ACR Meeting Abstracts

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Abstracts tagged "B cells"

  • Abstract Number: 1922 • 2015 ACR/ARHP Annual Meeting

    Peripheral B Lymphocytes Secrete Both Interleukin 6 and Transforming Growth Factor-Beta and Potentiate Fibroblast Activation in Systemic Sclerosis

    Nicolas Dumoitier1,2,3,4, Sebastien Lofek2,3,5, Alexis Regent6, Jonathan London7, Benjamin Chaigne1,2,3,8, Benjamin Terrier2,7,9,10, Nadine Varin-Blank4,11 and Luc Mouthon1,2,4,6, 1Infection, Immunité, Inflammation, Institut Cochin, INSERM U1016, Paris, France, 2CNRS, UMR8104, Paris, France, 3Université Paris Descartes, Paris, France, 4Labex Inflamex, Université Sorbonne Paris Cité, Paris, France, 5Infection,Immunité, Inflammation, Institut Cochin, INSERM U1016, Paris, France, 6Internal Medicine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, Paris, France, 7Internal Medecine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochin, Paris, France, 8Internal Medecine, National Referral Center for Rare Systemic Autoimmune Diseases, Hôpital Cochinl, Paris, France, 9Infection, Immunité, Inflammation, Institut Cochin INSERM U1016, Paris, France, 10Université Paris Descartes, paris, France, 11UFR SMBH, INSERM, UMR978, Bobigny, France

    Background/Purpose: Systemic sclerosis (SSc) is a rare connective tissue disease characterized by fibroblasts activation, increased extra-cellular matrix synthesis associated with autoimmunity. However, the potential role…
  • Abstract Number: 738 • 2015 ACR/ARHP Annual Meeting

    Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of the BCL-2 Inhibitor Venetoclax (ABT-199) in a Phase 1 Single and Multiple Ascending Dose Study in Female Patients with Systemic Lupus Erythematosus

    Peng Lu1, Roy Fleischmann2, Craig Curtis3, Stanislav Ignatenko4, Monali Desai5, Shekman L. Wong5, Kristie M. Grebe1, Jiewei Zeng5, Jeroen Medema5 and James Stolzenbach5, 1AbbVie Inc., Worcester, MA, 2University of Texas Southwestern Medical Center, Dallas, TX, 3Compass Research Center, Orlando, FL, 4Charité Research Organization, Berlin, Germany, 5AbbVie Inc., North Chicago, IL

    Background/Purpose: Apoptosis is needed to eliminate auto-reactive T and B cells during immune responses; failure of elimination is important in development of systemic lupus erythematosus…
  • Abstract Number: 1115 • 2015 ACR/ARHP Annual Meeting

    B Cell-Intrinsic Interferon Gamma Signals Promote the Development of Systemic Lupus Erythematosus By Enhancing the Formation of Spontaneous Autoimmune Germinal Centers

    Shaun Jackson, Nicole Scharping, Holly Jacobs, Tanvi Arkatkar, Socheath Khim and David Rawlings, Seattle Children's Research Institute, Seattle, WA

    Background/Purpose: Type 1 interferon (IFN) is strongly implicated in lupus pathogenesis, and SLE patients frequently express a “type 1 IFN gene signature”. The type 2…
  • Abstract Number: 1934 • 2015 ACR/ARHP Annual Meeting

    Autophagy Pathway As a Target of Therapeutic P140 Peptide Used in Lupus

    Maud Wilhelm1, Fengjuan Wang2, Nicolas Schall2, Michael Faludi3, Jean Francois Kleinmann4, Emil P. Nashi5, Thierry Martin6, Jean Sibilia7, Jean-Louis Pasquali8, Daniel Wallace9 and Sylviane Muller10, 1Immunopathologie & Chimie Thérapeutique, CNRS, Strasbourg, France, 2CNRS, Strasbourg, France, 3761 Graham, McGill University, Mont-Royal, QC, Canada, 4Rheumatology, Strasbourg University Hospital, Strasbourg, France, 5Rheumatology, McGill University Health Centre, Montreal, QC, Canada, 6Cnrs UPR9021, IBMC, Strasbourg, France, 7Department of Rheumatology, Strasbourg University Hospital, Strasbourg, France, 8Strasbourg University, Hospital, CNRS UPR 3572, Strasbourg, France, 9Cedars-Sinai/UCLA, Los Angeles, CA, 10CNRS Institut de Biologie Moléculaire et Cellulaire, Strasbourg, France

    Background/Purpose: P140 is a 21-mer peptide (sequence 131-151, phosphorylated at position 140) that is derived from the spliceosomal protein U1-70K. In a multicenter, randomized, placebo-controlled…
  • Abstract Number: 1052 • 2015 ACR/ARHP Annual Meeting

    Identification of Novel Sjogren’s Syndrome Risk Loci in the Regions of TNFAIP3 and PRDM1

    Christopher J. Lessard1,2, He Li1,2, John Ice2, Indra Adrianto3, Astrid Rasmussen2, Kiely Grundahl4, Jennifer A. Kelly5, Corinne Miceli6, Simon Bowman7, Susan Lester8, Johan G. Brun9,10, Lasse G. Goransson11, Erna Harboe11, Joel M. Guthridge2, Kenneth M. Kaufman12,13, Per Eriksson14, Maija-Leena Eloranta15, Marika Kvarnström16, Deborah S. Cunninghame-Graham17, A. Darise Farris2, Michael T. Brennan18, James Chodosh19, Raj Gopalakrishnan20, Andrew J.W. Huang21, Pamela Hughes22, David M. Lewis23, Lida Radfar24, Michael D. Rohrer25, Donald U. Stone26, Timothy J. Vyse17, Patrick M. Gaffney2, Judith A. James1,5,27, John B. Harley12,28, Roald Omdal11, Marie Wahren-Herlenius16, Gabor G. Illei29, Torsten Witte30, Roland Jonsson10,31, Maureen Rischmueller32,33, Lars Rönnblom34, Xavier Mariette35, Juan-Manuel Anaya36, Wan-Fai Ng37, Gunnel Nordmark34, Courtney G. Montgomery2, Nelson L. Rhodus38, Barbara M. Segal39, R. Hal Scofield2,27,40 and Kathy L. Sivils1,2, 1Department of Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 2Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma CIty, OK, 5Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 6Rheumatology, PARIS, France, 7Rheumatology Dept, University Hospital Birmingham, Birmingham, United Kingdom, 8Queen Elizabeth Hospital, Adelaide, Australia, 9Institute of Internal Medicine, University of Bergen, Bergen, Norway, 10Department of Rheumatology, Haukeland University Hospital, Bergen, Norway, 11Clinical Immunology Unit, Department of Internal Medicine, Stavanger University Hospital, Stavanger, Norway, 12US Department of Veterans Affairs Medical Center, Cincinnati, OH, 13Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 14Department of Clinical and Experimental Medicine, Rheumatology/AIR, Linköping University, Linköping, Sweden, Linköping, Sweden, 15Department of Medical Sciences, SciLife Lab, Rheumatology, Uppsala University, Uppsala, Sweden, Uppsala, Sweden, 16Department of Medicine, Karolinska Institutet, Stockholm, Sweden, 17Department of Medical and Molecular Genetics, King's College London, London, United Kingdom, 18Department of Oral Medicine, Carolinas Medical Center, Charlotte, NC, 19Ophthalmology, Massachusetts Eye and Ear Infirmary, Harvard Medical School, Boston, MA, 20Diagnostic and Biological Sciences, Division of Oral Pathology, University of Minnesota, Minneapolis, MN, 21Department of Ophthalmology and Visual Sciences, Washington University, St Louis, MO, 22Division of Oral and Maxillofacial Surgery, Department of Developmental and Surgical Science, University of Minnesota School of Dentistry, Minneapolis, MN, 23College of Dentistry, Department of Oral and Maxillofacial Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 24Oral Diagnosis and Radiology Department, University of Oklahoma Health Sciences Center College of Dentistry, Oklahoma City, OK, 25Hard Tissue Research Laboratory, University of Minnesota School of Dentistry, Minneapolis, MN, 26Department of Ophthalmology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 27Department of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 28Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 29National Institute of Dental and Craniofacial Research, NIH, Bethesda, MD, 30Hannover Medical School, Hanover, Germany, 31Broegelmann Research Laboratory, The Gade Institute, University of Bergen, Bergen, Norway, 32University of Adelaide, Adelaide, Australia, 33Department of Rheumatology, The Queen Elizabeth Hospital, Adelaide, Australia, 34Rheumatology, Department of Medical Sciences and Science for Life Laboratory, Uppsala University, Uppsala, Sweden, 35AP-HP, Hopitaux Universitaires Paris-Sud, Université Paris-Sud, Paris, France, 36Center for Autoimmune Diseases Research (CREA), Universidad del Rosario, Bogotá, Colombia, 37Institute of Cellular Medicine, Newcastle University, Newcastle upon Tyne, United Kingdom, 38Department of Oral Surgery, University of Minnesota School of Dentistry, Minneapolis, MN, 39Division of Rheumatology, University of Minnesota Medical School, Minneapolis, MN, 40US Department of Veterans Affairs Medical Center, Oklahoma City, OK

    Background/Purpose: Sjögren’s syndrome (SS) is a complex autoimmune disease with both environmental and genetic factors playing important roles in its pathophysiology. The goal of this…
  • Abstract Number: 1116 • 2015 ACR/ARHP Annual Meeting

    Decreased Expression of Negative Regulators of Toll-like Receptor Signaling and Increased TLR7 Responsiveness in Expanded IgD- CD27- B Cells from Systemic Lupus Erythematosus Patients

    Scott Jenks1, Benjamin Barwick2 and Ignacio Sanz3, 1Allergy, Immunology, and Rheumatology, Emory University School of Medicine, Atlanta, GA, 2Emory University, Altanta, GA, 3Medicine, Emory University, Atlanta, GA

    Background/Purpose: B cell homeostasis is perturbed in SLE patients; in particular many patients with active disease have a large expansion of IgD- CD27- B cells…
  • Abstract Number: 1942 • 2015 ACR/ARHP Annual Meeting

    B Cell Depletion By Rituximab in Lymphocyte Subpopulations from Peripheral Blood in Patients with Rheumatoid Arthritis

    Leticia Merino-Meléndez1, Jorge López-López2, Irene Llorente1, Santos Castañeda3, Federico Herrera2, Teresa Velasco4, Lorena Vega5, Francisco Rodriguez5, Jose María Alvaro-Gracia3, Rosario Garcia-Vicuña6, Cecilia Muñoz-Calleja2 and Isidoro Gonzalez-Alvaro7, 1Rheumatology, H.U. La Princesa, Madrid, Spain, 2Immunology, Hospital Universitario de La Princesa, Madrid, Spain, 3Hospital Universitario de La Princesa. IIS La Princesa, Madrid, Spain, 4Rheumatology, H.U La Princesa, Madrid, Spain, 5H.U. La Princesa, Madrid, Spain, 6Rheumatology, Hospital Universitario de La Princesa. IIS La Princesa, Madrid, Spain, 7Hospital Univ. de La Princesa, IIS Princesa, Madrid, Spain

    Background/Purpose: Rheumatoid arthritis (RA) is a chronic disease that leads to inflammation of the joints and other tissues. Rituximab (Rtx) is a therapeutic monoclonal antibody…
  • Abstract Number: 1073 • 2015 ACR/ARHP Annual Meeting

    B Cell Subsets Are Epigenetically and Transcriptionally Dysregulated in Systemic Lupus Erythematosus

    Emily Blalock1, Chris Scharer2, Ben Barwick2, Scott Jenks3, Bridget Neary3, Jeremy Boss2 and Ignacio Sanz3,4, 1Emory University School of Medicine, Atlanta, GA, 2Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, 3Rheumatology, Emory University School of Medicine, Atlanta, GA, 4Medicine, Emory University, Atlanta, GA

    Background/Purpose: Systemic lupus erythematosus (SLE) is characterized by multiple B cell abnormalities, including the production of autoantibodies, a major contributing factor to disease pathogenesis. Epigenetic…
  • Abstract Number: 1118 • 2015 ACR/ARHP Annual Meeting

    Role of the Chemokine Receptor CXCR3 in the Function of Regulatory B Cells in Patients with SLE

    Shun-ichiro Ota1,2, Hiroaki Niiro3, Naoko Ueki2,4, Yuri Hirosaki2, Hirofumi Tsuzuki2, Siamak Jabbarzadeh-Tabrizi2, Tsuyoshi Nakayama2, Koji Mishima2, Ayako Takaki2, Hiroki Mitoma2, Mitsuteru Akahoshi2, Yojiro Arinobu2, Hiroshi Tsukamoto2 and Koichi Akashi2, 1Department of Rheumatology, Internal medicine and connective tissue disorders, Shimonoseki City Hospital, Shimonoseki, Japan, 2Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan, 3Clinical Education Center, Kyushu University Hospital, Fukuoka, Japan, 4Division of Nephrology and Rheumatology, Fukuoka University, Fukuoka, Japan

    Background/Purpose: The emerging application of B-cell directed therapies in autoimmune diseases has led to the discovery of a novel B cell population, referred to as…
  • Abstract Number: 2460 • 2015 ACR/ARHP Annual Meeting

    B10 Cells May be Involved in Controlling Disease Activity in Polyarticular Juvenile Idiopathic Arthritis Patients

    Qianzi Zhao1 and Lawrence K. Jung2, 1Rheumatology, Children's National Medical Center, Washington, DC, 2Pediatric Rheumatology, Children's National Medical Center, Washington, DC

    Background/Purpose: In addition to antibodies production, B cells have been shown to have down-regulatory function on immune response in both mouse and human. The down-regulatory…
  • Abstract Number: 1096 • 2015 ACR/ARHP Annual Meeting

    B Cells Are Prime Producers of Tumor Necrosis Factor Alpha in Rheumatoid Arthritis

    Victor Wang1, Nida Meednu1, Wen Sun2, Javier Rangel-Moreno3, Lianping Xing2 and Jennifer H. Anolik1, 1Medicine- Allergy, Immunology and Rheumatology, University of Rochester Medical Center, Rochester, NY, 2Pathology & Lab Medicine, University of Rochester Medical Center, Rochester, NY, 3Medicine- Allergy, Immunology, and Rheumatology, University of Rochester Medical Center, Rochester, NY

    Background/Purpose: Rheumatoid arthritis (RA) is a systemic autoimmune disease, which causes joint inflammation and bone loss. Inflammation-mediated joint damage is linked to the imbalance of…
  • Abstract Number: 1120 • 2015 ACR/ARHP Annual Meeting

    Analysis of SLE Plasmablasts By High Throughput Pairing of the Immunoglobulin Heavy and Light Chain (VH-VL)

    Deepak Tomar1, Christopher Tipton1 and Ignacio Sanz2, 1Medicine/Rheumatology, Emory University School of Medicine, Atlanta, GA, 2Rheumatology, Emory University School of Medicine, Atlanta, GA

    Background/Purpose: In-depth analysis of the molecular and antigenic properties of antibody secreting cells (ASC) is critical for our understanding of autoimmune diseases.  This goal however…
  • Abstract Number: 3075 • 2015 ACR/ARHP Annual Meeting

    Salivary Gland FcRL4+ B-Cells Are a Potential Source of Progenitor Cells for MALT Lymphoma in Primary Sjögren’s Syndrome

    Erlin A. Haacke1, Frans G.M. Kroese2, Philip Kluin3, Petra M. Meiners4, Annie Visser5, Fred K.L. Spijkervet6 and Hendrika Bootsma7, 1Pathology, University Medical Center Groningen, Groningen, Netherlands, 2Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, Netherlands, 3Department of Pathology and Medical Biology, UMCG Groningen, Groningen, Netherlands, 4Oral and Maxillofacial Surgery, University Medical Center Groningen, University of Groningen, Groningen, Netherlands, 5Rheumatology and Clinical Immunology, UMC Groningen, Groningen, Netherlands, 6Oral and Maxillofacial Surgery, University Medical Center Groningen, Groningen, Netherlands, 7Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, Groningen, Netherlands

    Background/Purpose: Patients with primary Sjögren's Syndrome (pSS) have an increased risk of non-Hodgkin's lymphoma, predominantly of the Mucosa Associated Lymphoid Tissue (MALT) type, which commonly…
  • Abstract Number: 1097 • 2015 ACR/ARHP Annual Meeting

    Pre-Clinical Development of a Novel, Potent and Selective BTK Inhibitor for Autoimmune Disease and Inflammation Including Arthritis

    Stephen Morris, Alain Laurent, Lori Jerome, Alain Boudreault, Helen Ashdown, Yannick Rose, Patrick Bureau, Shou-Yun Yin, Patrick Cleroux, Delphine Labit, Nicholas Henry, Marie-Noelle Tremblay, Marlyna Guerard, Emilie Dumas Bérubé and Kosta Spathis, Pharmascience Inc., Ville St-Laurent, QC, Canada

    Background/Purpose: Bruton’s tyrosine kinase (BTK) is an important component of B cell and Fc receptor signaling and has been shown to be critical for B-cell…
  • Abstract Number: 1123 • 2015 ACR/ARHP Annual Meeting

    Regulatory B Cells Regulate Skin and Lung Fibrosis and Immunological Abnormalities in a Topoisomerase I and Complete Freund’s Adjuvant-Induced Scleroderma Model Via an Antigen-Specific Manner

    Ayumi Yoshizaki1, Takashi Taniguchi1, Kouki Nakamura1, Ryosuke Saigusa1, Takashi Yamashita1, Takehiro Takahashi1, Tetsuo Toyama1, Yohei Ichimura1, Yoshihide Asano2 and Shinichi Sato1, 1Dermatology, University of Tokyo Graduate School of Medicine, Tokyo, Japan, 2University of Tokyo Graduate School of Medicine, Tokyo, Japan

    Background/Purpose: Immune cells play a critical role in systemic sclerosis (SSc). B cells have more functions than producing antibodies, including antigen-presentation, various cytokine production, and…
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