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Differences and similarities in cytokine profiles of macrophage activation syndrome in systemic lupus erythematosus and adult-onset Still’s disease

Authors :
Tomoka, Hiyama
Kazuhiro, Kurasawa
Anna, Hasegawa
Tomoyuki, Miyao
Ayae, Tanaka
Satoko, Arai
Masafumi, Arima
Reika, Maezawa
Source :
Clinical and Experimental Medicine.
Publication Year :
2023
Publisher :
Springer Science and Business Media LLC, 2023.

Abstract

To clarify the differences and similarities in the cytokine profiles of macrophage activating syndrome (MAS) between systemic lupus erythematosus (SLE) and adult-onset Still's disease (AOSD). The study participants included 9 patients with MAS-SLE, 22 with non-MAS-SLE, 9 with MAS-AOSD, and 13 with non-MAS-AOSD. Serum cytokine levels were measured using a multiplex bead assay. Cytokine levels were compared between patients with SLE and AOSD with/without MAS. Moreover, cytokine patterns were examined using principal component analysis (PCA) and cluster analysis. IL-6, IL-8, IL-18, and TNF-α levels were elevated in patients with SLE and AOSD. IFN-α levels were elevated in SLE, whereas IL-1β and IL-18 levels were elevated in AOSD. In SLE, IFN-α and IL-10 levels were higher in MAS than in non-MAS and controls. PCA revealed distinctive cytokine patterns in SLE and AOSD, SLE with IFN-α and IP-10, AOSD with IL-1β, IL-6, and IL-18, and enhanced cytokine production in MAS. PCA and cluster analysis showed no differences in cytokine patterns between the MAS and non-MAS groups. However, serum ferritin levels were correlated with IFN-α levels in SLE. Cytokine profiles differed between SLE and AOSD but not between MAS and non-MAS. MAS is induced by the enhancement of underlying cytokine abnormalities rather than by MAS-specific cytokine profiles. Type I IFN may be involved in MAS development in patients with SLE.

Details

ISSN :
15919528
Database :
OpenAIRE
Journal :
Clinical and Experimental Medicine
Accession number :
edsair.doi.dedup.....5bb73dfde9ce4760fbaca35107d6c2c7
Full Text :
https://doi.org/10.1007/s10238-023-00988-4