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Sabrina Rizzo

Researcher at University of Ferrara

Publications -  18
Citations -  202

Sabrina Rizzo is an academic researcher from University of Ferrara. The author has contributed to research in topics: Medicine & Immunology. The author has an hindex of 3, co-authored 9 publications receiving 33 citations.

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TLR3 and TLR7 RNA Sensor Activation during SARS-CoV-2 Infection.

TL;DR: In this article, the authors investigated the role of pathogen-associated molecular patterns (PAMPs)-pattern recognition receptors (PRRs) interaction and showed that both TLR3 and TLR7 are involved in the control of innate immunity during lung SARS-CoV-2 infection.
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SARS-CoV-2 Spike 1 Protein Controls Natural Killer Cell Activation via the HLA-E/NKG2A Pathway.

TL;DR: It is shown for the first time that NK cells are affected by SP1 expression in lung epithelial cells via HLA-E/NKG2A interaction and the resulting NK cells’ exhaustion might contribute to immunopathogenesis in SARS-CoV-2 infection.
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Increased sHLA-G Is Associated with Improved COVID-19 Outcome and Reduced Neutrophil Adhesion.

TL;DR: In this article, the authors evaluated blood sHLA-E and HLA-G levels in hospitalized COVID-19 patients with respiratory failure and their relationship with clinical evolution, changes in endothelial activation biomarker profile, and neutrophil adhesion.
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Detailed In Vitro Pharmacological Characterization of the Clinically Viable Nociceptin/Orphanin FQ Peptide Receptor Antagonist BTRX-246040.

TL;DR: In all assays, BTRX-246040 behaves as a pure and selective antagonist at human recombinant and murine native NOP receptors displaying 3–10-fold higher potency than the standard antagonist SB-612111.
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Transparent Polymeric Formulations Effective against SARS-CoV-2 Infection.

TL;DR: In this article, two transparent polymeric compounds, containing silver and benzalkonium ions electrostatically bound to a polystyrene sulfonate backbone, were synthesized, through simple procedures, and evaluated for their antimicrobial properties against Gram-positive and Gram-negative bacteria and Candida albicans, and for their antiviral activity toward 229E and SARS-CoV-2 coronavirus.