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

  • Abstract Number: 2248 • 2012 ACR/ARHP Annual Meeting

    Serum Phosphatidylserine-Specific Phospholipase A1 (PS-PLA1) Identified As a Novel Biomarker for Systemic Lupus Erythematosus (SLE)

    Tetsuji Sawada1, Kazuhiro Nakamura2, Ryunosuke Ohkawa2, Aki Shoji1, Koichiro Tahara1, Haeru Hayashi1, Eri Kimura1, Koji Igarashi3, Junken Aoki4 and Yutaka Yatomi5, 1Rheumatology, Tokyo Medical University, Tokyo, Japan, 2Department of Clinical Laboratory, The University of Tokyo Hospital, Tokyo, Japan, 3AIA Research Group, TOSOH Corporation, Kanagawa, Japan, 4Department of Molecular and Cellular Biochemistry, Graduate School of Pharmaceutical Sciences, Tohoku University, Miyagi, Japan, 5Department of Clinical Laboratory Medicine, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan

    Background/Purpose: Lysophosphatidylserine (LPS), which is a degraded form of phosphatidylserine (PS), is an acidic lyso-glycerophospholipid, similar to lysophosphatidic acid (LPA). LPS is known to mediate…
  • Abstract Number: 2256 • 2012 ACR/ARHP Annual Meeting

    A Population of IL-21 Producing CD4+ T Cells Correlates with Disease Damage in Systemic Lupus Erythematosus (SLE) Patients

    Babak Noamani1, Stacey Morrison2, Dafna D. Gladman3, Jorge Sanchez-Guerrero4, Murray B. Urowitz5, Joan E. Wither6 and Carolina Landolt-Marticorena7, 1Genetics and developmental biology, Toronto Western Research Institute, Toronto, ON, Canada, 2Div Rheumatology Rm MP-10-304, The Toronto Western Hospital, Toronto, ON, Canada, 3Division of Rheumatology, Toronto Western Hospital and University of Toronto, Toronto, ON, Canada, 4UHN Toronto Western Hospital, Toronto, ON, Canada, 5Division of Rheumatology, University of Toronto, Toronto Western Hospital, Toronto, ON, Canada, 61E420/Div of Rheumatology, Toronto Western Research Institute, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada, 7Rheumatology, Toronto Western Hospital, University of Toronto, Toronto, ON, Canada

    Background/Purpose: SLE mice models implicate IL-21, a T cell-derived cytokine, in disease pathogenesis with cytokine over-expression promoting the development of auto-antibodies and lupus-like clinical syndromes.…
  • Abstract Number: 685 • 2012 ACR/ARHP Annual Meeting

    Using a Library of Synthetic Autoantigen Mimics to Discover Biomarkers of Systemic Lupus Erythematosus

    Akshai Lakhanpal1, Jiexia Quan2, Sayed Zaman1, Nancy J. Olsen3 and David R. Karp2, 1Rheumatic Diseases Divsion, UT Southwestern Medical Center, Dallas, TX, 2Rheumatic Diseases Division, UT Southwestern Medical Center, Dallas, TX, 3Medicine, Penn State MS Hershey Medical Center, Hershey, PA

    Background/Purpose:   The natural history of systemic lupus erythematosus (SLE) is felt to evolve from a state of normal immunity to serologic autoimmunity and then…
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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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