ACR Meeting Abstracts

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Abstracts tagged "SLE"

  • 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: 2631 • 2014 ACR/ARHP Annual Meeting

    Overall Cause and Cause-Specific Mortality in a Multinational Inception Cohort of SLE

    Murray B. Urowitz1, Dafna D. Gladman1, Nicole Anderson2, Dominique Ibanez3 and Systemic Lupus International Collaborating Clinics (SLICC)4, 1University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 2Rheumatology, Toronto Western Hospital Research Institute, Toronto, ON, Canada, 3Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 4Toronto Western Hospital, Division of Rheumatology, University of Toronto, Toronto Western Hospital (Coordinating Center), Toronto, ON, Canada

    Background/Purpose: A large multicenter multinational inception cohort was established initially to study risk factors for atherosclerosis (AS) in SLE.   The aim of this study was…
  • Abstract Number: 1828 • 2014 ACR/ARHP Annual Meeting

    Adverse Pregnancy Outcomes in Adolescents and Young Women with Systemic Lupus Erythematosus: A National Estimate

    Nicole Ling1, Isabel E. Allen2, Erica F. Lawson1 and Emily von Scheven3, 1Pediatrics, University of California, San Francisco, San Francisco, CA, 2Epidemiology and Biostatistics, University of California, San Francisco, San Francisco, CA, 3Pediatric Rheumatology, University of California, San Francisco, San Francisco, CA

    Background/Purpose: Pregnant women with SLE have increased risk of adverse outcomes including lupus flare, spontaneous abortion, preeclampsia/eclampsia, premature birth and maternal death, but pregnancy outcomes…
  • Abstract Number: 1294 • 2014 ACR/ARHP Annual Meeting

    Gender Differences in the Lupus Nephritis Biomarkers in Children

    Khalid Abulaban1, Hermine Brunner2, Michael Bennett3, Shannen L. Nelson4, Jun Ying5 and Prasad Devarajan3, 1Pediatric Rheumatology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 2Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 3Nephrology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 4Rheumatology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 5University of Cincinnati, Cincinnati, OH

    Background/Purpose:  Lupus nephritis (LN) is frequently associated with a poor long-term prognosis. The non-invasive traditional measures of LN (LN-TM) currently used to monitor LN have…
  • Abstract Number: 674 • 2014 ACR/ARHP Annual Meeting

    A Novel Strategy to  Identify and Evaluate Approved Drugs and Treatments for Repositioning As Therapies for Systemic Lupus Erythematosus (SLE)

    Peter E. Lipsky, Matthew Ryals, Jacob Smearman, Victoria Soler and Amrie Grammer, AMPEL BioSolutions, Charlottesville, VA

    Background/Purpose: Development of new SLE treatments has been slow with only one new treatment approved in the past half century. One way to increase the…
  • 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: 2623 • 2014 ACR/ARHP Annual Meeting

    Treatment Patterns and Resource Utilization of Systemic Lupus Erythematosus Patients Newly Initiating Standard of Care: United States Commercial and Medicare Supplemental Claims Analysis

    Shonda A Foster1, Emily Durden2, Brett Maiese2, Sarah Al Sawah1 and Kathleen Solotkin1, 1Eli Lilly and Company, Indianapolis, IN, 2Truven Health Analytics, Bethesda, MD

    Background/Purpose: Currently, there is not a standard treatment algorithm for the management of Systemic Lupus Erythematosus (SLE); however, there are medications that may be considered…
  • Abstract Number: 1813 • 2014 ACR/ARHP Annual Meeting

    DNA Sensors Regulate Inflammation in a Model of Autoimmune Arthritis

    Rebecca Baum1, Shruti Sharma2, Sudesh Pawaria3, Susan Carpenter4, Katherine A. Fitzgerald5, Ann Marshak-Rothstein6 and Ellen M. Gravallese7, 1Cell Biology, University of Massachusetts Medical School, Worcester, MA, 2Department of Medicine - Infectious Diseases Division, University of Massachusetts Medical School, Worcester, MA, 3Department of Medicine, University of Massachusetts Medical School, Worcester, MA, 4University of California, San Francisco, San Francisco, CA, 5Department of Medicine, Division of Infectious Diseases and Immunology, University of Massachusetts Medical School, Worcester, MA, 6Department of Medicine, Division of Rheumatology, University of Massachusetts Medical School, Worcester, MA, 7Department of Medicine, Division of Rheumatology, UMass Memorial Medical Center, Worcester, MA

    Background/Purpose: Innate immune sensors such as cytosolic DNA sensors and toll-like receptors (TLRs) detect viral or bacterial DNA, resulting in production of proinflammatory cytokines and…
  • Abstract Number: 1209 • 2014 ACR/ARHP Annual Meeting

    Anti-Scavenger Receptor Autoantibodies Disrupted Marginal Zone Macrophage Integrity Via Bruton’s Tyrosine Kinase

    Hao Li1,2, Qi Wu1, PingAr Yang1, Zheng Wang3, Jun Li1, Bao Luo1, Jeffrey C. Edberg1, Hui-Chen Hsu1, John D. Mountz1,4 and Robert P. Kimberly on behalf of PROFILE investigators5, 1Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 2Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 3Med - Pulmonary/Allergy/Critical Care, University of Alabama at Birmingham, Birmingham, AL, 4Birmingham VA Medical Center, Birmingham, AL, 5Clinical Immun & Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose Ibrutinib, a Btk kinase activity inhibitor, is a novel inhibitor under development for autoimmune disease therapy.  We have shown that Btk was significantly upregulated…
  • Abstract Number: 673 • 2014 ACR/ARHP Annual Meeting

    A Comparison of Rheumatoid Arthritis and Systemic Lupus Erythematosus Trial Design: Ways to Improve Positive Trials in Systemic Lupus Erythematosus

    Amy Miles1 and Janet E. Pope2, 1Medicine, University of Western Ontario and U of Toronto, London, ON, Canada, 2St Joseph Health Care, London, ON, Canada

    Background/Purpose: Recent SLE RCTs were examined and compared to rheumatoid arthritis (RA) RCT to suggest modifications to SLE RCTs that could improve the future success…
  • 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: 2432 • 2014 ACR/ARHP Annual Meeting

    Nutritional Assessment in Patients with Systemic Lupus Erythematosus and Systemic Sclerosis

    Sabrina Vagnani1, Chiara Tani2, Linda Carli3, Francesca Querci3, Alessandra Della Rossa3, Anna d'Ascanio3,4, Ilaria Ermini5, Marco Ceroti5, Saverio Caini5, Domenico Palli5, Stefano Bombardieri6 and Marta Mosca3, 1Department of Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy, 2Clinical and Experimental Medicine, Rheumatology Unit, University of Pisa, Pisa, Italy, 3Rheumatology Unit, University of Pisa, Pisa, Italy, 4Internal Medicine, University of Pisa, Pisa, Italy, 5Molecular and Nutritional Epidemiology Unit, Cancer Research and Prevention Institute, ISPO, Florence, Itay., Florence, Italy, 6Rheumatology Unit, Pisa, Italy

    Background/Purpose Systemic Lupus Erythematosus (SLE) and Systemic Sclerosis (SSc) can be both associated with various degrees and types of malnutrition, with different pathogenetic mechanisms.  It’s…
  • Abstract Number: 1825 • 2014 ACR/ARHP Annual Meeting

    Cognitive Performance Scores for the Pediatric Automated Neuropsychological Assessment Metrics in Childhood-Onset Systemic Lupus Erythematosus

    Patricia Vega-Fernandez1, Shana Vanderburgh2, Deborah M. Levy3, Frank A. Zelko4, Eyal Muscal5, Natasha M. Ruth6, Adam M. Huber7, Marisa S. Klein-Gitelman8, Kasha Wiley9, Wenjie Zheng10, Lori B. Tucker11, Tresa Roebuck-Spencer12, Jun Ying13 and Hermine Brunner14, 1Rheumatology, Cincinnati Children's Hospital, Cincinnati, OH, 2University of Cincinnati, Cincinnati, OH, 3Rheumatology, The Hospital for Sick Children and University of Toronto, Toronto, ON, Canada, 4Northwestern University Feinberg School of Medicine, Chicago, IL, 5Rheumatology, Texas Children's Hospital, Houston, TX, 6Pediatric Rheumatology, Medical University of South Carolina, Charleston, SC, 7IWK Health Centre, Halifax, NS, Canada, 8Division of Rheumatology, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL, 9Division of Rheumatology, Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 10Cincinnati Children's Hospital Medical Center, Cincinnati, OH, 11Rheumatology, BC Children's Hospital and University of British Columbia, Vancouver, BC, Canada, 12Cognitive Science Research Center, University of Oklahoma, Norman, OK, 13Medicine-Internal Medicine-General Medicine, University of Cincinnati, Cincinnati, OH, 14PRCSG, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

    Background/Purpose: Patients with childhood-onset SLE (cSLE) may experience neuropsychiatric SLE (NPSLE) manifested as neurocognitive dysfunction (NCD). Formal neurocognitive testing (FNCT) is the most accepted method…
  • Abstract Number: 1202 • 2014 ACR/ARHP Annual Meeting

    Type I Interferon Promotes Inflammatory Cytokine Production By Inhibiting Mir-146a Maturation in SLE

    Bo Qu1, Jianchang Cao2, Feifei Zhang2 and Nan Shen1,2,3, 1Shanghai Institute of Rheumatology, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China, Shanghai, China, 2Institute of Health Sciences, Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) & Shanghai Jiao Tong University School of Medicine (SJTUSM), Shanghai, China, Shanghai, China, 3The Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children’s Hospital Medical Center, Cincinnati, Ohio, United States of America, Cincinnati, OH

    Background/Purpose Systemic lupus erythematosus (SLE) is characterized by the uncontrolled inflammation along with over produced inflammatory cytokines, among which type I interferon (IFN) is recognized…
  • Abstract Number: 670 • 2014 ACR/ARHP Annual Meeting

    Decreased Disease Activity and Corticosteroid Usage and No Renal Flares during Belimumab Treatment in Patients with Systemic Lupus Erythematosus

    Ioannis Parodis1, Elisabet Svenungsson1, Magnus Axelsson2 and Iva Gunnarsson1, 1Department of Medicine, Rheumatology Unit, Karolinska Institutet, Stockholm, Sweden, 2AlbaNova, Stockholm University, Stockholm, Sweden

    Background/Purpose B cells have a central role in Systemic Lupus Erythematosus (SLE) and autoantibody production. B-Lymphocyte Stimulator (BLyS) is important for the activation and maintenance…
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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 ET on November 14, 2024. 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].

ACR Abstract Embargo Policy

Accepted abstracts are made available to the public online in advance of the meeting and are published in a special online supplement of Arthritis & Rheumatology. Information contained in those abstracts may not be released until the abstracts appear online. 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 a scientific presentation or presentation of additional new information that will be available at the time of the meeting) is under embargo until Saturday, November 11, 2023.

Violation of this policy may result in the abstract being withdrawn from the meeting and other measures deemed appropriate. Authors are responsible for notifying financial and other sponsors about this policy. If you have questions about the abstract embargo policy, please contact the public relations department at [email protected].

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