Local and systemic responses to SARS-CoV-2 infection in children and adults
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Peer-reviewed
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Abstract
It is not fully understood why COVID-19 is typically milder in children To examine differences in response to SARS-CoV-2 infection in children and adults, we analysed paediatric and adult COVID-19 patients and healthy controls (total n=93) using single-cell multi-omic profiling of matched nasal, tracheal, bronchial and blood samples. In healthy paediatric airways, we observed cells already in an interferon-activated state, that upon SARS-CoV-2 infection was further induced especially in airway immune cells. We postulate that higher paediatric innate interferon-responses restrict viral replication and disease progression. The systemic response in children was characterised by increases in naive lymphocytes and a depletion of natural killer cells, while in adults cytotoxic T cells and interferon-stimulated subpopulations were significantly increased. We provide evidence that dendritic cells initiate interferon signaling in early infection, and identify novel epithelial cell states that associate with COVID-19 and age. Our matching nasal and blood data showed a strong interferon response in the airways with the induction of systemic interferon-stimulated populations, which were massively reduced in paediatric patients. Together, we provide several mechanisms that explain the milder clinical syndrome observed in children.
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1476-4687
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European Commission Horizon 2020 (H2020) Societal Challenges (874656)
Medical Research Council (MR/S036113/1)
Medical Research Council (MC_PC_17230)
MRC (MR/W014556/1)
Medical Research Council (MR/R015635/1)
Medical Research Council (MR/S035842/1)