TY - JOUR
T1 - Viral infection triggers rapid differentiation of human blood monocytes into dendritic cells
AU - Hou, Wanqiu
AU - Gibbs, James S.
AU - Lu, Xiuju
AU - Brooke, Christopher B.
AU - Roy, Devika
AU - Modlin, Robert L.
AU - Bennink, Jack R.
AU - Yewdell, Jonathan W.
PY - 2012/3/29
Y1 - 2012/3/29
N2 - 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 infectionamongblood mononuclear cells, with the likely purpose of generating cells with enhanced capacity to activate innate and acquired antiviral immunity.
AB - 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 infectionamongblood mononuclear cells, with the likely purpose of generating cells with enhanced capacity to activate innate and acquired antiviral immunity.
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U2 - 10.1182/blood-2011-09-379479
DO - 10.1182/blood-2011-09-379479
M3 - Article
C2 - 22310910
AN - SCOPUS:84859341989
SN - 0006-4971
VL - 119
SP - 3128
EP - 3131
JO - Blood
JF - Blood
IS - 13
ER -