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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.
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.
Abstract:
Background: Kawasaki disease (KD) is the most common form of febrile coronary vasculitis disease to occur in children. Early diagnosis and proper therapy can prevent the complication of coronary artery lesions (CAL). The main pathogenesis of KD is an inflammatory process related to the host's genetic characteristics. In innate human immunity, the interaction of leukocytes and glycoprotein plays an important role against microbes. The purpose of our study was to understand the role of leukocytes' glycoprotein genes during the acute phase of KD. Materials and Methods: We enrolled a total of 97 subjects from a medical center. Of those, 24 subjects were healthy controls, and 24 subjects were fever controls; the other 49 subjects were KD patients who had had blood samples taken both before and after IVIG treatment. We collected the total RNA from leukocytes and performed a quantitative polymerase chain reaction for the HP, GRP84, and CLEC4D genes in real time. Results: Compared with both the healthy and fever controls, the upregulation of HP, GRP84, and CLEC4D genes was significant in peripheral leukocytes during acute-phase KD. The transcriptional level of these respective genes not only demonstrated a positive correlation with each other, but were also effective predictors for KD (all auROC >0.87) according to the ROC curve analysis. The hyper-expression of these three genes was significantly associated with IVIG resistance, but not CAL formation. Conclusions: Our study demonstrates that the expression of HP, GRP84, and CLEC4D genes of leukocytes play an important role in the pathogenesis and primary IVIG response during the acute inflammatory process of KD.
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