
pmid: 17675470
Abstract It is well recognized that IFN-γ plays a critical role in the control of CD8 T cell expansion and contraction during immune responses to several intracellular pathogens. However, our understanding of the mechanisms underlying the regulation of T cell fate by IFN-γ is sorely incomplete. Specifically, it is unclear whether regulation of CD8 T cell homeostasis occurs by a T cell intrinsic IFN-γ pathway. In this study, we have determined the role of the direct effects of IFN-γ on T cells in regulating the expansion, contraction, and memory phases of the polyclonal CD8 T cell response to an acute viral infection. Using two complementary approaches we demonstrate that the direct effects of IFN-γ suppress IL-7R expression on Ag-specific effector CD8 T cells, but clonal expansion or deletion of activated CD8 T cells in vivo can occur in the apparent absence of IFN-γR signaling in T cells. These findings have clarified fundamental features of control of T cell homeostasis by IFN-γ in the context of CD8 T cell memory and protective immunity.
Mice, Knockout, Receptors, Interleukin-7, CD8-Positive T-Lymphocytes, Lymphocytic Choriomeningitis, Interferon-gamma, Mice, Gene Expression Regulation, Acute Disease, Animals, Homeostasis, Lymphocytic choriomeningitis virus, Antigens, Viral, Immunologic Memory, Cell Proliferation, Signal Transduction
Mice, Knockout, Receptors, Interleukin-7, CD8-Positive T-Lymphocytes, Lymphocytic Choriomeningitis, Interferon-gamma, Mice, Gene Expression Regulation, Acute Disease, Animals, Homeostasis, Lymphocytic choriomeningitis virus, Antigens, Viral, Immunologic Memory, Cell Proliferation, Signal Transduction
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