High SARS-CoV-2 Viral Load and Low CCL5 Expression Levels in the Upper Respiratory Tract Are Associated With COVID-19 Severity

Abstract Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and progression of coronavirus disease 2019 (COVID-19). We analyzed SARS-CoV-2 RNA load and expression of se...

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Published in:The Journal of infectious diseases Vol. 225; no. 6; pp. 977 - 982
Main Authors: Pérez-García, Felipe, Martin-Vicente, María, Rojas-García, Rosa Lía, Castilla-García, Lucía, Muñoz-Gomez, María José, Hervás Fernández, Irene, González Ventosa, Victoria, Vidal-Alcántara, Erick Joan, Cuadros-González, Juan, Bermejo-Martin, Jesús F, Resino, Salvador, Martínez, Isidoro
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Language:English
Published: US Oxford University Press 15-03-2022
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Abstract Abstract Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and progression of coronavirus disease 2019 (COVID-19). We analyzed SARS-CoV-2 RNA load and expression of selected immune genes in the upper respiratory tract (nasopharynx) of 255 SARS-CoV-2–infected patients and evaluated their association with severe COVID-19. SARS-CoV-2 replication in nasopharyngeal mucosa induces expression of several innate immune genes. High SARS-CoV-2 viral load and low CCL5 expression levels were associated with intensive care unit admission or death, although CCL5 was the best predictor of COVID-19 severity. Graphical Abstract Graphical Abstract
AbstractList Abstract Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and progression of coronavirus disease 2019 (COVID-19). We analyzed SARS-CoV-2 RNA load and expression of selected immune genes in the upper respiratory tract (nasopharynx) of 255 SARS-CoV-2–infected patients and evaluated their association with severe COVID-19. SARS-CoV-2 replication in nasopharyngeal mucosa induces expression of several innate immune genes. High SARS-CoV-2 viral load and low CCL5 expression levels were associated with intensive care unit admission or death, although CCL5 was the best predictor of COVID-19 severity. Graphical Abstract Graphical Abstract
Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and progression of coronavirus disease 2019 (COVID-19). We analyzed SARS-CoV-2 RNA load and expression of selected immune genes in the upper respiratory tract (nasopharynx) of 255 SARS-CoV-2-infected patients and evaluated their association with severe COVID-19. SARS-CoV-2 replication in nasopharyngeal mucosa induces expression of several innate immune genes. High SARS-CoV-2 viral load and low CCL5 expression levels were associated with intensive care unit admission or death, although CCL5 was the best predictor of COVID-19 severity.
Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), and progression of coronavirus disease 2019 (COVID-19). We analyzed SARS-CoV-2 RNA load and expression of selected immune genes in the upper respiratory tract (nasopharynx) of 255 SARS-CoV-2–infected patients and evaluated their association with severe COVID-19. SARS-CoV-2 replication in nasopharyngeal mucosa induces expression of several innate immune genes. High SARS-CoV-2 viral load and low CCL5 expression levels were associated with intensive care unit admission or death, although CCL5 was the best predictor of COVID-19 severity. Graphical Abstract
Author González Ventosa, Victoria
Martin-Vicente, María
Vidal-Alcántara, Erick Joan
Pérez-García, Felipe
Rojas-García, Rosa Lía
Cuadros-González, Juan
Resino, Salvador
Martínez, Isidoro
Bermejo-Martin, Jesús F
Hervás Fernández, Irene
Castilla-García, Lucía
Muñoz-Gomez, María José
AuthorAffiliation 6 Group for Biomedical Research in Sepsis, Instituto de Investigación Biomédica de Salamanca , Salamanca , Spain
2 Servicio de Microbiología Clínica, Hospital Universitario Príncipe de Asturias , Madrid , Spain
8 Centro de Investigación Biomédica en Red en Enfermedades Respiratorias, Instituto de Salud Carlos III , Madrid , Spain
5 Servicio de Hematología y Hemoterapia, Hospital Universitario Príncipe de Asturias , Madrid , Spain
4 Centro de Investigación Biomédica en Red en Enfermedades Infecciosas, Instituto de Salud Carlos III , Madrid , Spain
1 Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III , Majadahonda , Spain
7 Hospital Universitario Río Hortega , Valladolid , Spain
3 Departamento de Biomedicina y Biotecnología, Facultad de Medicina, Universidad de Alcalá de Henares , Madrid , Spain
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  givenname: Lucía
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  givenname: Irene
  surname: Hervás Fernández
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  givenname: Victoria
  surname: González Ventosa
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  givenname: Erick Joan
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  fullname: Vidal-Alcántara, Erick Joan
  organization: Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Spain
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  surname: Cuadros-González
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  surname: Bermejo-Martin
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  surname: Resino
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  givenname: Isidoro
  surname: Martínez
  fullname: Martínez, Isidoro
  organization: Unidad de Infección Viral e Inmunidad, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Majadahonda, Spain
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ContentType Journal Article
Copyright The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2021
The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
Copyright_xml – notice: The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2021
– notice: The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.
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Keywords COVID-19
SARS-CoV-2
viral load
death
innate immunity
CCL5
ICU
nasopharynx
gene expression
Language English
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F. P.-G., M. M.-V., and R. L. R.-G. contributed equally.
J. F. B.-M., S. R., and I. M. contributed equally.
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Snippet Abstract Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory...
Mucosal immune response in the upper respiratory tract is crucial for initial control of viral replication, clearance of severe acute respiratory syndrome...
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SubjectTerms Body fluids
Chemokine CCL5 - genetics
Chemokine CCL5 - metabolism
Coronaviruses
COVID-19
COVID-19 - diagnosis
COVID-19 - mortality
Humans
Immune clearance
Immune response
Immune system
Intensive Care Units
Major and Brief Reports
Mucosal immunity
Nasopharynx
Nasopharynx - virology
Nose
Pathophysiology
Replication
Respiratory tract
RNA, Viral - genetics
SARS-CoV-2
Severe acute respiratory syndrome coronavirus 2
Severity of Illness Index
Viral Load
Title High SARS-CoV-2 Viral Load and Low CCL5 Expression Levels in the Upper Respiratory Tract Are Associated With COVID-19 Severity
URI https://www.ncbi.nlm.nih.gov/pubmed/34910814
https://www.proquest.com/docview/2640498924
https://search.proquest.com/docview/2610909132
https://pubmed.ncbi.nlm.nih.gov/PMC8754799
Volume 225
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