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Multisystem Inflammatory Syndrome in Children (MIS-C), Possibly Due to COVID-19 mRNA Vaccination
Alije Keka-Sylaj1,2, Atifete Ramosaj1,2, Arbana Baloku2
1Institute of Anatomy, Faculty of Medicine, University of Prishtina, 10000 Prishtina, Kosovo.
Insights
Multisystem inflammatory syndrome in children (MIS-C) can occur after COVID-19 vaccination. This case report details MIS-C in a fully vaccinated teen, suggesting a potential link between vaccination and the syndrome.
Area of Science:
- Pediatrics
- Immunology
- Infectious Diseases
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a serious condition linked to SARS-CoV-2.
- The relationship between COVID-19 vaccination and MIS-C remains unclear.
- Investigating potential vaccine-precipitated MIS-C is crucial for public health.
Observation:
- A 16-year-old girl developed MIS-C three weeks after her second Pfizer COVID-19 vaccine dose.
- She had no prior SARS-CoV-2 infection or known exposure.
- Clinical presentation included fever, multi-organ dysfunction, and elevated inflammatory markers.
Findings:
- Laboratory tests showed high SARS-CoV-2 IgG spike antibodies.
- Tests for acute SARS-CoV-2 infection and other inflammatory causes were negative.
- The temporal association suggested a possible vaccine-related etiology.
Implications:
- This case raises questions about whether COVID-19 vaccination can trigger MIS-C.
- Further research is needed to understand the role of vaccination in MIS-C development.
- Understanding this link is vital for vaccine safety monitoring and pediatric health.
Abstract:
Multisystem inflammatory syndrome in children (MIS-C) is a potentially life-threatening childhood disease caused by SARS-CoV-2 infection, manifested by the persistence of fever and multi-organ dysfunction, elevated inflammatory markers, and the lack of an alternative diagnosis. It is still unknown if vaccination can precipitate or abrogate MIS-C or if a natural infection preceding or occurring at the time of vaccination plays any role. We present one case of MIS-C in a 16-year-old girl who was fully immunized against COVID-19 (Pfizer), with the second dose received three weeks prior to onset of the disease. She had no history of COVID-19 disease or contact with COVID-19 patients. At admission, she was somnolent, pale, and dehydrated, with cyanotic lips and cold extremities; she was hypotensive with tachycardia and poorly palpable pulses. Initial laboratory results revealed elevated levels of inflammatory markers, and high level of SARS-CoV-2 IgG spike antibodies, while testing for SARS-CoV-2 acute infection and other inflammatory etiologies were negative. Vaccine-related MIS-C was suspected in our case due to the development of MIS-C three weeks following the second dose of the COVID-19 mRNA vaccine, the absence of previous infection or exposure to SARS-CoV-2, and a positive result for IgG anti-spike (S) antibodies.
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