Th1/17 cells, a subset of Th17 cells, are expanded in patients with active systemic lupus erythematosus

Skewed cytokine production characterizes T cells in Systemic Lupus Erythematosus (SLE). Among Th17 cells that are expanded in lupus, a subset (Th1/17) retains the ability to produce IFNγ. We aimed to analyze Th17 and Th1/17 cells in patients with SLE. Patients with active disease displayed increased...

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Veröffentlicht in:Clinical immunology (Orlando, Fla.) Fla.), 2018-10, Vol.195, p.101-106
Hauptverfasser: Tsanaktsi, Anastasia, Solomou, Elena E., Liossis, Stamatis-Nick C.
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Sprache:eng
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Zusammenfassung:Skewed cytokine production characterizes T cells in Systemic Lupus Erythematosus (SLE). Among Th17 cells that are expanded in lupus, a subset (Th1/17) retains the ability to produce IFNγ. We aimed to analyze Th17 and Th1/17 cells in patients with SLE. Patients with active disease displayed increased percentages of circulating Τh17 and Th1/17 cells. Stimulated T cells from patients with lupus secreted significantly more IL-17 compared to healthy donors. Also, T cells from patients with active SLE released significantly lower levels of IFN-γ compared to controls. However, following stimulation, levels of IFN-γ also rose significantly. Our data suggest that lupus Th1/17 cells are not only expanded but also functional. In summary, in this study it was shown that patients with active SLE display increased Th17 and functional Th1/17 cells. This impaired T-cell axis might represent a possible future therapeutic target.
ISSN:1521-6616
1521-7035
DOI:10.1016/j.clim.2018.08.005