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  • Abstract Number: 2854 • 2016 ACR/ARHP Annual Meeting

    Laboratory and Demographic Longitudinal Profile of a Large Cohort of Individuals Presenting with the ANA Nuclear Dense Fine Speckled Immunofluorescence Pattern

    Andressa Mathias1, Alessandra Dellavance2, José Sá3, Felipe Muramoto4, Valdecir Marvulle5 and Luis Eduardo C. Andrade6, 1Immunology Division, Fleury Medicine and Health Laboratories, SAO PAULO, Brazil, 2Research and Development Department, Fleury Medicine and Health Laboratories, São Paulo, Brazil, 3Infomation Technology Department, Fleury Medicine and Health Laboratories, SAO PAULO, Brazil, 4Information Technology Departmente, Fleury Medicine and Health Laboratories, SAO PAULO, Brazil, 5Statistics Department, Universidade Federal de São Paulo, SAO PAULO, Brazil, 6Rheumatology, Escola Paulista de Medicina, Universidade Federal de Sao Paulo, Sao Paulo, Brazil

    Background/Purpose:  The nuclear dense fine speckled (DFS) pattern observed in the ANA assay on HEp-2 cells is strongly associated with autoantibodies to the 70/75kD lens…
  • Abstract Number: 2855 • 2016 ACR/ARHP Annual Meeting

    The Long-Term Clinical Outcomes of Lupus Nephritis

    Julie Davidson1, Qinggong Fu2, Beulah Ji3, Sapna Rao4, David Roth5, Laurence S Magder6 and Michelle Petri7, 1Worldwide Epidemiology, GlaxoSmithKline R&D, Uxbridge, United Kingdom, 2Worldwide Epidemiology, GlaxoSmithKline, Collegeville, PA, 3Clinical Development, GlaxoSmithKline R&D, Uxbridge, United Kingdom, 4Real World Evidence, GlaxoSmithKline R&D, Research Triangle Park, NC, 5GSK, Philadelphia, PA, 6Epidemiology and Public Health, Division of Rheumatology, School of Medicine, Johns Hopkins University, Baltimore, MD, 7Rheumatology Division, Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Clinical trials in lupus nephritis have often been designed to demonstrate renal response (or remission) following therapy based on categorical remission endpoints (often no…
  • Abstract Number: 2856 • 2016 ACR/ARHP Annual Meeting

    Serum C5a Is Elevated in Lupus Nephritis and in Neuropsychiatric Systemic Lupus Erythematosus through Different Mechanisms

    Yuko Sakuma1, Tatsuo Nagai2, Taku Yoshio3 and Shunsei Hirohata4, 1Department of Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Kanagawa, Japan, 2Rheumatology and Infectious Diseases, Kitasato University School of Medicine, Sagamihara, Japan, 3Jichi Medical University, Tochigi, Japan, 4Kitasato University School of Medicine, Sagamihara, Japan

    Background/Purpose: Neuropsychiatric manifestation in systemic lupus erythematosus (NPSLE) is one of the most serious complications of the disease. We have recently demonstrated that the breakdown…
  • Abstract Number: 2857 • 2016 ACR/ARHP Annual Meeting

    Results from a Phase 0 Longitudinal Clinical Trial in Cutaneous Lupus Erythematosus: Analysis of the Type I IFN Signature in the Skin and Blood and Its Relationship with Disease Activity Scores and Autoantibody Profiles

    Jessica Schreiter1, Jarrat Jordan1, Matteo Cesaroni1, Marc Chevrier2, Alexa Piantone3, Ian Gourley3, Jacqueline Benson1 and Takahiro Sato1, 1Estrela Lupus Venture, Janssen Research and Development, LLC., Spring House, PA, 2Janssen Research and Development, LLC, Collegeville, PA, 3Immunology Translational Medicine, Janssen Pharmaceutical Research and Development, LLC, Spring House, PA

    Background/Purpose:  Type I IFN (IFN-I)-regulated gene expression is known to be elevated in blood and skin lesions of patients with two different forms of cutaneous…
  • Abstract Number: 2858 • 2016 ACR/ARHP Annual Meeting

    Urinary PF4 and E-Selectin As Novel Biomarkers for Disease Activity and Renal Damage in Lupus Nephritis

    Huihua Ding1, Ling Qin1, Samantha Stanley1, Ramesh Saxena2 and Chandra Mohan3, 1Biomedical Engineering Department, University of Houston, Houston, TX, 2Nephrology, University of Texas Southwestern Medical Center, Dallas, TX, 3Biomedical Engineering, University of Houston, Houston, TX

    Background/Purpose: Lupus nephritis (LN) is the leading cause of morbidity and mortality in systemic lupus erythematosus (SLE). The objective of this study is to validate…
  • Abstract Number: 2859 • 2016 ACR/ARHP Annual Meeting

    Health-Related Interference of Social Activities and Suicidal Ideation in Systemic Lupus Erythematosus:  Georgians Organized Against Lupus Cohort

    Charmayne M. Dunlop-Thomas1, Gaobin Bao2, S. Sam Lim2 and Cristina Drenkard3, 1Medicine/Rheumatology, Emory University, Atlanta, GA, 2Medicine, Emory University School of Medicine, Atlanta, GA, 3Emory University School of Medicine, Atlanta, GA

    Background/Purpose:   Social integration has been found to be a protective factor from suicide-related ideation even after adjusting for mental health predictors. This is especially…
  • Abstract Number: 2860 • 2016 ACR/ARHP Annual Meeting

    Exercise Significantly Improves Cardiorespiratory Fitness and Reduces Disease-Related Fatigue without Adverse Effects on Disease Activity in Systemic Lupus Erythematosus: a Systematic Review with Meta-Analysis

    Tom O'Dwyer1, Laura Durcan2 and Fiona Wilson3, 1Physiotherapy, Trinity College Dublin, Dublin, Ireland, 2University of Washington, Seattle, WA, 3Physiotherapy, Trinity College, Dublin, Ireland

    Background/Purpose: Systemic lupus erythematous (SLE) associates with accelerated mortality, frequently attributable to cardiovascular (CV) causes, which is not fully explained by traditional CV risk factors.…
  • Abstract Number: 2861 • 2016 ACR/ARHP Annual Meeting

    Proportions of Circulating Follicular Helper T Cells and Complement Levels, White Blood Cell Counts, and Skin Manifestations in Patients with Active Systemic Lupus Erythematosus

    Jun Kikuchi1, Masaru Takeshita1, Katsuya Suzuki2, Yoshiaki Kassai3, Takahiro Miyazaki3 and Tsutomu Takeuchi2, 1Division of Rheumatology, Department of Internal Medicine, Keio University School of Medicine, Tokyo, Japan, 2Keio University School of Medcine, Division of Rheumatology, Department of Internal Medicine, Tokyo, Japan, 3Inflammation Drug Discovery Unit, Pharmaceutical Research Division, Takeda Pharmaceutical Company Ltd., Kanagawa, Japan

    Background/Purpose:  Although circulating B cells and T cells, including follicular helper T (Tfh) cells, are reported to be involved in systemic lupus erythematosus (SLE) 1,2),…
  • Abstract Number: 2862 • 2016 ACR/ARHP Annual Meeting

    Whole Blood Phenotyping and Innate and Adaptive Stimulation Reveal Unique Differences in Granulocytes and Innate Pathways of African American SLE Patients with Variable Disease Activity

    Samantha Slight-Webb1, Krista M. Bean1, Joseph Kheir1, Bolanle Adebayo1, Holden T. Maecker2, Paul J. Utz3, Judith A. James4 and Joel M. Guthridge5, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Division of Immunology and Rheumatology, Stanford University School of Medicine, Stanford, CA, 3Medicine, Stanford University School of Medicine, Stanford, CA, 4Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 5Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a systemic autoimmune disorder characterized by periods of heightened disease activity. Disease flares significantly affect quality of life and…
  • Abstract Number: 2863 • 2016 ACR/ARHP Annual Meeting

    High Frequency of Terminally Differentiated CD8+ T Cells Characterize Systemic Lupus Erythematosus Patients with Renal Involvement

    Nataly Manjarrez-Orduño1, Laurence Menard1, Julie Carman1, Suzanne Suchard1, Francesca Casano1, Deborah Lee1, Sium Habte1, Sherif Daouti2, Selena Kansal3, Dana Banas3, Can Jiang3, Dawn Stetsko3, Mark Cunningham3, Vivek Jayaswal4, Somnath Bandyopadhyay3, Sarah Hu3, Richard A. Furie5 and Steven G. Nadler6, 1Discovery Translational Sciences Group, Bristol-Myers Squibb, Princeton, NJ, 2Bristol-Myers Squibb, Princeton, NY, 3Bristol-Myers Squibb, Princeton, NJ, 4Biocon Bristol-Myers Squibb Research Center, Bangalore, India, 5Division of Rheumatology, Northwell Health, Great Neck, NY, 6Immunosciences Translational Research, Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: SLE is a highly heterogeneous disease. The identification of disease subtypes with different pathological mechanisms is crucial to identify subjects with different disease progression…
  • Abstract Number: 2864 • 2016 ACR/ARHP Annual Meeting

    Identifying Dysregulated and Co-Dysregulated Markers in Systemic Lupus Erythematosus Using Multi-Modal Biomarker Data from a Large Pre-Clinical Study

    Yanhua Sarah Hu1, S Bandyopadhyay1, Julie Carman2, Nataly Manjarrez-Orduño2, Can Jiang1, Suzanne Suchard2, Laurence Menard2, sium habte1, selena kansal1, vivek jayaswal3, Richard A. Furie4 and Steven G. Nadler5, 1Bristol-Myers Squibb, Princeton, NJ, 2Discovery Translational Sciences Group, Bristol-Myers Squibb, Princeton, NJ, 3Biocon Bristol-Myers Squibb Research Center, Bangalore, NJ, India, 4Division of Rheumatology, North Shore LIJ Health System, Great Neck, NY, 5Immunosciences Translational Research, Bristol-Myers Squibb, Princeton, NJ

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic, relapsing autoimmune disease affecting multiple organs and is a highly heterogeneous condition, with wide variations in the…
  • Abstract Number: 2865 • 2016 ACR/ARHP Annual Meeting

    Apoptotic Microparticles, but Not Exosomes, Induce an Inflammatory Response in Synoviocytes

    Brittany Bettendorf1, Elizabeth Mitton-Fitzgerald2, Claudia Gohr3 and Ann K. Rosenthal4, 1Rheumatology, Medical College of Wisconsin, MIlwaukee, WI, 2Rheumatology, Medical College of Wisconsin, Milwaukee, WI, 3Medicine, Medical College of Wisconsin, Milwaukee, WI, 4Division of Rheumatology, Medical College of WI, Milwaukee, WI

    Background/Purpose: Circulating microparticles (MPs) and exosomes modulate immune responses and play a role in the pathogenesis of systemic lupus erythematosus (SLE). Exosomes are 50-250 nm…
  • Abstract Number: 2866 • 2016 ACR/ARHP Annual Meeting

    Lupus HDL Induces Pro-Inflammatory Responses in Macrophages By Binding LOX1Rand Failing to Promote ATF3 Activity

    Carolyne K. Smith1, Nickie Seto1, Anuradha Vivekanandan-Giri2, Wenmin Yuan3, Martin Playford4, Zerai G. Manna5, Sarfaraz A. Hasni6, Rui Kuai3, Nehal N. Mehta4, Anna Schwendeman3, Subramaniam Pennathur2 and Mariana Kaplan7, 1Systemic Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Internal Medicine/Nephrology, University of Michigan Nephrology, Ann Arbor, MI, 3Department of Medicinal Chemistry and the Biointerfaces Institute, University of Michigan, Ann Arbor, MI, 4NHLBI, National Institutes of Health, Bethesda, MD, 5National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 6Lupus Clinical Research Program, Office of the Clinical Director, NIAMS/NIH, Bethesda, MD, 7NIAMS/NIH, Bethesda, MD

    Background/Purpose: Recent evidence indicates that high-density lipoprotein (HDL) exerts vasculoprotective activities by promoting activating transcription factor 3 (ATF3), leading to down-regulation of TLR-induced inflammatory responses.…
  • Abstract Number: 2867 • 2016 ACR/ARHP Annual Meeting

    Aberrant Epigenetic Alterations at the Promoter up-Regulate cAMP Responsive Element Modulator Alpha in CD4+ T Cells from Patients with Systemic Lupus Erythematosus

    Qing Zhang1, Huilin Zhang2, Shu Ding3, Hai Long4, Yi Zhan2, Xiangning Qiu4 and Qianjin Lu4, 1Department of Dermatology, The Second Xiangya Hospital of Central South University, Changsha, China, 2Second Xiangya Hospital, Central South University, Changsha, China, 3Department of Dermatology, The Third Xiangya Hospital of Central South University, Changsha, China, 4Department of Dermatology, Second Xiangya Hospital, Central South University, Changsha, China

    Background/Purpose:  Recently, accumulating studies have documented that up-regulated cAMP responsive element modulator α (CREMα) which can inhibit IL-2 and induce IL-17A in T cells plays…
  • Abstract Number: 2868 • 2016 ACR/ARHP Annual Meeting

    NK Cell Characterization in Patients with Systemic Lupus Erythematosus: Increased Frequency of Ki67+ NK Cells Associated with Disease Activity and Type I Interferon Signature

    Kelly Hudspeth1, Shu Wang2, Jingya Wang2, Saifur Rahman2, Michael Smith2, Kerry Casey2, Geoffrey Stephens3, Miguel Sanjuan2, Autoimmunity Molecular Medicine group2, Zerai G. Manna4, Sarfaraz Hasni4, Rachel Ettinger5 and Richard Siegel6, 1Immunoregulation Section, Autoimmunity Branch, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 2Respiratory, Inflammation, and Autoimmunity Group, MedImmune LLC, Gaithersburg, MD, 3Respiratory, Inflammatory, and Autoimmune Diseases Research, Medimmune, LLC, Gaithersburg, MD, 4National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 5Respiratory, Inflammation and Autoimmunity (RIA), MedImmune, LLC, Gaithersburg, MD, 6Immunoregulation Section, Autoimmunity Branch and Office of the Clinical Director National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, MD

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is a complex autoimmune disorder whose pathology appears to involve many immune cell types. While it is clear that autoantibody…
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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.).

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