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Systemic Inflammation and Microbial Translocation Are Characteristic Features of SARS-CoV-2-Related Multisystem
Nathella Pavan Kumar1, Aishwarya Venkataraman1,2, Luke Elizabeth Hanna1
1ICMR-National Institute for Research in Tuberculosis, Chennai,India.
Background:
Multisystem inflammatory syndrome in children (MIS-C) is a rare manifestation of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in children that can result in increased morbidity and mortality. The inflammatory underpinnings of MIS-C have not been examined in detail.
Methods:
We examined the plasma levels of acute phase proteins and microbial translocation markers in children with MIS-C, children with acute coronavirus disease 2019 (COVID-19) infection, SARS-CoV-2-seropositive children, and controls.
Results:
MIS-C children exhibited significantly higher levels of C-reactive protein (CRP), alpha2 macroglobulin (α2M), serum amyloid P (SAP), lipopolysaccharide (LPS), sCD14, and LPS binding protein (LBP) and significantly lower levels of haptoglobin (Hp) in comparison with seropositive, control, and/or COVID-19 children. In addition, COVID-19 children exhibited significantly higher levels of most of the above markers in comparison with seropositive and control children. Principal component analysis using a set of these markers could clearly discriminate MIS-C and COVID-19 from seropositive and control children. MIS-C children requiring pediatric intensive care unit admission and COVID-19 children with severe disease had higher levels of CRP, SAP, and/or sCD14 at admission.
Conclusions:
Our study describes the role of systemic inflammation and microbial translocation markers in children with MIS-C and COVID-19 and therefore helps in advancing our understanding of the pathogenesis of different presentations of SARS-CoV-2 infection in children.
Insights
Multisystem inflammatory syndrome in children (MIS-C) involves heightened inflammation and microbial translocation markers. These markers help distinguish MIS-C and COVID-19 from other SARS-CoV-2 infections in children.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Virology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) is a rare but serious complication of SARS-CoV-2 infection.
- The detailed inflammatory mechanisms underlying MIS-C remain largely unexplored.
Purpose of the Study:
- To investigate the role of systemic inflammation and microbial translocation markers in children with MIS-C.
- To compare these markers in children with MIS-C, acute COVID-19, SARS-CoV-2 seropositivity, and healthy controls.
Main Methods:
- Plasma levels of acute phase proteins (e.g., CRP, α2M, SAP, Hp) and microbial translocation markers (e.g., LPS, sCD14, LBP) were measured.
- Statistical analyses and principal component analysis were employed to differentiate between groups.
Main Results:
- Children with MIS-C showed significantly elevated levels of CRP, α2M, SAP, LPS, sCD14, and LBP, and lower Hp levels compared to other groups.
- COVID-19 children also had higher marker levels than seropositive and control children.
- Principal component analysis effectively distinguished MIS-C and COVID-19 cases from seropositive and control children.
Conclusions:
- Systemic inflammation and microbial translocation are key features differentiating MIS-C and COVID-19 in children.
- These findings enhance understanding of the pathogenesis of diverse SARS-CoV-2 presentations in pediatric populations.
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