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Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China
BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in children is associated with better outcomes than in adults. The inflammatory response to COVID-19 infection in children remains poorly characterised. METHODS: We retrospectively analysed the medical records of...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049192/ https://www.ncbi.nlm.nih.gov/pubmed/33880437 http://dx.doi.org/10.1016/j.eclinm.2021.100831 |
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author | Qian, Guoqing Zhang, Yong Xu, Yang Hu, Weihua Hall, Ian P. Yue, Jiang Lu, Hongyun Ruan, Liemin Ye, Maoqing Mei, Jin |
author_facet | Qian, Guoqing Zhang, Yong Xu, Yang Hu, Weihua Hall, Ian P. Yue, Jiang Lu, Hongyun Ruan, Liemin Ye, Maoqing Mei, Jin |
author_sort | Qian, Guoqing |
collection | PubMed |
description | BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in children is associated with better outcomes than in adults. The inflammatory response to COVID-19 infection in children remains poorly characterised. METHODS: We retrospectively analysed the medical records of 127 laboratory-confirmed COVID-19 patients aged 1 month to 16 years from Wuhan and Jingzhou of Hubei Province. Patients presented between January 25th and March 24th 2020. Information on clinical features, laboratory results, plasma cytokines/chemokines and lymphocyte subsets were analysed. FINDINGS: Children admitted to hospital with COVID-19 were more likely to be male (67.7%) and the median age was 7.3 [IQR 4.9] years. All but one patient with severe disease was aged under 2 and the majority (5/7) had significant co-morbidities. Despite 53% having viral pneumonia on computed tomography (CT) scanning only 2 patients had low lymphocyte counts and no differences were observed in the levels of plasma proinflammatory cytokines, including interleukin (IL)-2, IL-4, IL-6, tumour necrosis factor (TNF)- [Formula: see text] , and interferon (IFN)- [Formula: see text] between patients with mild, moderate or severe disease. INTERPRETATIONS: We observed that the immune responses of children to COVID-19 infection is significantly different from that seen in adults. Our evidence suggests that SARS-CoV-2 does not trigger a robust inflammatory response or ‘cytokine storm’ in children with COVID-19, and this may underlie the generally better outcomes seen in children with this disease. |
format | Online Article Text |
id | pubmed-8049192 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-80491922021-04-16 Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China Qian, Guoqing Zhang, Yong Xu, Yang Hu, Weihua Hall, Ian P. Yue, Jiang Lu, Hongyun Ruan, Liemin Ye, Maoqing Mei, Jin EClinicalMedicine Research Paper BACKGROUND: Infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) in children is associated with better outcomes than in adults. The inflammatory response to COVID-19 infection in children remains poorly characterised. METHODS: We retrospectively analysed the medical records of 127 laboratory-confirmed COVID-19 patients aged 1 month to 16 years from Wuhan and Jingzhou of Hubei Province. Patients presented between January 25th and March 24th 2020. Information on clinical features, laboratory results, plasma cytokines/chemokines and lymphocyte subsets were analysed. FINDINGS: Children admitted to hospital with COVID-19 were more likely to be male (67.7%) and the median age was 7.3 [IQR 4.9] years. All but one patient with severe disease was aged under 2 and the majority (5/7) had significant co-morbidities. Despite 53% having viral pneumonia on computed tomography (CT) scanning only 2 patients had low lymphocyte counts and no differences were observed in the levels of plasma proinflammatory cytokines, including interleukin (IL)-2, IL-4, IL-6, tumour necrosis factor (TNF)- [Formula: see text] , and interferon (IFN)- [Formula: see text] between patients with mild, moderate or severe disease. INTERPRETATIONS: We observed that the immune responses of children to COVID-19 infection is significantly different from that seen in adults. Our evidence suggests that SARS-CoV-2 does not trigger a robust inflammatory response or ‘cytokine storm’ in children with COVID-19, and this may underlie the generally better outcomes seen in children with this disease. Elsevier 2021-04-15 /pmc/articles/PMC8049192/ /pubmed/33880437 http://dx.doi.org/10.1016/j.eclinm.2021.100831 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Research Paper Qian, Guoqing Zhang, Yong Xu, Yang Hu, Weihua Hall, Ian P. Yue, Jiang Lu, Hongyun Ruan, Liemin Ye, Maoqing Mei, Jin Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title | Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title_full | Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title_fullStr | Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title_full_unstemmed | Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title_short | Reduced inflammatory responses to SARS-CoV-2 infection in children presenting to hospital with COVID-19 in China |
title_sort | reduced inflammatory responses to sars-cov-2 infection in children presenting to hospital with covid-19 in china |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8049192/ https://www.ncbi.nlm.nih.gov/pubmed/33880437 http://dx.doi.org/10.1016/j.eclinm.2021.100831 |
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