Deep immune profiling uncovers novel associations with clinical phenotypes of multisystem inflammatory syndrome in children (MIS-C)
Journal
Annals of the Rheumatic Diseases
ISSN
0003-4967
1468-2060
Date Issued
2022
Author(s)
Christopher John Redmond
Moses M Kitakule
Aran Son
McKella Sylvester
Keith Sacco
Ottavia Delmonte
Francesco Licciardi
Riccardo Castagnoli
Yasmin Espinoza
Camila Astudillo
Sarah E Weber
Gina A Montealegre Sanchez
Karyl S Barron
Mary Magliocco
Kerry Dobbs
Yu Zhang
Helen Matthews
Cihan Oguz
Helen C Su
Luigi D Notarangelo
Pamela Frischmeyer-Guerrerio
Daniella M Schwartz
Type
Resource Types::text::journal::journal article
Cite this document
Redmond, C. J., Kitakule, M. M., Son, A., Sylvester, M., Sacco, K., Delmonte, O., Licciardi, F., Castagnoli, R., Poli, M. C., Espinoza, Y., Astudillo, C., Weber, S. E., Montealegre Sanchez, G. A., Barron, K. S., Magliocco, M., Dobbs, K., Zhang, Y., Matthews, H., Oguz, C., … Schwartz, D. M. (2023). Deep immune profiling uncovers novel associations with clinical phenotypes of multisystem inflammatory syndrome in children (Mis-c). Annals of the Rheumatic Diseases, 82(3), 442-445. https://doi.org/10.1136/ard-2022-223269
Subjects
covid-19
;
immune system diseases
;
inflammation
;
covid-19
;
humans
;
systemic inflammatory response syndrome
;
alpha4 integrin
;
beta interferon
;
cd28 antigen
;
cd4 antigen
;
cd45ro antigen
;
interleukin 10
;
interleukin 17
;
interleukin 2
;
tumor necrosis factor
;
cardiogenic shock
;
cd4+ t lymphocyte
;
cd8+ t lymphocyte
;
coronavirus disease 2019
;
diarrhea
;
disease association
;
fever
;
flow cytometry
;
human
;
immune response
;
immunophenotyping
;
letter
;
macrophage
;
mucocutaneous lymph node syndrome
;
pediatric multisystem inflammatory syndrome
;
peripheral blood mononuclear cell
;
protein expression level
;
th1 cell
;
systemic inflammatory response syndrome