Dysregulation in neutrophil extracellular trap (NET) formation and degradation may play a role in the pathogenesis and severity of COVID-19; however, its role in the pediatric manifestations of this disease including multisystem inflammatory syndrome in children (MIS-C) and chilblain-like lesions (CLL), otherwise known as "COVID toes", remains unclear. Studying multinational cohorts, we found that, in CLL, NETs were significantly increased in serum and skin. There was geographic variability in the prevalence of increased NETs in MIS-C, in association with disease severity. MIS-C and CLL serum samples displayed decreased NET degradation ability, in association with C1q and G-actin or anti-NET antibodies, respectively, but not with genetic variants of DNases. In adult COVID-19, persistent elevations in NETs post-disease diagnosis were detected but did not occur in asymptomatic infection. COVID-19-affected adults displayed significant prevalence of impaired NET degradation, in association with anti-DNase1L3, G-actin, and specific disease manifestations, but not with genetic variants of DNases. NETs were detected in many organs of adult patients who died from COVID-19 complications. Infection with the Omicron variant was associated with decreased levels of NETs when compared to other SARS-CoV-2 strains. These data support a role for NETs in the pathogenesis and severity of COVID-19 in pediatric and adult patients.

Carmona-Rivera, C., Zhang, Y., Dobbs, K., Markowitz, T., Dalgard, C., Oler, A., et al. (2022). Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19. JCI INSIGHT [10.1172/jci.insight.160332].

Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19

Biondi, Andrea;Bonfanti, Paolo;
2022

Abstract

Dysregulation in neutrophil extracellular trap (NET) formation and degradation may play a role in the pathogenesis and severity of COVID-19; however, its role in the pediatric manifestations of this disease including multisystem inflammatory syndrome in children (MIS-C) and chilblain-like lesions (CLL), otherwise known as "COVID toes", remains unclear. Studying multinational cohorts, we found that, in CLL, NETs were significantly increased in serum and skin. There was geographic variability in the prevalence of increased NETs in MIS-C, in association with disease severity. MIS-C and CLL serum samples displayed decreased NET degradation ability, in association with C1q and G-actin or anti-NET antibodies, respectively, but not with genetic variants of DNases. In adult COVID-19, persistent elevations in NETs post-disease diagnosis were detected but did not occur in asymptomatic infection. COVID-19-affected adults displayed significant prevalence of impaired NET degradation, in association with anti-DNase1L3, G-actin, and specific disease manifestations, but not with genetic variants of DNases. NETs were detected in many organs of adult patients who died from COVID-19 complications. Infection with the Omicron variant was associated with decreased levels of NETs when compared to other SARS-CoV-2 strains. These data support a role for NETs in the pathogenesis and severity of COVID-19 in pediatric and adult patients.
Articolo in rivista - Articolo scientifico
Scientifica
Infectious disease; Inflammation; Neutrophils;
English
Carmona-Rivera, C., Zhang, Y., Dobbs, K., Markowitz, T., Dalgard, C., Oler, A., et al. (2022). Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19. JCI INSIGHT [10.1172/jci.insight.160332].
Carmona-Rivera, C; Zhang, Y; Dobbs, K; Markowitz, T; Dalgard, C; Oler, A; Claybaugh, D; Draper, D; Truong, M; Delmonte, O; Licciardi, F; Ramenghi, U; Crescenzio, N; Imberti, L; Sottini, A; Quaresima, V; Fiorini, C; Discepolo, V; Lo Vecchio, A; Guarino, A; Pierri, L; Catzola, A; Biondi, A; Bonfanti, P; Poli Harlowe, M; Espinosa, Y; Astudillo, C; Rey-Jurado, E; Vial, C; De la Cruz, J; Gonzalez, R; Pinera, C; Mays, J; Ng, A; Platt, A; Drolet, B; Moon, J; Cowen, E; Kenney, H; Weber, S; Castagnoli, R; Magliocco, M; Stack, M; Montealegre Sanchez, G; Barron, K; Fink, D; Kuhns, D; Hewitt, S; Arkin, L; Chertow, D; Su, H; Notarangelo, L; Kaplan, M
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Utilizza questo identificativo per citare o creare un link a questo documento: http://hdl.handle.net/10281/388966
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