ACR Meeting Abstracts

ACR Meeting Abstracts

  • Meetings
    • ACR Convergence 2024
    • ACR Convergence 2023
    • 2023 ACR/ARP PRSYM
    • ACR Convergence 2022
    • ACR Convergence 2021
    • ACR Convergence 2020
    • 2020 ACR/ARP PRSYM
    • 2019 ACR/ARP Annual Meeting
    • 2018-2009 Meetings
    • Download Abstracts
  • Keyword Index
  • Advanced Search
  • Your Favorites
    • Favorites
    • Login
    • View and print all favorites
    • Clear all your favorites
  • ACR Meetings
  • Abstract Number: 1086 • 2018 ACR/ARHP Annual Meeting

    Low-Dose IL-2 Combined with Rapamycin Efficiently Promotes Remission of Refractory Systemic Lupus Erythematosus

    Zhaoyun Liang1, Xiaona Jing1, Meihua Hao1, Chong Gao2, Xiao-Feng Li3 and Junwei Chen1, 1The Second Hospital of Shanxi Medical University, Taiyuan, China, 2Department of Pathology, Brigham and Women’s Hospital, Harvard Medical School, Boston, MA, Cambridge, MA, 3Rheumatology, the Second Hospital of Shanxi Medical University, Taiyuan, China

    Background/Purpose: Systemic lupus erythematosus (SLE) is a potentially fatal autoimmune disease. Regulatory T (Treg) cells and T helper type 17 (Th17) cells play opposite roles…
  • Abstract Number: 1087 • 2018 ACR/ARHP Annual Meeting

    Association between Cigarette Smoking and Systemic Lupus Erythematosus – a Bayesian Multivariate Meta-Analysis of Case-Control and Cohort Studies

    Monica Hui Yan Chua1, Irene Ai Ting Ng1, Mike Wai-Leung Cheung2 and Anselm Mak3, 1Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore, 2Psychology, Faculty of Arts and Social Sciences, National University of Singapore, Singapore, Singapore, 3Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore

    Background/Purpose: The association between cigarette smoking and the occurrence of SLE has been studied over the past two decades but results are conflicting. The global…
  • Abstract Number: 1088 • 2018 ACR/ARHP Annual Meeting

    Pro-Inflammatory and Regulatory Soluble Mediator Pathways Vary between African American and European American SLE Patients

    Samantha Slight-Webb1, Miles C. Smith1, Holden T. Maecker2, Paul J. Utz3, Joel M. Guthridge1 and Judith A. James4, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Stanford University, Stanford, CA, 3Medicine, Stanford University School of Medicine, Stanford, CA, 4Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: Systemic lupus erythematosus (SLE) is an autoimmune disease that primarily affects women, and is associated with periods of elevated and suppressed clinical symptoms. SLE…
  • Abstract Number: 1089 • 2018 ACR/ARHP Annual Meeting

    Commensal Gut Bacteria of Anti-Ro Positive Mothers of Children with Neonatal Lupus in Aggregate Resemble Healthy Subjects without Overt Dysbiosis of Abundance of Microorganisms

    Robert M. Clancy1, Carl Langefeld2, Hannah C. Ainsworth3, H. Michael Belmont1, Martin Blaser4, Peter M. Izmirly5, Corey Lacher1, Miranda C Marion6, Mala Masson1, Gregg Silverman7 and Jill P. Buyon1, 1NYU School of Medicine, New York, NY, 2Wake Forest School of Medicine, Winston-Salem, NC, 3Biostatistical Sciences, Wake Forest School of Medicine, Winston-Salem, NC, 4Director of the NYU Human Microbiome Program, NYU School of Medicine, New York, NY, 5Medicine, Division of Rheumatology, NYU School of Medicine, New York, NY, 6Biostatistical Sciences and Center for Public Health Genomics, Wake Forest School of Medicine, Winston-Salem, NC, 7Rheumatology, NYU School of Medicine, New York, NY

    Background/Purpose: Anti-Ro60 autoantibodies are present in asymptomatic individuals years before onset of disease. We hypothesize that differences in autoreactivity-inducing commensal abundances may drive progression to…
  • Abstract Number: 1090 • 2018 ACR/ARHP Annual Meeting

    Cell-Free Mitochondrial DNA As a Novel Biomarker in Systemic Lupus Erythematosus

    Bhargavi Duvvuri1, Richard Moore1 and Christian Lood2, 1Division of Rheumatology, University of Washington, Seattle, WA, 2Department of Medicine, Division of Rheumatology, University of Washington, Seattle, WA

    Background/Purpose: We recently described a fundamental role for mitochondrial (mt)-mediated inflammation in systemic lupus erythematosus (SLE). Briefly, mtROS promoted formation of neutrophil extracellular traps (NETs),…
  • Abstract Number: 1091 • 2018 ACR/ARHP Annual Meeting

    Serine Arginine-Rich Splicing Factor 1 (SRSF1) Is Essential for T Lymphocyte Homeostasis and Decreased Levels of SRSF1 Correlate with Lymphopenia in SLE Patients

    Takayuki Katsuyama1, Kotaro Iida2 and Vaishali R. Moulton1, 1Division of Rheumatology, Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, 2Beth Israel Deaconess Medical Center, Harvard Medical School, Division of Rheumatology, Department of Medicine, Boston, MA

    Background/Purpose: Lymphopenia is one of the most common clinical features in patients with systemic lupus erythematosus (SLE), and associates with severe disease and comorbidities such…
  • Abstract Number: 1092 • 2018 ACR/ARHP Annual Meeting

    Immune Complex-Driven Neutrophil Activation and BAFF Production Promote B Cell Activation and Autoantibody Production in Human SLE

    Andrew Vasconcellos1, John Marken1, Sladjana Skopelja-Gardner1, Christian Lood2 and Natalia V. Giltiay1, 1Division of Rheumatology, Department of Medicine, University of Washington, Seattle, WA, 2Division of Rheumatology, Division of Rheumatology, Department of Medicine, University of Washington, Seattle, WA

    Background/Purpose: The production of anti-nuclear auto-antibodies (Ab) and the formation of immune complexes (IC) are hallmarks of Systemic Lupus Erythematosus (SLE). Enhanced neutrophil (PMN) activation…
  • Abstract Number: 1093 • 2018 ACR/ARHP Annual Meeting

    Serologic Evidence Linking Epstein Barr Virus Reactivation, Heightened Interferon Pathway Activation and Increased Disease Activity in Patients with Systemic Lupus Erythematosus

    Rebecca Wood1, Lauren Guthridge1, Carla J. Guthridge2, Rebecka L. Bourn1, Hua Chen1, Wade DeJager1, Susan R. Macwana1, Stan Kamp1, Rufei Lu1,3, Cristina Arriens1, Eliza Chakravarty1, Katherine Thanou1, Joan T. Merrill1, Joel M. Guthridge1,4 and Judith A. James4,5, 1Arthritis and Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 2Arthritis & Clinical Immunology, Oklahoma Medical Research Foundation, Oklahoma City, OK, 3Medicine and Pathology, University of Oklahoma Health Sciences Center, Oklahoma City, OK, 4University of Oklahoma Health Sciences Center, Oklahoma City, OK, 5Arthritis and Clinical Immunology Program, Oklahoma Medical Research Foundation, Oklahoma City, OK

    Background/Purpose: SLE is a clinically heterogeneous disease oftentimes characterized by a waxing and waning course. Mechanisms of SLE flare remain elusive. This study examined relationships…
  • Abstract Number: 1094 • 2018 ACR/ARHP Annual Meeting

    Endogenous Ifnβ Production Is Required for Efficient BCR Crosslinking and Survival of SLE B Cells

    John D. Mountz1, Shanrun Liu2, PingAr Yang3, Qi Wu4, Bao Luo5, W. Winn Chatham6 and Hui-Chen Hsu4, 1University of Alabama at Birmingham and Birmingham VA Medical center, Birmingham, AL, 2Biochemistry & Molecular Genetics, University of Alabama at Birmingham, Birmingham, AL, 3Department of Medicine, Clinical Immunology & Rheumatology, University of Alabama at Birmingham, Birmingham, AL, 4Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 5Division of Clinical Immunology and Rheumatology, Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 6Medcine/Clinical Immunology and Rheumatology, University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Increased type I interferon (IFN) has been shown to affect survival and activation of B cells in SLE. This study investigated novel mechanisms of…
  • Abstract Number: 1095 • 2018 ACR/ARHP Annual Meeting

    IFN Gene Expression Correlates with Frequency of Circulating Switched Memory B-Cells in Patients with Incomplete Systemic Lupus Erythematosus

    Wietske Lambers1, Geert Lanting1, Wayel H. Abdulahad2, Hendrika Bootsma2, Johanna Westra2 and Karina de Leeuw3, 1Rheumatology/Clinical Immunology, University Medical Center Groningen, Groningen, Netherlands, 2Rheumatology and Clinical Immunology, University of Groningen, University Medical Center Groningen, Groningen, Netherlands, 3Rheumatology and Clinical Immunology, University Medical Center Groningen, Groningen, Netherlands

    Background/Purpose: Incomplete systemic lupus erythematosus (iSLE) includes patients with typical features of SLE, who do not meet classification criteria. Still, up to 50% will develop…
  • Abstract Number: 1096 • 2018 ACR/ARHP Annual Meeting

    Unexpected Association between Health-Related Quality of Life and the Blood Interferon Modular Transcriptional Signatures in Patients with Systemic Lupus Erythematosus

    Laurent Chiche1, julie seguier2, stephanie gentile2, stephane burtey2, bertrand dussol2, philippe halfon3, wahiba bidaut3, elisabeth jouve2 and Noémie Jourde-Chiche4, 1Internal medicine, Hopital europeen, Marseille, France, 2aphm, marseille, France, 3hopital europeen, marseille, France, 4Vascular Research Center of Marseille, Aix-Marseille Univ., Vascular Research Center of Marseille, Marseille, France

    Background/Purpose: SLE has important effects on health-related quality of life (HRQOL) and is not well correlated to disease activity. As most SLE patients in remission…
  • Abstract Number: 1097 • 2018 ACR/ARHP Annual Meeting

    Spatial-Time Cluster Analysis of SLE Disease Activity

    George Stojan1, Anton Kvit2, Frank Curriero2 and Michelle Petri3, 1Division of Rheumatology, Johns Hopkins University, Baltimore, MD, 2Bloomberg School of Public Health, Baltimore, MD, 3Johns Hopkins University School of Medicine, Baltimore, MD

    Background/Purpose: Cluster detection is an essential tool in the public health domain with the goal of detecting anomalous clusters of disease cases. We performed a…
  • Abstract Number: 1098 • 2018 ACR/ARHP Annual Meeting

    Comparative Analysis of the Total Proteome of the Skin Lesions from Cutaneous Lupus Erythematosus (CLE) and Dermatomyositis (DM)

    Timothy B. Niewold1, Alexander Meves2, Julia S. Lehman3, Karin Popovic-Silwerfeldt4, Cristine Charlesworth5, Marie Wahren-Herlenius6, Elisabet Svenungsson7 and Vilija Oke8, 1Colton Center for Autoimmunity, New York University, New York, NY, 2Cancer Cenetr, Dermatology, Mayo Clinic, Rochester, MN, 3Pathology and Dermatology, Mayo Clinic College of Medicine and Science, Rochester, MN, MN, 4Department of Clinical Sciences, Dermatology Clinic, Danderyds Hospital,, Stockholm, Sweden, 5Mayo Clinic, Rochester, MN, 6Unit of Rheumatology, Department of Medicine, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden, 7Division of Rheumatology, Department of Medicine, Karolinska Institutet, Stockholm, Sweden, Stockholm, Sweden, 8Department of Medicine, Rheumatology Unit, Karolinska Institutet, Karolinska University Hospital, Stockholm, Sweden, Stockholm, Sweden

    Background/Purpose: Cutaneous lupus erythematosus (CLE) and dermatomyositis (DM) are autoimmune diseases. The histopathological pattern of skin involvement can be similar, i.e. interface dermatitis, but the…
  • Abstract Number: 1099 • 2018 ACR/ARHP Annual Meeting

    Ongoing DNA Damage, Chromatin Deregulation and Defective DNA Damage Response in Systemic Autoimmune Rheumatic Diseases

    Maria Pappa1, Nikolaos I. Vlachogiannis1, Alexandra Argyriou1, Vassilis L. Souliotis2 and Petros Sfikakis3, 1National Kapodistrian University of Athens Medical School, Athens, Greece, First Department of Propaedeutic and Internal Medicine & Rheumatology Unit, National Kapodistrian University of Athens Medical School, Athens, Greece, Athens, Greece, 2National Hellenic Research Foundation, Athens, Greece, Institute of Biology, Medicinal Chemistry and Biotechnology, National Hellenic Research Foundation, Athens, Greece, Athens, Greece, 3Rheumatology Unit, 1st Dept. of Propaedeutic Internal Medicine, Joint Academic Rheumatology Program, Athens University Medical School, Athens, Greece

    Background/Purpose: Recent data highlight that patients with Systemic Lupus Erythematosus (SLE) have defects in two main DNA repair pathways, namely nucleotide excision repair (NER) and…
  • Abstract Number: 1100 • 2018 ACR/ARHP Annual Meeting

    The Frequencies and Molecular Profiles of CD16+ Monocyte Subsets in Patients with Systemic Lupus Erythematosus, Primary Antiphospholipid Syndrome, and Antiphospholipid Syndrome with Lupus, Identify Specific Clinical Features of These Diseases

    Chary Lopez-Pedrera1, Maria Ángeles Aguirre Zamorano1, Nuria Barbarroja2, Patricia Ruiz-Limon3, Maria Carmen Abalos-Aguilera4, Yolanda Jiménez-Gómez2, Ivan Arias de la Rosa4, Pedro Segui5, Rafaela Ortega-Castro2, Eduardo Collantes Estevez1, Alejandro Escudero-Contreras4, Lucas Le Lann6, Christophe Jamin6, Concepcion Marañón7, Marta Alarcón-Riquelme8, Jacques-Olivier Pers6 and Carlos Perez-Sanchez2, 1IMIBIC/Reina Sofia Hospital/University of Cordoba, Cordoba, Spain, 2Rheumatology service, IMIBIC/Reina Sofia Hospital/University of Cordoba, Cordoba, Spain, 3Research Group of Endocrine Diseases, Research Laboratory. Biomedical Research Institute of Malaga (IBIMA).Virgen de la Victoria Universitary Hospital, Malaga, Spain., Málaga, MA, Spain, 4Rheumatology Service, IMIBIC/Reina Sofia Hospital/University of Cordoba, Cordoba, Spain, 5Radiology, IMIBIC/Reina Sofia Hospital/University of Cordoba, Cordoba, Spain, 6U1227, Université de Brest, Inserm, Labex IGO, CHU de Brest, Brest, France, 7GENYO, Centre for Genomics and Oncological Research Pfizer, University of Granada, Andalusian Regional Government, Granada, Spain, 8Medical Genomics, Center for Genomics and Oncological Research (GENYO), Granada, Spain

    Background/Purpose: This study, developed within the IMI-JU project PRECISESADS framework, aimed to determine the enrichment on CD14+ and CD16+ monocyte subpopulations in SLE, APS and…
  • « Previous Page
  • 1
  • …
  • 1075
  • 1076
  • 1077
  • 1078
  • 1079
  • …
  • 2425
  • Next Page »
Advanced Search

Your Favorites

You can save and print a list of your favorite abstracts during your browser session by clicking the “Favorite” button at the bottom of any abstract. View your favorites »

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].

Wiley

  • Online Journal
  • Privacy Policy
  • Permissions Policies
  • Cookie Preferences

© Copyright 2025 American College of Rheumatology