Neutrophil Profiles of Pediatric COVID-19 and Multisystem Inflammatory Syndrome in Children

Brittany P. Boribong, Thomas J. LaSalle,Yannic C. Bartsch, Felix Ellett,Maggie E. Loiselle, Jameson P. Davis,Anna L. K. Gonye, Soroush Hajizadeh,Johannes Kreuzer, Shiv Pillai,Wilhelm Haas, Andrea Edlow,Alessio Fasano, Galit Alter,Daniel Irimia,Moshe Sade-Feldman,Lael M. Yonker

biorxiv(2021)

引用 19|浏览14
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摘要
Multisystem Inflammatory Syndrome in Children (MIS-C) is a delayed-onset, COVID-19-related hyperinflammatory systemic illness characterized by SARS-CoV-2 antigenemia, cytokine storm and immune dysregulation; however, the role of the neutrophil has yet to be defined. In adults with severe COVID-19, neutrophil activation has been shown to be central to overactive inflammatory responses and complications. Thus, we sought to define neutrophil activation in children with MIS-C and acute COVID-19. We collected samples from 141 children: 31 cases of MIS-C, 43 cases of acute pediatric COVID-19, and 67 pediatric controls. We found that MIS-C neutrophils display a granulocytic myeloid-derived suppressor cell (G-MDSC) signature with highly altered metabolism, which is markedly different than the neutrophil interferon-stimulated gene (ISG) response observed in pediatric patients during acute SARS-CoV-2 infection. Moreover, we identified signatures of neutrophil activation and degranulation with high levels of spontaneous neutrophil extracellular trap (NET) formation in neutrophils isolated from fresh whole blood of MIS-C patients. Mechanistically, we determined that SARS-CoV-2 immune complexes are sufficient to trigger NETosis. Overall, our findings suggest that the hyperinflammatory presentation of MIS-C could be mechanistically linked to persistent SARS-CoV-2 antigenemia through uncontrolled neutrophil activation and NET release in the vasculature. One Sentence Summary Circulating SARS-CoV-2 antigen:antibody immune complexes in Multisystem Inflammatory Syndrome in Children (MIS-C) drive hyperinflammatory and coagulopathic neutrophil extracellular trap (NET) formation and neutrophil activation pathways, providing insight into disease pathology and establishing a divergence from neutrophil signaling seen in acute pediatric COVID-19. ### Competing Interest Statement Moshe Sade-Feldman receives funding from Bristol-Myers Squibb. Galit Alter is a founder of Seromyx Systems Inc. Alessio Fasano is co-founder of and stockholder in Alba Therapeutics.
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