The Journal of Immunology · 2008 · 125 citations · 20 references
Life SciencesEndocrinologyImmunologyImmunoregulationInnate ImmunityReproductive ImmunologyAntiviral ImmunityDendritic Cell BiologyDendritic Cell RegulationInnate Immune ModulationInnate Immune ResponseInnate Immune Signaling PathwaysAntiviral Innate SignalingDendritic Cell Antiviral ResponsesInhibition Of Interferon ResponsesPlasmacytoid Dendritic Cell Interferon ResponsesPlasmacytoid Dendritic Cell ResponsesProgesterone ImmunomodulationProgesterone-mediated Immune ModulationSteroid Hormone Action
Use of the progesterone (Pg) birth control depot medroxyprogesterone acetate (DMPA) increases a woman's risk for sexually transmitted infection with HIV or HSV-2 via unknown mechanisms. Plasmacytoid dendritic cells (pDCs) are circulating and tissue-resident sentinels capable of making large quantities of IFN-alpha upon recognizing viruses through TLRs 7 and 9. In this study, we show that Pg inhibits TLR9-induced IFN-alpha production by human and mouse pDCs and that DMPA impairs TLR9- and virus-induced IFN-alpha production by pDCs in mice, providing a potential explanation for how DMPA impairs innate antiviral immunity in women. Pg failed to inhibit the Mda-5 pathway of IFN-alpha induction in dendritic cells, suggesting that Pg regulates select antiviral DC programs. This may occur through selective blockade of IFN regulatory factor-7 activation, a novel steroid action. Thus, through inhibition of TLR-mediated IFN-alpha production by pDCs, Pg may regulate antiviral immunity.
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