The mechanism that is responsible for generating and maintaining memory T cell populations is not known. It is hypothesized that specific cytokines may facilitate the differentiation and survival of CD8 memory T cells. The objective of this proposal is to determine whether the cytokines that use the common gamma chain (gammac) receptor subunit are required for generating or maintaining memory CD8+ T cells. IL-2, IL-7, and IL-15 are cytokines that signal through receptors that contain the gammac and have been shown to increase survival of T cells. Therefore, the in vivo requirements for IL-2, IL-7, and IL-15 for CD8 T cell activation and memory generation will be examined. OT-I T cells (transgenic for a TCR that recognizes an ovalbumin peptide in the context of MHC class I) which cannot produce IL-2 (OT-1/IL-2-/-) will be adoptively transferred into normal mice and their ability to expand and differentiate into memory T cells will be measured. Furthermore. OT-I T cells that cannot respond to IL-7 or IL-15 will also be produced (OT-I/IL-7Ralpha-/-, OT-I/IL-15Ralpha--). These OT-I T cells will be used in the adoptive transfer system and their ability to expand and differentiate into memory T cells will also be determined. These studies will help define the requirements for the generation of memory T cells and thus would facilitate vaccine development.
| Robinson, Tanya O; Schluns, Kimberly S (2017) The potential and promise of IL-15 in immuno-oncogenic therapies. Immunol Lett 190:159-168 |
| D'Souza, Warren N; Schluns, Kimberly S; Masopust, David et al. (2002) Essential role for IL-2 in the regulation of antiviral extralymphoid CD8 T cell responses. J Immunol 168:5566-72 |
