PI3Kδ Regulates the Magnitude of CD8+ T Cell Responses after Challenge with Listeria monocytogenes

• Published in: The Journal of immunology (1950) 2015-10, Vol.195 (7), p.3206-3217
• Main Authors: Pearce, Verity Q, Bouabe, Hicham, MacQueen, Amy R, Carbonaro, Valentina, Okkenhaug, Klaus
• Format: Article
• Language: English
• Subjects: Adoptive Transfer; Animals; CD8-Positive T-Lymphocytes - immunology; CD8-Positive T-Lymphocytes - transplantation; Class I Phosphatidylinositol 3-Kinases; Cytokines - biosynthesis; Granzymes - biosynthesis; Immunologic Memory - genetics; Immunologic Memory - immunology; Immunosenescence - immunology; Infectious Disease and Host Response; Interferon-gamma - biosynthesis; Listeria monocytogenes; Listeria monocytogenes - immunology; Listeriosis - immunology; Listeriosis - microbiology; Mice; Mice, Inbred C57BL; Mice, Transgenic; Phosphatidylinositol 3-Kinases - immunology; Phosphoinositide-3 Kinase Inhibitors; Phosphorylation; Proto-Oncogene Proteins c-akt - metabolism
• ISSN: 0022-1767; 1550-6606
• DOI: 10.4049/jimmunol.1501227

PI3Ks regulate diverse immune cell functions by transmitting intracellular signals from Ag, costimulatory receptors, and cytokine receptors to control cell division, differentiation, survival, and migration. In this study, we report the effect of inhibiting the p110δ subunit of PI3Kδ on CD8(+) T cell responses to infection with the intracellular bacteria Listeria monocytogenes. A strong dependency on PI3Kδ for IFN-γ production by CD8(+) T cells in vitro was not recapitulated after Listeria infection in vivo. Inactivation of PI3Kδ resulted in enhanced bacterial elimination by the innate immune system. However, the magnitudes of the primary and secondary CD8 +: T cell responses were reduced. Moreover, PI3Kδ activity was required for CD8(+) T cells to provide help to other responding CD8(+) cells. These findings identify PI3Kδ as a key regulator of CD8(+) T cell responses that integrates extrinsic cues, including those from other responding cells, to determine the collective behavior of CD8(+) T cell populations responding to infection.