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The interferon landscape along the respiratory tract impacts the severity of COVID-19

Articolo
Data di Pubblicazione:
2021
Citazione:
The interferon landscape along the respiratory tract impacts the severity of COVID-19 / Sposito, Benedetta; Broggi, Achille; Pandolfi, Laura; Crotta, Stefania; Clementi, Nicola; Ferrarese, Roberto; Sisti, Sofia; Criscuolo, Elena; Spreafico, Roberto; Long, Jaclyn M.; Ambrosi, Alessandro; Liu, Enju; Frangipane, Vanessa; Saracino, Laura; Bozzini, Sara; Marongiu, Laura; Facchini, Fabio A.; Bottazzi, Andrea; Fossali, Tommaso; Colombo, Riccardo; Clementi, Massimo; Tagliabue, Elena; Chou, Janet; Pontiroli, Antonio E.; Meloni, Federica; Wack, Andreas; Mancini, Nicasio; Zanoni, Ivan. - In: CELL. - ISSN 0092-8674. - 184:19(2021), pp. 4953-4968. [10.1016/j.cell.2021.08.016]
Abstract:
Severe coronavirus disease 2019 (COVID-19) is characterized by overproduction of immune mediators, but the role of interferons (IFNs) of the type I (IFN-I) or type III (IFN-III) families remains debated. We scrutinized the production of IFNs along the respiratory tract of COVID-19 patients and found that high levels of IFN-III, and to a lesser extent IFN-I, characterize the upper airways of patients with high viral burden but reduced disease risk or severity. Production of specific IFN-III, but not IFN-I, members denotes patients with a mild pathology and efficiently drives the transcription of genes that protect against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In contrast, compared to subjects with other infectious or noninfectious lung pathologies, IFNs are overrepresented in the lower airways of patients with severe COVID-19 that exhibit gene pathways associated with increased apoptosis and decreased proliferation. Our data demonstrate a dynamic production of IFNs in SARS-CoV-2-infected patients and show IFNs play opposing roles at distinct anatomical sites.
Tipologia CRIS:
1.1 Articolo in rivista
Elenco autori:
Sposito, Benedetta; Broggi, Achille; Pandolfi, Laura; Crotta, Stefania; Clementi, Nicola; Ferrarese, Roberto; Sisti, Sofia; Criscuolo, Elena; Spreafico, Roberto; Long, Jaclyn M.; Ambrosi, Alessandro; Liu, Enju; Frangipane, Vanessa; Saracino, Laura; Bozzini, Sara; Marongiu, Laura; Facchini, Fabio A.; Bottazzi, Andrea; Fossali, Tommaso; Colombo, Riccardo; Clementi, Massimo; Tagliabue, Elena; Chou, Janet; Pontiroli, Antonio E.; Meloni, Federica; Wack, Andreas; Mancini, Nicasio; Zanoni, Ivan
Autori di Ateneo:
AMBROSI ALESSANDRO
CLEMENTI NICOLA
CLEMENTI MASSIMO
CRISCUOLO ELENA
Link alla scheda completa:
https://iris.unisr.it/handle/20.500.11768/118259
Link al Full Text:
https://iris.unisr.it//retrieve/handle/20.500.11768/118259/83173/1-s2.0-S0092867421009909-main.pdf
https://iris.unisr.it//retrieve/handle/20.500.11768/118259/84844/PIIS0092867421009909.pdf
Pubblicato in:
CELL
Journal
  • Dati Generali

Dati Generali

URL

https://www.cell.com/action/showPdf?pii=S0092-8674(21)00990-9; https://pubmed.ncbi.nlm.nih.gov/34492226/
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