The Expression of Glycoprotein Genes in the Inflammatory Process of Kawasaki Disease

Kuang-Che Kuo1, Ya-Ling Yang2, Mao-Hung Lo1,3

  • 1Department of Pediatrics, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.

Frontiers in Pediatrics
|December 21, 2020
PubMed

Insights

Investigating leukocyte glycoprotein genes in Kawasaki disease (KD) revealed HP, GRP84, and CLEC4D gene upregulation in acute phases. These genes predict KD and correlate with IVIG resistance, aiding understanding of KD pathogenesis.

Area of Science:

  • Pediatric rheumatology
  • Immunology
  • Genetics

Background:

  • Kawasaki disease (KD) is a leading cause of febrile coronary vasculitis in children.
  • Prompt diagnosis and treatment are crucial to prevent coronary artery lesions (CAL).
  • Genetic factors influence KD pathogenesis, particularly leukocyte-glycoprotein interactions in innate immunity.

Purpose of the Study:

  • To investigate the role of leukocyte glycoprotein genes during the acute phase of Kawasaki disease.
  • To assess the diagnostic and prognostic significance of specific gene expressions in KD.

Main Methods:

  • Quantitative real-time PCR was used to analyze HP, GRP84, and CLEC4D gene expression in leukocytes.
  • Study included 97 subjects: 24 healthy controls, 24 fever controls, and 49 KD patients (pre- and post-IVIG treatment).
  • ROC curve analysis was performed to evaluate predictive values.

Main Results:

  • HP, GRP84, and CLEC4D genes were significantly upregulated in peripheral leukocytes during acute KD compared to controls.
  • These genes showed positive correlations with each other and were effective KD predictors (auROC >0.87).
  • Gene hyper-expression correlated with IVIG resistance but not CAL formation.

Conclusions:

  • Leukocyte HP, GRP84, and CLEC4D gene expression are important in KD pathogenesis.
  • These genes play a role in the acute inflammatory process and primary IVIG response in KD.
  • Findings suggest potential biomarkers for KD diagnosis and treatment response.

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