Abstract
Systemic sclerosis (SSc) is characterised by systemic fibrosis, vascular dysfunction, and the presence of antinuclear autoantibodies. The major SSc-associated antinuclear antibodies include anticentromere, antitopoisomerase I, anti–RNA polymerase III and antifibrillarin autoantibodies [1]. These autoantibodies are generally mutually exclusive and define clinically relevant subgroups.
Original language | English |
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Journal | Annals of the Rheumatic Diseases |
Early online date | 19 Jun 2025 |
DOIs | |
Publication status | E-pub ahead of print - 19 Jun 2025 |
Acknowledgements
We thank An Knoops for performing the indirect immunofluorescence assay.Funding
JB Vulsteke held a Research Foundation—Flanders (FWO) SB Fellowship (1S62419N). This study was supported by the Research Fund KU Leuven (C3/20/042) and by FWO-Applied Biomedical research (TBM) (T004821N).