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Cutting Edge: Progesterone Regulates IFN-α Production by Plasmacytoid Dendritic Cells
Author(s) -
Grant C. Hughes,
Sunil Thomas,
Chang Li,
Murali-Krishna Kaja,
Edward A. Clark
Publication year - 2008
Publication title -
the journal of immunology
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.737
H-Index - 372
eISSN - 1550-6606
pISSN - 0022-1767
DOI - 10.4049/jimmunol.180.4.2029
Subject(s) - tlr9 , plasmacytoid dendritic cell , medroxyprogesterone acetate , innate immune system , immunology , biology , interferon , virus , immunity , microbiology and biotechnology , dendritic cell , immune system , estrogen , endocrinology , gene , gene expression , genetics , dna methylation
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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