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Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19

Compared to adults, children with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have predominantly mild or asymptomatic infections, but the underlying immunological differences remain unclear. Here, we describe clinical features, virology, longitudinal cellular, and cytokine immune pr...

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Autores principales: Tosif, Shidan, Neeland, Melanie R., Sutton, Philip, Licciardi, Paul V., Sarkar, Sohinee, Selva, Kevin J., Do, Lien Anh Ha, Donato, Celeste, Quan Toh, Zheng, Higgins, Rachel, Van de Sandt, Carolien, Lemke, Melissa M., Lee, Christina Y., Shoffner, Suzanne K., Flanagan, Katie L., Arnold, Kelly B., Mordant, Francesca L., Mulholland, Kim, Bines, Julie, Dohle, Kate, Pellicci, Daniel G., Curtis, Nigel, McNab, Sarah, Steer, Andrew, Saffery, Richard, Subbarao, Kanta, Chung, Amy W., Kedzierska, Katherine, Burgner, David P., Crawford, Nigel W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658256/
https://www.ncbi.nlm.nih.gov/pubmed/33177504
http://dx.doi.org/10.1038/s41467-020-19545-8
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author Tosif, Shidan
Neeland, Melanie R.
Sutton, Philip
Licciardi, Paul V.
Sarkar, Sohinee
Selva, Kevin J.
Do, Lien Anh Ha
Donato, Celeste
Quan Toh, Zheng
Higgins, Rachel
Van de Sandt, Carolien
Lemke, Melissa M.
Lee, Christina Y.
Shoffner, Suzanne K.
Flanagan, Katie L.
Arnold, Kelly B.
Mordant, Francesca L.
Mulholland, Kim
Bines, Julie
Dohle, Kate
Pellicci, Daniel G.
Curtis, Nigel
McNab, Sarah
Steer, Andrew
Saffery, Richard
Subbarao, Kanta
Chung, Amy W.
Kedzierska, Katherine
Burgner, David P.
Crawford, Nigel W.
author_facet Tosif, Shidan
Neeland, Melanie R.
Sutton, Philip
Licciardi, Paul V.
Sarkar, Sohinee
Selva, Kevin J.
Do, Lien Anh Ha
Donato, Celeste
Quan Toh, Zheng
Higgins, Rachel
Van de Sandt, Carolien
Lemke, Melissa M.
Lee, Christina Y.
Shoffner, Suzanne K.
Flanagan, Katie L.
Arnold, Kelly B.
Mordant, Francesca L.
Mulholland, Kim
Bines, Julie
Dohle, Kate
Pellicci, Daniel G.
Curtis, Nigel
McNab, Sarah
Steer, Andrew
Saffery, Richard
Subbarao, Kanta
Chung, Amy W.
Kedzierska, Katherine
Burgner, David P.
Crawford, Nigel W.
author_sort Tosif, Shidan
collection PubMed
description Compared to adults, children with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have predominantly mild or asymptomatic infections, but the underlying immunological differences remain unclear. Here, we describe clinical features, virology, longitudinal cellular, and cytokine immune profile, SARS-CoV-2-specific serology and salivary antibody responses in a family of two parents with PCR-confirmed symptomatic SARS-CoV-2 infection and their three children, who tested repeatedly SARS-CoV-2 PCR negative. Cellular immune profiles and cytokine responses of all children are similar to their parents at all timepoints. All family members have salivary anti-SARS-CoV-2 antibodies detected, predominantly IgA, that coincide with symptom resolution in 3 of 4 symptomatic members. Plasma from both parents and one child have IgG antibody against the S1 protein and virus-neutralizing activity detected. Using a systems serology approach, we demonstrate higher levels of SARS-CoV-2-specific antibody features of these family members compared to healthy controls. These data indicate that children can mount an immune response to SARS-CoV-2 without virological confirmation of infection, raising the possibility that immunity in children can prevent the establishment of SARS-CoV-2 infection. Relying on routine virological and serological testing may not identify exposed children, with implications for epidemiological and clinical studies across the life-span.
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spelling pubmed-76582562020-11-17 Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19 Tosif, Shidan Neeland, Melanie R. Sutton, Philip Licciardi, Paul V. Sarkar, Sohinee Selva, Kevin J. Do, Lien Anh Ha Donato, Celeste Quan Toh, Zheng Higgins, Rachel Van de Sandt, Carolien Lemke, Melissa M. Lee, Christina Y. Shoffner, Suzanne K. Flanagan, Katie L. Arnold, Kelly B. Mordant, Francesca L. Mulholland, Kim Bines, Julie Dohle, Kate Pellicci, Daniel G. Curtis, Nigel McNab, Sarah Steer, Andrew Saffery, Richard Subbarao, Kanta Chung, Amy W. Kedzierska, Katherine Burgner, David P. Crawford, Nigel W. Nat Commun Article Compared to adults, children with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) have predominantly mild or asymptomatic infections, but the underlying immunological differences remain unclear. Here, we describe clinical features, virology, longitudinal cellular, and cytokine immune profile, SARS-CoV-2-specific serology and salivary antibody responses in a family of two parents with PCR-confirmed symptomatic SARS-CoV-2 infection and their three children, who tested repeatedly SARS-CoV-2 PCR negative. Cellular immune profiles and cytokine responses of all children are similar to their parents at all timepoints. All family members have salivary anti-SARS-CoV-2 antibodies detected, predominantly IgA, that coincide with symptom resolution in 3 of 4 symptomatic members. Plasma from both parents and one child have IgG antibody against the S1 protein and virus-neutralizing activity detected. Using a systems serology approach, we demonstrate higher levels of SARS-CoV-2-specific antibody features of these family members compared to healthy controls. These data indicate that children can mount an immune response to SARS-CoV-2 without virological confirmation of infection, raising the possibility that immunity in children can prevent the establishment of SARS-CoV-2 infection. Relying on routine virological and serological testing may not identify exposed children, with implications for epidemiological and clinical studies across the life-span. Nature Publishing Group UK 2020-11-11 /pmc/articles/PMC7658256/ /pubmed/33177504 http://dx.doi.org/10.1038/s41467-020-19545-8 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Tosif, Shidan
Neeland, Melanie R.
Sutton, Philip
Licciardi, Paul V.
Sarkar, Sohinee
Selva, Kevin J.
Do, Lien Anh Ha
Donato, Celeste
Quan Toh, Zheng
Higgins, Rachel
Van de Sandt, Carolien
Lemke, Melissa M.
Lee, Christina Y.
Shoffner, Suzanne K.
Flanagan, Katie L.
Arnold, Kelly B.
Mordant, Francesca L.
Mulholland, Kim
Bines, Julie
Dohle, Kate
Pellicci, Daniel G.
Curtis, Nigel
McNab, Sarah
Steer, Andrew
Saffery, Richard
Subbarao, Kanta
Chung, Amy W.
Kedzierska, Katherine
Burgner, David P.
Crawford, Nigel W.
Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title_full Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title_fullStr Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title_full_unstemmed Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title_short Immune responses to SARS-CoV-2 in three children of parents with symptomatic COVID-19
title_sort immune responses to sars-cov-2 in three children of parents with symptomatic covid-19
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7658256/
https://www.ncbi.nlm.nih.gov/pubmed/33177504
http://dx.doi.org/10.1038/s41467-020-19545-8
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