Article

Viral infection triggers rapid differentiation of human blood monocytes into dendritic cells.

Laboratory of Viral Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD 20892, USA.
Blood (impact factor: 9.9). 02/2012; 119(13):3128-31. DOI:10.1182/blood-2011-09-379479 pp.3128-31
Source: PubMed

ABSTRACT Surprisingly little is known about the interaction of human blood mononuclear cells with viruses. Here, we show that monocytes are the predominant cell type infected when peripheral blood mononuclear cells are exposed to viruses ex vivo. Remarkably, infection with vesicular stomatitis virus, vaccinia virus, and a variety of influenza A viruses (including circulating swine-origin virus) induces monocytes to differentiate within 18 hours into CD16(-)CD83(+) mature dendritic cells with enhanced capacity to activate T cells. Differentiation into dendritic cells does not require cell division and occurs despite the synthesis of viral proteins, which demonstrates that monocytes counteract the capacity of these highly lytic viruses to hijack host cell biosynthetic capacity. Indeed, differentiation requires infectious virus and viral protein synthesis. These findings demonstrate that monocytes are uniquely susceptible to viral infection among blood mononuclear cells, with the likely purpose of generating cells with enhanced capacity to activate innate and acquired antiviral immunity.

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Keywords

activate innate
 
activate T cells
 
antiviral immunity
 
blood mononuclear cells
 
cell division
 
dendritic cells
 
differentiate
 
hijack host cell biosynthetic capacity
 
human blood mononuclear cells
 
infectious virus
 
likely purpose
 
lytic viruses
 
monocytes
 
peripheral blood mononuclear cells
 
predominant cell type
 
vesicular stomatitis virus
 
viral infection
 
viral protein synthesis
 
viral proteins
 
viruses ex vivo
 

Wanqiu Hou