Le Page M E L, Goodridge J P, Zhang G, Holt P G, Sly P, Witt C S
School of Pathology and Laboratory Medicine, University of Western Australia, Perth, WA,, Australia.
Tissue Antigens. 2013 Oct;82(4):276-9. doi: 10.1111/tan.12185. Epub 2013 Aug 23.
Human leukocyte antigen (HLA)-G is upregulated on the bronchial epithelium of asthma patients and genetic polymorphism affecting expression of HLA-G has been reported to influence susceptibility to asthma. As the NK cell receptor KIR2DL4 has been reported to induce interferon gamma (IFNγ) secretion when ligated with HLA-G, we postulated that the 9A/10A genetic polymorphism of KIR2DL4 which influences receptor structure may influence susceptibility to asthma. KIR2DL4 genotypes were determined in two cohorts of children (n = 219 and n = 1356) in whom total serum IgE, allergen-specific IgE, atopy, bronchial reactivity and asthma symptoms had been studied between birth and 14 years. No reproducible associations with KIR2DL4 genotype were identified, leading us to conclude that the KIR2DL4 9A/10A polymorphism has no influence on susceptibility to asthma.
人类白细胞抗原(HLA)-G在哮喘患者的支气管上皮细胞上表达上调,据报道,影响HLA-G表达的基因多态性会影响哮喘易感性。由于据报道自然杀伤(NK)细胞受体KIR2DL4与HLA-G结合时会诱导γ干扰素(IFNγ)分泌,我们推测影响受体结构的KIR2DL4 9A/10A基因多态性可能会影响哮喘易感性。在两个儿童队列(n = 219和n = 1356)中确定了KIR2DL4基因型,这两个队列在出生至14岁期间研究了总血清IgE、过敏原特异性IgE、特应性、支气管反应性和哮喘症状。未发现与KIR2DL4基因型有可重复的关联,由此我们得出结论,KIR2DL4 9A/10A多态性对哮喘易感性没有影响。