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Published on: April 4, 2018
Genetic variants of CD209 associated with Kawasaki disease susceptibility
Ho-Chang Kuo1, Ying-Hsien Huang1, Shu-Chen Chien2
1Department of Pediatrics and Kawasaki Disease Center, Kaohsiung Chang Gung Memorial Hospital and Chang Gung University College of Medicine, Kaohsiung, Taiwan.
Insights
Genetic variations in CD209 are linked to Kawasaki disease susceptibility in children. These specific CD209 polymorphisms increase the risk of developing this inflammatory condition.
Area of Science:
- Immunology
- Genetics
- Pediatrics
Background:
- Kawasaki disease (KD) is a systemic vasculitis of unknown cause, predominantly affecting children in Asian countries.
- Dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin (DC-SIGN, CD209) plays a role in anti-inflammatory responses and is associated with KD susceptibility.
Purpose of the Study:
- To investigate the association between genetic polymorphisms of CD209 and the risk of developing Kawasaki disease.
- To determine if CD209 polymorphisms influence coronary artery lesion formation or treatment response to intravenous immunoglobulin (IVIG).
Main Methods:
- A total of 948 participants (381 KD patients, 567 controls) were analyzed.
- Nine tagging single nucleotide polymorphisms (SNPs) in the CD209 gene were genotyped using TaqMan allelic discrimination assays.
- Clinical data, including coronary artery lesions (CAL) and IVIG treatment outcomes, were collected.
Main Results:
- Significant associations were identified between specific CD209 polymorphisms (rs4804800, rs2287886, rs735240) and the risk of KD.
- Haplotype analysis revealed that A/A/G and G/A/G haplotypes in rs2287886/rs735239/rs735240 were associated with an increased risk of KD.
- No significant associations were found between CD209 polymorphisms and CAL formation or IVIG treatment responsiveness.
Conclusions:
- CD209 gene polymorphisms are associated with susceptibility to Kawasaki disease.
- These genetic variations do not appear to influence the risk of coronary artery lesion formation or the effectiveness of IVIG treatment in KD patients.
Background:
Kawasaki disease (KD) is a systemic vasculitis with unknown etiology mainly affecting children in Asian countries. Dendritic cell-specific intercellular adhesion molecule-3 grabbing non-integrin (DC-SIGN, CD209) in humans was showed to trigger an anti-inflammatory cascade and associated with KD susceptibility. This study was conducted to investigate the association between genetic polymorphisms of CD209 and the risk KD.
Methods:
A total of 948 subjects (381 KD and 567 controls) were recruited. Nine tagging SNPs (rs8112310, rs4804800, rs11465421, rs1544766, rs4804801, rs2287886, rs735239, rs735240, rs4804804) were selected for TaqMan allelic discrimination assay. Clinical phenotypes, coronary artery lesions (CAL) and intravenous immunoglobulin (IVIG) treatment outcomes were collected for analysis.
Results:
Significant associations were found between CD209 polymorphisms (rs4804800, rs2287886, rs735240) and the risk of KD. Haplotype analysis for CD209 polymorphisms showed that A/A/G haplotype (P = 0.0002, OR = 1.61) and G/A/G haplotype (P = 0.0365, OR = 1.52) had higher risk of KD as compared with G/G/A haplotype in rs2287886/rs735239/rs735240 pairwise allele analysis. There were no significant association in KD with regards to CAL formation and IVIG treatment responses.
Conclusion:
CD209 polymorphisms were responsible for the susceptibility of KD, but not CAL formation and IVIG treatment responsiveness.
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