HLA DPB1*0201 allele is negatively associated with immunoglobulin E responsiveness specific for house dust mite allergens in Taiwan

Abstract
Background: House dust mite (HDM) Dermatophagoides pteronyssinus is the most important source of indoor allergens that cause allergic diseases in Taiwan. We prepared purified HDM allergens (Der p 1, Der p 2 and Der p 5) to detect allergen‐specific immunoglobulin (Ig) E responsiveness among a large number of test subjects. The robust genetic typing system for HLA class II genes also facilitated the study on association of HLA and allergic response toward HDM.Objective: This study intended to investigate the association between HLA class II alleles and the IgE responsiveness to the major allergens from HDM, D. pteronyssinus.Methods: Two hundred and forty‐eight subjects were selected for HLA association study. Plasma HDM allergen (Der p 1, Der p 2, Der p 5) ‐specific IgE and Der p 2‐specific IgG antibodies were detected by ELISA, while HLA class II ‐DRB1, ‐DQA1, ‐DQB1, ‐DPB1 genetic polymorphism was determined by polymerase chain reaction/sequence‐specific oligonucleotide probe hybridization (PCR/SSOPH). Statistical comparison of the allelic distribution of each HLA class II genes among the individuals with/without HDM allergen‐specific IgE and IgG antibodies were performed.Results: There was no significant association between HLA DRB1, DQB1, DQA1 alleles and HDM‐specific IgE responsiveness noted. Only DRB1*0803 and the linked DQA1*0103 alleles showed positive association with Der p 5‐specific IgE responsiveness. However, we found that HLA‐DPB1*1301 predisposed subjects to IgE responsiveness to HDM Der p 5. HLA DPB1*0501 was weakly associated with the IgE responsiveness to HDM Der p 1 and Der p 5. There was a strong negative association between the HLA‐DPB1*0201 allele with IgE responsiveness to Der p 1 (OR: 0.30, P ≤ 0.0001, P ≤ 0.0007, Pc ≤ 0.010).Conclusion: We clearly observed the association between HLA DPB1 alleles and specific IgE responsiveness to HDM major allergens. The molecular mechanism of HLA‐DPB1*0201 involvement in protecting subjects from HDM‐specific IgE responsiveness awaits further investigation.

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