Cargando…

Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome

While adults with Down syndrome (DS) are at increased risk of severe COVID-19 pneumonia, little is known about COVID-19 in children with DS. In children without DS, SARS-CoV-2 can rarely cause severe COVID-19 pneumonia, or an even rarer and more typically pediatric condition, multisystem inflammator...

Descripción completa

Detalles Bibliográficos
Autores principales: Malle, Louise, Bastard, Paul, Martin-Nalda, Andrea, Carpenter, Taya, Bush, Douglas, Patel, Roosheel, Colobran, Roger, Soler-Palacin, Pere, Casanova, Jean-Laurent, Gans, Melissa, Rivière, Jacques G., Bogunovic, Dusan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178650/
https://www.ncbi.nlm.nih.gov/pubmed/34089457
http://dx.doi.org/10.1007/s10875-021-01078-4
_version_ 1783703616527269888
author Malle, Louise
Bastard, Paul
Martin-Nalda, Andrea
Carpenter, Taya
Bush, Douglas
Patel, Roosheel
Colobran, Roger
Soler-Palacin, Pere
Casanova, Jean-Laurent
Gans, Melissa
Rivière, Jacques G.
Bogunovic, Dusan
author_facet Malle, Louise
Bastard, Paul
Martin-Nalda, Andrea
Carpenter, Taya
Bush, Douglas
Patel, Roosheel
Colobran, Roger
Soler-Palacin, Pere
Casanova, Jean-Laurent
Gans, Melissa
Rivière, Jacques G.
Bogunovic, Dusan
author_sort Malle, Louise
collection PubMed
description While adults with Down syndrome (DS) are at increased risk of severe COVID-19 pneumonia, little is known about COVID-19 in children with DS. In children without DS, SARS-CoV-2 can rarely cause severe COVID-19 pneumonia, or an even rarer and more typically pediatric condition, multisystem inflammatory syndrome in children (MIS-C). Although the underlying mechanisms are still unknown, MIS-C is thought to be primarily immune-mediated. Here, we describe an atypical, severe form of MIS-C in two infant girls with DS who were hospitalized for over 4 months. Immunological evaluation revealed pronounced neutrophilia, B cell depletion, increased circulating IL-6 and IL-8, and elevated markers of immune activation ICAM1 and FcɣRI. Importantly, uninfected children with DS presented with similar but less stark immune features at steady state, possibly explaining risk of further uncontrolled inflammation following SARS-CoV-2 infection. Overall, a severe, atypical form of MIS-C may occur in children with DS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10875-021-01078-4.
format Online
Article
Text
id pubmed-8178650
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-81786502021-06-05 Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome Malle, Louise Bastard, Paul Martin-Nalda, Andrea Carpenter, Taya Bush, Douglas Patel, Roosheel Colobran, Roger Soler-Palacin, Pere Casanova, Jean-Laurent Gans, Melissa Rivière, Jacques G. Bogunovic, Dusan J Clin Immunol Original Article While adults with Down syndrome (DS) are at increased risk of severe COVID-19 pneumonia, little is known about COVID-19 in children with DS. In children without DS, SARS-CoV-2 can rarely cause severe COVID-19 pneumonia, or an even rarer and more typically pediatric condition, multisystem inflammatory syndrome in children (MIS-C). Although the underlying mechanisms are still unknown, MIS-C is thought to be primarily immune-mediated. Here, we describe an atypical, severe form of MIS-C in two infant girls with DS who were hospitalized for over 4 months. Immunological evaluation revealed pronounced neutrophilia, B cell depletion, increased circulating IL-6 and IL-8, and elevated markers of immune activation ICAM1 and FcɣRI. Importantly, uninfected children with DS presented with similar but less stark immune features at steady state, possibly explaining risk of further uncontrolled inflammation following SARS-CoV-2 infection. Overall, a severe, atypical form of MIS-C may occur in children with DS. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s10875-021-01078-4. Springer US 2021-06-05 2021 /pmc/articles/PMC8178650/ /pubmed/34089457 http://dx.doi.org/10.1007/s10875-021-01078-4 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021 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 Original Article
Malle, Louise
Bastard, Paul
Martin-Nalda, Andrea
Carpenter, Taya
Bush, Douglas
Patel, Roosheel
Colobran, Roger
Soler-Palacin, Pere
Casanova, Jean-Laurent
Gans, Melissa
Rivière, Jacques G.
Bogunovic, Dusan
Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title_full Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title_fullStr Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title_full_unstemmed Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title_short Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
title_sort atypical inflammatory syndrome triggered by sars-cov-2 in infants with down syndrome
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8178650/
https://www.ncbi.nlm.nih.gov/pubmed/34089457
http://dx.doi.org/10.1007/s10875-021-01078-4
work_keys_str_mv AT mallelouise atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT bastardpaul atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT martinnaldaandrea atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT carpentertaya atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT bushdouglas atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT patelroosheel atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT colobranroger atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT solerpalacinpere atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT casanovajeanlaurent atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT gansmelissa atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT rivierejacquesg atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome
AT bogunovicdusan atypicalinflammatorysyndrometriggeredbysarscov2ininfantswithdownsyndrome