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The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age

Coronavirus disease 19 (COVID-19) is clinically less severe in children, even if the wide variety and degree of severity of symptoms reported in children pose a still-unresolved challenge for clinicians. We performed an in-depth analysis of the immunological profiles of 18 hospitalized SARS-CoV-2-in...

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Autores principales: Vanetti, Claudia, Lampasona, Vito, Stracuzzi, Marta, Fenizia, Claudio, Biasin, Mara, Saulle, Irma, Limanaqi, Fiona, Abdelsalam, Ahmed, Loretelli, Cristian, Paradiso, Laura, Longoni, Emma, Barcellini, Lucia, Piemonti, Lorenzo, Marzinotto, Ilaria, Dispinseri, Stefania, Amendola, Antonella, Fappani, Clara, Tanzi, Elisabetta, Clerici, Mario Salvatore, Scarlatti, Gabriella, Zuccotti, Gian Vincenzo, Giacomet, Vania, Trabattoni, Daria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095251/
https://www.ncbi.nlm.nih.gov/pubmed/37047752
http://dx.doi.org/10.3390/ijms24076779
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author Vanetti, Claudia
Lampasona, Vito
Stracuzzi, Marta
Fenizia, Claudio
Biasin, Mara
Saulle, Irma
Limanaqi, Fiona
Abdelsalam, Ahmed
Loretelli, Cristian
Paradiso, Laura
Longoni, Emma
Barcellini, Lucia
Piemonti, Lorenzo
Marzinotto, Ilaria
Dispinseri, Stefania
Amendola, Antonella
Fappani, Clara
Tanzi, Elisabetta
Clerici, Mario Salvatore
Scarlatti, Gabriella
Zuccotti, Gian Vincenzo
Giacomet, Vania
Trabattoni, Daria
author_facet Vanetti, Claudia
Lampasona, Vito
Stracuzzi, Marta
Fenizia, Claudio
Biasin, Mara
Saulle, Irma
Limanaqi, Fiona
Abdelsalam, Ahmed
Loretelli, Cristian
Paradiso, Laura
Longoni, Emma
Barcellini, Lucia
Piemonti, Lorenzo
Marzinotto, Ilaria
Dispinseri, Stefania
Amendola, Antonella
Fappani, Clara
Tanzi, Elisabetta
Clerici, Mario Salvatore
Scarlatti, Gabriella
Zuccotti, Gian Vincenzo
Giacomet, Vania
Trabattoni, Daria
author_sort Vanetti, Claudia
collection PubMed
description Coronavirus disease 19 (COVID-19) is clinically less severe in children, even if the wide variety and degree of severity of symptoms reported in children pose a still-unresolved challenge for clinicians. We performed an in-depth analysis of the immunological profiles of 18 hospitalized SARS-CoV-2-infected children, whose results were compared to those obtained from 13 age- and sex-matched healthy controls (HC). The patients were categorized as paucisymptomatic/moderate (55.6%) or severe/critical (44.5%) according to established diagnostic criteria and further stratified into the categories of infants (1–12 months), children (1–12 years), and adolescents (>12 years). We assessed SARS-CoV-2-specific RBD antibodies (Ab), neutralizing antibodies (nAb), and circulating cytokines/chemokines in the plasma, and the SARS-CoV-2-specific immune response was measured in PBMCs by gene expression and secretome analyses. Our results showed peculiar circulating cytokine/chemokine profiles among patients sharing a similar clinical phenotype. A cluster of patients consisting of infants with severe symptoms presented hyperinflammatory profiles, together with extremely polarized antibody profiles. In a second cluster consisting of paucisymptomatic patients, a less pronounced increase in the level of inflammatory cytokines, together with an association between the selected cytokines and humoral responses, was observed. A third cluster, again consisting of paucisymptomatic patients, showed a circulating cytokine/chemokine profile which overlapped with that of the HC. The SARS-CoV-2-stimulated production of pro-inflammatory proteins, T lymphocyte activation, and migration-specific proteins, were significantly increased in SARS-CoV-2-infected children compared to the HC. Our findings suggest that immune response activation in the course of SARS-CoV-2 infection in children is directly correlated with clinical severity and, to a lesser extent, age.
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spelling pubmed-100952512023-04-13 The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age Vanetti, Claudia Lampasona, Vito Stracuzzi, Marta Fenizia, Claudio Biasin, Mara Saulle, Irma Limanaqi, Fiona Abdelsalam, Ahmed Loretelli, Cristian Paradiso, Laura Longoni, Emma Barcellini, Lucia Piemonti, Lorenzo Marzinotto, Ilaria Dispinseri, Stefania Amendola, Antonella Fappani, Clara Tanzi, Elisabetta Clerici, Mario Salvatore Scarlatti, Gabriella Zuccotti, Gian Vincenzo Giacomet, Vania Trabattoni, Daria Int J Mol Sci Article Coronavirus disease 19 (COVID-19) is clinically less severe in children, even if the wide variety and degree of severity of symptoms reported in children pose a still-unresolved challenge for clinicians. We performed an in-depth analysis of the immunological profiles of 18 hospitalized SARS-CoV-2-infected children, whose results were compared to those obtained from 13 age- and sex-matched healthy controls (HC). The patients were categorized as paucisymptomatic/moderate (55.6%) or severe/critical (44.5%) according to established diagnostic criteria and further stratified into the categories of infants (1–12 months), children (1–12 years), and adolescents (>12 years). We assessed SARS-CoV-2-specific RBD antibodies (Ab), neutralizing antibodies (nAb), and circulating cytokines/chemokines in the plasma, and the SARS-CoV-2-specific immune response was measured in PBMCs by gene expression and secretome analyses. Our results showed peculiar circulating cytokine/chemokine profiles among patients sharing a similar clinical phenotype. A cluster of patients consisting of infants with severe symptoms presented hyperinflammatory profiles, together with extremely polarized antibody profiles. In a second cluster consisting of paucisymptomatic patients, a less pronounced increase in the level of inflammatory cytokines, together with an association between the selected cytokines and humoral responses, was observed. A third cluster, again consisting of paucisymptomatic patients, showed a circulating cytokine/chemokine profile which overlapped with that of the HC. The SARS-CoV-2-stimulated production of pro-inflammatory proteins, T lymphocyte activation, and migration-specific proteins, were significantly increased in SARS-CoV-2-infected children compared to the HC. Our findings suggest that immune response activation in the course of SARS-CoV-2 infection in children is directly correlated with clinical severity and, to a lesser extent, age. MDPI 2023-04-05 /pmc/articles/PMC10095251/ /pubmed/37047752 http://dx.doi.org/10.3390/ijms24076779 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Vanetti, Claudia
Lampasona, Vito
Stracuzzi, Marta
Fenizia, Claudio
Biasin, Mara
Saulle, Irma
Limanaqi, Fiona
Abdelsalam, Ahmed
Loretelli, Cristian
Paradiso, Laura
Longoni, Emma
Barcellini, Lucia
Piemonti, Lorenzo
Marzinotto, Ilaria
Dispinseri, Stefania
Amendola, Antonella
Fappani, Clara
Tanzi, Elisabetta
Clerici, Mario Salvatore
Scarlatti, Gabriella
Zuccotti, Gian Vincenzo
Giacomet, Vania
Trabattoni, Daria
The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title_full The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title_fullStr The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title_full_unstemmed The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title_short The Immunological Profile of SARS-CoV-2 Infection in Children Is Linked to Clinical Severity and Age
title_sort immunological profile of sars-cov-2 infection in children is linked to clinical severity and age
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10095251/
https://www.ncbi.nlm.nih.gov/pubmed/37047752
http://dx.doi.org/10.3390/ijms24076779
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