Cargando…
Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19
The coronavirus disease 2019 (COVID-19) has spread globally and variants continue to emerge, with children are accounting for a growing share of COVID-19 cases. However, the establishment of immune memory and the long-term health consequences in asymptomatic or mildly symptomatic children after seve...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779549/ https://www.ncbi.nlm.nih.gov/pubmed/35062289 http://dx.doi.org/10.3390/v14010085 |
_version_ | 1784637604527865856 |
---|---|
author | Tian, Xiaodong Bai, Zhihua Cao, Ying Liu, Haizhou Liu, Di Liu, Wenjun Li, Jing |
author_facet | Tian, Xiaodong Bai, Zhihua Cao, Ying Liu, Haizhou Liu, Di Liu, Wenjun Li, Jing |
author_sort | Tian, Xiaodong |
collection | PubMed |
description | The coronavirus disease 2019 (COVID-19) has spread globally and variants continue to emerge, with children are accounting for a growing share of COVID-19 cases. However, the establishment of immune memory and the long-term health consequences in asymptomatic or mildly symptomatic children after severe acute respiratory syndrome coronavirus 2 infection are not fully understood. We collected clinical data and whole blood samples from discharged children for 6–8 months after symptom onset among 0-to-14-year-old children. Representative inflammation signs returned to normal in all age ranges. The infants and young children (0–4 years old) had lung lesions that persisted for 6–8 months and were less responsive for antigen-specific IgG secretion. In the 5-to-14-year-old group, lung imaging abnormalities gradually recovered, and the IgG-specific antibody response was strongest. In addition, we found a robust IgM(+) memory B cell response in all age. Memory T cells specific for the spike or nucleocapsid protein were generated, with no significant difference in IFN-γ response among all ages. Our study highlights that although lung lesions caused by COVID-19 can last for at least 6–8 months in infants and young children, most children have detectable residual neutralizing antibodies and specific cellular immune responses at this stage. |
format | Online Article Text |
id | pubmed-8779549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87795492022-01-22 Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 Tian, Xiaodong Bai, Zhihua Cao, Ying Liu, Haizhou Liu, Di Liu, Wenjun Li, Jing Viruses Article The coronavirus disease 2019 (COVID-19) has spread globally and variants continue to emerge, with children are accounting for a growing share of COVID-19 cases. However, the establishment of immune memory and the long-term health consequences in asymptomatic or mildly symptomatic children after severe acute respiratory syndrome coronavirus 2 infection are not fully understood. We collected clinical data and whole blood samples from discharged children for 6–8 months after symptom onset among 0-to-14-year-old children. Representative inflammation signs returned to normal in all age ranges. The infants and young children (0–4 years old) had lung lesions that persisted for 6–8 months and were less responsive for antigen-specific IgG secretion. In the 5-to-14-year-old group, lung imaging abnormalities gradually recovered, and the IgG-specific antibody response was strongest. In addition, we found a robust IgM(+) memory B cell response in all age. Memory T cells specific for the spike or nucleocapsid protein were generated, with no significant difference in IFN-γ response among all ages. Our study highlights that although lung lesions caused by COVID-19 can last for at least 6–8 months in infants and young children, most children have detectable residual neutralizing antibodies and specific cellular immune responses at this stage. MDPI 2022-01-04 /pmc/articles/PMC8779549/ /pubmed/35062289 http://dx.doi.org/10.3390/v14010085 Text en © 2022 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 Tian, Xiaodong Bai, Zhihua Cao, Ying Liu, Haizhou Liu, Di Liu, Wenjun Li, Jing Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title | Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title_full | Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title_fullStr | Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title_full_unstemmed | Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title_short | Evaluation of Clinical and Immune Responses in Recovered Children with Mild COVID-19 |
title_sort | evaluation of clinical and immune responses in recovered children with mild covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8779549/ https://www.ncbi.nlm.nih.gov/pubmed/35062289 http://dx.doi.org/10.3390/v14010085 |
work_keys_str_mv | AT tianxiaodong evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT baizhihua evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT caoying evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT liuhaizhou evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT liudi evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT liuwenjun evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 AT lijing evaluationofclinicalandimmuneresponsesinrecoveredchildrenwithmildcovid19 |