ACR Meeting Abstracts

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Abstracts tagged "SLE"

  • Abstract Number: 25 • 2013 ACR/ARHP Annual Meeting

    SLE Flares Are Characterized By Generalized Polyclonal Expansions Of Antibody Secreting Cells Without Preference For Autoimmune Responses

    H. Travis Ichikawa, Medicine, Emory University, Atlanta, GA

    Background/Purpose: Increased circulating antibody secreting cells (ASC), including both CD138- plasmablasts and CD138+ plasma cells (PB/PC), correlate with SLE activity and are prominent during Lupus…
  • Abstract Number: 2796 • 2013 ACR/ARHP Annual Meeting

    Effects Of BAFF Inhibition On B Cell Selection In Murine SLE

    Alexis Boneparth1,2, Ramalingam Bethunaickan3, Weiqing Huang4 and Anne Davidson4, 1Pediatrics, The Children's Hospital at Montefiore, Bronx, NY, 2Feinstein Institute for medical Research, Manhasset, NY, 3Autoimmunity, Feinstein Institute for Medical Research, Manhasset, NY, 4Autoimmunity and Musculoskeletal Diseases, Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: BAFF inhibition is a new B cell targeted therapy approved for the treatment of moderately active SLE. Although BAFF regulates selection of naïve autoreactive…
  • Abstract Number: 1646 • 2013 ACR/ARHP Annual Meeting

    Alterations In Circulating T Follicular Helper Cells and T Regulatory Cells In Autoimmune Rheumatic Diseases Treated With B Cell Depletion Therapy: Rituximab

    Pamela M.K Lutalo1,2, Yuan Zhao2, Lee Meng Choong1, Shirish Sangle1, Jo Spencer3 and David P. D'Cruz4, 1Louise Coote Lupus Unit, St Thomas' Hospital, London, United Kingdom, 2Peter Gorer Department of Immunobiology, School of Medicine, King's College London, London, United Kingdom, 3Peter Gorer Department of Immunobiology, King's College London, School of Medicine, London, United Kingdom, 4Louise Coote Lupus Unit, Louise Coote Lupus Unit, St Thomas' Hospital, London, United Kingdom

    Background/Purpose: Granulomatosis with polyangiitis (GPA) and systemic lupus erythematosus (SLE) are autoimmune rheumatic diseases which develop due to failure of immune self-tolerance. T follicular helper…
  • Abstract Number: 1571 • 2013 ACR/ARHP Annual Meeting

    Efficacy Of Tacrolimus Combination Therapy During The Maintenance Phase Of Systemic Lupus Erythematosus

    Kumiko Ohtsuka1, Yusuke Miwa1, Nao Oguro2, Yoko Miura1, Sho Ishii1, Shinya Seki1, Hidekazu Furuya1, Ryo Yanai1, Ryo Takahashi1, Kuninobu Wakabayashi1, Nobuyuki Yajima1 and Tsuyoshi Kasama1, 1Div of Rheumatology, Showa University School of Med, Shinagawa-ku Tokyo, Japan, 2Div of Rhemuatology, Showa University School of Med, Shinagawa-ku Tokyo, Japan

    Background/Purpose: In Japan, a placebo-controlled clinical trial was undertaken to investigate the efficacy and safety of tacrolimus (TAC) for lupus nephritis. Based on the results…
  • Abstract Number: 637 • 2013 ACR/ARHP Annual Meeting

    Proteomic Approach and Validation Of Urinary Biomarkers In Lupus Nephritis

    Joo Youn Lee1, Sung Hae Chang2, Hye Jin Oh3, Yong Yook Lee1, Min Jueng Kang1, Eun Young Lee4, Eun Bong Lee5, Eugene C. Yi1 and Young Wook Song1,5, 1Department of Molecular Medicine and Biopharmaceutical Sciences, Seoul National University, Seoul, South Korea, 2Internal Medicine Rheumatology, Seoul National University Bundang Hospital, Seongnam-si, South Korea, 3Seoul National University, Seoul, South Korea, 4Internal medicine, Division of Rheumatology, Department of Internal Medicine, Seoul National University, Seoul, South Korea, 5Division of Rheumatology, Department of Internal Medicine, Seoul National University, Seoul, South Korea

    Background/Purpose: Renal involvement occurs in about half of systemic lupus erythematosus (SLE) patients. A number of biochemical markers are currently used to clinically assess lupus…
  • Abstract Number: 31 • 2013 ACR/ARHP Annual Meeting

    IgD- CD27- B Cells From Systemic Lupus Erythematous Patients Have Increased Expression Of Genes Involved In RNA Sensing and Toll-Like Receptor 3 Signaling Pathways

    Scott Jenks1, Edward Ramos2 and Ignacio Sanz3, 1Allergy, Immunology, and Rheumatology, Emory University School of Medicine, Atlanta, GA, 2Biology, Emory University, Atlanta, GA, 3Allergy, Immunology and Rheumatology, Emory University School of Medicine, Atlanta, GA

    Background/Purpose: SLE patients have perturbations in B cell subsets including a large expansion of IgD-CD27- B cells (DN) in patients with active disease. Patients also…
  • Abstract Number: 2797 • 2013 ACR/ARHP Annual Meeting

    B-Lymphocyte Stimulator and A Proliferation Inducing Ligand In Lupus Nephritis: Low Serum Levels Of BLyS Predict Treatment Response

    Ioannis Parodis1, Agneta Zickert1, Elisabet Svenungsson2, Vivianne Malmström2 and Iva Gunnarsson1, 1Department of Medicine, Rheumatology Unit, Karolinska Institutet, Stockholm, Sweden, 2Rheumatology Unit, Department of Medicine, Karolinska Institutet, Stockholm, Sweden

    Background/Purpose: B-lymphocytes have a pivotal role in the pathogenesis of Systemic Lupus Erythematosus (SLE). B-Lymphocyte Stimulator (BLyS) has an important role in the activation, differentiation…
  • Abstract Number: 1630 • 2013 ACR/ARHP Annual Meeting

    Association Of TREM-Like Transcript-1 With Systemic Lupus Erythematosus

    Yerania Rodríguez-Navedo1, Karina Vilá -Rivera1, Mariely Nieves-Plaza2, Martha Ricaurte3, A. Valance Washington3 and Luis M. Vilá1, 1Department of Medicine, Division of Rheumatology, University of Puerto Rico Medical Sciences Campus, San Juan, PR, 2University of Pittsburgh, Pittsburgh, PA, 3University of Puerto Rico, Río Piedras Campus, San Juan, PR

    Background/Purpose:  Recent studies suggest that a platelet α-granule protein named TREM-like transcript-1 (TLT-1) is a key molecule in modulating the inflammatory response. TLT-1 has been…
  • Abstract Number: 1572 • 2013 ACR/ARHP Annual Meeting

    High Type I Interferon In Systemic Lupus Erythematosus Plasma Predicts Future Renal Disease

    Kyriakos A. Kirou1, Mikhail Olferiev1, Elzbieta E. Jacek1, Mari Lliguicota1, Margaret Robotham1, Wei-Ti Huang2, Elena Gkrouzman1 and Mary K. Crow3, 1Hospital for Special Surgery, New York, NY, 2Biostatistics, Hospital for Special Surgery, New York, NY, 3Department of Medicine, Hospital for Special Surgery, New York, NY

    Background/Purpose: Type I interferon (IFN-I) is elevated in many patients with SLE and is associated with more severe disease. However, the relationship between elevated levels…
  • Abstract Number: 640 • 2013 ACR/ARHP Annual Meeting

    Systemic Lupus Erythematosus Patients With Atherosclerosis Are Characterised By a Distinct Invariant Natural Killer T Cell Phenotype and Altered CD1d-Mediated Lipid Antigen Presentation

    Edward Smith1, Sara Croca2, Andrew Pitcher1, D.A. Isenberg1, Anisur Rahman3 and Elizabeth C. Jury4, 1Centre for Rheumatology Research, University College London, London, United Kingdom, 2Centre for Rheumatology Research, Division of Medicine, University College London, London, United Kingdom, 3Centre for Rheumatology Research,Rayne Institute, 4th Floor, University College London, London, United Kingdom, 4Division of Medicine, Centre for Rheumatology Research, University College London, London, United Kingdom

    Background/Purpose: It is widely reported that systemic lupus erythematosus (SLE) patients have an increased risk of atherosclerosis compared to the general population, irrespective of traditional…
  • Abstract Number: 32 • 2013 ACR/ARHP Annual Meeting

    Understanding The Stimulatory Pathways Responsible For Naïve B Cell Activation In Systemic Lupus Erythematosus

    Emily Blalock1, Chris Scharer2, Scott Jenks1, Jeremy Boss2 and Ignacio Sanz3, 1Allergy, Immunology, and Rheumatology, Emory University School of Medicine, Atlanta, GA, 2Microbiology and Immunology, Emory University School of Medicine, Atlanta, GA, 3Allergy, Immunology and Rheumatology, Emory University School of Medicine, Atlanta, GA

    Background/Purpose: Systemic lupus erythematosus (SLE) is a recurrent autoimmune disease characterized by multiple B cell abnormalities, including the activation of naïve B cells. However, gaps…
  • Abstract Number: 2737 • 2013 ACR/ARHP Annual Meeting

    In Vivo MiR-146a Administration Ameliorates Murine Lupus Nephritis

    Dong Liang1, Shiyu Zhou2, Zheng Liu3, Zhengyuan Shan1, Philip Brohawn3, Yihong Yao3, Indu Raman4, Quan-Zhen Li4, John B. Harley5,6 and Nan Shen1,2,7, 1Division of Rheumatology & the Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 2Shanghai Institutes for Biological Sciences Chinese Academy of Sciences & Shanghai Jiao Tong University School of Medicine, Shanghai, China, 3Translational Sciences, MedImmune, LLC, Gaithersburg, MD, 4Department of Immunology and Microarray Core Facility, University of Texas Southwestern Medical Center, Dallas, TX, 5Division of Rheumatology and The Center for Autoimmune Genomics & Etiology, University of Cincinnati, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH, 6US Department of Veterans Affairs Medical Center, Cincinnati, OH, 7Shanghai Institute of Rheumatology, Shanghai Institute of Rheumatology, Renji Hospital, Shanghai Jiaotong University School of Medicine, Shanghai, China

    Background/Purpose: New Zealand black and white F1 (NZBW/F1) is a classic mouse model of systemic lupus erythematosus (SLE). Type I interferon (IFN) infusion accelerates lupus…
  • Abstract Number: 1631 • 2013 ACR/ARHP Annual Meeting

    Transcription Activation-Like Effector Nuclease-Mediated Enhancer Knockout Influences TNFAIP3 Gene Expression and Mimics a Functional Phenotype Associated With Systemic Lupus Erythematosus

    Shaofeng Wang1, Feng Wen2, Bo He3 and Patrick M. Gaffney4, 1Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Pathology, The University of Oklahoma Health Sciences Center, Oklahoma City, OK, 4Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Emerging technologies for precise, targeted genome editing provide new opportunities for the functional elucidation of causal genetic variants and genomic elements without the confounding…
  • Abstract Number: 1581 • 2013 ACR/ARHP Annual Meeting

    Lipid Lowering Medication Use Is Associated With Reduced Muscle Strength In Systemic Lupus Erythematosus

    James S. Andrews1 and Patricia P. Katz2, 1Rheumatology, University of California San Francisco, San Francisco, CA, 2Medicine, University of California, San Francisco, San Francisco, CA

    Background/Purpose: Premature atherosclerotic coronary artery disease is a major source of morbidity for women with systemic lupus erythematosus (SLE).  Lipid lowering medications (LLM) are among…
  • Abstract Number: 604 • 2013 ACR/ARHP Annual Meeting

    Mycophenolate Mofetil Is Not Associated With Reduced Cardiovascular Or Lupus Damage Accumulation In a Cross-Sectional Lupus Cohort Study

    Maureen A. McMahon1, Maria Dall'era2, Eliza Chakravarty3, Joseph E. Craft4, Gary S. Gilkeson5, Kenneth C. Kalunian6, R. John Looney7, Gerald McGwin Jr.8 and Meggan Mackay9, 1Division of Rheumatology, UCLA David Geffen School of Medicine, Los Angeles, CA, 2Medicine/Rheumatology, University of California, San Francisco, San Francisco, CA, 3Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Yale University School of Medicine, Internal Medicine, Section of Rheumatology, New Haven, CT, 5Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 6UCSD School of Medicine, La Jolla, CA, 7Allergy, Immunology and Rheumatology, University of Rochester, Rochester, NY, 8Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 9Autoimmune & Musculoskeletal Disease, Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: Mycophenolate mofetil (MMF) is frequently used for the treatment of lupus.  The immune-modulating effects of MMF extend beyond effects on lymphocyte proliferation, and include…
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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.

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