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Hum Immunol ; 78(2): 88-94, 2017 Feb.
Article in English | MEDLINE | ID: mdl-27780790

ABSTRACT

BACKGROUND: Type I hypersensitivity, also known as IgE-mediated allergy, is a complex, multifactorial condition whose onset and severity are influenced by both genetic and environmental factors. Mite allergens stimulate the production of humoral response (IgE), especially in children, which is closely involved in atopic asthma and rhinitis. OBJECTIVE: This study aimed to investigate the association between HLA class I (-A, -B, and -C), and HLA class II (-DRB1) genes in individuals sensitive to dust mites (Dermatophagoides farinae, Dermatophagoides pteronyssinus, or Blomia tropicalis) and mite-insensitive controls. METHODS: 396 participants were grouped as mite-sensitive and mite-insensitive according to immediate hypersensitivity as determined by skin-prick tests, and to HLA genotyping by polymerase chain reaction-sequence specific oligonucleotide (PCR-SSO). RESULTS: After chi-square heterogeneity testing no significant differences were observed in HLA-A, B, and C genes, except for the HLA-DRB1 locus, which, showed a negative association for DRB1∗04, between mite-sensitive and mite-insensitive individuals. In high resolution, DRB1∗04:11 allele was significantly different from all other results (P=0.0042, OR=0.26, and 95%CI=0.09-0.70). The analysis stratified by etiologic agent confirmed these associations. CONCLUSION: Our results suggest a possible association between HLA-DRB1 genes and hypersensitivity to dust mites.


Subject(s)
Asthma/genetics , HLA-DRB1 Chains/genetics , Hypersensitivity/genetics , Adolescent , Adult , Animals , Antigens, Dermatophagoides/adverse effects , Antigens, Dermatophagoides/immunology , Asthma/etiology , Brazil , Child , Child, Preschool , Dermatophagoides pteronyssinus , Female , Gene Frequency , Gene-Environment Interaction , Genetic Association Studies , Genetic Predisposition to Disease , Genotype , Humans , Hypersensitivity/complications , Immunoglobulin E/blood , Male , Middle Aged , Polymorphism, Genetic , Young Adult
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