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SARS-CoV-2 infection induces a pro-inflammatory cytokine response through cGAS-STING and NF-κB
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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Covid-on-the-Web dataset
title
SARS-CoV-2 infection induces a pro-inflammatory cytokine response through cGAS-STING and NF-κB
Creator
Bartenschlager, Ralf
Cortese, Mirko
Lee, Ji-Young
Neufeldt, Christopher
Binder, Marco
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source
BioRxiv
abstract
SARS-CoV-2 is a novel virus that has rapidly spread, causing a global pandemic. In the majority of infected patients, SARS-CoV-2 leads to mild disease; however, in a significant proportion of infections, individuals develop severe symptoms that can lead to permanent lung damage or death. These severe cases are often associated with high levels of pro-inflammatory cytokines and low antiviral responses which can lead to systemic complications. We have evaluated transcriptional and cytokine secretion profiles from infected cell cultures and detected a distinct upregulation of inflammatory cytokines that parallels samples taken from infected patients. Building on these observations, we found a specific activation of NF-κB and a block of IRF3 nuclear translocation in SARS-CoV-2 infected cells. This NF-κB response is mediated by cGAS-STING activation and could be attenuated through STING targeting drugs. Our results show that SARS-CoV-2 curates a cGAS-STING mediated NF-κB driven inflammatory immune response in epithelial cells that likely contributes to inflammatory responses seen in patients and might be a target to suppress severe disease symptoms.
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2020-07-21
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10.1101/2020.07.21.212639
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biorxiv
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86f6646d3ad9776d1b58fe1894f69df7534baf93
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https://doi.org/10.1101/2020.07.21.212639
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SARS-CoV-2 infection induces a pro-inflammatory cytokine response through cGAS-STING and NF-κB
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bioRxiv
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covid:86f6646d3ad9776d1b58fe1894f69df7534baf93#body_text
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