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http://conacyt.repositorioinstitucional.mx/jspui/handle/1000/2126
Type 2 and interferon inflammation strongly regulate SARS-CoV-2 related gene expression in the airway epithelium | |
Satria P Sajuthi. Peter DeFord. Nathan D Jackson. Michael T Montgomery. Jamie L Everman. Cydney L Rios. Elmar Pruesse. James D Nolin. Elizabeth G Plender. Michael E Wechsler. Angel CY Mak. Celeste Eng. Sandra Salazar. Vivian Medina. Eric M Wohlford. Scott Huntsman. Deborah A Nickerson. Soren Germer. Michael C Zody. Goncalo Abecasis. Hyun Min Kang. Kenneth M Rice. Sam Oh. Jose Rodriguez-Santana. Esteban G Burchard. Max A Seibold. | |
Acceso Abierto | |
Atribución-NoComercial-SinDerivadas | |
10.1101/2020.04.09.034454 | |
Coronavirus disease 2019 (COVID-19) outcomes vary from asymptomatic infection to death. This disparity may reflect different airway levels of the SARS-CoV-2 receptor, ACE2, and the spike protein activator, TMPRSS2. Here we explore the role of genetics and co-expression networks in regulating these genes in the airway, through the analysis of nasal airway transcriptome data from 695 children. We identify expression quantitative trait loci (eQTL) for both ACE2 and TMPRSS2, that vary in frequency across world populations. Importantly, we find TMPRSS2 is part of a mucus secretory network, highly upregulated by T2 inflammation through the action of interleukin-13, and that interferon response to respiratory viruses highly upregulates ACE2 expression. Finally, we define airway responses to coronavirus infections in children, finding that these infections upregulate IL6 while also stimulating a more pronounced cytotoxic immune response relative to other respiratory viruses. Our results reveal mechanisms likely influencing SARS-CoV-2 infectivity and COVID-19 clinical outcomes. | |
www.biorxiv.org | |
2020 | |
Artículo | |
https://www.biorxiv.org/content/10.1101/2020.04.09.034454v1.full.pdf | |
Inglés | |
VIRUS RESPIRATORIOS | |
Aparece en las colecciones: | Artículos científicos |
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