Cutting Edge: Intravascular Staining Redefines Lung CD8 T Cell Responses

被引:243
作者
Anderson, Kristin G. [1 ]
Sung, Heungsup [1 ]
Skon, Cara N. [1 ]
Lefrancois, Leo [2 ]
Deisinger, Angela [1 ]
Vezys, Vaiva [1 ]
Masopust, David [1 ]
机构
[1] Univ Minnesota, Ctr Immunol, Dept Microbiol, Minneapolis, MN 55455 USA
[2] Univ Connecticut, Ctr Hlth, Dept Immunol, Farmington, CT 06030 USA
基金
美国国家卫生研究院;
关键词
RESPIRATORY VIRUS-INFECTIONS; RESIDENT MEMORY; TISSUE; PROTECTION; MIGRATION; IMMUNITY; DIFFERENTIATION; PATHOGEN; INNATE; ORGANS;
D O I
10.4049/jimmunol.1201682
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nonlymphoid T cell populations control local infections and contribute to inflammatory diseases, thus driving efforts to understand the regulation of their migration, differentiation, and maintenance. Numerous observations indicate that T cell trafficking and differentiation within the lung are starkly different from what has been described in most nonlymphoid tissues, including intestine and skin. After systemic infection, we found that >95% of memory CD8 T cells isolated from mouse lung via standard methods were actually confined to the pulmonary vasculature, despite perfusion. A respiratory route of challenge increased virus-specific T cell localization within lung tissue, although only transiently. Removing blood-borne cells from analysis by the simple technique of intravascular staining revealed distinct phenotypic signatures and chemokine-dependent trafficking restricted to Ag-experienced T cells. These results precipitate a revised model for pulmonary T cell trafficking and differentiation and a re-evaluation of studies examining the contributions of pulmonary T cells to protection and disease. The Journal of Immunology, 2012, 189: 2702-2706.
引用
收藏
页码:2702 / 2706
页数:5
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