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1.
J Allergy Clin Immunol ; 149(3): 912-922, 2022 03.
Artículo en Inglés | MEDLINE | ID: covidwho-1536619

RESUMEN

BACKGROUND: Multisystem inflammatory syndrome in children (MIS-C) is an acute, febrile, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-associated syndrome, often with cardiohemodynamic dysfunction. Insight into mechanism of disease is still incomplete. OBJECTIVE: Our objective was to analyze immunologic features of MIS-C patients compared to febrile controls (FC). METHODS: MIS-C patients were defined by narrow criteria, including having evidence of cardiohemodynamic involvement and no macrophage activation syndrome. Samples were collected from 8 completely treatment-naive patients with MIS-C (SARS-CoV-2 serology positive), 3 patients with unclassified MIS-C-like disease (serology negative), 14 FC, and 5 MIS-C recovery (RCV). Three healthy controls (HCs) were used for comparisons of normal range. Using spectral flow cytometry, we assessed 36 parameters in antigen-presenting cells (APCs) and 29 in T cells. We used biaxial analysis and uniform manifold approximation and projection (UMAP). RESULTS: Significant elevations in cytokines including CXCL9, M-CSF, and IL-27 were found in MIS-C compared to FC. Classic monocytes and type 2 dendritic cells (DCs) were downregulated (decreased CD86, HLA-DR) versus HCs; however, type 1 DCs (CD11c+CD141+CLEC9A+) were highly activated in MIS-C patients versus FC, expressing higher levels of CD86, CD275, and atypical conventional DC markers such as CD64, CD115, and CX3CR1. CD169 and CD38 were upregulated in multiple monocyte subtypes. CD56dim/CD57-/KLRGhi/CD161+/CD38- natural killer (NK) cells were a unique subset in MIS-C versus FC without macrophage activation syndrome. CONCLUSION: Orchestrated by complex cytokine signaling, type 1 DC activation and NK dysregulation are key features in the pathophysiology of MIS-C. NK cell findings may suggest a relationship with macrophage activation syndrome, while type 1 DC upregulation implies a role for antigen cross-presentation.


Asunto(s)
COVID-19/complicaciones , Células Dendríticas/inmunología , Células Dendríticas/virología , SARS-CoV-2/inmunología , Síndrome de Respuesta Inflamatoria Sistémica/inmunología , Síndrome de Respuesta Inflamatoria Sistémica/virología , ADP-Ribosil Ciclasa 1/sangre , Adolescente , Antígenos Virales/inmunología , COVID-19/inmunología , COVID-19/virología , Estudios de Casos y Controles , Niño , Preescolar , Reactividad Cruzada , Citocinas/sangre , Células Dendríticas/clasificación , Femenino , Antígenos HLA-DR/sangre , Humanos , Inmunofenotipificación , Interferón gamma/sangre , Interleucinas/sangre , Células Asesinas Naturales/inmunología , Masculino , Glicoproteínas de Membrana/sangre , Modelos Inmunológicos , Monocitos/inmunología , Lectina 1 Similar a Ig de Unión al Ácido Siálico/sangre , Linfocitos T/inmunología , Linfocitos T/virología , Regulación hacia Arriba
2.
Pediatrics ; 146(3)2020 09.
Artículo en Inglés | MEDLINE | ID: covidwho-742563

RESUMEN

We describe 2 patients with coronavirus disease who had multiple clinical features suggestive of Kawasaki disease (KD). Both patients presented with fever lasting >5 days and were found to have rash, conjunctival injection, and swollen lips. One patient also had extremity swelling, whereas the other developed desquamation of the fingers. In both cases, laboratory results were similar to those seen in KD. These patients had highly unusual but similar features, and both appeared to respond favorably to treatment. It remains unclear whether these patients had true KD or manifestations of coronavirus disease that resembled KD.


Asunto(s)
Infecciones por Coronavirus/diagnóstico , Infecciones por Coronavirus/terapia , Inmunoglobulinas Intravenosas/administración & dosificación , Síndrome Mucocutáneo Linfonodular/diagnóstico , Neumonía Viral/diagnóstico , Neumonía Viral/terapia , Síndrome de Respuesta Inflamatoria Sistémica/diagnóstico , COVID-19 , Preescolar , Terapia Combinada , Diagnóstico Diferencial , Femenino , Humanos , Masculino , Síndrome Mucocutáneo Linfonodular/terapia , Pandemias , Medición de Riesgo , Muestreo , Síndrome de Respuesta Inflamatoria Sistémica/terapia , Resultado del Tratamiento
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