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Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19

Coronavirus disease 2019 (COVID‐19), can present with a wide spectrum of severity. Elderly patients with cardiac, pulmonary and metabolic comorbidities are more likely to develop the severe manifestations of COVID‐19, which are observed in less than 5% of the pediatric patients. Severe acute respira...

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Autores principales: Costagliola, Giorgio, Spada, Erika, Consolini, Rita
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8014746/
https://www.ncbi.nlm.nih.gov/pubmed/33566457
http://dx.doi.org/10.1002/iid3.404
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author Costagliola, Giorgio
Spada, Erika
Consolini, Rita
author_facet Costagliola, Giorgio
Spada, Erika
Consolini, Rita
author_sort Costagliola, Giorgio
collection PubMed
description Coronavirus disease 2019 (COVID‐19), can present with a wide spectrum of severity. Elderly patients with cardiac, pulmonary and metabolic comorbidities are more likely to develop the severe manifestations of COVID‐19, which are observed in less than 5% of the pediatric patients. Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) is able to induce an immune impairment and dysregulation, finally resulting in the massive release of inflammatory mediators, strongly contributing to the pulmonary and systemic manifestations in COVID‐19. In children, the immune dysregulation following SARS‐CoV‐2 can also be responsible of a severe disease phenotype defined as multisystem inflammatory syndrome in children. As the immune system undergoes a complex process of maturation from birth to adult age, differences in the immune and inflammatory response could have a significant impact in determining the spectrum of severity of COVID‐19. Indeed, children show a higher ability to respond to viral infections and a reduced baseline pro‐inflammatory state compared with elderly patients. Age and comorbidities contribute to disease severity through immune‐mediated mechanisms, since they are associated with a chronic increase of pro‐inflammatory mediators, and cause an enhanced susceptibility to develop an immune dysregulation following SARS‐CoV‐2 infection. Also the expression of ACE2, the receptor of SARS‐CoV‐2, varies with age, and is linked to the immune and inflammatory response through a complex, and not completely elucidated, network. This paper reviews the peculiar immunopathogenic aspects of COVID‐19, with a focus on the differences between adult and pediatric patients.
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spelling pubmed-80147462021-04-01 Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19 Costagliola, Giorgio Spada, Erika Consolini, Rita Immun Inflamm Dis Reviews Coronavirus disease 2019 (COVID‐19), can present with a wide spectrum of severity. Elderly patients with cardiac, pulmonary and metabolic comorbidities are more likely to develop the severe manifestations of COVID‐19, which are observed in less than 5% of the pediatric patients. Severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2) is able to induce an immune impairment and dysregulation, finally resulting in the massive release of inflammatory mediators, strongly contributing to the pulmonary and systemic manifestations in COVID‐19. In children, the immune dysregulation following SARS‐CoV‐2 can also be responsible of a severe disease phenotype defined as multisystem inflammatory syndrome in children. As the immune system undergoes a complex process of maturation from birth to adult age, differences in the immune and inflammatory response could have a significant impact in determining the spectrum of severity of COVID‐19. Indeed, children show a higher ability to respond to viral infections and a reduced baseline pro‐inflammatory state compared with elderly patients. Age and comorbidities contribute to disease severity through immune‐mediated mechanisms, since they are associated with a chronic increase of pro‐inflammatory mediators, and cause an enhanced susceptibility to develop an immune dysregulation following SARS‐CoV‐2 infection. Also the expression of ACE2, the receptor of SARS‐CoV‐2, varies with age, and is linked to the immune and inflammatory response through a complex, and not completely elucidated, network. This paper reviews the peculiar immunopathogenic aspects of COVID‐19, with a focus on the differences between adult and pediatric patients. John Wiley and Sons Inc. 2021-02-10 /pmc/articles/PMC8014746/ /pubmed/33566457 http://dx.doi.org/10.1002/iid3.404 Text en © 2021 The Authors. Immunity, Inflammation and Disease published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Reviews
Costagliola, Giorgio
Spada, Erika
Consolini, Rita
Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title_full Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title_fullStr Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title_full_unstemmed Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title_short Age‐related differences in the immune response could contribute to determine the spectrum of severity of COVID‐19
title_sort age‐related differences in the immune response could contribute to determine the spectrum of severity of covid‐19
topic Reviews
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8014746/
https://www.ncbi.nlm.nih.gov/pubmed/33566457
http://dx.doi.org/10.1002/iid3.404
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