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Abstracts tagged "C1q"

  • Abstract Number: 1744 • 2016 ACR/ARHP Annual Meeting

    Expression of C1q By Podocytes at Late Stages of Proliferative Lupus Glomerulonephritis

    Hongyang Wang1, Ou Jin2, Niansheng Yang3, Chao Dai1, Sun-sang Sung1, Felicia Gaskin4 and Shu Man Fu5, 1Center for Immunity, Inflammation, and Regenerative Medicine, University of Virginia, Charlottesville, VA, 2Rheumatology, Sun Yat-sen University Third Affiliated Hospital, Guangzhou, China, 3Rheumatology, Sun Yat-sen University First Affiliated Hospital, Guangzhou, China, 4Psychiatry and Neurobehavioral Sciences, University of Virginia, Charlottesville, VA, 5Department of Medicine, University of Virginia, Charlottesville, VA

    Background/Purpose: In NZM2328 (NZM), a mouse model of proliferative lupus glomerulonephritis (GN), lupus GN can be categorized to four stages, i.e. normal, acute GN (aGN),…
  • Abstract Number: 1747 • 2016 ACR/ARHP Annual Meeting

    Dissecting the Role of Single Complement Deficiencies in a Novel Model for Apoptotic Cell-Induced Lupus

    Lucrezia Colonna1, Clayton J. Sontheimer2, Lena M. Tanaka3, Kelly L. Hudkins4, Charles E. Alpers4, Keith B. Elkon1 and YuFeng Peng3, 1Department of Medicine, Division of Rheumatology, University of Washington, Seattle, WA, 2Pediatric Rheumatology, University of Washington, Seattle, WA, 3Division of Rheumatology, University of Washington, Seattle, WA, 4Pathology, University of Washington, Seattle, WA

    Background/Purpose: The role of complement in Systemic Lupus Erythematosus (SLE) is complex as complement deficiencies in early components of the classical pathway cause lupus with…
  • Abstract Number: 2036 • 2016 ACR/ARHP Annual Meeting

    Whole Exome Sequencing in Early Onset Systemic Lupus Erythematosus

    Ezgi Deniz Batu1, Can Kosukcu2, Ekim Z. Taskiran2, Sema Akman3, Kubra Ozturk4, Betul Sozeri5, Erbil Unsal6, Zelal Ekinci4, Yelda Bilginer7, Mehmet Alikasifoglu2 and Seza Ozen8, 1Department of Pediatrics, Divison of Rheumatology, Hacettepe University Faculty of Medicine, ANKARA, Turkey, 2Department of Medical Genetics, Hacettepe University Faculty of Medicine, ANKARA, Turkey, 3Department of Pediatrics, Division of Nephrology-Rheumatology, Akdeniz University Faculty of Medicine, Antalya, Turkey, 4Department of Pediatrics, Division of Rheumatology, Kocaeli University Faculty of Medicine, Kocaeli, Turkey, 5Pediatric Rheumatology, Erciyes University Faculty of Medicine, Kayseri, Turkey, 6Dokuz Eylul University, Izmir, Turkey, 7Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, Ankara, Turkey, 8Department of Pediatrics, Division of Rheumatology, Hacettepe University Faculty of Medicine, ANKARA, Turkey

    Background/Purpose:  Systemic lupus erythematosus (SLE) is a multisystemic autoimmune disorder with different genetic and environmental factors playing role in its pathogenesis. Early onset SLE, familial…
  • Abstract Number: 2958 • 2016 ACR/ARHP Annual Meeting

    Hypocomplementemic Urticarial Vasculitis (HUV) Syndrome in Two Geographically Defined Populations of Sweden

    Christopher Sjöwall1, Thomas Mandl2 and Aladdin Mohammad3,4, 1Linköping University, Department of Clinical and Experimental Medicine Rheumatology/AIR, Linköping, Sweden, 2Department of Clinical Sciences Malmö, Lund University, Skåne University Hospital, Rheumatology, Malmö, Sweden, Malmö, Sweden, 3Department of Clinical Sciences Lund, Lund University, Skåne University Hospital, Rheumatology, Lund, Sweden, Lund, Sweden, 4Addenbrooke’s Hospital, Vasculitis and Lupus Clinic, Cambridge, UK, Cambridge, United Kingdom

    Background/Purpose: Since first described by McDuffie et al. in 1973, hypocomplementemic urticarial vasculitis (HUV) syndrome has been recognized as a specific autoimmune disorder involving at…
  • Abstract Number: 2777 • 2014 ACR/ARHP Annual Meeting

    Clinical-Biological Spectrum and Therapeutic Management of Hypocomplementemic Urticarial Vasculitis: Data from a French Nationwide Study on 57 Patients

    Marie Jachiet1, Alain Le Quellec2, Alban Deroux3, Pascal Godmer4, Mikael Ebbo5, Leonardo Astudillo6, Beatrice Flageul7, Nicolas Dupin8, Selim Aractingi1, Loïc Guillevin for the French Vasculitis Study Group9, Luc Mouthon9 and Benjamin Terrier10, 1Dermatology, Cochin Hospital, Paris, France, 2Division of internal Medicine, Hôpital Saint-Eloi, Centre Hospitalier Universitaire de Montpellier, Montpellier, Montpellier, France, 3Internal Medicine, CHU Grenoble, Grenoble, France, 4Department of Internal Medicine, Centre Hospitalier Bretagne Atlantique de Vannes, Vannes, France, 5Internal Medicine, CHU, Marseille, France, 6Internal Medicine, CHU, Toulouse, France, 7Dermatology, Saint Louis, Paris, France, 8Service de Dermatologie, Hôpital Cochin, AP-HP, Paris, France, 9National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, AP–HP, Université Paris Descartes, Paris, Paris, France, 10National Referral Center for Rare Systemic Autoimmune Diseases, Cochin Hospital, Paris, France

    Background/Purpose Hypocomplementemic urticarial vasculitis (HUV), an uncommon vasculitis of unknown etiology, is rarely reported. It is also called anti-C1q vasculitis in the 2012 revised International…
  • Abstract Number: 1618 • 2014 ACR/ARHP Annual Meeting

    Suppression of IFN-α Production from Systemic Lupus Erythematosus Immune Complexes Via C1 Complex Enzymatic Properties

    Jing Yao Leong1, Joo Guan Yeo1, Thaschawee Arkachaisri2 and Jinhua Lu3, 1Children Intensive Care Unit (CICU), KK Women's and Children's Hospital, Singapore, Singapore, 2Rheumatology & Immunology, KK Women's and Children's Hospital, Singapore, Singapore, 3Microbiology Department, National University of Singapore, Singapore, Singapore

    Background/Purpose Systemic Lupus Erythematosus (SLE) is an autoimmune disease associated with the development of auto-antibodies particularly against nuclear antigens. Previous studies have revealed the possible…
  • Abstract Number: 938 • 2014 ACR/ARHP Annual Meeting

    C1q Is Mandatory for Disease Development in Experimental Arthritis and Expression of Its Receptors Correlates with Disease Activity in Patients

    Matthieu Ribon1, Julie Mussard1, Roxane Herve1, Marina Botto2, Marie-Christophe Boissier3 and Patrice Decker1, 1INSERM UMR 1125, Li2P, University Paris 13, Sorbonne Paris Cité and Rheumatology Department, Avicenne Hospital, Assistance Publique-Hôpitaux de Paris (AP-HP), Bobigny, France, 2Centre for Complement & Inflammation Research, Imperial College, London, United Kingdom, 3INSERM UMR 1125, Li2P, University Paris 13, Sorbonne Paris Cité, Bobigny, France

    Background/Purpose The complement system is a major effector mechanism of innate and adaptive immunity. It is activated in rheumatoid arthritis (RA) patients but the pathway…
  • Abstract Number: 17 • 2013 ACR/ARHP Annual Meeting

    Autoantibodies Against Component Of Complement One Contribute To The Complement Activation and Clinical Manifestation Of Antiphospholipid Syndrome (APS) Especially In Refractory Cases

    Kenji Oku1, Olga Amengual1, Ikuma Nakagawa1, Toshiyuki Watanabe2, Yusaku Kanetsuka1, Toshiyuki Bohgaki1, Tetsuya Horita1, Shinsuke Yasuda1 and Tatsuya Atsumi1, 1Division of Rheumatology, Endocrinology and Nephrology, Hokkaido University Graduate School of Medicine, Sapporo, Japan, 2Division of Rheumatology, Endocrinology and Nephrology, Hokkaido University Graduate School of Medicine, Hokkaido, Japan

    Background/Purpose: In the pathogenic mechanisms of antiphospholipid syndrome (APS), it is recognized that pathogenicity of antiphospholipid antibodies (aPL) has dominant effects. Complement is the part…
  • Abstract Number: 2521 • 2012 ACR/ARHP Annual Meeting

    Immunoglobulin G Fc Receptor Activity in Vivo Is Under Complement Control

    Eveline Y. Wu1, Haixiang Jiang2, C. Garren Hester3 and Michael M. Frank2, 1DUMC Box 3212, Duke Univ Med Ctr, Durham, NC, 2Pediatrics, Duke Univ Med Ctr, Durham, NC, 3Duke Univ Med Ctr, Durham, NC

    Background/Purpose: Immunoglobulin G receptors (FcγR) are critical in the development of autoimmunity and pathogenesis of immune complex (IC) diseases. Although ICs activate complement, contributing to…
  • Abstract Number: 1637 • 2012 ACR/ARHP Annual Meeting

    A Novel Peptide Inhibiting the Binding Between C1q and Immunoglobulin Ameliorates Joint Destruction in Rats with Collagen-Induced Arthritis

    Yu Moriguichi and Tetsuya Tomita, Department of Orthopaedic Surgery, Osaka University Graduate School of Medicine, Suita, Japan

    Background/Purpose: C1q is the major subcomponent of the first component of complement protein. The activation of the complement is triggered by binding of C1q to…
  • Abstract Number: 661 • 2012 ACR/ARHP Annual Meeting

    Co-Localization of C-Reactive Protein, Immunoglobulin G and Complement in Renal Subendothelial Immune Deposits of Proliferative Lupus Nephritis Detected Using Immunogold Electron Microscopy

    Christopher Sjöwall1, Anders I. Olin2, Thomas Skogh3, Jonas Wetterö4, Mattias Mörgelin2, Ola Nived5, Gunnar Sturfelt6 and Anders A. Bengtsson7, 1Deparment of clinical and experimental medicine, Linkoping University, Linkoping, Sweden, 2Infection Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden, Lund, Sweden, 3Deparment of clinical and experimental medicine, Linköping University, Linköping, Sweden, 4Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden, 5Department of Rheumatology, University Hospital Lund, Lund, Sweden, 6Department of Clinical Sciences Lund, Section of Rheumatology, Lund University, Lund, Sweden, 7Department of Clinical Sciences, Section of Rheumatology, Lund University, Lund, Sweden

    Background/Purpose: The pattern recognition molecules C-reactive protein (CRP) and complement protein 1q (C1q) are pivotal parts of the innate immune system and display relevant biological…
  • Abstract Number: 662 • 2012 ACR/ARHP Annual Meeting

    Increased C1q, C4 and C3 Deposition On Platelets in Patients with Systemic Lupus Erythematosus – A Possible Link to Venous Thrombosis?

    Christian Lood1, Sam Eriksson1, Birgitta Gullstrand2, Andreas Jönsen1, Gunnar Sturfelt3, Lennart Truedsson2 and Anders A. Bengtsson4, 1Department of Clinical Sciences Lund, Section of Rheumatology, Lund, Sweden, 2Department of Laboratory Medicine, Section of Microbiology, Immunology and Glycobiology, Lund University, Lund, Sweden, 3Department of Clinical Sciences Lund, Section of Rheumatology, Lund University, Lund, Sweden, 4Department of Clinical Sciences, Section of Rheumatology, Lund University, Lund, Sweden

    Background/Purpose: Patients with systemic lupus erythematosus (SLE) have an increased risk of developing vascular diseases (VD) such as myocardial infarction, stroke and venous thrombosis, which…
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