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Virology. 2009 Aug 1;390(2):330-7. doi: 10.1016/j.virol.2009.05.013. Epub 2009 Jun 13.

Human cytomegalovirus suppresses type I interferon secretion by plasmacytoid dendritic cells through its interleukin 10 homolog.

Author information

1
Center for Comparative Medicine, University of California, Davis, CA 95616, USA. wlchang@ucdavis.edu

Abstract

Type I interferons (IFNs) are innate cytokines with potent antiviral and immunoregulatory activities. It remains unclear how human cytomegalovirus (HCMV) can establish persistence in the face of these strongly antagonistic cytokines. In this study, we confirm that IFN-alpha efficiently suppresses the penetration of HCMV into susceptible cells, including monocytes, the major cell population in peripheral blood that is highly susceptible to HCMV infection. We further demonstrate that the HCMV-derived interleukin 10 (IL-10) homolog functions similar to cellular IL-10 and broadly inhibits TLR-induced transcriptional activation of IFN-alpha/beta genes in plasmacytoid dendritic cells (PDCs), a major type I IFN-producer in vivo that is highly resistant to HCMV infection in vitro. These results suggest that HCMV subverts innate immunity by suppressing type I IFN production of PDCs during primary viral infection via its IL-10 homolog.

PMID:
19524994
PMCID:
PMC2747589
DOI:
10.1016/j.virol.2009.05.013
[Indexed for MEDLINE]
Free PMC Article

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