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: 2544

Serum Mediated Phagocytosis Of Necrotic Material By Polymorphonuclear Leukocytes May Be Used As a Tool To Predict Clinical Manifestations In Systemic Lupus Erythematosus

Michele Compagno1, Birgitta Gullstrand2, Andreas Jönsen3, Lennart Truedsson2, Gunnar Sturfelt4 and Anders A. Bengtsson3, 1Department of clinical sciences - Rheumatology, Lund University, Lund, Sweden, 2Department of Laboratory Medicine, Section of Microbiology, Immunology and Glycobiology, Lund University, Lund, Sweden, 3Department of Clinical Sciences, Section of Rheumatology, Lund University, Lund, Sweden, 4Department of Clinical Sciences Lund, Section of Rheumatology, Lund University, Lund, Sweden

Meeting: 2013 ACR/ARHP Annual Meeting

Keywords: Clinical research, flow cytometry, leukocytes, phagocytosis and systemic lupus erythematosus (SLE)

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print
Session Information

Title: Systemic Lupus Erythematosus-Clinical Aspects III: Biomarkers, Quality of Life and Disease Indicators, Late Complications

Session Type: Abstract Submissions (ACR)

Background/Purpose:

Polymorphonuclear (PMNs) leukocytes with engulfed necrotic cell material (NCM), as formerly used in the LE-cell test, are frequently seen in SLE and associated to severe clinical manifestations.

The aim of this study was to investigate if phagocytosis of NCM could predict or was associated with specific clinical phenotypes and/or disease activity in patients affected by SLE.

Methods:

Sixty-nine SLE-patients were followed longitudinally for a median time of 2.1 years. A total of 1074 serum samples were taken approximately every 60 days together with registration of an extensive set of clinical and laboratory variables. NCM was generated by heat treatment of mononuclear cells from healthy donors, and PMNs from healthy donors were isolated by density gradient centrifugation. Sera from SLE-patients were incubated with PMNs and NCM, and phagocytosis was assessed by flow cytometry. Association and prediction of relevant clinical phenotypes were evaluated with logistic regression and odds ratio (OR) and 95% confidence intervals (CI) were calculated.

Results:

In serum samples from 46 of the 69 SLE patients, phagocytosis of NCM by PMNs was seen at least once and totally 417 times. Significant association between phagocytosis of NCM by PMNs was found with clinical phenotypes such as lupus nephritis (OR=1.7, CI=1.2-2.5), mucocutaneous involvement (OR=1.45, CI=1.1-1.9) and also with increased disease activity (SLEDAI score) (OR=1.41, CI=1.0-2.0). Arthritis, though, was inversely associated with phagocytosis of NCM (OR=0.51, CI= 0.3 -0.8). Furthermore, phagocytosis of NCM by PMNs could predict alopecia (OR=2.22, CI=1.3-3.7) while arthritis was inversely related (OR=0.38, CI=0.1-1.0).

Conclusion:

In SLE, high capacity of serum mediated phagocytosis of NCM by PMNs is commonly seen. It is associated with disease activity and certain clinical phenotypes and was a predictor for alopecia and inversely related to arthritis. The assessment of phagocytosis of NCM by PMNs may be used as a complementary laboratory tool in management of SLE-patients.


Disclosure:

M. Compagno,
None;

B. Gullstrand,
None;

A. Jönsen,
None;

L. Truedsson,
None;

G. Sturfelt,
None;

A. A. Bengtsson,
None.

  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to 2013 ACR/ARHP Annual Meeting

ACR Meeting Abstracts - https://acrabstracts.org/abstract/serum-mediated-phagocytosis-of-necrotic-material-by-polymorphonuclear-leukocytes-may-be-used-as-a-tool-to-predict-clinical-manifestations-in-systemic-lupus-erythematosus/

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