Tissue resident memory T cells (T) 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 reside permanently within tissues. As the main surveyors of non-lymphoid tissues, T are positioned to rapidly respond upon reinfection at barrier sites. During a viral reinfection, T 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 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 in multiple viral challenge models and contextualize the implications of these findings for vaccine development.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5346042 | PMC |
http://dx.doi.org/10.1016/j.coviro.2016.11.011 | DOI Listing |
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