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Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution

BACKGROUND: The coronavirus disease-19 (COVID-19) pandemic has cost lives and economic hardships globally. Various studies have found a number of different factors, such as hyperinflammation and exhausted/suppressed T cell responses to the etiological SARS coronavirus-2 (SARS-CoV-2), being associate...

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Autores principales: Ong, Eugenia Z, Kalimuddin, Shirin, Chia, Wen Chong, Ooi, Sarah H, Koh, Clara WT, Tan, Hwee Cheng, Zhang, Summer L, Low, Jenny G, Ooi, Eng Eong, Chan, Kuan Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937043/
https://www.ncbi.nlm.nih.gov/pubmed/33691247
http://dx.doi.org/10.1016/j.ebiom.2021.103262
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author Ong, Eugenia Z
Kalimuddin, Shirin
Chia, Wen Chong
Ooi, Sarah H
Koh, Clara WT
Tan, Hwee Cheng
Zhang, Summer L
Low, Jenny G
Ooi, Eng Eong
Chan, Kuan Rong
author_facet Ong, Eugenia Z
Kalimuddin, Shirin
Chia, Wen Chong
Ooi, Sarah H
Koh, Clara WT
Tan, Hwee Cheng
Zhang, Summer L
Low, Jenny G
Ooi, Eng Eong
Chan, Kuan Rong
author_sort Ong, Eugenia Z
collection PubMed
description BACKGROUND: The coronavirus disease-19 (COVID-19) pandemic has cost lives and economic hardships globally. Various studies have found a number of different factors, such as hyperinflammation and exhausted/suppressed T cell responses to the etiological SARS coronavirus-2 (SARS-CoV-2), being associated with severe COVID-19. However, sieving the causative from associative factors of respiratory dysfunction has remained rudimentary. METHODS: We postulated that the host responses causative of respiratory dysfunction would track most closely with disease progression and resolution and thus be differentiated from other factors that are statistically associated with but not causative of severe COVID-19. To track the temporal dynamics of the host responses involved, we examined the changes in gene expression in whole blood of 6 severe and 4 non-severe COVID-19 patients across 15 different timepoints spanning the nadir of respiratory function. FINDINGS: We found that neutrophil activation but not type I interferon signaling transcripts tracked most closely with disease progression and resolution. Moreover, transcripts encoding for protein phosphorylation, particularly the serine-threonine kinases, many of which have known T cell proliferation and activation functions, were increased after and may thus contribute to the upswing of respiratory function. Notably, these associative genes were targeted by dexamethasone, but not methylprednisolone, which is consistent with efficacy outcomes in clinical trials. INTERPRETATION: Our findings suggest neutrophil activation as a critical factor of respiratory dysfunction in COVID-19. Drugs that target this pathway could be potentially repurposed for the treatment of severe COVID-19. FUNDING: This study was sponsored in part by a generous gift from The Hour Glass. EEO and JGL are funded by the National Medical Research Council of Singapore, through the Clinician Scientist Awards awarded by the National Research Foundation of Singapore.
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spelling pubmed-79370432021-03-08 Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution Ong, Eugenia Z Kalimuddin, Shirin Chia, Wen Chong Ooi, Sarah H Koh, Clara WT Tan, Hwee Cheng Zhang, Summer L Low, Jenny G Ooi, Eng Eong Chan, Kuan Rong EBioMedicine Research paper BACKGROUND: The coronavirus disease-19 (COVID-19) pandemic has cost lives and economic hardships globally. Various studies have found a number of different factors, such as hyperinflammation and exhausted/suppressed T cell responses to the etiological SARS coronavirus-2 (SARS-CoV-2), being associated with severe COVID-19. However, sieving the causative from associative factors of respiratory dysfunction has remained rudimentary. METHODS: We postulated that the host responses causative of respiratory dysfunction would track most closely with disease progression and resolution and thus be differentiated from other factors that are statistically associated with but not causative of severe COVID-19. To track the temporal dynamics of the host responses involved, we examined the changes in gene expression in whole blood of 6 severe and 4 non-severe COVID-19 patients across 15 different timepoints spanning the nadir of respiratory function. FINDINGS: We found that neutrophil activation but not type I interferon signaling transcripts tracked most closely with disease progression and resolution. Moreover, transcripts encoding for protein phosphorylation, particularly the serine-threonine kinases, many of which have known T cell proliferation and activation functions, were increased after and may thus contribute to the upswing of respiratory function. Notably, these associative genes were targeted by dexamethasone, but not methylprednisolone, which is consistent with efficacy outcomes in clinical trials. INTERPRETATION: Our findings suggest neutrophil activation as a critical factor of respiratory dysfunction in COVID-19. Drugs that target this pathway could be potentially repurposed for the treatment of severe COVID-19. FUNDING: This study was sponsored in part by a generous gift from The Hour Glass. EEO and JGL are funded by the National Medical Research Council of Singapore, through the Clinician Scientist Awards awarded by the National Research Foundation of Singapore. Elsevier 2021-03-07 /pmc/articles/PMC7937043/ /pubmed/33691247 http://dx.doi.org/10.1016/j.ebiom.2021.103262 Text en © 2021 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research paper
Ong, Eugenia Z
Kalimuddin, Shirin
Chia, Wen Chong
Ooi, Sarah H
Koh, Clara WT
Tan, Hwee Cheng
Zhang, Summer L
Low, Jenny G
Ooi, Eng Eong
Chan, Kuan Rong
Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title_full Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title_fullStr Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title_full_unstemmed Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title_short Temporal dynamics of the host molecular responses underlying severe COVID-19 progression and disease resolution
title_sort temporal dynamics of the host molecular responses underlying severe covid-19 progression and disease resolution
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7937043/
https://www.ncbi.nlm.nih.gov/pubmed/33691247
http://dx.doi.org/10.1016/j.ebiom.2021.103262
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