PMID- 25749780 OWN - NLM STAT- PubMed-not-MEDLINE DCOM- 20150404 LR - 20201001 IS - 2092-7355 (Print) IS - 2092-7363 (Electronic) IS - 2092-7355 (Linking) VI - 7 IP - 3 DP - 2015 May TI - Association of Single Nucleotide Polymorphisms in the MD-2 Gene Promoter Region With Der p 2 Allergy. PG - 249-55 LID - 10.4168/aair.2015.7.3.249 [doi] AB - PURPOSE: Sensitization to house dust mite (Dermatophagoides pteronyssinus) is a considerable risk factor for the progression of allergic disease. The group 2 allergen from Dermatophagoides pteronyssinus, Der p 2, is considered a major one in patients with specific immunoglobulin E (IgE) to Der p 2. Der p 2 has structural homology with myeloid differentiation 2 (MD-2), which is involved in the lipopolysaccharide-binding component of the Toll-like receptor 4 signaling pathway and the development of inflammation. The aim of this study was to examine the genetic association of single nucleotide polymorphisms (SNPs) in the promoter region of MD-2 with Der p 2-sensitive allergy. METHODS: We investigated associations between cohort's characteristics, including 280 allergic and 80 healthy subjects by examining total IgE, eosinophils, D. pteronyssinus-specific IgE, Der p 2-specific IgE, the number of IgE-producing B cells induced by Der p 2, and the odds ratio of allergic symptoms. RESULTS: Based on the 1,000 genome project data, the minor allele frequencies of the rs1809441 and rs1809442 are 0.467 and 0.474, respectively. However, the correlation of linkage disequilibrium (LD) between these 2 SNPs is D'=1, the genotype frequencies of the 2 MD-2 (LY96) SNPs (rs1809441 and rs1809442) that are located nearby were significantly different between allergic and health subjects: the TT genotype of rs1809441 and the GG genotype of rs1809442 were more frequent in allergic subjects than in healthy subjects (16.1% vs 2.5% in both genotypes). The allergic patients with these genotypes exhibited significantly higher levels of D. pteronyssinus-specific IgE and Der p 2-specific Ig E, and a larger number of Der p 2-activated B cells. In addition, these 2 SNPs in the MD-2 promoter region were significantly associated with the prevalence of nasal, skin, and asthmatic allergic symptoms. CONCLUSIONS: Our results indicated that 2 SNPs in the MD-2 promoter region were significantly associated with Der p 2-specific Ig E, and thereby suggest that these SNPs may play a major role in susceptibility to Der p 2-triggered immune responses in a Taiwanese population. FAU - Liao, En Chih AU - Liao EC AD - Center for Translational Medicine, Department of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan.; Department of BioIndustry Technology, Da Yeh University, Changhua, Taiwan.; Department of Medical Technology, Jen-Ten College of Medicine, Nursing and Management, Miaoli, Taiwan. FAU - Chang, Ching Yun AU - Chang CY AD - Division of Allergy, Immunology & Rheumatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan. FAU - Wu, Chia Che AU - Wu CC AD - Department of Mechanical Engineering, National Chung-Hsing University, Taichung, Taiwan. FAU - Wang, Gou Jen AU - Wang GJ AD - Graduate Institute of Biomedical Engineering, National Chung-Hsing University, Taichung, Taiwan. FAU - Tsai, Jaw Ji AU - Tsai JJ AD - Division of Allergy, Immunology & Rheumatology, Department of Internal Medicine, Taichung Veterans General Hospital, Taichung, Taiwan.; College of Life Sciences, National Chung-Hsing University, Taichung, Taiwan.; Institute of Clinical Medicine, National Yang Ming University, Taipei, Taiwan. jawji@vghtc.gov.tw. LA - eng PT - Journal Article DEP - 20150305 PL - Korea (South) TA - Allergy Asthma Immunol Res JT - Allergy, asthma & immunology research JID - 101518382 PMC - PMC4397365 OTO - NOTNLM OT - Der p 2 OT - Dermatophagoides pteronyssinus OT - mite allergy OT - myeloid differentiation-2 (MD-2) OT - single nucleotide polymorphisms (SNPs) COIS- There are no financial or other issues that might lead to conflict of interest. EDAT- 2015/03/10 06:00 MHDA- 2015/03/10 06:01 PMCR- 2015/05/01 CRDT- 2015/03/10 06:00 PHST- 2014/09/01 00:00 [received] PHST- 2014/10/31 00:00 [revised] PHST- 2014/11/10 00:00 [accepted] PHST- 2015/03/10 06:00 [entrez] PHST- 2015/03/10 06:00 [pubmed] PHST- 2015/03/10 06:01 [medline] PHST- 2015/05/01 00:00 [pmc-release] AID - 7.e24 [pii] AID - 10.4168/aair.2015.7.3.249 [doi] PST - ppublish SO - Allergy Asthma Immunol Res. 2015 May;7(3):249-55. doi: 10.4168/aair.2015.7.3.249. Epub 2015 Mar 5.