ACR Meeting Abstracts

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Abstracts tagged "cytokines and systemic lupus erythematosus (SLE)"

  • Abstract Number: 1081 • 2018 ACR/ARHP Annual Meeting

    Associations between Daily Alcohol Intake and SLE-Related Cytokines and Chemokines U.S. Female Nurses without SLE

    Cianna Leatherwood1, Xinyi Liu1, Susan Malspeis2, Andrea Roberts3, Jeffrey A. Sparks1, Elizabeth Karlson1, Candace H. Feldman1, Judith A. James4, Laura Kubzansky5 and Karen Costenbader1, 1Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital, Boston, MA, 2Brigham and Women's Hospital, Boston, MA, 3Harvard T.H. Chan School of Public Health, Boston, MA, 4OMRF & OUHSC, Oklahoma City, OK, 5Social and Behavioral Sciences, Harvard T.H. Chan School of Public Health, Boston, MA

    Background/Purpose: Low or no alcohol intake (0-5 gm/day or <0.5 drinks/day) has been associated with increased SLE risk among women.  Several cytokines and chemokines are…
  • Abstract Number: 1693 • 2018 ACR/ARHP Annual Meeting

    Innate, Adaptive, and TNF-Superfamily Immune Pathways Inform a Lupus Disease Activity Immune Index That Characterizes Disease Activity in SLE

    Melissa E. Munroe1,2, Joel M. Guthridge1, Rufei Lu1,3, Joseph M. Kheir1, Bolanle Adebayo1, Susan R. Macwana1, Hua Chen1, Virginia C. Roberts1, Mohan Purushothaman2, Sanjiv Sharma2, Teresa Aberle1, Stan Kamp1, Cristina Arriens1, Eliza Chakravarty1, Katherine Thanou1, Joan T. Merrill1 and Judith A. James4,5, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Progentec Diagnostics, Inc., Oklahoma City, OK, 3Medicine and Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 4University of Oklahoma Health Sciences Center, Oklahoma City, OK, 5Clinical Arthritis and Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a complex autoimmune disease marked by immune dysregulation. A comprehensive but cost-effective tool to track relevant mediators of altered…
  • Abstract Number: 1743 • 2017 ACR/ARHP Annual Meeting

    Serine Arginine/Rich Splicing Factor 1 (SRSF1) Increases IL-2 Production in T Cells By Increasing the Expression of NFAT and c-Fos

    Takayuki Katsuyama1, Michael W. Mosho1, George C. Tsokos1 and Vaishali R. Moulton2, 1Division of Rheumatology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 2Rheumatology, Beth Israel Deaconess Medical Center, Boston, MA

    Background/Purpose: T cells from patients with systemic lupus erythematosus (SLE) produce insufficient amounts of the vital cytokine IL-2, and the molecular mechanisms leading to this…
  • Abstract Number: 1776 • 2016 ACR/ARHP Annual Meeting

    Analysis of Progressive Brain and Corpus Callosum Atrophy and Association with Th1 and Th2 Cytokines in Systemic Lupus Erythematosus

    Mariana Postal1, Aline Tamires Lapa1, Karina O. Peliçari1, Nailu A. Sinicato2, Fernando A. Peres1, Wesley Geraldo Ferreira3, Lilian TL Costallat3, Fernando Cendes3 and Simone Appenzeller4, 1Medicine, State University of Campinas, Campinas, Brazil, 2Pediatrics, State University of Campinas, Campinas, Brazil, 3State University of Campinas, Campinas, Brazil, 4Division of Rheumatology, Faculty of Medical Science, State University of Campinas, São Paulo, Brazil

    Background/Purpose:  The pathophysiology of brain damage SLE is complex. The aim of this study was to determine brain atrophy progression and the association with Th1…
  • Abstract Number: 2818 • 2016 ACR/ARHP Annual Meeting

    High Sensitivity Multiplex ELISA Reveals Cytokine Expression Heterogeneity in Active SLE

    John A. Reynolds1, Sahena Haque2, Eoghan M. McCarthy3, Jamie C Sergeant4, Elaine Lee5, Eileen Holling Lee5, Steven Kilfeather5, Benjamin Parker6 and Ian N. Bruce7, 1NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester University Hospitals NHS Foundation Trust, Manchester, United Kingdom, 2Rheumatology department, University Hospitals of South Manchester NHS Foundation Trust, Manchester, United Kingdom, 3NIHR Manchester Musculoskeletal Biomedical Research Unit, Central Manchester University Hospital NHS Foundation Trust, Manchester, United Kingdom, 4Arthritis Research UK Centre for Epidemiology, Centre for Musculoskeletal Research, Manchester Academic Health Science Centre, University of Manchester, Manchester, UK, Manchester, United Kingdom, 5Aeirtec Limited, UK, North Shields, United Kingdom, 6Centre for Musculoskeletal Research, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom, 7Central Manchester University Hospital NHS Foundation Trust and Manchester Academic Health Science Centre, Arthritis Research UK Epidemiology Unit, The University of Manchester, Manchester Academic Health Sciences Centre, Manchester, United Kingdom

    Background/Purpose: Patients with SLE have a broad clinical and immunological phenotype in which multiple immune pathways may be sequentially or simultaneously activated.  No reliable biomarkers…
  • Abstract Number: 2835 • 2016 ACR/ARHP Annual Meeting

    Longitudinal Analysis of Th1 and Th2 Cytokines in Systemic Lupus Erythematosus

    Mariana Postal1, Karina O. Peliçari1, Nailu A. Sinicato2, Aline Tamires Lapa1, Fernando A. Peres1, André Moreno Morcillo3, Lilian TL Costallat3 and Simone Appenzeller4, 1Medicine, State University of Campinas, Campinas, Brazil, 2Pediatrics, State University of Campinas, Campinas, Brazil, 3State University of Campinas, Campinas, Brazil, 4Division of Rheumatology, Faculty of Medical Science, State University of Campinas, São Paulo, Brazil

    Background/Purpose:  While autoantibodies production and immune complex deposition are cornered as hallmark features of systemic lupus erythematosus (SLE), there is growing evidence to propose the…
  • Abstract Number: 2935 • 2016 ACR/ARHP Annual Meeting

    Activation Status of Mucosal-Associated Invariant T Cells Sensitively Reflects Disease Activity of Systemic Lupus Erythematosus

    Asako Chiba1, Goh Murayama2, Mie Kitagaichi3, Naoto Tamura4, Ken Yamaji2, Yoshinari Takasaki4 and Sachiko Miyake1, 1Immunology, Juntendo University School of Medicine, Tokyo, Japan, 2Department of Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 3Department of Rheumatology, Juntendo University School of Medicine, Tokyo, Japan, 4Internal Medicine and Rheumatology, Juntendo University School of Medicine, Tokyo, Japan

    Background/Purpose: Mucosal-associated invariant T (MAIT) cells are innate-like lymphocytes that express a semi-invariant TCRα chain: Vα7.2-Jα33 in humans and Vα19-Jα33 in mice. MAIT cells are…
  • Abstract Number: 1829 • 2015 ACR/ARHP Annual Meeting

    Heart Rate Variability Is Associated with SLE Flare and with TNF- and IFN-Mediated Signaling

    Aikaterini Thanou1, Stavros Stavrakis2, John Dyer2, Stan Kamp3, Melissa E. Munroe1, David Albert4, Judith A. James5 and Joan T. Merrill3, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Heart Rhythm Institute, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 3Clinical Pharmacology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4AliveCor, Inc., San Francisco, CA, 5Arthritis and Clinical Immunology, University of Oklahoma Health Sciences Center and Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Decreased heart rate variability (HRV), associated with adverse outcomes in cardiovascular diseases, is frequently seen in patients with SLE. The LF/HF ratio, a HRV…
  • Abstract Number: 1855 • 2015 ACR/ARHP Annual Meeting

    Systemic Lupus Erythematosus Exosomes Contain Distinct RNA Transcripts That Differentiate Disease Activity and Modulate Cellular Function

    Samantha Slight-Webb1, Krista M. Bean1, Nicolas Dominguez1, Mikhail G. Dozmorov2, Judith A. James3 and Joel M. Guthridge1, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis and Clincial Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Arthritis & Clinical Immunology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is a complex autoimmune disease involving multiple organ systems and periods of waxing and waning disease activity. The lack of…
  • Abstract Number: 2066 • 2015 ACR/ARHP Annual Meeting

    Elevated Innate, Adaptive, and TNF-Superfamily Soluble Inflammatory Mediators Mark Impending Disease Flare, While Regulatory Mediators Distinguish Lack of Impending Disease Flare in African-American SLE Patients with Active Disease

    Melissa E. Munroe1, Evan G. Vista2, Joan T. Merrill3, Joel M. Guthridge1, Virginia C. Roberts1 and Judith A. James4, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Rheumatology and Clinical Immunology, University of Santo Tomas, Taguig City, Philippines, 3Clinical Pharmacology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 4Arthritis and Clinical Immunology, University of Oklahoma Health Sciences Center and Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: SLE is a multifaceted disease characterized by immune dysregulation and varied disease activity. Identifying mechanistic mediators of altered disease activity would help prevent damage…
  • Abstract Number: 3156 • 2015 ACR/ARHP Annual Meeting

    IL17 Promotes Development of Autoreactive Early Stage B Cells in Distinct Regions of the Spleen Follicle

    Jennie Hamilton1, Qi Wu2, PingAr Yang3, Jun Li4, Yanna Ding1, Bao Luo5, John Mountz6 and Hui-Chen Hsu2, 1University 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, 4Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 6Dept of Med/Rheumatology Div, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: The early stage transitional B cell has been shown to be the key peripheral B-cell tolerance control point defect in SLE patients.  Anti-RNP Abs can…
  • Abstract Number: 2734 • 2014 ACR/ARHP Annual Meeting

    B55β Regulates T Cell Survival through the Modulation of AKT during Cytokine Deprivation

    José C. Crispin1, Sokratis A. Apostolidis2, Noe Rodriguez Rodriguez1, Tran Nguyen2 and George C. Tsokos3, 1Medicine/Rheumatology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 2Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 3Rheumatology, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA

    Background/Purpose . The abundance of cytokines controls the length of immune responses through poorly defined mechanisms. B55β is a molecule that triggers apoptosis in activated…
  • Abstract Number: 1944 • 2014 ACR/ARHP Annual Meeting

    Targeting CD22 with Epratuzumab Impacts Cytokine Production By B Cells

    Vanessa Fleischer1,2, Julia Sieber1,2, Sarah J. Fleischer3,4, Anthony Shock5, Guido Heine6, Capucine Daridon1,2 and Thomas Dörner1,2, 1CC12, Dept. Medicine/Rheumatology and Clinical Immunology, Charité University Medicine Berlin, Berlin, Germany, 2German Rheumatism Research Centre Berlin, Berlin, Germany, 3Charité University Medicine, Dept. Medicine/Rheumatology and Clinical Immunology/German Rheumatism Research Center (DRFZ), Berlin, Germany, 4Department of Medicine/Rheumatology and Clinical Immunology, Charité University Medicine Berlin, Berlin, Germany, 5UCB Pharma, Slough, United Kingdom, 6Department of Dermatology, Venerology and Allergology, Charité University Medicine Berlin, Berlin, Germany

    Background/Purpose CD22 is a negative co-receptor of the B-cell receptor (BCR) and, when targeted by epratuzumab, partially inhibits BCR signaling, for example by reducing Syk…
  • Abstract Number: 1942 • 2014 ACR/ARHP Annual Meeting

    Regulation of the Responses of Human B Cell Subsets to Innate Immune Signals By Epratuzumab, a Humanized Monoclonal Antibody Targeting CD22

    Natalia V. Giltiay1, Geraldine L. Shu2, Anthony Shock3 and Edward A. Clark4, 1Department of Immunology, Division of Rheumatology, University of Washington, Seattle, WA, 2Department of Immunology, University of Washington, Seattle, WA, 3UCB Pharma, Slough, United Kingdom, 4Department of Immunology and Division of Rheumatology, University of Washington, Seattle, WA

    Background/Purpose The B cell-associated receptor, CD22, functions to regulate adhesion and signaling through both the B cell receptor (BCR) and Toll-like receptors (TLRs) expressed in…
  • Abstract Number: 1602 • 2013 ACR/ARHP Annual Meeting

    Autoantibodies, Cytokines and Chemokines In Serum and Cerebrospinal Fluid Of SLE Patients With Cognitive Dysfunction

    Hilda Fragoso-Loyo1, Alí Duarte-García2, Sandra Juárez-Arellano3, Alba Cicero-Casarrubias4, Juanita Romero-Díaz5, Luis LLorente-Peters1 and Jorge Sánchez-Guerrero6, 1Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico, Mexico, 2Department of Medicine, Tufts Medical Center, Boston, MA, 3Department of Neurology, Instituto Nacional de Ciencias Medicas y Nutricion S.Z., Mexico city, Mexico, 4Immunology and Rheumatology, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Mexico City, Mexico, 5Immunology and Rheumatology, Instituto Nacional de Ciencias Medicas y Nutricion, Mexico City, Mexico, 6Rheumatology, Mount Sinai Hospital and University Health Network, Toronto Canada, Toronto, ON, Canada

    Background/Purpose: The nature and pathogenesis and cognitive dysfunction (CD) in patients with SLE is unkown.To determine the presence and levels of autoantibodies, cytokines and chemokines…
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