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    Plasmacytoid dendritic cell interferon-alpha production to R-848 stimulation is decreased in male infants

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    Authors
    Wang, Jennifer P.
    Zhang, Lei
    Madera, Rachel F.
    Woda, Marcia
    Libraty, Daniel H.
    UMass Chan Affiliations
    Department of Medicine, Division of Infectious Diseases and Immunology
    Document Type
    Journal Article
    Publication Date
    2012-07-06
    Keywords
    Interferon-alpha
    Dendritic Cells
    Imidazoles
    Immunology and Infectious Disease
    Life Sciences
    Medicine and Health Sciences
    
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    Abstract
    BACKGROUND: Sex differences in response to microbial infections, especially viral ones, may be associated with Toll-like receptor (TLR)-mediated responses by plasmacytoid dendritic cells (pDCs). RESULTS: In this study, we identified sex differences in human infant pDC interferon-alpha production following challenge with the TLR7/8 agonist R-848. Male pDC responses were significantly lower than those of females during early infancy. This difference may be attributed to the androgen surge experienced by males during the early infancy period. Pretreatment of human pDCs with dihydrotestosterone produced a significant reduction in interferon-alpha production following R-848 challenge. CONCLUSIONS: Androgen-mediated regulation of pDC TLR7-driven innate immune responses may contribute to the observed sex differences in response to infections during early infancy.
    Source
    BMC Immunol. 2012 Jul 6;13:35. Link to article on publisher's site
    DOI
    10.1186/1471-2172-13-35
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/39520
    PubMed ID
    22769054
    Related Resources
    Link to Article in PubMed
    Rights
    © 2012 Wang et al.; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
    ae974a485f413a2113503eed53cd6c53
    10.1186/1471-2172-13-35
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