Neutrophils sustain effective CD8+ T-cell responses in the respiratory tract following influenza infection

被引:69
作者
Tate, Michelle D. [2 ]
Brooks, Andrew G. [2 ]
Reading, Patrick C. [2 ,3 ]
Mintern, Justine D. [1 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Div Immunol, Melbourne, Vic 3010, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Melbourne, Vic, Australia
[3] WHO Collaborating Ctr Reference & Res Influenza, Melbourne, Vic, Australia
基金
英国医学研究理事会;
关键词
influenza; CD8(+) T cell; neutrophil and lung; SIMPLEX-VIRUS TYPE-1; ANTIGEN PRESENTATION; DENDRITIC CELLS; IN-VIVO; POLYMORPHONUCLEAR NEUTROPHILS; MONOCLONAL-ANTIBODY; PULMONARY INFECTION; RESTRICTED ANTIGEN; MICE; EXPRESSION;
D O I
10.1038/icb.2011.26
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Neutrophils have an important role in early host protection during influenza A virus infection. Their ability to modulate the virus-specific adaptive immune response is less clear. Here, we have used a mouse model to examine the impact of neutrophils on CD8(+) T-cell responses during influenza virus infection. CD8(+) T-cell priming, expansion, migration, cytokine secretion and cytotoxic capacity were investigated in the virus-infected airways and secondary lymphoid organs. To do this, we utilised a Ly6G-specific monoclonal antibody (mAb; 1A8) that specifically depletes neutrophils in vivo. Neutrophil depletion early after infection with influenza virus strain HKx31 (H3N2) did not alter influenza virus-derived antigen presentation or naive CD8(+) T-cell expansion in the secondary lymphoid organs. Trafficking of virus-specific CD8(+) T cells into the infected pulmonary airways was also unaltered. Instead, early neutropenia reduced both the overall magnitude of influenza virus-specific CD8(+) T cells, together with impaired cytokine production and cytotoxic effector function. Therefore, neutrophils are important participants in anti-viral mechanisms that sustain effective CD8(+) T-cell responses in the respiratory tract of influenza virus-infected mice. Immunology and Cell Biology (2012) 90, 197-205; doi:10.1038/icb.2011.26; published online 12 April 2011
引用
收藏
页码:197 / 205
页数:9
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