: The cytokines which utilize receptors containing the common gamma chain (gammac) are required at proscribed steps of T cell development and during the immune response. One of these, IL-15, is important for CD8 T cell, NK, NK-T, and intestinal intraepithelial lymphocyte development. However, the precise role of lL-15 in CD8 T cell development and function is not known. Mice lacking expression of IL-15 or lL-l5Ra lack memory phenotype CD8 T cells, but our preliminary data shows that CD8 memory T cells can be generated in these mice. This result questions the origin of memory-phenotype cells in normal mice and provides a strong rationale for the in-depth studies proposed here to determine the role of IL-15 in CD8 T cell development and immune response.
The specific aims of the application are:
Aim 1. To determine the requirements for IL-15 in CD8 T cell development. Studies will examine thymocyte subsets during fetal, neonatal and adult life to determine whether a defect in CD8 T cell development can be identified. Experiments will then focus on identifying the source of IL-15, hematopoietic or non-hematopoietic, needed for normal CD8 T cell production. Studies will examine whether CD8 T cell production/survival requires IL-15 expressed in the thymus versus the peripheral tissues.
Aim 2. To determine the role of IL-15 in control of CD8 T cell immune responses. Our preliminary results show that virus infection of IL-1 5-/-IL-15Ralpha-/- mice generates CD44high memory CD8 T cells. Yet, uninfected IL-15-/-/IL- 5Ra-/- mice lack the CD44high CD8 T cell subset. We hypothesize that the strength of the initial activation signal regulates the level of IL-15 dependence of the immune response, and this theory will be tested by using a variety of immunization regimens and by examining whether CD4 T cell activation is IL-15 dependent. Model systems will also be used to determine the relevant source of IL-15 in controlling the magnitude of the response.
Aim 3. To determine the role of IL-15 in generation and survival of CD8 memory T cells. Experiments in this aim will test whether antiviral memory CD8 T cells or memory-phenotype CD8 T cells from uninfected mice are IL-15-dependent once generated. Studies measuring turnover and survival in the presence or absence of IL-i5 will be performed. In addition, the expression pattern of IL-15R components during an immune response will be assessed. Transgenic mice expressing inducible IL-15Ralpha will be generated in order to distinguish between thymic and peripheral effects of IL-15Ralpha on CD8 T cell biology. These studies will provide a comprehensive analysis of the role of lL-15 in regulation of CD8 T cells.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
1R01AI051583-01
Application #
6466499
Study Section
Immunobiology Study Section (IMB)
Program Officer
Macchiarini, Francesca
Project Start
2002-09-01
Project End
2007-02-28
Budget Start
2002-09-01
Budget End
2003-02-28
Support Year
1
Fiscal Year
2002
Total Cost
$181,250
Indirect Cost
Name
University of Connecticut
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Farmington
State
CT
Country
United States
Zip Code
06030
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Colpitts, Sara L; Stonier, Spencer W; Stoklasek, Thomas A et al. (2013) Transcriptional regulation of IL-15 expression during hematopoiesis. J Immunol 191:3017-24
Colpitts, Sara L; Stoklasek, Thomas A; Plumlee, Courtney R et al. (2012) Cutting edge: the role of IFN-? receptor and MyD88 signaling in induction of IL-15 expression in vivo. J Immunol 188:2483-7
Wu, Carol A; Paveglio, Sara A; Lingenheld, Elizabeth G et al. (2011) Transmission of murine cytomegalovirus in breast milk: a model of natural infection in neonates. J Virol 85:5115-24
Obar, Joshua J; Lefrancois, Leo (2010) Early events governing memory CD8+ T-cell differentiation. Int Immunol 22:619-25
Lefrancois, Leo; Obar, Joshua J (2010) Once a killer, always a killer: from cytotoxic T cell to memory cell. Immunol Rev 235:206-18
Obar, Joshua J; Lefrancois, Leo (2010) Memory CD8+ T cell differentiation. Ann N Y Acad Sci 1183:251-66
Stoklasek, Thomas A; Colpitts, Sara L; Smilowitz, Henry M et al. (2010) MHC class I and TCR avidity control the CD8 T cell response to IL-15/IL-15Rýý complex. J Immunol 185:6857-65
Stoklasek, Thomas A; Schluns, Kimberly S; Lefrancois, Leo (2006) Combined IL-15/IL-15Ralpha immunotherapy maximizes IL-15 activity in vivo. J Immunol 177:6072-80
Klonowski, Kimberly D; Williams, Kristina J; Marzo, Amanda L et al. (2006) Cutting edge: IL-7-independent regulation of IL-7 receptor alpha expression and memory CD8 T cell development. J Immunol 177:4247-51

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