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Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection

BACKGROUND: The basis of the less severe clinical presentation of coronavirus disease 2019 (COVID-19) in children as compared with adults remains incompletely understood. Studies have suggested that a more potent boosting of immunity to endemic common cold coronaviruses (HCoVs) may protect children....

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Autores principales: Tomasi, Lisa, Thiriard, Anais, Heyndrickx, Leo, Georges, Daphnée, Van den Wijngaert, Sigi, Olislagers, Véronique, Sharma, Shilpee, Matagne, André, Ackerman, Margaret E, Ariën, Kevin K, Goetghebuer, Tessa, Marchant, Arnaud
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709628/
https://www.ncbi.nlm.nih.gov/pubmed/36467295
http://dx.doi.org/10.1093/ofid/ofac554
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author Tomasi, Lisa
Thiriard, Anais
Heyndrickx, Leo
Georges, Daphnée
Van den Wijngaert, Sigi
Olislagers, Véronique
Sharma, Shilpee
Matagne, André
Ackerman, Margaret E
Ariën, Kevin K
Goetghebuer, Tessa
Marchant, Arnaud
author_facet Tomasi, Lisa
Thiriard, Anais
Heyndrickx, Leo
Georges, Daphnée
Van den Wijngaert, Sigi
Olislagers, Véronique
Sharma, Shilpee
Matagne, André
Ackerman, Margaret E
Ariën, Kevin K
Goetghebuer, Tessa
Marchant, Arnaud
author_sort Tomasi, Lisa
collection PubMed
description BACKGROUND: The basis of the less severe clinical presentation of coronavirus disease 2019 (COVID-19) in children as compared with adults remains incompletely understood. Studies have suggested that a more potent boosting of immunity to endemic common cold coronaviruses (HCoVs) may protect children. METHODS: To test this hypothesis, we conducted a detailed analysis of antibodies induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children aged 2 months to 14 years. RESULTS: Younger children had higher titers of antibodies to SARS-CoV-2 receptor binding domain (RBD), S1 but not S2 domain, and total spike (S) protein, higher avidity RBD immunoglobulin G, and higher titers of neutralizing and complement-activating antibodies as compared with older children. In contrast, older children had higher titers of antibodies to HCoVs, which correlated with antibodies to the SARS-CoV-2 S2 domain but not with neutralizing or complement-activating antibodies. CONCLUSIONS: These results reveal a unique capacity of young children to develop effector antibody responses to SARS-CoV-2 infection independently of their immunity to HCoVs.
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spelling pubmed-97096282022-12-01 Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection Tomasi, Lisa Thiriard, Anais Heyndrickx, Leo Georges, Daphnée Van den Wijngaert, Sigi Olislagers, Véronique Sharma, Shilpee Matagne, André Ackerman, Margaret E Ariën, Kevin K Goetghebuer, Tessa Marchant, Arnaud Open Forum Infect Dis Major Article BACKGROUND: The basis of the less severe clinical presentation of coronavirus disease 2019 (COVID-19) in children as compared with adults remains incompletely understood. Studies have suggested that a more potent boosting of immunity to endemic common cold coronaviruses (HCoVs) may protect children. METHODS: To test this hypothesis, we conducted a detailed analysis of antibodies induced by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children aged 2 months to 14 years. RESULTS: Younger children had higher titers of antibodies to SARS-CoV-2 receptor binding domain (RBD), S1 but not S2 domain, and total spike (S) protein, higher avidity RBD immunoglobulin G, and higher titers of neutralizing and complement-activating antibodies as compared with older children. In contrast, older children had higher titers of antibodies to HCoVs, which correlated with antibodies to the SARS-CoV-2 S2 domain but not with neutralizing or complement-activating antibodies. CONCLUSIONS: These results reveal a unique capacity of young children to develop effector antibody responses to SARS-CoV-2 infection independently of their immunity to HCoVs. Oxford University Press 2022-11-30 /pmc/articles/PMC9709628/ /pubmed/36467295 http://dx.doi.org/10.1093/ofid/ofac554 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Article
Tomasi, Lisa
Thiriard, Anais
Heyndrickx, Leo
Georges, Daphnée
Van den Wijngaert, Sigi
Olislagers, Véronique
Sharma, Shilpee
Matagne, André
Ackerman, Margaret E
Ariën, Kevin K
Goetghebuer, Tessa
Marchant, Arnaud
Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title_full Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title_fullStr Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title_full_unstemmed Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title_short Younger Children Develop Higher Effector Antibody Responses to SARS-CoV-2 Infection
title_sort younger children develop higher effector antibody responses to sars-cov-2 infection
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9709628/
https://www.ncbi.nlm.nih.gov/pubmed/36467295
http://dx.doi.org/10.1093/ofid/ofac554
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