Primed antigen-specific CD4+ T cells are required for NK cell activation in vivo upon Leishmania major infection

F Bihl, J Pecheur, B Bréart, G Poupon… - The Journal of …, 2010 - journals.aai.org
F Bihl, J Pecheur, B Bréart, G Poupon, J Cazareth, V Julia, N Glaichenhaus, VM Braud
The Journal of Immunology, 2010journals.aai.org
The ability of NK cells to rapidly produce IFN-γ is an important innate mechanism of
resistance to many pathogens including Leishmania major. Molecular and cellular
components involved in NK cell activation in vivo are still poorly defined, although a central
role for dendritic cells has been described. In this study, we demonstrate that Ag-specific
CD4+ T cells are required to initiate NK cell activation early on in draining lymph nodes of L.
major-infected mice. We show that early IFN-γ secretion by NK cells is controlled by IL-2 and …
Abstract
The ability of NK cells to rapidly produce IFN-γ is an important innate mechanism of resistance to many pathogens including Leishmania major. Molecular and cellular components involved in NK cell activation in vivo are still poorly defined, although a central role for dendritic cells has been described. In this study, we demonstrate that Ag-specific CD4+ T cells are required to initiate NK cell activation early on in draining lymph nodes of L. major-infected mice. We show that early IFN-γ secretion by NK cells is controlled by IL-2 and IL-12 and is dependent on CD40/CD40L interaction. These findings suggest that newly primed Ag-specific CD4+ T cells could directly activate NK cells through the secretion of IL-2 but also indirectly through the regulation of IL-12 secretion by dendritic cells. Our results reveal an unappreciated role for Ag-specific CD4+ T cells in the initiation of NK cell activation in vivo upon L. major infection and demonstrate bidirectional regulations between innate and adaptive immunity.
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