimmune disease defined by autoantibody production, immune dysregulation, and end-organ damage. Our laboratory previously showed that MyD88,…
  • Abstract Number: 2789 • 2016 ACR/ARHP Annual Meeting

    Novel Glucocorticoid Prodrug Effectively Attenuates Late Stage Lupus Nephritis with Improved Safety Profile

    Xiaobei Wang1, Zhenshan Jia2, Yangsheng Yu3, Kaihong Su3, James R. O'Dell4 and Dong Wang5, 1Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE, 2University of Nebraska Medical Center, Omaha, NE, 3Pathology and Microbiology, University of Nebraska Medical Center, Omaha, NE, 4Department of Internal Medicine, University of Nebraska Medical Center, Omaha, NE, 5Department of Pharmaceutical Sciences, University of Nebraska Medical Center, Omaha, NE

    Background/Purpose: Lupus nephritis (LN) is a severe complication of systemic lupus erythematosus (SLE). Glucocorticoids (GCs) are recommended by ACR as one of the first line…
  • Abstract Number: 2790 • 2016 ACR/ARHP Annual Meeting

    Selective Disruption of Estrogen Receptor Alpha Expression in Dendritic Cells of Lupus-Prone Mice Results in Increased Female-Specific Death

    Melissa A. Cunningham1, Jena R. Wirth2, Jackie G. Eudaly2 and Gary S. Gilkeson3, 1Rheumatology and Immunology, Medical University of South Carolina, Charleston, SC, 2Med/Rheumatology, Medical University of South Carolina, Charleston, SC, 3Department of Medicine, Medical University of South Carolina, Charleston, SC

    Background/Purpose: SLE is a disease that disproportionately affects females. The etiology of the sex bias in this disease is unclear. We previously showed that a…
  • Abstract Number: 2791 • 2016 ACR/ARHP Annual Meeting

    Targeting Micro-RNAs Derived from Extracellular Vesicles to Inhibit of TLR7 and TLR8 Signaling Suppresses Inflammation in a Novel Human-Mouse Chimeric Model of Systemic Lupus Erythematosus

    Nicholas A. Young1, Giancarlo R. Valiente2, Holly Steigelman3, Jeffrey Hampton4 and Wael N. Jarjour5, 1Immunology and Rheumatology, The Ohio State University Wexner Medical Center, Columbus, OH, 2Rheumatology & Immunology, The Ohio State University Wexner Medical Center, Columbus, OH, 3The Ohio State University, Columbus, OH, 4Immunology and Rheumatoloty, The Ohio State University Wexner Medical Center, Columbus, OH, 5Department of Rheumatology/Medicine, Ohio State University, Columbus, OH

    Background/Purpose:  Systemic lupus erythematosus (SLE) is a prototypic autoimmune disease displaying a heavy female predominance during reproductive years. We have previously shown that toll-like receptor…
  • Abstract Number: 2792 • 2016 ACR/ARHP Annual Meeting

    Hyperhomocysteinemia in SLE

    Michelle Petri1 and Wei Fu2, 1Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD, 2Rheumatology, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Hyperhomocysteinemia has been correlated with the occurrence of blood clots, heart attacks and strokes. We investigated the association of the Hyperhomocysteinemia with other clinical…
  • Abstract Number: 2793 • 2016 ACR/ARHP Annual Meeting

    The Predictors of Sustained Complete Remission in Lupus Nephritis

    Rattapol Pakchotanon1, Dafna D. Gladman2, Jiandong Su2 and Murray Urowitz3, 1Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 3Medicine, Centre for Prognosis Studies in the Rheumatic Diseases, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada

    Background/Purpose: Sustained complete remission is an independent predictor of good long term prognosis in lupus nephritis (LN). We aimed to examine the predictors of sustained…
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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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