Deep immune profiling of MIS-C demonstrates marked but transient immune activation compared with adult and pediatric COVID-19

Immunocompetence
DOI: 10.1126/sciimmunol.abf7570 Publication Date: 2021-03-02T20:05:11Z
ABSTRACT
Pediatric COVID-19 following SARS-CoV-2 infection is associated with fewer hospitalizations and often milder disease than in adults. A subset of children, however, present Multisystem Inflammatory Syndrome Children (MIS-C) that can lead to vascular complications shock, but rarely death. The immune features MIS-C compared pediatric or adult remain poorly understood. We analyzed peripheral blood responses hospitalized infected patients (pediatric COVID-19) MIS-C. had patterns T cell-biased lymphopenia cell activation similar severely ill adults, all spike-specific antibodies at admission. distinct feature was robust patrolling CX3CR1+ CD8+ cells correlated the use vasoactive medication. Finally, whereas acute respiratory distress syndrome (ARDS) sustained activation, displayed clinical improvement over time, concomitant decreasing activation. Thus, non-MIS-C versus illnesses are characterized by divergent signatures temporally from one another implicate presentation trajectory
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