Tissue resident memory T cells and viral immunity

被引:97
作者
Rosato, Pamela C. [1 ,2 ]
Beura, Lalit K. [1 ,2 ]
Masopust, David [1 ,2 ]
机构
[1] Univ Minnesota, Dept Microbiol & Immunol, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Immunol, Minneapolis, MN 55455 USA
基金
美国国家卫生研究院;
关键词
HSV-1; REACTIVATION; NONLYMPHOID TISSUE; LOCAL ANTIGEN; RM CELLS; HERPES; MIGRATION; MAINTENANCE; DIFFERENTIATION; PROTECTION; INFECTION;
D O I
10.1016/j.coviro.2016.11.011
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Tissue resident memory T cells (T-RM) constitute a recently identified T cell lineage that is responsible for frontline defense against viral infections. In contrast to central and effector memory T cells, which constitutively recirculate between tissues and blood, T-RM reside permanently within tissues. As the main surveyors of non-lymphoid tissues, T-RM are positioned to rapidly respond upon reinfection at barrier sites. During a viral reinfection, T-RM trigger the local tissue environment to activate and recruit immune cells and establish an antiviral state. Consistent with this function, there is empirical evidence that T-RM accelerate control in the event of reinfection or possible reactivation of latent infections in solid organs and barrier tissues. Here we review recent literature highlighting the protective functions of T-RM in multiple viral challenge models and contextualize the implications of these findings for vaccine development.
引用
收藏
页码:44 / 50
页数:7
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