Antigen persistence and the control of local T cell memory by migrant respiratory dendritic cells after acute virus infection

被引:150
作者
Kim, Taeg S. [1 ,3 ]
Hufford, Matthew M. [1 ,2 ]
Sun, Jie [1 ]
Fu, Yang-Xin [4 ]
Braciale, Thomas J. [1 ,2 ,3 ]
机构
[1] Univ Virginia, Beirne B Carter Ctr Immunol Res, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Microbiol, Charlottesville, VA 22908 USA
[3] Univ Virginia, Dept Pathol, Charlottesville, VA 22908 USA
[4] Univ Chicago, Dept Pathol, Chicago, IL 60637 USA
基金
美国国家卫生研究院;
关键词
INFLUENZA-VIRUS; VIRAL PERSISTENCE; LYMPHOID ORGANS; SYNCYTIAL VIRUS; HELPER-CELLS; IMMUNITY; LUNG; MIGRATION; SUBSETS; TISSUE;
D O I
10.1084/jem.20092017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Acute viral infections induce robust adaptive immune responses resulting in virus clearance. Recent evidence suggests that there may be depots of viral antigen that persist in draining lymph nodes (DLNs) after virus clearance and could, therefore, affect the adaptive immune response and memory T cell formation. The nature of these residual antigen depots, the mechanism of antigen persistence, and the impact of the persistent antigen on memory T cells remain ill defined. Using a mouse model of influenza virus infection of the respiratory tract, we identified respiratory dendritic cells (RDCs) as essential for both sampling and presenting residual viral antigen. RDCs in the previously infected lung capture residual viral antigen deposited in an irradiation-resistant cell type. RDCs then transport the viral antigen to the LNs draining the site of infection, where they present the antigen to T cells. Lastly, we document preferential localization of memory T cells to the DLNs after virus clearance as a consequence of presentation of residual viral antigen by the migrant RDC.
引用
收藏
页码:1161 / 1172
页数:12
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