Cargando…
Pathophysiology of COVID-19: Why Children Fare Better than Adults?
The world is facing Coronavirus Disease-2019 (COVID-19) pandemic, which is causing a large number of deaths and burden on intensive care facilities. It is caused by Severe Acute Respiratory Syndrome coronavirus-2 (SARS-CoV-2) originating in Wuhan, China. It has been seen that fewer children contract...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer India
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221011/ https://www.ncbi.nlm.nih.gov/pubmed/32410003 http://dx.doi.org/10.1007/s12098-020-03322-y |
_version_ | 1783533280041107456 |
---|---|
author | Dhochak, Nitin Singhal, Tanu Kabra, S. K. Lodha, Rakesh |
author_facet | Dhochak, Nitin Singhal, Tanu Kabra, S. K. Lodha, Rakesh |
author_sort | Dhochak, Nitin |
collection | PubMed |
description | The world is facing Coronavirus Disease-2019 (COVID-19) pandemic, which is causing a large number of deaths and burden on intensive care facilities. It is caused by Severe Acute Respiratory Syndrome coronavirus-2 (SARS-CoV-2) originating in Wuhan, China. It has been seen that fewer children contract COVID-19 and among infected, children have less severe disease. Insights in pathophysiological mechanisms of less severity in children could be important for devising therapeutics for high-risk adults and elderly. Early closing of schools and day-care centers led to less frequent exposure and hence, lower infection rate in children. The expression of primary target receptor for SARS-CoV-2, i.e. angiotensin converting enzyme-2 (ACE-2), decreases with age. ACE-2 has lung protective effects by limiting angiotensin-2 mediated pulmonary capillary leak and inflammation. Severe COVID-19 disease is associated with high and persistent viral loads in adults. Children have strong innate immune response due to trained immunity (secondary to live-vaccines and frequent viral infections), leading to probably early control of infection at the site of entry. Adult patients show suppressed adaptive immunity and dysfunctional over-active innate immune response in severe infections, which is not seen in children. These could be related to immune-senescence in elderly. Excellent regeneration capacity of pediatric alveolar epithelium may be contributing to early recovery from COVID-19. Children, less frequently, have risk factors such as co-morbidities, smoking, and obesity. But young infants and children with pre-existing illnesses could be high risk groups and need careful monitoring. Studies describing immune-pathogenesis in COVID-19 are lacking in children and need urgent attention. |
format | Online Article Text |
id | pubmed-7221011 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer India |
record_format | MEDLINE/PubMed |
spelling | pubmed-72210112020-05-14 Pathophysiology of COVID-19: Why Children Fare Better than Adults? Dhochak, Nitin Singhal, Tanu Kabra, S. K. Lodha, Rakesh Indian J Pediatr Review Article The world is facing Coronavirus Disease-2019 (COVID-19) pandemic, which is causing a large number of deaths and burden on intensive care facilities. It is caused by Severe Acute Respiratory Syndrome coronavirus-2 (SARS-CoV-2) originating in Wuhan, China. It has been seen that fewer children contract COVID-19 and among infected, children have less severe disease. Insights in pathophysiological mechanisms of less severity in children could be important for devising therapeutics for high-risk adults and elderly. Early closing of schools and day-care centers led to less frequent exposure and hence, lower infection rate in children. The expression of primary target receptor for SARS-CoV-2, i.e. angiotensin converting enzyme-2 (ACE-2), decreases with age. ACE-2 has lung protective effects by limiting angiotensin-2 mediated pulmonary capillary leak and inflammation. Severe COVID-19 disease is associated with high and persistent viral loads in adults. Children have strong innate immune response due to trained immunity (secondary to live-vaccines and frequent viral infections), leading to probably early control of infection at the site of entry. Adult patients show suppressed adaptive immunity and dysfunctional over-active innate immune response in severe infections, which is not seen in children. These could be related to immune-senescence in elderly. Excellent regeneration capacity of pediatric alveolar epithelium may be contributing to early recovery from COVID-19. Children, less frequently, have risk factors such as co-morbidities, smoking, and obesity. But young infants and children with pre-existing illnesses could be high risk groups and need careful monitoring. Studies describing immune-pathogenesis in COVID-19 are lacking in children and need urgent attention. Springer India 2020-05-14 2020 /pmc/articles/PMC7221011/ /pubmed/32410003 http://dx.doi.org/10.1007/s12098-020-03322-y Text en © Dr. K C Chaudhuri Foundation 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Review Article Dhochak, Nitin Singhal, Tanu Kabra, S. K. Lodha, Rakesh Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title | Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title_full | Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title_fullStr | Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title_full_unstemmed | Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title_short | Pathophysiology of COVID-19: Why Children Fare Better than Adults? |
title_sort | pathophysiology of covid-19: why children fare better than adults? |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7221011/ https://www.ncbi.nlm.nih.gov/pubmed/32410003 http://dx.doi.org/10.1007/s12098-020-03322-y |
work_keys_str_mv | AT dhochaknitin pathophysiologyofcovid19whychildrenfarebetterthanadults AT singhaltanu pathophysiologyofcovid19whychildrenfarebetterthanadults AT kabrask pathophysiologyofcovid19whychildrenfarebetterthanadults AT lodharakesh pathophysiologyofcovid19whychildrenfarebetterthanadults |