SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?

Multisystem inflammatory syndrome in children (MIS-C) emerged in April 2020 in communities with high COVID-19 rates. This new condition is heterogenous but resembles Kawasaki disease (KD), a well-known but poorly understood and clinically heterogenous pediatric inflammatory condition for which weak...

ver descrição completa

Detalhes bibliográficos
Autores: Sancho-Shimizu, Vanessa, Brodin, Petter, Cobat, Aurélie, Biggs, Catherine M., Toubiana, Julie, Lucas, Carrie L., Henrickson, Sarah E., Belot, Alexandre, MIS-C@CHGE, Tangye, Stuart G., Milner, Joshua D., Levin, Michael, Abel, Laurent, Bogunovic, Dusan, Casanova, Jean-Laurent, Zhang, Shen-Ying, Gut, Marta
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2021
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositório:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10230/53114
Acesso em linha:http://hdl.handle.net/10230/53114
http://dx.doi.org/10.1084/jem.20210446
Access Level:Acceso aberto
Palavra-chave:COVID-19 (Malaltia)
Malaltia de Kawasaki
Genètica
Pediatria
id ES_c988dafcc3b21ab2af675dafcff4e032
oai_identifier_str oai:recercat.cat:10230/53114
network_acronym_str ES
network_name_str España
repository_id_str
spelling SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?Sancho-Shimizu, VanessaBrodin, PetterCobat, AurélieBiggs, Catherine M.Toubiana, JulieLucas, Carrie L.Henrickson, Sarah E.Belot, AlexandreMIS-C@CHGETangye, Stuart G.Milner, Joshua D.Levin, MichaelAbel, LaurentBogunovic, DusanCasanova, Jean-LaurentZhang, Shen-YingGut, MartaCOVID-19 (Malaltia)Malaltia de KawasakiGenèticaPediatriaMultisystem inflammatory syndrome in children (MIS-C) emerged in April 2020 in communities with high COVID-19 rates. This new condition is heterogenous but resembles Kawasaki disease (KD), a well-known but poorly understood and clinically heterogenous pediatric inflammatory condition for which weak associations have been found with a myriad of viral illnesses. Epidemiological data clearly indicate that SARS-CoV-2 is the trigger for MIS-C, which typically occurs about 1 mo after infection. These findings support the hypothesis of viral triggers for the various forms of classic KD. We further suggest that rare inborn errors of immunity (IEIs) altering the immune response to SARS-CoV-2 may underlie the pathogenesis of MIS-C in some children. The discovery of monogenic IEIs underlying MIS-C would shed light on its pathogenesis, paving the way for a new genetic approach to classic KD, revisited as a heterogeneous collection of IEIs to viruses.The studies are funded by the Howard Hughes Medical Institute, the Rockefeller University, the St. Giles Foundation, the National Institutes of Health (R01AI088364 to J.-L. Casanova and S.-Y. Zhang; R01AI148963, R01AI151029, and R01AI150300 to D. Bogunovic; K08AI135091 to S.E. Henrickson; R21AI144315-02S1 to C.L. Lucas), the National Center for Advancing Translational Sciences, National Institutes of Health Clinical and Translational Science Award program (UL1 TR001866), the Yale Center for Mendelian Genomics and the GSP Coordinating Center funded by the National Human Genome Research Institute (UM1HG006504 and U24HG008956), Institut National de la Santé et de la Recherche Médicale and Université de Paris, the French National Research Agency (ANR) Résilience-Covid-19 grant GenMIS-C, the ANR “Investments for the Future” program (ANR-10-IAHU-01), the Integrative Biology of Emerging Infectious Diseases Laboratory of Excellence (ANR-10-LABX-62-IBEID), the ANR project AABIFNCOV (ANR-20-CO11-0001), the French Foundation for Medical Research (EQU201903007798), the French Foundation for Medical Research and ANR GENCOVID project, the ANRSCOV05 project, the Square Foundation, Grandir - Fonds de solidarité pour l’enfance, the Fondation du Souffle, the SCOR Corporate Foundation for Science, UK Research and Innovation Future Leader’s Fellowship (MR/S032304/1), the NIHR Imperial Biomedical Research Centre at Imperial College Healthcare NHS Trust (70931), the Burroughs Wellcome Fund Career Awards for Medical ScientistsRockefeller University Press202220222021info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttp://hdl.handle.net/10230/53114http://dx.doi.org/10.1084/jem.20210446reponame:Recercat. Dipósit de la Recerca de Catalunyainstname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)Inglés© 2021 Vanessa Sancho-Shimizu et al. This article is distributed under the terms of a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 International license, as described at https://creativecommons.org/licenses/by-nc-sa/4.0/)https://creativecommons.org/licenses/by-nc-sa/4.0/info:eu-repo/semantics/openAccessoai:recercat.cat:10230/531142026-05-29T05:05:01Z
dc.title.none.fl_str_mv SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
title SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
spellingShingle SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
Sancho-Shimizu, Vanessa
COVID-19 (Malaltia)
Malaltia de Kawasaki
Genètica
Pediatria
title_short SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
title_full SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
title_fullStr SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
title_full_unstemmed SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
title_sort SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease?
dc.creator.none.fl_str_mv Sancho-Shimizu, Vanessa
Brodin, Petter
Cobat, Aurélie
Biggs, Catherine M.
Toubiana, Julie
Lucas, Carrie L.
Henrickson, Sarah E.
Belot, Alexandre
MIS-C@CHGE
Tangye, Stuart G.
Milner, Joshua D.
Levin, Michael
Abel, Laurent
Bogunovic, Dusan
Casanova, Jean-Laurent
Zhang, Shen-Ying
Gut, Marta
author Sancho-Shimizu, Vanessa
author_facet Sancho-Shimizu, Vanessa
Brodin, Petter
Cobat, Aurélie
Biggs, Catherine M.
Toubiana, Julie
Lucas, Carrie L.
Henrickson, Sarah E.
Belot, Alexandre
MIS-C@CHGE
Tangye, Stuart G.
Milner, Joshua D.
Levin, Michael
Abel, Laurent
Bogunovic, Dusan
Casanova, Jean-Laurent
Zhang, Shen-Ying
Gut, Marta
author_role author
author2 Brodin, Petter
Cobat, Aurélie
Biggs, Catherine M.
Toubiana, Julie
Lucas, Carrie L.
Henrickson, Sarah E.
Belot, Alexandre
MIS-C@CHGE
Tangye, Stuart G.
Milner, Joshua D.
Levin, Michael
Abel, Laurent
Bogunovic, Dusan
Casanova, Jean-Laurent
Zhang, Shen-Ying
Gut, Marta
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv COVID-19 (Malaltia)
Malaltia de Kawasaki
Genètica
Pediatria
topic COVID-19 (Malaltia)
Malaltia de Kawasaki
Genètica
Pediatria
description Multisystem inflammatory syndrome in children (MIS-C) emerged in April 2020 in communities with high COVID-19 rates. This new condition is heterogenous but resembles Kawasaki disease (KD), a well-known but poorly understood and clinically heterogenous pediatric inflammatory condition for which weak associations have been found with a myriad of viral illnesses. Epidemiological data clearly indicate that SARS-CoV-2 is the trigger for MIS-C, which typically occurs about 1 mo after infection. These findings support the hypothesis of viral triggers for the various forms of classic KD. We further suggest that rare inborn errors of immunity (IEIs) altering the immune response to SARS-CoV-2 may underlie the pathogenesis of MIS-C in some children. The discovery of monogenic IEIs underlying MIS-C would shed light on its pathogenesis, paving the way for a new genetic approach to classic KD, revisited as a heterogeneous collection of IEIs to viruses.
publishDate 2021
dc.date.none.fl_str_mv 2021
2022
2022
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/10230/53114
http://dx.doi.org/10.1084/jem.20210446
url http://hdl.handle.net/10230/53114
http://dx.doi.org/10.1084/jem.20210446
dc.language.none.fl_str_mv Inglés
language_invalid_str_mv Inglés
dc.rights.none.fl_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0/
info:eu-repo/semantics/openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/4.0/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Rockefeller University Press
publisher.none.fl_str_mv Rockefeller University Press
dc.source.none.fl_str_mv reponame:Recercat. Dipósit de la Recerca de Catalunya
instname:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
reponame_str Recercat. Dipósit de la Recerca de Catalunya
collection Recercat. Dipósit de la Recerca de Catalunya
repository.name.fl_str_mv
repository.mail.fl_str_mv
_version_ 1869419379327762432
score 15,811543