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Single-cell Analysis of Immunophenotype and Cytokine Production in Peripheral Whole Blood via Mass Cytometry
Published on: June 26, 2018
Laboratory parameters between multisystem inflammatory syndrome in children and Kawasaki disease
Chunling Zhou1, Yan Zhao1, Xia Wang2
1Department of Pediatrics, People's Hospital of Chongqing Banan District, Chongqing, China.
Insights
Multisystem inflammatory syndrome in children (MIS-C) and Kawasaki disease (KD) show distinct laboratory findings. MIS-C patients exhibit lower leukocytes, lymphocytes, and platelets but higher C-reactive protein and ferritin compared to KD.
Area of Science:
- Pediatric rheumatology
- Infectious diseases
- Clinical immunology
Background:
- Multisystem inflammatory syndrome in children (MIS-C) shares clinical similarities with Kawasaki disease (KD).
- Distinguishing MIS-C from KD is crucial for appropriate patient management and understanding disease pathogenesis.
- Laboratory parameters offer potential biomarkers to differentiate these conditions.
Purpose of the Study:
- To systematically review and meta-analyze laboratory parameters in MIS-C.
- To compare laboratory findings of MIS-C with those of KD and Kawasaki disease shock syndrome (KDSS).
- To identify key laboratory differences aiding in the diagnosis and understanding of MIS-C.
Main Methods:
- Systematic review and meta-analysis of published studies.
- Searched databases for laboratory parameters (hematology, inflammatory, cardiac, biochemistry) of MIS-C.
- Included twelve studies with 3073 participants (969 MIS-C patients).
Main Results:
- MIS-C patients had lower leukocytes, lymphocyte count, and platelet count (PLT) than KD patients.
- MIS-C patients showed higher C-reactive protein, D-dimer, and ferritin, but similar procalcitonin and erythrocyte sedimentation rate (ESR) compared to KD.
- Differences in cardiac markers (higher CPK in MIS-C) and biochemistry (lower albumin, sodium; higher creatinine in MIS-C) were observed.
Conclusions:
- Laboratory parameters significantly differ between MIS-C and KD.
- Distinct hematological and inflammatory profiles may help differentiate MIS-C from KD and KDSS.
- Further research into these laboratory markers can aid clinical evaluation and mechanistic studies of MIS-C.
Abstract:
Multisystem inflammatory syndrome in children (MIS-C) associated with coronavirus disease 2019 (COVID-19) has been described to partially overlap with Kawasaki disease (KD) with regard to clinical symptoms, but they are unlikely to share the same disease entity. We conducted a systematic review and meta-analysis to characterize the laboratory parameters of MIS-C compared with those of KD and Kawasaki disease shock syndrome (KDSS). Databases were searched for studies on laboratory parameters of MIS-C (hematology, inflammatory markers, cardiac markers, and biochemistry) through May 31, 2021. Twelve studies with 3073 participants yielded 969 MIS-C patients. In terms of hematology, MIS-C patients had lower levels of leukocytes, absolute lymphocyte count and platelet count (PLT) than KD patients and had similar absolute neutrophil count (ANC) and hemoglobin (Hb) levels. In terms of inflammatory markers, MIS-C patients had higher levels of C-reactive protein, D-dimer and ferritin than KD patients and had similar levels of procalcitonin and erythrocyte sedimentation rate (ESR). In terms of cardiac markers, MIS-C patients had higher CPK levels than KD patients. The levels of N-terminal pro-brain natriuretic peptide, troponin and aspartate aminotransferase were not significantly different between MIS-C and KD patients. In terms of biochemistry, MIS-C patients had lower levels of albumin, sodium and alanine aminotransferase and higher levels of creatinine than KD patients. In addition, MIS-C patients had lower levels of PLT, Hb and ESR and higher levels of ANC than KDSS patients. Measurement of laboratory parameters might assist clinicians with accurate evaluation of MIS-C and further mechanistic research.
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