| Literature DB >> 26519527 |
Morgane Griesbeck1, Susanne Ziegler2, Sophie Laffont3, Nikaïa Smith4, Lise Chauveau5, Phillip Tomezsko6, Armon Sharei7, Georgio Kourjian6, Filippos Porichis6, Meghan Hart6, Christine D Palmer6, Michael Sirignano6, Claudia Beisel8, Heike Hildebrandt2, Claire Cénac3, Alexandra-Chloé Villani9, Thomas J Diefenbach6, Sylvie Le Gall6, Olivier Schwartz5, Jean-Philippe Herbeuval4, Brigitte Autran10, Jean-Charles Guéry3, J Judy Chang11, Marcus Altfeld12.
Abstract
Increased IFN-α production contributes to the pathogenesis of infectious and autoimmune diseases. Plasmacytoid dendritic cells (pDCs) from females produce more IFN-α upon TLR7 stimulation than pDCs from males, yet the mechanisms underlying this difference remain unclear. In this article, we show that basal levels of IFN regulatory factor (IRF) 5 in pDCs were significantly higher in females compared with males and positively correlated with the percentage of IFN-α-secreting pDCs. Delivery of recombinant IRF5 protein into human primary pDCs increased TLR7-mediated IFN-α secretion. In mice, genetic ablation of the estrogen receptor 1 (Esr1) gene in the hematopoietic compartment or DC lineage reduced Irf5 mRNA expression in pDCs and IFN-α production. IRF5 mRNA levels furthermore correlated with ESR1 mRNA levels in human pDCs, consistent with IRF5 regulation at the transcriptional level by ESR1. Taken together, these data demonstrate a critical mechanism by which sex differences in basal pDC IRF5 expression lead to higher IFN-α production upon TLR7 stimulation in females and provide novel targets for the modulation of immune responses and inflammation.Entities:
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Year: 2015 PMID: 26519527 PMCID: PMC4654231 DOI: 10.4049/jimmunol.1501684
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422