Robust innate responses to SARS-CoV-2 in children resolve faster than in adults without compromising adaptive immunity
COVID-19 / virology
info:eu-repo/classification/ddc/616.07
COVID-19 / genetics
Monocytes / metabolism
ddc:616.07
Adaptive Immunity
Antibodies, Viral
Monocytes
Gene profile
info:eu-repo/classification/ddc/616
info:eu-repo/classification/ddc/618
antibodies
Inflammation / virology
info:eu-repo/classification/ddc/613
Longitudinal Studies
Biology (General)
Child
Children
Innate responses
ddc:616
B-Lymphocytes
0303 health sciences
ddc:618
interferon
Viral Load
Middle Aged
3. Good health
innate responses
Child, Preschool
Interferon
Cytokines
monocytes
Adult
Adolescent
QH301-705.5
Sciences de l'ingénieur
Antibodies
Article
Granulocyte-Macrophage Colony-Stimulating Factor / metabolism
Young Adult
03 medical and health sciences
children
COVID-19 / immunology
Chemokine CXCL10 / metabolism
Humans
ddc:613
Inflammation
B cells
Sequence Analysis, RNA
SARS-CoV-2
resolution
COVID-19
Granulocyte-Macrophage Colony-Stimulating Factor
Infant
Interferons / metabolism
B-Lymphocytes / metabolism
gene profile
Immunity, Innate
Chemokine CXCL10
Cytokines / metabolism
Antibodies, Viral / immunology
Interferons
Resolution
Transcriptome
SARS-CoV-2 / immunology
DOI:
10.1016/j.celrep.2021.109773
Publication Date:
2021-09-15T05:17:45Z
AUTHORS (20)
ABSTRACT
SARS-CoV-2 infection in children is less severe than it is in adults. We perform a longitudinal analysis of the early innate responses in children and adults with mild infection within household clusters. Children display fewer symptoms than adults do, despite similar initial viral load, and mount a robust anti-viral immune signature typical of the SARS-CoV-2 infection and characterized by early interferon gene responses; increases in cytokines, such as CXCL10 and GM-CSF; and changes in blood cell numbers. When compared with adults, the antiviral response resolves faster (within a week of symptoms), monocytes and dendritic cells are more transiently activated, and genes associated with B cell activation appear earlier in children. Nonetheless, these differences do not have major effects on the quality of SARS-CoV-2-specific antibody responses. Our findings reveal that better early control of inflammation as observed in children may be key for rapidly controlling infection and limiting the disease course.
SUPPLEMENTAL MATERIAL
Coming soon ....
REFERENCES (70)
CITATIONS (76)
EXTERNAL LINKS
PlumX Metrics
RECOMMENDATIONS
FAIR ASSESSMENT
Coming soon ....
JUPYTER LAB
Coming soon ....