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Multisystem Inflammatory Syndrome Following SARS-CoV-2 Vaccination in Two Children
Christos Karatzios1,2, Rosie Scuccimarri1,3, Gaëlle Chédeville1,3
1Department of Pediatrics, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Insights
Two children developed multisystem inflammatory syndrome post-vaccination (MIS-V) after their first SARS-CoV-2 vaccine dose. Differentiating antibodies (anti-S vs. anti-NC) help distinguish MIS-V from MIS-C.
Area of Science:
- Pediatric immunology
- Vaccine adverse events
- Infectious disease
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a rare but serious condition following SARS-CoV-2 infection.
- Vaccination against SARS-CoV-2 is crucial for pediatric protection, but surveillance for rare adverse events is necessary.
Observation:
- Two pediatric cases of multisystem inflammatory syndrome post-vaccination (MIS-V) occurred within six weeks of the first Pfizer-BioNTech SARS-CoV-2 vaccine dose.
- One child presented with peri-myocarditis and shock, while the other exhibited Kawasaki disease features.
- Both patients tested positive only for SARS-CoV-2 antispike (anti-S) antibodies, indicating a post-vaccine event.
Findings:
- Both MIS-V cases responded well to standard treatments like intravenous immunoglobulins and corticosteroids.
- Measuring both anti-S and anti-nucleocapsid (anti-NC) antibodies is crucial for differentiating MIS-V from MIS-C post-infection.
Implications:
- This report underscores the importance of continued surveillance for rare adverse events following immunization in children.
- Accurate antibody testing can distinguish between post-vaccine and post-infection inflammatory syndromes, aiding clinical management.
- Understanding MIS-V is vital, especially with expanding SARS-CoV-2 vaccination eligibility in younger age groups.
Abstract:
This report presents 2 pediatric cases of multisystem inflammatory syndrome in children and adults (MIS-C/A) post severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) vaccination (MIS-V). Both children presented with MIS-V within 6 weeks of receiving their first and only dose of Pfizer-BioNTech's SARS-CoV-2 vaccine. The first patient had symptoms of MIS-C/A with peri-myocarditis and shock, and the second 1 had classic Kawasaki disease features. Both responded well to intravenous immunoglobulins and/or systemic corticosteroids. Both children were positive only for SARS-2-CoV antispike (S) (and not for antinucleocapsid [NC]) antibodies consistent with a postvaccine, and not a postinfection, event. Surveillance for rare adverse events following immunization should continue, especially now that SARS-CoV-2 vaccination is approved in the 5 to 11 year age group that has had the highest risk of developing MIS-C post SARS-CoV-2 infection. Our patients did not receive any further SARS-CoV-2 vaccines. Our report highlights the importance of measuring differentiating antibodies (anti-S and anti-NC) that can be used within a specific timeframe to help determine if a patient has MIS-V post vaccine (only anti-S present), or MIS-C/A post SARS-CoV-2 infection (both anti-S and anti-NC present).
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