首页> 外文期刊>Clinical and Experimental Immunology: An Official Journal of the British Society for Immunology >Polymorphisms of interleukin (IL)-4 receptor alpha and signal transducer and activator of transcription-6 (Stat6) are associated with increased IL-4Ralpha-Stat6 signalling in lymphocytes and elevated serum IgE in patients with Graves' disease.
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Polymorphisms of interleukin (IL)-4 receptor alpha and signal transducer and activator of transcription-6 (Stat6) are associated with increased IL-4Ralpha-Stat6 signalling in lymphocytes and elevated serum IgE in patients with Graves' disease.

机译:白细胞介素(IL)-4受体α和信号转导和转录激活因子6(Stat6)的多态性与Graves病患者淋巴细胞中IL-4Ralpha-Stat6信号的增加和血清IgE的升高有关。

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摘要

Activated interleukin (IL)-4Ralpha stimulates production of IgE through signal transducer and activator of transcription-6 (Stat6) activation in lymphocytes. Genetic studies have shown an association between polymorphisms in the genes encoding IL-4Ralpha and Stat6 and elevated serum IgE in patients with atopic disease. Some authors, including us, have reported an association of Graves' disease and elevated serum IgE. To analyse the relationship between IL-4Ralpha and Stat6 polymorphisms and elevated serum IgE in patients with Graves' disease, 169 patients with Graves' disease were studied. We investigated whether these polymorphisms affect IL-4Ralpha-Stat6 signalling in cultured human lymphocytes. A high frequency of both the Ile50 polymorphism in IL-4Ralpha and 13GT repeat variants of the Stat6 gene was observed in patients with Graves' disease and elevated serum IgE (Ile50 allele; P < 0.05, 13GT allele; P < 0.01 versus controls) but not in subjects with normal IgE. Cultured human lymphocytes with theIle50 IL-4Ralpha polymorphism and the 13GT repeat variant of Stat6 showed increased IL-4 (and/or IL-13)-induced Stat6 activation (2.7-fold; P < 0.05 and 2.2-fold; P < 0.05, respectively). These findings suggest that polymorphisms in the IL-4Ralpha and Stat6 genes play an important role in elevation of serum IgE through increased Stat6 action in patients with Graves' disease.
机译:活化的白介素(IL)-4Ralpha通过信号转导和淋巴细胞中的转录6(Stat6)激活剂来刺激IgE的产生。遗传学研究表明,特应性疾病患者的IL-4Ralpha和Stat6编码基因多态性与血清IgE升高之间存在关联。包括我们在内的一些作者报告说,格雷夫斯病与血清IgE升高有关。为了分析Graves病患者的IL-4Ralpha和Stat6多态性与血清IgE升高之间的关系,研究了169例Graves病患者。我们调查了这些多态性是否影响培养的人类淋巴细胞中的IL-4Ralpha-Stat6信号传导。在患有Graves病和血清IgE升高的患者中观察到Stat6基因的IL-4Ralpha和13GT重复变异体中Ile50多态性的高频率(Ile50等位基因; P <0.05,13GT等位基因; P <0.01与对照) IgE正常的受试者不适合。具有Ile50IL-4Rα多态性和Stat6的13GT重复变体的培养人淋巴细胞显示IL-4(和/或IL-13)诱导的Stat6激活增加(2.7倍; P <0.05和2.2倍; P <0.05,分别)。这些发现表明,IL-4Ralpha和Stat6基因的多态性在Graves病患者中通过增加Stat6的作用在提高血清IgE中起重要作用。

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