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Atypical Inflammatory Syndrome Triggered by SARS-CoV-2 in Infants with Down Syndrome
Louise Malle1,2,3,4,5, Paul Bastard6,7,8, Andrea Martin-Nalda9,10
1Center for Inborn Errors of Immunity, Icahn School of Medicine At Mount Sinai, New York, NY, USA.
Children with Down syndrome (DS) may experience a severe form of multisystem inflammatory syndrome in children (MIS-C) after SARS-CoV-2 infection. Immune findings in these children suggest a heightened risk for severe inflammatory responses.
Area of Science:
- Pediatric Immunology
- Infectious Diseases
Background:
- Adults with Down syndrome (DS) face higher risks for severe COVID-19 pneumonia.
- COVID-19 in children with DS is not well understood, though SARS-CoV-2 can cause severe pneumonia or multisystem inflammatory syndrome in children (MIS-C) in the general pediatric population.
Observation:
- Two infant girls with DS developed an atypical, severe form of MIS-C requiring prolonged hospitalization (>4 months).
- Immunological assessments revealed significant neutrophilia, B cell depletion, elevated IL-6, IL-8, ICAM1, and FcɣRI.
Findings:
- Children with DS, even when uninfected, showed similar but less pronounced immune alterations at baseline.
- These baseline immune characteristics may predispose children with DS to exaggerated inflammation post-SARS-CoV-2 infection.
Implications:
- A severe, atypical MIS-C presentation is possible in infants with Down syndrome.
- Understanding these immune dysregulations is crucial for managing COVID-19 and MIS-C in children with DS.
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