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Massimo Vitale

Researcher at University of Genoa

Publications -  110
Citations -  16986

Massimo Vitale is an academic researcher from University of Genoa. The author has contributed to research in topics: Receptor & Interleukin 21. The author has an hindex of 53, co-authored 104 publications receiving 15758 citations. Previous affiliations of Massimo Vitale include University of Brescia.

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Activating receptors and coreceptors involved in human natural killer cell-mediated cytolysis.

TL;DR: The discovery of MHC-specific inhibitory receptors in mouse and in human clarified the molecular basis of this important NK cell function, and some of these receptors have now been identified in humans, thus shedding some light on the molecular mechanisms involved in NK cell activation during the process of natural cytotoxicity.
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Receptors for hla class-i molecules in human natural killer cells

TL;DR: These receptors exert an inhibiting activity on T cell receptor- mediated functions and offer a valuable model to analyze the regulatory mechanisms involved in receptor-mediated cell activation and inactivation.
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Identification of PVR (CD155) and Nectin-2 (CD112) as Cell Surface Ligands for the Human DNAM-1 (CD226) Activating Molecule

TL;DR: The surface expression of PVR or Nectin-2 in cell transfectants resulted in DNAM-1–dependent enhancement of NK-mediated lysis of these target cells, and this lysis was inhibited or even virtually abrogated upon mAb-mediated masking of DNam-1 (on NK cells) or PVR and NectIn-2 ligands (on celltransfectants).
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Characterization of an Antigen That Is Recognized on a Melanoma Showing Partial HLA Loss by CTL Expressing an NK Inhibitory Receptor

TL;DR: CTL, active against tumor cells showing partial HLA loss, may constitute an intermediate line of anti-tumor defense between the CTL, which recognizes highly specific tumor antigens, and the NK cells, which recognize HLA Loss variants.
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NKp44, a Novel Triggering Surface Molecule Specifically Expressed by Activated Natural Killer Cells, Is Involved in Non–Major Histocompatibility Complex–restricted Tumor Cell Lysis

TL;DR: It is shown that p46 and NKp44 are coupled to the intracytoplasmic transduction machinery via the association with CD3ζ or KARAP/DAP12, respectively; these associated molecules are tyrosine phosphorylated upon NK cell stimulation.