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: 0575

Combined Testing of anti-CD74 IgA and Anti-UH-axSpA Antibodies Increases the Diagnostic Potential for axSpA

Kurt de Vlam1, Pieter Ruytinx2, Elien luyten2, Anouk Agten2, Frank Vandenabeele2 and Veerle somers2, 1Department of Rheumatology, UZ Leuven, and Department of Development and Regeneration, Skeletal Biology and Engineering Research Center, KU Leuven, Leuven, Belgium, 2Universiteit Hasselt, Hasselt, Belgium

Meeting: ACR Convergence 2024

Keywords: Autoantibody(ies), Biomarkers, spondyloarthritis, Spondyloarthropathies

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

Date: Saturday, November 16, 2024

Title: SpA Including PsA – Diagnosis, Manifestations, & Outcomes Poster I

Session Type: Poster Session A

Session Time: 10:30AM-12:30PM

Background/Purpose: Diagnosis of axial spondyloarthritis (axSpA) is challenging and a specific laboratory diagnostic test is lacking. Previously, we identified novel immunoglobulin G (IgG) and IgA antibodies to 4 Hasselt University (UH)-axSpA antigens (UH-axSpA-IgG 4, 8 and UH-axSpA-IgA 1,10), corresponding to non-physiological peptides and to a novel axSpA autoantigen, Double homeobox protein 4 (DUX4). Validation of antibody reactivity in plasma samples of axSpA patients from the Leuven spondyloarthritis biologics cohort (BIOSPAR) cohort revealed antibody reactivity against at least one of these 4 peptide targets in 15.9 % of axSpA patients (26/164). In addition, IgA antibodies against CD74, involved in the assembly of and the prevention of premature peptide-binding to major histocompatibility complex (MHC) class II has been shown in patients with axSpA. 

Here we aim to determine the diagnostic potential of the anti-CD74 IgA antibodies in combination with previously determined IgG and IgA antibodies against the 4 UH-axSpA antigens.

Methods: Anti-CD74 IgA antibodies were measured using the AESKULISA SpA Detect Kit (AESKU Diagnostics, Wendelsheim, Germany) in axSpA patients from the BIOSPAR cohort and patients with chronic low back pain (CLBP) served as the control group. The cut-off of the ELISA was 20 U/ml.

Results: In the BIOSPAR cohort, anti-CD74 IgA antibodies were present in 29.3% of axSpA patients (48/164) versus no presence in the CLBP patients (0/58) (p< 0.0001). Additional testing for the presence of antibodies against the 4 UH-axSpA peptides further increased the antibody reactivity in 40.2 % of the patients (66/164) and only in 3.4% of the CLBP patients (2/58) (p< 0.0001). Interestingly, we found a significant increase in age, disease duration and Bath Ankylosing Spondylitis Functional Index (BASFI) in axSpA patients who tested positive for antibodies against at least one of the 4 UH-axSpA antigens or CD74 compared to seronegative patients.

Conclusion: Combined testing for antibody reactivity against the 4 novel UH-axSpA peptides and  anti-CD74 results in improved diagnosis of axSpA. Including this set of antibody reactivities increases the post-test probability for axial spondyloarthritis considerably in patients with chronic back pain


Disclosures: K. de Vlam: AbbVie, 2, 6, Amgen, 2, 5, 6, Galapagos, 2, 6, Lilly, 2, 6, 12, Paid instructor, Novartis, 2, 6, Pfizer, 2, 6, UCB, 2, 6; P. Ruytinx: None; E. luyten: None; A. Agten: None; F. Vandenabeele: None; V. somers: None.

To cite this abstract in AMA style:

de Vlam K, Ruytinx P, luyten E, Agten A, Vandenabeele F, somers V. Combined Testing of anti-CD74 IgA and Anti-UH-axSpA Antibodies Increases the Diagnostic Potential for axSpA [abstract]. Arthritis Rheumatol. 2024; 76 (suppl 9). https://acrabstracts.org/abstract/combined-testing-of-anti-cd74-iga-and-anti-uh-axspa-antibodies-increases-the-diagnostic-potential-for-axspa/. Accessed .
  • Tweet
  • Click to email a link to a friend (Opens in new window) Email
  • Click to print (Opens in new window) Print

« Back to ACR Convergence 2024

ACR Meeting Abstracts - https://acrabstracts.org/abstract/combined-testing-of-anti-cd74-iga-and-anti-uh-axspa-antibodies-increases-the-diagnostic-potential-for-axspa/

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