Polymorphisms of human leukocyte antigen genes in korean children with Kawasaki disease
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Updated: Jul 9, 2026

qKAT: Quantitative Semi-automated Typing of Killer-cell Immunoglobulin-like Receptor Genes
Published on: March 6, 2019
Jin Hee Oh1, Ji Whan Han, Soon Ju Lee
1Department of Pediatrics, College of Medicine, The Catholic University of Korea, Seoul, Republic of Korea.
Insights
Human leukocyte antigen (HLA) gene variations are linked to Kawasaki disease in Korean children. Specific HLA-B and HLA-C alleles increase susceptibility, while certain HLA-DRB1 alleles are associated with coronary complications.
Area of Science:
- Immunogenetics
- Pediatric Cardiology
- Molecular Genetics
Background:
- Kawasaki disease is a primary cause of acquired heart disease in children.
- Prevalence of Kawasaki disease differs across ethnic groups.
- Human Leukocyte Antigen (HLA) polymorphisms are increasingly linked to various diseases via DNA analysis.
Purpose of the Study:
- To investigate the association between HLA alleles and the risk of developing Kawasaki disease in Korean children.
- To determine if specific HLA alleles are linked to coronary complications in pediatric patients with Kawasaki disease.
Main Methods:
- DNA was extracted from 74 children diagnosed with Kawasaki disease.
- HLA-A, -B, -C, and -DRB1 allele polymorphisms were analyzed using PCR-ARMS and PCR-SSP.
- Patient polymorphisms were compared against 159 healthy control subjects.
Main Results:
- Significant increases in HLA-B35, -B75, and -Cw09 allele frequencies were observed in Kawasaki disease patients versus controls.
- No significant increase in HLA-DRB1 allele frequency was found in Kawasaki disease patients compared to controls.
- Kawasaki disease patients with coronary complications showed increased frequencies of HLA-DRB1*11 and HLA-DRB1*09 compared to healthy controls and subgroups.
Conclusions:
- Polymorphisms in specific HLA class I alleles (B and C) are associated with Kawasaki disease susceptibility in Korean children.
- Certain HLA-DRB1 alleles may be linked to the development of coronary complications in Kawasaki disease.
Background:
Kawasaki disease is a leading cause of acquired heart disease in children. The prevalence rate varies in different ethnic groups. Recently, with the clinical application of molecular genetic technology, human leukocyte antigen (HLA) polymorphisms associated with several diseases have been identified by DNA analysis. This study aimed to assess the association of HLA alleles with susceptibility and complications of Kawasaki disease in Korean children.
Methods:
In this study, DNA was extracted from 74 children with a diagnosis of Kawasaki disease. The polymorphisms of the HLA-A, -B, -C, and -DRB1 alleles of patients with Kawasaki disease were determined by polymerase chain reaction (PCR)-amplification refractory mutation system (ARMS) and PCR-sequence-specific primer (SSP) analysis. The polymorphisms identified were compared with those of 159 normal healthy control subjects.
Results:
There was a significant increase in the frequencies of the HLA-B35, -B75, and -Cw09 alleles in patients with Kawasaki disease compared with the healthy control group. There was no increase in the frequency of HLA-DRB1 alleles among the Kawasaki disease patients compared with a healthy control group. When the patients with Kawasaki disease were divided into two subgroups, with or without coronary complications, the Kawasaki disease patients with coronary complications showed a significantly increased frequency of the HLA-DRB1*11 allele compared with the healthy control group and increased frequency of HLA-DRB1*09 in a comparison of the subgroups.
Conclusions:
This study suggests that polymorphisms in some alleles of B and C in HLA class I genes are associated with Kawasaki disease in Korean children.
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