Title | SARS-CoV-2-related MIS-C: A key to the viral and genetic causes of Kawasaki disease? |
Publication Type | Journal Article |
Year of Publication | 2021 |
Authors | Sancho-Shimizu, V, Brodin, P, Cobat, A, Biggs, CM, Toubiana, J, Lucas, CL, Henrickson, SE, Belot, A, Tangye, SG, Milner, JD, Levin, M, Abel, L, Bogunovic, D, Casanova, J-L, Zhang, S-Y |
Corporate Authors | MIS-C@CHGE |
Journal | J Exp Med |
Volume | 218 |
Issue | 6 |
Date Published | 2021 06 07 |
ISSN | 1540-9538 |
Keywords | Biomarkers, Child, COVID-19, Cytokines, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Inflammation, Inflammation Mediators, Lymphohistiocytosis, Hemophagocytic, Models, Biological, Mucocutaneous Lymph Node Syndrome, Pandemics, SARS-CoV-2, Systemic Inflammatory Response Syndrome |
Abstract | 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. |
DOI | 10.1084/jem.20210446 |
Alternate Journal | J Exp Med |
PubMed ID | 33904890 |
PubMed Central ID | PMC8080850 |
Grant List | UM1 HG006504 / HG / NHGRI NIH HHS / United States R01 AI148963 / AI / NIAID NIH HHS / United States R21 AI144315 / AI / NIAID NIH HHS / United States UL1 TR001866 / TR / NCATS NIH HHS / United States R01 AI150300 / AI / NIAID NIH HHS / United States R01 AI151029 / AI / NIAID NIH HHS / United States U24 HG008956 / HG / NHGRI NIH HHS / United States R01 AI088364 / AI / NIAID NIH HHS / United States K08 AI135091 / AI / NIAID NIH HHS / United States |