Abstract
Dendritic cells (DCs), the most abundant antigen-presenting cells in the lung, have been drawing attention for their roles in specific allergic responses to aeroallergens with support of Th lymphocytes, and in persistent inflammatory changes in allergic asthma. To identify genetic factors that may be involved in the asthma susceptibility and development of the disease phenotypes, we examined association of DC-specific DCNP1 polymorphisms with the disease risk. The case-control study revealed association of the nucleotide variants with serum immunoglobulin E (IgE) levels specific for Dermatophagoides farinae (Der f 1) and Dermatophagoides pteronyssinus (Der p 1), major aeroallergens of dust mites, among subjects with asthma. In particular, the T-allele-carrying genotype frequencies for one of the variants (c.-1289C>T) located in the promoter region were found increased in the asthmatic group with low levels of the mite-specific IgE (odds ratio (OR)=0.63 (0.48-0.83) for Der p 1). Results from functional analyses indicated that the promoter variant would affect the gene expression by modulating DNA-protein interaction. We propose that the genetic polymorphism of DCNP1 may influence production of specific IgE by altering DC functions in the mite allergen presenting and/or processing. The functional relevance of the genetic variation would provide an important insight into the genetic basis of allergic response to the mite antigens.
Original language | English |
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Pages (from-to) | 369-378 |
Number of pages | 10 |
Journal | Genes and Immunity |
Volume | 8 |
Issue number | 5 |
DOIs | |
Publication status | Published - Jul 2007 |
Bibliographical note
Funding Information:We are grateful to Dr Akira Takashima from University of Texas Southwestern Medical Center for generously donating us XS106 and NS47 cells for this study. We also thank Dr Yasuharu Nishimura’s group from Kumamoto University for advices concerning DC line selection for transfection. We appreciate Hye Ree Han and Min Jin Go’s helpful comments on the association analyses. This work was supported by the National Institute of Health (National Budget Code 348-6111-221), Korea Health 21 R&D Project (00-PJ3-PG6-GN07-001) and the Ministry of Health & Welfare, Republic of Korea (01-PJ3-PG6-01GN04-003).