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

  • Abstract Number: 2313 • 2012 ACR/ARHP Annual Meeting

    The Autoantibody-Inducing CD4 T Cell (aiCD4 T cell) Belongs to CCR4+CD45RBlo122lo CD4 Subpopulation: A Novel ‘Self-Organized Criticality Theory’ Explains the Cause of Systemic Lupus Erythematosus (SLE)

    Yumi Miyazaki1, Ken Tsumiyama2 and Shunichi Shiozawa2, 1Kyushu University Beppu Hospital/ Kobe University Graduate School of Health Sciences, Beppu/ Kobe, Japan, 2Kyushu University Beppu Hospital, Beppu, Japan

    Background/Purpose:  We found that systemic lupus erythematosus (SLE) was induced experimentally by repeatedly immunizing the mice normally not prone to autoimmune diseases by any exogenous…
  • Abstract Number: 1725 • 2012 ACR/ARHP Annual Meeting

    ANTI-Factor Xa Antibodies ARE Significantly Increased in Patients with Systemic LUPUS Erythematosus and Antiphospholipid Syndrome

    Bahar Artim-Esen1, Charis Pericleous2, Ian Mackie3, Yiannis Ioannou4, Anisur Rahman5, David A. Isenberg6 and Ian Giles5, 1Division of Medicine, Centre for Rheumatology, University College London, London, United Kingdom, 2Centre for Rheumatology, Division of Medicine, Centre for Rheumatology, University College London, London, United Kingdom, 3Haemostasis Research Unit, 1st Floor, 51 Chenies Mews, Haemostasis Research Unit, University College London, London, United Kingdom, 4Arthritis Research UK Centre for Adolescent Rheumatology at University College London, Great Ormond Street Hospital and UCLH, University College London, London, United Kingdom, 5Centre for Rheumatology Research,Rayne Institute, 4th Floor, University College London, London, United Kingdom, 6Centre for Rheumatology Research, Rayne Building, 4th Floor, Centre for Rheumatology, Department of Medicine, University College London, London, United Kingdom

    Background/Purpose: Increased levels of antibodies against different serine proteases (SP) have been identified in patients with the Antiphospholipid Syndrome (APS) compared with healthy controls. These…
  • Abstract Number: 1450 • 2012 ACR/ARHP Annual Meeting

    MEDI-551 Depletes a Majority of Murine B Cells and Reduces Serum Titers of Autoantibodies in the SLE1-huCD19 TG Mice

    Sandra Gallagher1, Yue Wang1, Isharat Yusuf1, Thomas McCaughtry1, Ronald Herbst2 and Laura Carter1, 1Respiratory, Inflammation and Autoimmune, MedImmune, Gaithersburg, MD, 2Respiration, Inflammation and Autoimmunity, MedImmune, Gaithersburg, MD

    Background/Purpose: Systemic Lupus Erythematosus (SLE) is characterized by chronic inflammation that can affect various organs.  Hyperactive B cells appear to be key drivers in SLE…
  • Abstract Number: 1422 • 2012 ACR/ARHP Annual Meeting

    Clinical Associations of Anti-Smith Antibodies in Profile: A Multiethnic Lupus Cohort

    Yesenia C. Santiago-Casas1, Luis M. Vila1, Gerald McGwin Jr.2, Ryan S. Cantor2, Michelle Petri3, Rosalind Ramsey-Goldman4, John D. Reveille5, Robert P. Kimberly6, Graciela S. Alarcon7 and Elizabeth E. Brown8, 1Department of Medicine, Division of Rheumatology, University of Puerto Rico Medical Sciences Campus, San Juan, PR, 2Epidemiology, University of Alabama at Birmingham, Birmingham, AL, 3Johns Hopkins University School of Medicine, Baltimore, MD, 4Medicine/Rheumatology, Northwestern University Feinberg School of Medicine, Chicago, IL, 5Internal Medicine/Rheumatology, Univ of Texas Health Science Center at Houston, Houston, TX, 6Department of Medicine, University of Alabama at Birmingham, Birmingham, AL, 7Medicine, University of Alabama at Birmingham, Birmingham, AL, 8University of Alabama at Birmingham, Birmingham, AL

    Background/Purpose: Anti-Smith (anti-Sm) antibodies are highly specific for systemic lupus erythematosus (SLE) and have an important value in the diagnosis of this disease.  However, whether…
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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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