Local and systemic responses to SARS-CoV-2 infection in children and adults
Author:
Yoshida MasahiroORCID, Worlock Kaylee B.ORCID, Huang Ni, Lindeboom Rik G. H.ORCID, Butler Colin R., Kumasaka NatsuhikoORCID, Dominguez Conde CeciliaORCID, Mamanova LiraORCID, Bolt LiamORCID, Richardson LauraORCID, Polanski KrzysztofORCID, Madissoon Elo, Barnes Josephine L.ORCID, Allen-Hyttinen JessicaORCID, Kilich Eliz, Jones Brendan C.ORCID, de Wilton Angus, Wilbrey-Clark Anna, Sungnak WaradonORCID, Pett J. PatrickORCID, Weller JulianeORCID, Prigmore ElenaORCID, Yung Henry, Mehta Puja, Saleh Aarash, Saigal Anita, Chu VivianORCID, Cohen Jonathan M.ORCID, Cane ClareORCID, Iordanidou Aikaterini, Shibuya SoichiORCID, Reuschl Ann-Kathrin, Herczeg Iván T.ORCID, Argento A. Christine, Wunderink Richard G.ORCID, Smith Sean B., Poor Taylor A., Gao Catherine A.ORCID, Dematte Jane E., Budinger G. R. Scott, Donnelly Helen K., Markov Nikolay S., Lu Ziyan, Reynolds GaryORCID, Haniffa MuzlifahORCID, Bowyer Georgina S.ORCID, Coates Matthew, Clatworthy Menna R., Calero-Nieto Fernando J.ORCID, Göttgens BertholdORCID, O’Callaghan Christopher, Sebire Neil J., Jolly ClareORCID, De Coppi PaoloORCID, Smith Claire M.ORCID, Misharin Alexander V.ORCID, Janes Sam M.ORCID, Teichmann Sarah A.ORCID, Nikolić Marko Z.ORCID, Meyer Kerstin B.ORCID,
Abstract
AbstractIt is not fully understood why COVID-19 is typically milder in children1–3. Here, to examine the differences between children and adults in their response to SARS-CoV-2 infection, we analysed paediatric and adult patients with COVID-19 as well as healthy control individuals (total n = 93) using single-cell multi-omic profiling of matched nasal, tracheal, bronchial and blood samples. In the airways of healthy paediatric individuals, we observed cells that were already in an interferon-activated state, which after 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 characterized by increases in naive lymphocytes and a depletion of natural killer cells, whereas, in adults, cytotoxic T cells and interferon-stimulated subpopulations were significantly increased. We provide evidence that dendritic cells initiate interferon signalling in early infection, and identify epithelial cell states associated with COVID-19 and age. Our matching nasal and blood data show a strong interferon response in the airways with the induction of systemic interferon-stimulated populations, which were substantially reduced in paediatric patients. Together, we provide several mechanisms that explain the milder clinical syndrome observed in children.
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Reference82 articles.
1. Swann, O. V. et al. Clinical characteristics of children and young people admitted to hospital with covid-19 in United Kingdom: prospective multicentre observational cohort study. Brit. Med. J. 370, m3249 (2020). 2. Castagnoli, R. et al. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children and adolescents: a systematic review. JAMA Pediatr. 174, 882–889 (2020). 3. Ledford, H. Deaths from COVID ‘incredibly rare’ among children. Nature 595, 639–639 (2021). 4. Hoffmann, M. et al. SARS-CoV-2 cell entry depends on ACE2 and TMPRSS2 and is blocked by a clinically proven protease inhibitor. Cell 181, 271–280 (2020). 5. Pang, L. et al. Influence of aging on deterioration of patients with COVID-19. Aging 12, 26248–26262 (2020).
Cited by
220 articles.
订阅此论文施引文献
订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
|
|