346 The contribution of interferon lambda to sle

Background and aimsInterferon lambda (IFN-λ) is a novel type of interferon produced by dendritic cells (DC). Despite its binding to a different receptor, IFN-λ shares functional similarities with type I IFN (IFN-I) by upregulating the expression of IFN-stimulated genes. The role of IFN-λ in DC biolo...

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Veröffentlicht in:Lupus science & medicine 2017-03, Vol.4 (Suppl 1), p.A152
Hauptverfasser: Macri, C, Pang, ES, Pooley, J, Radford, K, O’Keeffe, M
Format: Artikel
Sprache:eng
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Zusammenfassung:Background and aimsInterferon lambda (IFN-λ) is a novel type of interferon produced by dendritic cells (DC). Despite its binding to a different receptor, IFN-λ shares functional similarities with type I IFN (IFN-I) by upregulating the expression of IFN-stimulated genes. The role of IFN-λ in DC biology and in autoimmunity remains unknown.to identify the DC subsets producing IFN-λ.to investigate the role of IFN-λ in DC functions.to investigate the role of IFN-λ in SLE.MethodsMouse and human DC subsets were stimulated ex vivo and the IFN-λ expression was measured.The maturation and the capacity of DC to cross-prime T cells was compared in WT and IFN-λR-/- mice. T cell cross-priming by human DCs was measured ex vivo in the presence of exogenous IFN-λ.Serum levels of IFN-λ was measured in lupus-prone mice and in SLE patients. The phenotype of the blood DC subsets from SLE patients was also characterised.ResultsMouse plasmacytoid DC (pDC) and CD8+ DC highly secrete IFN-λ. In humans, the CD141+ DC are the major IFN-λ producers.IFN-λ enhances the capacities of mouse and human DCs to maturate and to cross-prime T cells.High serum levels of IFN-λ were detected in lupus-prone mice and in some SLE patients. SLE patients display increased activation of the IFN-producing DC subsets: the pDCs (producing IFN-I) and the CD141+ DCs (producing IFN-λ).ConclusionsIFN-λ is produced by some DC subsets and enhances their functions. Furthermore, IFN-λ is expressed during SLE, suggesting a potential role of the cytokine in the aetiology of SLE.
ISSN:2053-8790
DOI:10.1136/lupus-2017-000215.346