Natural killer (NK) cells represent a distinct lymphoid population characterized by unique phenotypic and functional features. NK cells were originally identified on a functional basis as this denomination was assigned to lymphoid cells capable of lysing tumor cell lines in the absence of prior stimulation in vivo or in vitro.1 Both their origin and the mechanism(s) mediating their function remained mysterious until recently. Regarding their origin, it has been shown that NK cells derive from a precursor common to T cells and expressing the CD34þCD7þ phenotype. In addition, functional NK cells can be obtained in vitro and in vivo from (CD34þ) haematopoietic precursors isolated from several different sources.26 The cell maturation in vitro has been shown to require appropriate feeder cells and/or IL-15. The molecular mechanisms underlying the ability of NK cells to discriminate between normal and tumor cells, predicted by the ‘‘missing self hypothesis’’,7 have been clarified only during the past decade. It has been shown that NK cells recognize MHCclass I molecules through surface receptors delivering inhibitory, rather than activating, signals. Accordingly, NK cells lyse target cells that have lost (or express low amounts of) MHC class I molecules. This event occurs frequently in tumors or in cells infected by some viruses such as certain herpesviruses or adenoviruses. In addition to provide a first line of defence against viruses, NK cells release various cytokines and chemokines. These released cytokines can control bacterial spreading but also induce or modulate inflammatory responses, hematopoiesis, and control the growth and function of monocytes and granulocytes. Finally, the functional links between NK and dendritic cells (DCs) have been widely investigated in recent years and different studies have demonstrated that reciprocal activations ensue upon NK/DC interactions. More recently, the anatomical sites where these interactions take place have been identified together with the related cell subsets involved.8 Remarkably, there is now ‘‘in vivo’’ evidence that this cellular cross-talk occurring during the innate phase of the immune response against bacteria or bacterial products can deeply affect the magnitude and the quality of the subsequent adaptive response. These new experimental evidences emphasize the relevance of the interplay between DCs and NK cells during bacterial infections.

Interactions between natural killer and dendritic cells during bacterial infections

FERLAZZO, Guido
2007-01-01

Abstract

Natural killer (NK) cells represent a distinct lymphoid population characterized by unique phenotypic and functional features. NK cells were originally identified on a functional basis as this denomination was assigned to lymphoid cells capable of lysing tumor cell lines in the absence of prior stimulation in vivo or in vitro.1 Both their origin and the mechanism(s) mediating their function remained mysterious until recently. Regarding their origin, it has been shown that NK cells derive from a precursor common to T cells and expressing the CD34þCD7þ phenotype. In addition, functional NK cells can be obtained in vitro and in vivo from (CD34þ) haematopoietic precursors isolated from several different sources.26 The cell maturation in vitro has been shown to require appropriate feeder cells and/or IL-15. The molecular mechanisms underlying the ability of NK cells to discriminate between normal and tumor cells, predicted by the ‘‘missing self hypothesis’’,7 have been clarified only during the past decade. It has been shown that NK cells recognize MHCclass I molecules through surface receptors delivering inhibitory, rather than activating, signals. Accordingly, NK cells lyse target cells that have lost (or express low amounts of) MHC class I molecules. This event occurs frequently in tumors or in cells infected by some viruses such as certain herpesviruses or adenoviruses. In addition to provide a first line of defence against viruses, NK cells release various cytokines and chemokines. These released cytokines can control bacterial spreading but also induce or modulate inflammatory responses, hematopoiesis, and control the growth and function of monocytes and granulocytes. Finally, the functional links between NK and dendritic cells (DCs) have been widely investigated in recent years and different studies have demonstrated that reciprocal activations ensue upon NK/DC interactions. More recently, the anatomical sites where these interactions take place have been identified together with the related cell subsets involved.8 Remarkably, there is now ‘‘in vivo’’ evidence that this cellular cross-talk occurring during the innate phase of the immune response against bacteria or bacterial products can deeply affect the magnitude and the quality of the subsequent adaptive response. These new experimental evidences emphasize the relevance of the interplay between DCs and NK cells during bacterial infections.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11567/1117989
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