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  • Abstract Number: 2871 • 2014 ACR/ARHP Annual Meeting

    Break of Anergy in Human Autoreactive B Cells By T Helper Signals Restores B Cell Receptor Signaling Capacity and Is Dependent on Upregulation of CD45 Phosphatase Activity-a Possible Novel Mechanism of Breech of B Cell Tolerance in Rheumatic Diseases

    Peter Szodoray1, Stephanie M. Stanford2, Nunzio Bottini2 and Britt Nakken1, 1Institute of immunology, Rikshospitalet, Oslo University Hospital, Oslo, Norway, 2Cellular Biology, La Jolla Institute for Allergy and Immunology, La Jolla, CA

    Background/Purpose : We recently identified a human B cell population, which is naturally autoreactive and tolerized by functional anergy. This population was naïve, fully mature,…
  • Abstract Number: 2872 • 2014 ACR/ARHP Annual Meeting

    B-Cell Autoepitope and Tetramer Analysis Reveals Expansion of Apoptotic Autoantigen La and snRNP Reactive B Cells in BXD2 Mice

    Jennie Hamilton1, Jun Li2, Qi Wu3, PingAr Yang3, Bao Luo3, Hao Li4, Troy Randall5, John Edwin Bradley5, Justin J. Taylor6, John D. Mountz7,8 and Hui-Chen Hsu3,4, 1University of Alabama at Birmingham, Birmingham, AL, 2Med - Immunology/Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 4Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 5Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 6Vaccine and Infectious Disease Division, Fred Hutchinson Cancer Research Center, Seattle, WA, 7Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL, 8Birmingham VA Medical Center, Birmingham, AL

    Background/Purpose Systemic lupus erythematous (SLE) is characterized by production of highly pathogenic IgG autoantibodies (autoAbs).  While serum autoAb profiling is standard, it remains challenging to…
  • Abstract Number: 2873 • 2014 ACR/ARHP Annual Meeting

    Epratuzumab Induces Broad Inhibition of B Cell Receptor Proximal Signaling but Has Opposing Effects on Distal Signaling in B Cell Subsets: A Profile of Effects on Functional Immune Signaling By Single Cell Network Profiling

    Alison Maloney1, Drew Hotson2, Stephen Rapecki1, Gianluca Fossati1, Simon Lumb1, David Rosen2, Santosh Putta2, Nikil Wale2, David Spellmeyer2, Alessandra Cesano2, Rachael Hawtin2 and Anthony Shock1, 1UCB Pharma, Slough, United Kingdom, 2Nodality Inc., South San Francisco, CA

    Background/Purpose Epratuzumab is a humanized monoclonal antibody targeting the B cell-specific protein CD22 and is in Phase 3 clinical trials in patients with systemic lupus…
  • Abstract Number: 2874 • 2014 ACR/ARHP Annual Meeting

    Pro-Inflammatory FcRL4+ Memory B Cells in Joints of RA Patients: Immunoglobulin Gene Characteristics and Antigen Specificity

    Khaled Amara1, Lorraine Yeo2, Natalie Sippl1, Philip Titcombe1, Andrew Filer3, Karim Raza3, Dagmar Scheel-Toellner2 and Vivianne Malmström4, 1Rheumatology Unit, Department of Medicine, Karolinska University Hospital, Karolinska Institutet, SE-17176 Solna, Stockholm, Sweden., Stockholm, Sweden, 2Rheumatology Research Group, Centre for Translational Inflammation Research, College of Medical and Dental Sciences, University of Birmingham, Birmingham B15 2TT, UK, Birmingham, United Kingdom, 3Rheumatology Research Group, MRC Centre for Immune Regulation, School of Immunity and Infection, University of Birmingham, Birmingham, United Kingdom, 4Medicine, Rheumatology Unit, Karolinska University Hospital, Solna, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose:    Our recent findings identified a subset of pro-inflammatory memory B cells in the RA synovium characterized by the expression of the surface protein…
  • Abstract Number: 2835 • 2014 ACR/ARHP Annual Meeting

    A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Proof-of-Concept Study to Evaluate the Efficacy and Safety of Sirukumab in Patients with Active Lupus Nephritis

    Cynthia Aranow1, R. van Vollenhoven2, Brad H. Rovin3, Carrie Wagner4, Bei Zhou4, Robert Gordon4 and Benjamin Hsu4, 1The Feinstein Institute for Medical Research, Manhasset, NY, 2The Karolinska Institute, Stockholm, Sweden, 3Division of Nephrology, Ohio State University Medical Center, Columbus, OH, 4Janssen Research & Development, LLC., Spring House, PA

    Background/Purpose:   IL-6 is a pro-inflammatory cytokine that is over-expressed in lupus nephritis(LN). This proof-of-concept study examined the efficacy and safety of sirukumab, an anti-interleukin-6…
  • Abstract Number: 2836 • 2014 ACR/ARHP Annual Meeting

    Effects of Blisibimod, an Inhibitor of B Cell Activating Factor, on Patient Reported Outcomes and Disease Activity in Patients with Systemic Lupus Erythematosus

    Michelle Petri1, Renee S. Martin2, Colin Hislop2, Morton A. Scheinberg3 and Richard Furie4, 1Johns Hopkins University School of Medicine, Baltimore, MD, 2Anthera Pharmaceuticals Inc, Hayward, CA, 3Rheumatology Hospital Abreu Sodre Pesquisa Clínica, São Paulo, Brazil, 4Division of Rheumatology and Allergy-Clinical Immunology, North Shore - Long Island Jewish Health System, Great Neck, NY

    Background/Purpose: To conduct secondary endpoint analyses of the effects of subcutaneously-administered blisibimod (A-623, AMG 623), an inhibitor of B-cell activating factor (BAFF), on patient-reported outcomes and…
  • Abstract Number: 2837 • 2014 ACR/ARHP Annual Meeting

    Induction of Clinical Remission By Low-Dose Interleukin-2 in Refractory SLE

    Jens Y. Humrich1, Caroline von Spee-Mayer1, Elise Siegert1, Angelika Rose1, Tobias Alexander2, Falk Hiepe1, Andreas Radbruch3, Gerd Burmester4 and Gabriela Riemekasten1, 1Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Germany, 2Department of Rheumatology and Clinical Immunology, Charité – University Hospital, Berlin, Germany, 3German Rheumatism Research Centre Berlin (DRFZ), an institute of the Leibniz Association, Berlin, Germany, 4Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology, Berlin, Germany

    Background/Purpose Interleukin-2 (IL-2) is crucial for the growth and survival of regulatory T cells (Treg), and thus for the control of autoimmunity. In previous studies…
  • Abstract Number: 2838 • 2014 ACR/ARHP Annual Meeting

    Exploratory Analysis of Pharmacokinetic Effects of Atacicept in Patients with Moderate to Severe Systemic Lupus Erythematosus

    David Wofsy1, Caroline Gordon2, Yong Li3, Stephen D. Wax4 and David Isenberg5, 1Division of Rheumatology, University of California, San Francisco, CA, 2Rheumatology Research Group, School of Immunity and Infection, College of Medical and Dental Sciences, University of Birmingham, Birmingham, United Kingdom, 3R&D Global BioStatistics, EMD Serono, Billerica, MA, 4Global Clinical Development Center - Immunology, EMD Serono Inc, Rockland, MA, 5Centre for Rheumatology Research, University College Hospital London, London, United Kingdom

    Background/Purpose: Atacicept is a fusion protein that inhibits B-cell stimulating factors BLyS and APRIL. We previously reported the clinical effects of atacicept in lupus patients…
  • Abstract Number: 2839 • 2014 ACR/ARHP Annual Meeting

    BCL-2 As a Potential Therapeutic Target in Human Lupus Tubulointerstitial Inflammation

    Kichul Ko1, Denisse Yanez1, Natalya Kaverina1, Vladimir M. Liarski1, Yahui Peng2, Li Lan3, Stuart Perper4, Annette Schwartz5, Liz O'connor6, Andrew Souers7, Steven Elmore7, Lisa Olson5, Maryellen L. Giger3, Li Chun Wang4 and Marcus R. Clark1, 1Rheumatology and Knapp Center for Lupus Research, University of Chicago, Chicago, IL, 2School of Electronic and Information Engineering, Beijing Jiaotong University, Beijing, China, 3Radiology, University of Chicago, Chicago, IL, 4Immunology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 5AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 6Toxicology, AbbVie Inc, AbbVie Bioresearch Center, Worcester, MA, 7AbbVie Inc, North Chicago, IL

    Background/Purpose Lupus nephritis (LuN) is the most common, severe manifestation of systemic lupus erythematosus (SLE). We have previously shown that glomerulonephritis appears to be a…
  • Abstract Number: 2840 • 2014 ACR/ARHP Annual Meeting

    Targeting the RhoA-Rock Pathway to Reverse T Cell Dysfunction in SLE

    Cristina T. Rozo1, Laura Leuenberger2, Kyriakos A. Kirou3, Margaret Robotham1, Sanjay Gupta4, Reena Khianey2, Alessandra B. Pernis4 and Jane E. Salmon2, 1535 East 70th Street, Hospital for Special Surgery, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Hospital for Special Surgery, New York, NY, 4Autoimmunity & Inflammation Research Program, Hospital for Special Surgery, New York, NY

    Background/Purpose Aberrant expansion of TH-17 cells and deregulated production of IL-17 and IL-21 are involved in the pathogenesis of SLE. Production of IL-17 and IL-21…
  • Abstract Number: 2841 • 2014 ACR/ARHP Annual Meeting

    Identifying Novel Lupus Severity Risk Variants through Identification of Alleles with High Ethnic Variability Worldwide

    Belinda A. Waltman1, Kimberly E. Taylor2, Julio Molineros3, Sarah French4, Joanne Nitiham1, Jennifer Kelly3, Adam Adler5, Judith A. James3, Swapan Nath6, Marta Alarcon-Riquelme3,7 and Lindsey A. Criswell1, 1Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 2Department of Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 3Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4School of Medicine, University of California, San Francisco, Rosalind Russell / Ephraim P. Engleman Rheumatology Research Center, San Francisco, CA, 5Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 6Oklahoma Medical Research Foundation, Oklahoma City, OK, 7GENYO. Center for Genomics and Oncological Research, Granada, Spain

    Background/Purpose: Substantial epidemiologic evidence demonstrates that SLE disproportionately affects minority patients in terms of incidence, prevalence, and disease severity. European ancestry has been associated with…
  • Abstract Number: 2842 • 2014 ACR/ARHP Annual Meeting

    An Anti CD123 Monoclonal Antibody (CSL362) Depletes Plasmacytoid Dendritic Cells and Inhibits CpG Upregulated IFNα Production and IFNα-Inducible Gene Expression in Peripheral Blood Mononuclear Cells from Patients with Systemic Lupus Erythematosus

    Shereen Oon1,2,3, Nicholas Wilson4,5 and Ian Wicks1,2,3, 1Inflammation, The Walter and Eliza Hall Institute of Medical Research, Melbourne, Australia, 2Rheumatology, The Royal Melbourne Hospital, Melbourne, Australia, 3Medical Biology, The University of Melbourne, Melbourne, Australia, 4Cell Biology and Physiology, CSL Limited, Melbourne, Australia, 5Honorary appointment, The University of Melbourne, Melbourne, Australia

    Background/Purpose Plasmacytoid dendritic cells (pDCs) contribute to systemic lupus erythematosus (SLE) pathogenesis by producing Type 1 interferon (IFN), most likely induced by endosomal Toll like…
  • Abstract Number: 2843 • 2014 ACR/ARHP Annual Meeting

    SLE Patients Carrying a Disease-Associated PTPN22 R620W Variant Show Reduced Interferon-Inducing Capacity

    Yaya Wang1, David Ewart2, Ami Yamamoto2, Emily C. Baechler1, Parastoo Fazeli3 and Erik J. Peterson2, 1Medicine, University of Minnesota, Minneapolis, MN, 2University of Minnesota, Minneapolis, MN, 3Division of Rheumatic and Autoimmune Diseases, University of Minnesota, Minneapolis, MN

    Background/Purpose Type 1 interferons (IFN) are implicated in the pathogenesis of systemic lupus erythematosus (SLE). Increased expression of IFN-regulated genes, termed the IFN-signature, correlates with…
  • Abstract Number: 2844 • 2014 ACR/ARHP Annual Meeting

    Intracellular Complement C3 Is Exposed on the Cell Surface upon Apoptosis Induction and Participates in the Clearance of Apoptotic Cells By Phagocytes

    Lucrezia Colonna1, Christian Lood1, YuFeng Peng2, Xizhang Sun3, Lena Tanaka3, Sandip Panicker4 and Keith B. Elkon3, 1Department of Medicine, Division of Rheumatology, University of Washington, Seattle, WA, 2Rheumatology, University of Washington, Seattle, WA, 3Division of Rheumatology, University of Washington, Seattle, WA, 4True North Therapeutics, South San Francisco, CA

    Background/Purpose The complement system has been viewed as a predominantly serum-derived host defense mechanism with multiple functions, including clearance of apoptotic cells. Defective function of…
  • Abstract Number: 2845 • 2014 ACR/ARHP Annual Meeting

    Altered Plasticity of Inflammatory CD4 T Cells Contributing to Th17 Shift in Rheumatoid Arthritis

    Jan Leipe, Fausto Pirronello, Simon Hermann, Matthias Witt, Hendrik Schulze-Koops and Alla Skapenko, Division of Rheumatology and Clinical Immunology, University of Munich, Munich, Germany

    Background/Purpose Whereas T helper (Th) cell subsets were previously regarded as irreversibly differentiated endpoints, evidence suggests that Th cell differentiation is a plastic process in…
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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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