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IL-15 Complexes Induce Migration of Resting Memory CD8 T Cells into Mucosal Tissues.

Identifieur interne : 000822 ( Main/Exploration ); précédent : 000821; suivant : 000823

IL-15 Complexes Induce Migration of Resting Memory CD8 T Cells into Mucosal Tissues.

Auteurs : Ryan T. Sowell [États-Unis] ; Josef W. Goldufsky [États-Unis] ; Magdalena Rogozinska [États-Unis] ; Zurisaday Quiles [États-Unis] ; Yanxia Cao [États-Unis] ; Eliseo F. Castillo [États-Unis] ; Alison Finnegan [États-Unis] ; Amanda L. Marzo [États-Unis]

Source :

RBID : pubmed:28814601

Descripteurs français

English descriptors

Abstract

IL-15 is an essential cytokine known to promote T cell survival and activate the effector function of memory phenotype CD8 T cells. Blocking IL-15 signals also significantly impacts tissue-specific effector and memory CD8 T cell formation. In this study, we demonstrate that IL-15 influences the generation of memory CD8 T cells by first promoting their accumulation into mucosal tissues and second by sustaining expression of Bcl-6 and T-bet. We show that the mechanism for this recruitment is largely dependent on mammalian target of rapamycin and its subsequent inactivation of FoxO1. Last, we show that IL-15 complexes delivered locally to mucosal tissues without reinfection is an effective strategy to enhance establishment of tissue resident memory CD8 T cells within mucosal tissues. This study provides mechanistic insight into how IL-15 controls the generation of memory CD8 T cells and influences their trafficking and ability to take up residence within peripheral tissues.

DOI: 10.4049/jimmunol.1501638
PubMed: 28814601
PubMed Central: PMC5605445


Affiliations:


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Le document en format XML

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<div type="abstract" xml:lang="en">IL-15 is an essential cytokine known to promote T cell survival and activate the effector function of memory phenotype CD8 T cells. Blocking IL-15 signals also significantly impacts tissue-specific effector and memory CD8 T cell formation. In this study, we demonstrate that IL-15 influences the generation of memory CD8 T cells by first promoting their accumulation into mucosal tissues and second by sustaining expression of Bcl-6 and T-bet. We show that the mechanism for this recruitment is largely dependent on mammalian target of rapamycin and its subsequent inactivation of FoxO1. Last, we show that IL-15 complexes delivered locally to mucosal tissues without reinfection is an effective strategy to enhance establishment of tissue resident memory CD8 T cells within mucosal tissues. This study provides mechanistic insight into how IL-15 controls the generation of memory CD8 T cells and influences their trafficking and ability to take up residence within peripheral tissues.</div>
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