Information will be sought on the factors controlling the turnover (rate of proliferation) and survival of memory T-cells. In normal mice, memory CD4+ and CD8+ cells have a characteristic phenotype, typified by high expression of CD44 (CD44hi). Labeling studies with DNA precursors such as bromodeoxyuridine (BrdU) have shown that the turnover of memory-phenotype T-cells in vitro is far higher than for naive-phenotype cells. The high turnover of memory-phenotype T-cells may reflect (a) continuous TCR-mediated immune responses to foreign (or self) antigens, or (b) TCR-independent """"""""bystander"""""""" stimulation elicited by cytokines, or both. In favor of this second possibility, injecting mice with various cytokines considerably augments the turnover of memory-phenotype T-cells. Some cytokines, notably IL-15, elicit selective proliferation of CD44hi cells both in vivo and in vitro. However, other cytokines such as type I interferon (IFN-I) stimulate T-cell proliferation only in vivo and not in vitro. These and other data have led to a scenario where """"""""inducer"""""""" cytokines such as IFN-I cause T-cell proliferation in vivo by stimulating production of """"""""effector"""""""" cytokines (possibly IL-15) by antigen-presenting cells (APC). To assess this idea, three broad avenues of investigation are proposed. First, the possibility that IL-15 is an important effector cytokine for bystander T-cell proliferation initiated by IFN-I will be tested by using IL-15-'- or IL-15-unresponsive mice as host for normal T-cells. In addition, the capacity of IL-15 to potentiate the survival of memory T-cells will be explored. Second, a variety of different cytokines will be assessed for their capacity to act as effector cytokine inducers in vivo. Third, IFN-I and other cytokines will be tested for their ability to act as adjuvants for T-cell responses to specific antigen; the issue of whether the adjuvant function of cytokines operates at the level of APC, or T-cells or both will be explored.
| Boyman, Onur; Ramsey, Chris; Kim, David M et al. (2008) IL-7/anti-IL-7 mAb complexes restore T cell development and induce homeostatic T Cell expansion without lymphopenia. J Immunol 180:7265-75 |
| Ramsey, Chris; Rubinstein, Mark P; Kim, David M et al. (2008) The lymphopenic environment of CD132 (common gamma-chain)-deficient hosts elicits rapid homeostatic proliferation of naive T cells via IL-15. J Immunol 180:5320-6 |
| Purton, Jared F; Tan, Joyce T; Rubinstein, Mark P et al. (2007) Antiviral CD4+ memory T cells are IL-15 dependent. J Exp Med 204:951-61 |
| Boyman, Onur; Cho, Jae-Ho; Tan, Joyce T et al. (2006) A major histocompatibility complex class I-dependent subset of memory phenotype CD8+ cells. J Exp Med 203:1817-25 |
| Surh, Charles D; Boyman, Onur; Purton, Jared F et al. (2006) Homeostasis of memory T cells. Immunol Rev 211:154-63 |
| Kovar, Marek; Boyman, Onur; Shen, Xuefei et al. (2006) Direct stimulation of T cells by membrane vesicles from antigen-presenting cells. Proc Natl Acad Sci U S A 103:11671-6 |
| Rubinstein, Mark P; Kovar, Marek; Purton, Jared F et al. (2006) Converting IL-15 to a superagonist by binding to soluble IL-15R{alpha}. Proc Natl Acad Sci U S A 103:9166-71 |
| Ishimaru, Naozumi; Kishimoto, Hidehiro; Hayashi, Yoshio et al. (2006) Regulation of naive T cell function by the NF-kappaB2 pathway. Nat Immunol 7:763-72 |
| Surh, Charles D; Sprent, Jonathan (2005) Regulation of mature T cell homeostasis. Semin Immunol 17:183-91 |
| Sprent, Jonathan (2005) Direct stimulation of naive T cells by antigen-presenting cell vesicles. Blood Cells Mol Dis 35:17-20 |
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