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Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis

BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clini...

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Autores principales: Koch, Clarissa M., Prigge, Andrew D., Setar, Leah, Anekalla, Kishore R., Do-Umehara, Hahn Chi, Abdala-Valencia, Hiam, Politanska, Yuliya, Shukla, Avani, Chavez, Jairo, Hahn, Grant R., Coates, Bria M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540395/
https://www.ncbi.nlm.nih.gov/pubmed/36211387
http://dx.doi.org/10.3389/fimmu.2022.924792
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author Koch, Clarissa M.
Prigge, Andrew D.
Setar, Leah
Anekalla, Kishore R.
Do-Umehara, Hahn Chi
Abdala-Valencia, Hiam
Politanska, Yuliya
Shukla, Avani
Chavez, Jairo
Hahn, Grant R.
Coates, Bria M.
author_facet Koch, Clarissa M.
Prigge, Andrew D.
Setar, Leah
Anekalla, Kishore R.
Do-Umehara, Hahn Chi
Abdala-Valencia, Hiam
Politanska, Yuliya
Shukla, Avani
Chavez, Jairo
Hahn, Grant R.
Coates, Bria M.
author_sort Koch, Clarissa M.
collection PubMed
description BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clinical outcomes. METHODS: Nasal scrape biopsies were obtained from 33 infants admitted to the pediatric intensive care unit (PICU) with critical RSV bronchiolitis requiring non-invasive respiratory support (NIS) or invasive mechanical ventilation (IMV), and RNA sequencing (RNA-seq) was performed. Gene expression in participants who required shortened NIS (</= 3 days), prolonged NIS (> 3 days), and IMV was compared. FINDINGS: Increased expression of ciliated cell genes and estimated ciliated cell abundance, but not immune cell abundance, positively correlated with duration of hospitalization in infants with critical bronchiolitis. A ciliated cell signature characterized infants who required NIS for > 3 days while a basal cell signature was present in infants who required NIS for </= 3 days, despite both groups requiring an equal degree of respiratory support at the time of sampling. Infants who required invasive mechanical ventilation had increased expression of genes involved in neutrophil activation and cell death. INTERPRETATION: Increased expression of cilia-related genes in clinically indistinguishable infants with critical RSV may differentiate between infants who will require prolonged hospitalization and infants who will recover quickly. Validation of these findings in a larger cohort is needed to determine whether a cilia-related gene signature can predict duration of illness in infants with critical bronchiolitis. The ability to identify which infants with critical RSV bronchiolitis may require prolonged hospitalization using non-invasive nasal samples would provide invaluable prognostic information to parents and medical providers.
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spelling pubmed-95403952022-10-08 Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis Koch, Clarissa M. Prigge, Andrew D. Setar, Leah Anekalla, Kishore R. Do-Umehara, Hahn Chi Abdala-Valencia, Hiam Politanska, Yuliya Shukla, Avani Chavez, Jairo Hahn, Grant R. Coates, Bria M. Front Immunol Immunology BACKGROUND: Respiratory syncytial virus (RSV) can cause life-threatening respiratory failure in infants. We sought to characterize the local host response to RSV infection in the nasal mucosa of infants with critical bronchiolitis and to identify early admission gene signatures associated with clinical outcomes. METHODS: Nasal scrape biopsies were obtained from 33 infants admitted to the pediatric intensive care unit (PICU) with critical RSV bronchiolitis requiring non-invasive respiratory support (NIS) or invasive mechanical ventilation (IMV), and RNA sequencing (RNA-seq) was performed. Gene expression in participants who required shortened NIS (</= 3 days), prolonged NIS (> 3 days), and IMV was compared. FINDINGS: Increased expression of ciliated cell genes and estimated ciliated cell abundance, but not immune cell abundance, positively correlated with duration of hospitalization in infants with critical bronchiolitis. A ciliated cell signature characterized infants who required NIS for > 3 days while a basal cell signature was present in infants who required NIS for </= 3 days, despite both groups requiring an equal degree of respiratory support at the time of sampling. Infants who required invasive mechanical ventilation had increased expression of genes involved in neutrophil activation and cell death. INTERPRETATION: Increased expression of cilia-related genes in clinically indistinguishable infants with critical RSV may differentiate between infants who will require prolonged hospitalization and infants who will recover quickly. Validation of these findings in a larger cohort is needed to determine whether a cilia-related gene signature can predict duration of illness in infants with critical bronchiolitis. The ability to identify which infants with critical RSV bronchiolitis may require prolonged hospitalization using non-invasive nasal samples would provide invaluable prognostic information to parents and medical providers. Frontiers Media S.A. 2022-09-23 /pmc/articles/PMC9540395/ /pubmed/36211387 http://dx.doi.org/10.3389/fimmu.2022.924792 Text en Copyright © 2022 Koch, Prigge, Setar, Anekalla, Do-Umehara, Abdala-Valencia, Politanska, Shukla, Chavez, Hahn and Coates https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Immunology
Koch, Clarissa M.
Prigge, Andrew D.
Setar, Leah
Anekalla, Kishore R.
Do-Umehara, Hahn Chi
Abdala-Valencia, Hiam
Politanska, Yuliya
Shukla, Avani
Chavez, Jairo
Hahn, Grant R.
Coates, Bria M.
Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title_full Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title_fullStr Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title_full_unstemmed Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title_short Cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
title_sort cilia-related gene signature in the nasal mucosa correlates with disease severity and outcomes in critical respiratory syncytial virus bronchiolitis
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9540395/
https://www.ncbi.nlm.nih.gov/pubmed/36211387
http://dx.doi.org/10.3389/fimmu.2022.924792
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