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Phosphatidylinositol 3-Kinase p110? Isoform Regulates CD8+ T Cell Responses during Acute Viral and Intracellular Bacterial Infections.


ABSTRACT: The p110? isoform of PI3K is known to play an important role in immunity, yet its contribution to CTL responses has not been fully elucidated. Using murine p110?-deficient CD8(+) T cells, we demonstrated a critical role for the p110? subunit in the generation of optimal primary and memory CD8(+) T cell responses. This was demonstrated in both acute viral and intracellular bacterial infections in mice. We show that p110? signaling is required for CD8(+) T cell activation, proliferation and effector cytokine production. We provide evidence that the effects of p110? signaling are mediated via Akt activation and through the regulation of TCR-activated oxidative phosphorylation and aerobic glycolysis. In light of recent clinical trials that employ drugs targeting p110? in certain cancers and other diseases, our study suggests caution in using these drugs in patients, as they could potentially increase susceptibility to infectious diseases. These studies therefore reveal a novel and direct role for p110? signaling in in vivo CD8(+) T cell immunity to microbial pathogens.

SUBMITTER: Gracias DT 

PROVIDER: S-EPMC4761756 | biostudies-literature | 2016 Feb

REPOSITORIES: biostudies-literature

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Phosphatidylinositol 3-Kinase p110δ Isoform Regulates CD8+ T Cell Responses during Acute Viral and Intracellular Bacterial Infections.

Gracias Donald T DT   Boesteanu Alina C AC   Fraietta Joseph A JA   Hope Jennifer L JL   Carey Alison J AJ   Mueller Yvonne M YM   Kawalekar Omkar U OU   Fike Adam J AJ   June Carl H CH   Katsikis Peter D PD  

Journal of immunology (Baltimore, Md. : 1950) 20160106 3


The p110δ isoform of PI3K is known to play an important role in immunity, yet its contribution to CTL responses has not been fully elucidated. Using murine p110δ-deficient CD8(+) T cells, we demonstrated a critical role for the p110δ subunit in the generation of optimal primary and memory CD8(+) T cell responses. This was demonstrated in both acute viral and intracellular bacterial infections in mice. We show that p110δ signaling is required for CD8(+) T cell activation, proliferation and effect  ...[more]

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