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Guido Ferlazzo

Researcher at University of Messina

Publications -  137
Citations -  9646

Guido Ferlazzo is an academic researcher from University of Messina. The author has contributed to research in topics: Interleukin 21 & Interleukin 12. The author has an hindex of 45, co-authored 126 publications receiving 8514 citations. Previous affiliations of Guido Ferlazzo include Cornell University & Wayne State University.

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Human dendritic cells activate resting natural killer (NK) cells and are recognized via the NKp30 receptor by activated NK cells.

TL;DR: It is suggested that DCs are able to control directly the expansion of NK cells and that the lysis of immature DCs can regulate the afferent limb of innate and adaptive immunity.
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The Abundant NK Cells in Human Secondary Lymphoid Tissues Require Activation to Express Killer Cell Ig-Like Receptors and Become Cytolytic

TL;DR: It is hypothesized that IL-2 can mobilize the NK cells of secondary lymphoid tissues to mediate natural killing during immune responses, and this newly characterized per forin− NK cell compartment in lymph nodes and related tissues probably outnumbers perforin+ NK cells.
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Distinct roles of IL-12 and IL-15 in human natural killer cell activation by dendritic cells from secondary lymphoid organs.

TL;DR: In this paper, the capacity of Dendritic cells to interact with NK cells in human lymphoid organs and identify the role of specific DC-derived cytokines was identified. And they demonstrated that DCs colocalize with NKs in the T cell areas of lymph nodes.
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CD56brightCD16− Killer Ig-Like Receptor− NK Cells Display Longer Telomeres and Acquire Features of CD56dim NK Cells upon Activation

TL;DR: The results suggest that CD56brightCD16− KIR− and CD56dimCD16+KIR+/− NK cells correspond to sequential steps of differentiation and support the hypothesis that secondary lymphoid organs can be sites of NK cell final maturation and self-tolerance acquisition during immune reaction.
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NK cells at the interface between innate and adaptive immunity

TL;DR: This work has shown that the recruitment of CD56low CD16+ NK cells into inflamed peripheral tissues is orchestrated by various chemochines including the newly identified Chemerin and this process appears to play a crucial role in shaping both innate and adaptive immune responses.