Abstract |
Type I interferons (IFNs) have broad and potent antiviral activity. We review the interplay between type I IFNs and SARS-CoV-2. Human cells infected with SARS-CoV-2 in vitro produce low levels of type I IFNs, and SARS-CoV-2 proteins can inhibit various steps in type I IFN production and response. Exogenous type I IFNs inhibit viral growth in vitro. In various animal species infected in vivo, type I IFN deficiencies underlie higher viral loads and more severe disease than in control animals. The early administration of exogenous type I IFNs improves infection control. In humans, inborn errors of, and auto- antibodies against type I IFNs underlie life-threatening COVID-19 pneumonia. Overall, type I IFNs are essential for host defense against SARS-CoV-2 in individual cells and whole organisms.
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Authors | Paul Bastard, Qian Zhang, Shen-Ying Zhang, Emmanuelle Jouanguy, Jean-Laurent Casanova |
Journal | Current opinion in immunology
(Curr Opin Immunol)
Vol. 74
Pg. 172-182
(02 2022)
ISSN: 1879-0372 [Electronic] England |
PMID | 35149239
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't, Review)
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Copyright | Copyright © 2022 The Authors. Published by Elsevier Ltd.. All rights reserved. |
Chemical References |
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Topics |
- Animals
- COVID-19
(immunology)
- Humans
- Interferon Type I
(immunology)
- SARS-CoV-2
(immunology)
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