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  • Abstract Number: 2869 • 2016 ACR/ARHP Annual Meeting

    Critical Roles of IRAK4 Kinase Activity in Inflammation but Not B Cell Response in SLE  

    Chia Chi Sun1, Gang Chen2, Nuruddeen Lewis1, Andrew T Bender1, Changling Sia3, Ling Zhang2, Catherine Jorand Lebrun4, Herbert Y Lin5, Ravi I Thadhani6, Harsukh Parmar1 and Julie A DeMartino1, 1TIP Immunology, EMD Serono, Inc, Billerica, MA, 2EMD Serono, Inc, Billerica, MA, 3TIP Immunology, EMD Serono, Inc, Billeria, MA, 4Discovery Technology, EMD Serono, Inc, Billerica, MA, 5Division of Nephrology, Massachusetts General Hospital, Boston, MA, 6Divison of Nephrology, Massachusetts General Hospital, Boston, MA

    Background/Purpose: Interleukin-1 receptor (IL-1R)-associated kinase 4 (IRAK4) is a key component of the Myddosome complex, which is essential for signalling downstream of IL-1R and most…
  • Abstract Number: 2870 • 2016 ACR/ARHP Annual Meeting

    Overexpression of EZH2 at the microRNA-142 Regulatory Region Contributes to Down-Regulation of microRNA-142-3p/5p in Systemic Lupus Erythematosus

    Shu Ding1, Qing Zhang2, Shuangyan Luo2, Lina Tan1, Hai Long3, Ming Zhao3, Yunsheng Liang2 and Qianjin Lu3, 1Department of Dermatology, The Third Xiangya Hospital of Central South University, Changsha, China, 2Department of Dermatology, The Second Xiangya Hospital of Central South University, Changsha, China, 3The Second Xiangya Hospital of Central South University, Changsha, China

    Background/Purpose: Recently, our group has demonstrated that decreased microRNA-142-3p/5p (miR-142-3p/5p) which contributes to T cell overactivation and B cell hyperstimulation plays an essential role in…
  • Abstract Number: 2871 • 2016 ACR/ARHP Annual Meeting

    Unaffected Lupus Relatives Are Distinguished from SLE Patients and Unaffected Individuals Not Related to SLE Patients By Lupus-Specific Connective Tissue Disease Questionnaire Scores, Autoantibodies, and Distinct Soluble Mediators

    Melissa E. Munroe1, Kendra A. Young2, Jill M. Norris2, Teresa Aberle1, Virginia C. Roberts1, Joel M. Guthridge3, Diane L. Kamen4, Gary S. Gilkeson5, Michael Weisman6, Mariko Ishimori6, Daniel J Wallace7, David Karp8, Kathy L. Sivils1, John B. Harley9,10 and Judith A. James11,12, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Epidemiology, Colorado School of Public Health, Aurora, CO, 3Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 5Department of Medicine, Division of Rheumatology, Medical University of South Carolina, Charleston, SC, 6Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 7Division of Rheumatology, Cedars-Sinai Medical Center, Los Angeles, CA, 8Internal Medicine/Division of Rheumatic Diseases, University of Texas Southwestern Medical Center, Dallas, TX, 9US Department of Veterans Affairs Medical Center, Cincinnati, OH, 10Center for Autoimmune Genomics and Etiology (CAGE), Cincinnati Childrens Hospital, Cincinnati, OH, 11Arthritis and Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 12Department of Medicine, University of Oklahoma Health Sciences Center, Oklahoma City, OK

    Background/Purpose:  Identifying populations at risk of SLE is essential to curtail inflammatory damage and select individuals for prevention trials. Blood relatives (Rel) of lupus patients…
  • Abstract Number: 2872 • 2016 ACR/ARHP Annual Meeting

    SLE Subjects Express High Levels of Intracellular Interferon-β That Acts in an Autocrine Fashion to Promote Survival of Transitional Stage B Cells

    Jennie Hamilton1, Qi Wu2, PingAr Yang3, Bao Luo4, Shanrun Liu5, Jun Li6, Ignacio Sanz7, W. Winn Chatham8, Hui-Chen Hsu2 and John D. Mountz9, 1Medicine/Division of Clinical Immunology and Rhematology, University of Alabama at Birmingham, Birmingham, AL, 2Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 3Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Biochemistry & Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, 6Medicine, University of Alabama at Birmingham, Birmingham, AL, 7Rheumatology and Lowance Center for Human Immunology, Emory University School of Medicine and Lowance Center for Human Immunology, Atlanta, GA, 8Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 9Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham and Birmingham VA Medical center, Birmingham, AL

    Background/Purpose:  Upregulation of interferon-β (IFNβ) is an important step in promoting maturation and survival of B cells. Secretion and autocrine action of IFNβ requires assembly…
  • Abstract Number: 2873 • 2016 ACR/ARHP Annual Meeting

    B-Cell activating Factor Genetic Variants in Systemic Lupus Erythematosus and Lupus Related Atherosclerosis

    Evangelos Theodorou1, Adrianos Nezos2, Pinelopi Kostantopoulou3, Maria Tektonidou4, Michael Koutsilieris5 and Clio P. Mavragani5, 1Rheumatology, 251 Hellenic (Greek) Air Force Hospital, Athens, Greece, 2Physiology, Department of Physiology, School of Medicine, National Kapodistrian University of Athens, Athens, Greece, 3Rheumatology Department, General Hospital of Athens "G.Gennimatas", Αthens, Greece, 4Laikon Hospital, Athens University Medical School, Athens, Greece, 5Department of Physiology, School of Medicine, National Kapodistrian University of Athens, Athens, Greece

    Background/Purpose: Systemic lupus erythematosus (SLE) is a chronic systemic autoimmune disease with an increased atherosclerotic risk compared to healthy population, partially explained by traditional cardiovascular…
  • Abstract Number: 2874 • 2016 ACR/ARHP Annual Meeting

    CD16+monocytes Are Enriched and Functionally Exacerbated in Driving B Cell Activation Under Systemic Lupus Erythematosus Condition

    Huaqun Zhu1, Yin Su2, Fanlei Hu3 and Liling Xu3, 1Department of Rheumatology and Immunology/Clinical Immunology Center, Peking University People's Hospital, Beijing, China, 2Department of Rheumatology and Immunology,Clinical Immunology Center, Peking University People's Hospital, Beijing, China, 3Peking University People's Hospital, Beijing, China

    Background/Purpose: Systemic lupus erythematosus(SLE) was an autoimmune disease characterized by extensive B cell activation and autoantibody production. Human peripheral monocytes could be categorized into three subsets…
  • Abstract Number: 2875 • 2016 ACR/ARHP Annual Meeting

    Depressed Serum IgM Levels in SLE Are Restricted to Defined Subgroups

    Caroline Grönwall1, Uta Hardt1, Iva Gunnarsson2, Gregg J. Silverman3 and Elisabet Svenungsson1, 1Department of Medicine, Rheumatology Unit, Karolinska Institutet, Stockholm, Sweden, 2Karolinska Institutet, Department of Medicine, Unit of Rheumatology, Stockholm, Sweden, 3Department of Medicine, Division of Rheumatology, New York University School of Medicine, New York, NY

    Background/Purpose: Natural IgM autoantibodies have been proposed to have protective properties, and decreased levels of IgM to phosphorylcholine (PC) in SLE are associated with higher…
  • Abstract Number: 2876 • 2016 ACR/ARHP Annual Meeting

    SLE Serum Impairs NO Production in Huvecs through Induction of eNOS Uncoupling

    Jim Oates1,2, Diane L. Kamen3 and Joy N Jones Buie4, 1Medical Service, Ralph H. Johnson VAMC, Charleston, SC, 2Medicine/Rheumatology & Immunology, Medical University of South Carolina, Charleston, SC, 3Department of Medicine, Division of Rheumatology and Immunology, Medical University of South Carolina, Charleston, SC, 4Rheumatology and Immunology, Medical University of South Carolina, Charleston, SC

    Background/Purpose: Systemic lupus erythematosus (SLE) induces endothelial cell dysfunction (ECD) that can manifest as glomerulonephritis or atherosclerosis. Lupus-prone mice lacking endothelial nitric oxide synthase (eNOS,…
  • Abstract Number: 2877 • 2016 ACR/ARHP Annual Meeting

    Notch Ligand Delta-like Ligand 4 (DLL4) Expression on Dendritic Cells Is Increased in Systemic Lupus Erythematosus

    Jevon Fragoso1, Lijun Meng2, Yi Zhang2 and Roberto Caricchio3, 1Rheumatology Medicine, Lewis Katz School of Medicine, Philadelphia, PA, 2Fels Institute for Cancer Research & Molecular Biology, Lewis Katz School of Medicine, Philadephia, PA, 3Medicine Rheumatology, Lewis Katz School of Medicine, Philadelphia, PA

    Background/Purpose: Dendritic cells (DCs) activate the immune system with a variety of cytokines and co-stimulatory molecules. Our group recently described the Notch ligand Delta-like Ligand…
  • Abstract Number: 2878 • 2016 ACR/ARHP Annual Meeting

    Major Lymphocyte Populations Share a Common Interferon Signature but Express Cell Type-Specific Interferon Pathway Genes in SLE

    Mikhail Olferiev1, Kyriakos A. Kirou2, David Fernandez3, Khalili Leila1, Dina Greenman1 and Mary K. Crow4, 1Mary Kirkland Center for Lupus Research, Hospital for Special Surgery, New York, NY, 2Rheumatology, Hospital for Special Surgery, New York, NY, 3Rheumatology, New York Presbyterian - Cornell Campus - HSS, New York, NY, 4Department of Medicine, Mary Kirkland Center for Lupus Research, Hospital for Special Surgery, New York, NY

    Background/Purpose: All lymphocyte populations contribute to SLE pathogenesis, but little is known of the specific gene transcripts particularly involved in each cell type. Activation of…
  • Abstract Number: 2879 • 2016 ACR/ARHP Annual Meeting

    Genome-Wide Pathway Analysis Reveals That VEGF Genetic Pathway Is Associated with Oral Ulcers in Systemic Lupus Erythematosus

    Antonio Julià1, Patricia Carreira2, Ricardo Blanco3, Victor Martinez Taboada4, Luis Carreño5, Jose Javier Perez Venegas6, Alejandro Olivé7, Jose Luis Andreu8, Maria Ángeles Aguirre Zamorano9, Paloma Vela10, Joan Miquel Nolla11, José Luis Marenco de la Fuente12, Antonio Zea13, JM Pego-Reigosa14, Mercedes Freire15, Elvira Diez Alvarez16, Adrìa Aterido1, Arnald Alonso1, Maria López-Lasanta17, Mireia López18, Raül Tortosa1, Sara Marsal19 and Antonio Fernandez-Nebro20, 1Rheumatology Research Group, Vall d'Hebron Hospital Research Institute, Barcelona, Spain, 2Department of Rheumatology, Hospital Universitario 12 de Octubre, Madrid, Spain, 3Rheumatology, Hospital Universitario Marqués de Valdecilla. IDIVAL, Santander, Spain, 4Hospital Marqués de Valdecilla., Santander, Spain, 5Rheumatology, HGU Gregorio Marañón, Madrid, Spain, 6Rheumatology, Hospital de Jerez de la Frontera, Jerez de la Frontera, Spain, 7Rheumatology, Hospital Universitario Germans Trias i Pujol, Barcelona, Spain, 8Rheumatology, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain, 9Rheumatology service, IMIBIC/Reina Sofia Hospital/University of Cordoba, Cordoba, Spain, 10Dpt. Rheumatology, Hospital General Universitario Alicante, Alicante, Spain, 11Rheumatology, Bellvitge University Hospital, Barcelona, Spain, 12Rheumatology, Hospital de Valme, Seville, Spain, 13Hospital Ramón y Cajal. Madrid, Madrid, Spain, 14Rheumatology Section, Hospital de Meixoeiro, Pontevedra, Spain, Vigo, Spain, 15Servicio de Reumatología. Instituto de Investigación Biomédica de A Coruña (INIBIC). Complexo HospitalarioUniversitario de A Coruña (CHUAC), Sergas. Universidade da Coruña (UDC), A Coruña, Spain, 16Rheumatology, Hospital de León, León, Spain, 17Vall d'Hebron Hospital Research Institute, Barcelona, Spain, 18Servicio de Reumatología, Hospital Universitario Vall d´Hebron, Barcelona, Spain, 19Rheumatology Research Unit, Vall d'Hebron Hospital, Barcelona, Spain, 20Rheumatology, Hospital Universitario Carlos Haya, Malaga, Spain

    Background/Purpose: Systemic lupus erythematosus (SLE) is a genetically complex rheumatic disease with heterogeneous clinical manifestations. Recent studies have suggested the existence of a genetic basis…
  • Abstract Number: 2880 • 2016 ACR/ARHP Annual Meeting

    Distinct Metabolic Pathways Regulate Lipid Antigen Presentation By Monocytes and B Cells: Implications for SLE Patients with Pre-Clinical Atherosclerotic Plaque

    Kirsty Waddington1, Edward Smith2, Sara Croca3, David A. Isenberg4, Anisur Rahman5, Ines Pineda Torra6 and Elizabeth Jury7, 1Clinical Pharmacology and Rheumatology, University College London, London, United Kingdom, 2Centre for Rheumatology Research, University College London, London, United Kingdom, 3Rheumatology, University College London, London, United Kingdom, 4Centre for Rheumatology Research, University College Hospital London, UK, London, United Kingdom, 5Rayne Institute, Centre for Rheumatology Research, UCL Division of Medicine, London, United Kingdom, 6Clinical Pharmacology, University College London, London, United Kingdom, 7Division of Medicine, Centre for Rheumatology Research, University College London, London, United Kingdom

    Background/Purpose:  Systemic lupus erythematosus (SLE) patients have an increased risk of developing clinically apparent cardiovascular disease (CVD) and subclinical atherosclerotic plaque, detectable by vascular ultrasound…
  • Abstract Number: 2881 • 2016 ACR/ARHP Annual Meeting

    Reduced Hippocampal-Thalamic Fiber Tracts in Systemic Lupus Erythematosus

    Meggan Mackay1, Pooneh Heshmati2, An Vo2, Cynthia Aranow2, Bruce Volpe2, Betty Diamond3 and David Eidelberg2, 1Autoimmune & Musculoskeletal Disorders, The Feinstein Institute for Medical Research, Manhasset, NY, 2The Feinstein Institute for Medical Research, Manhasset, NY, 3Feinstein Institute for Medical Research, Manhasset, NY

    Background/Purpose: SLE patients experience deterioration in cognitive function over time but attribution to disease-related mechanisms is confounded by medication effects, psychiatric disease, hormonal influences and…
  • Abstract Number: 2882 • 2016 ACR/ARHP Annual Meeting

    CD4+ T Helper Cells and Regulatory T Cells in Active Lupus Nephritis – an Imbalance Towards a Predominant Th1 Response?

    Danilo Mesquita Jr.1, Marcello Fabiano Franco2, Gianna Mastroianni Kirsztajn1, Luciana Aparecida Reis1, Sandro Perazzio3, Fernanda Vieira Mesquita1, Vanessa Ferreira1, Luis E C Andrade4 and Alexandre W.S. Souza5, 1Internal Medicine, Universidade Federal de São Paulo, São Paulo, Brazil, 2Pathology, Universidade Federal de São Paulo, São Paulo, Brazil, 3Rheumatology Division, Universidade Federal de São Paulo, Sao Paulo, Brazil, 4Pediatric Rheumatology Unit, Universidade Federal de São Paulo, São Paulo, Brazil, 5Universidade Federal de São Paulo, São Paulo, Brazil

    Background/Purpose:  Systemic lupus erythematosus (SLE) is a chronic inflammatory disease characterized by the involvement of multiple organs and systems with aberrations in T cell response,…
  • Abstract Number: 2883 • 2016 ACR/ARHP Annual Meeting

    The CD4+CD52low T Cell Contributes to the Development of Systemic Lupus Erythematosus through the CCR8/TARC Pathway

    Tomohito Sato1, Masataka Umeda1, Tomohiro Koga2, Takashi Igawa1, Syota Kurushima1, Ayuko Takatani1, Toshimasa Shimizu1, Shoichi Fukui1, Ayako Nishino1, Yoshiro Horai1, Shinya Kawashiri1, Naoki Iwamoto1, Yasuko Hirai1, Mami Tamai1, Hideki Nakamura1, Tomoki Origuchi3 and Atsushi Kawakami4, 1Department of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan, 2Department of Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki, Japan, 3Department of Rehabilitation Sciences, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan, 4Department of Immunology and Rheumatology, Unit of Translational Medicine, Graduate School of Biomedical Sciences, Nagasaki University, Nagasaki City, Japan

    Background/Purpose: CD52 is a cell-surface glycoprotein that is widely expressed in lymphocytes, monocytes and eosinophils. CD4+CD52high T cells inhibit the activation of CD4+CD52low T cells…
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