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Distinct roles for IL-2 and IL-15 in the differentiation and survival of CD8+ effector and memory T cells.


ABSTRACT: IL-2 provides a memory differentiation signal to CD8+ T cells during the primary response that impacts the ability of the subsequent memory pool to mount a successful recall response. In this study, we find that although primary effector CTL development is modestly decreased in the absence of IL-2, the persistence of short-term and long-term effector memory CD8+ T cells on pathogen clearance is greatly diminished. Furthermore, secondary challenge of CD8+ memory T cells lacking the high-avidity IL-2R results in a failure to repopulate the effector pool. The role of IL-2 in promoting effector differentiation is not shared with the highly related cytokine, IL-15. Although IL-15 supports the survival of effector CD8+ T cells after pathogen clearance, its absence does not impair either primary or secondary effector CTL differentiation, nor does it impact the differentiation of long-term effector memory CD8+ T cells. These findings indicate a unique role for IL-2, but not IL-15, in promoting the differentiation not only of primary effector CD8+ T cells, but also of CD8+ memory T cells capable of secondary effector differentiation.

SUBMITTER: Mitchell DM 

PROVIDER: S-EPMC2950111 | biostudies-literature | 2010 Jun

REPOSITORIES: biostudies-literature

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Distinct roles for IL-2 and IL-15 in the differentiation and survival of CD8+ effector and memory T cells.

Mitchell Diana M DM   Ravkov Eugene V EV   Williams Matthew A MA  

Journal of immunology (Baltimore, Md. : 1950) 20100514 12


IL-2 provides a memory differentiation signal to CD8+ T cells during the primary response that impacts the ability of the subsequent memory pool to mount a successful recall response. In this study, we find that although primary effector CTL development is modestly decreased in the absence of IL-2, the persistence of short-term and long-term effector memory CD8+ T cells on pathogen clearance is greatly diminished. Furthermore, secondary challenge of CD8+ memory T cells lacking the high-avidity I  ...[more]

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