Toll-like receptor-mediated activation of neutrophils by influenza A virus

被引:130
作者
Wang, Jennifer P. [1 ]
Bowen, Glennice N. [1 ]
Padden, Carolyn [2 ]
Cerny, Anna [1 ]
Finberg, Robert W. [1 ]
Newburger, Peter E. [2 ]
Kurt-Jones, Evelyn A. [1 ]
机构
[1] Univ Massachusetts, Sch Med, Dept Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA 01605 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1182/blood-2008-01-132860
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Influenza virus infection of the respiratory tract is characterized by a neutrophil infiltrate accompanied by inflammatory cytokine and chemokine production. We and others have reported that Toll-like receptor (TLR) proteins are present on human neutrophils and that granulocyte-macrophage colony-stimulating factor (GM-CSF) treatment enhances IL-8 (CXCL8) secretion in response to stimulation with TLR ligands. We demonstrate that influenza virus can induce IL-8 and other inflammatory cytokines from GM-CSF-primed human neutrophils. Using heat inactivation of influenza virus, we show that viral entry but not replication is required for cytokine induction. Furthermore, endosomal acidification and viral uncoating are necessary. Finally, using single-cell analysis of intracellular cytokine accumulation in neutrophils from knockout mice, we prove that TLR7 is essential for influenza viral recognition and inflammatory cytokine production by murine neutrophils. These studies demonstrate neutrophil activation by influenza virus and highlight the importance of TLR7 and TLR8 in that response.
引用
收藏
页码:2028 / 2034
页数:7
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