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首页> 外文期刊>Annals of allergy, asthma, and immunology >A familial study of filaggrin mutation in atopic dermatitis
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A familial study of filaggrin mutation in atopic dermatitis

机译:特征性皮炎中叶虫突变突变的家族研究

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with any severity of egg allergy and that these patients can be vaccinated safely with a single dose of IIV, without requiring administration by an allergist, which otherwise poses an unnecessary barrier to immunization and is not justified based on available safety data.Two new influenza vaccines not grown in eggs have been approved for patients 18 years and older; Flucelvax,6 prepared from virus propagated in cell culture, and Flublok,7 recombinant hemagglutinin proteins produced in an insect cell line.Filaggrin is an epidermal structural protein critical for the development of a functional skin barrier. People who have null mutations in the FLG gene are at increased susceptibility of atopic dermatitis (AD), peanut allergy, and asthma associated with AD.1-4 AD has a high familial occurrence evidenced by concordance rates of 0.72 to 0.77 in monozygotic and 0.15 to 0.23 in dizygotic twin pairs.5 These studies were primarily carried out in Northern Europe, particularly in large cohorts in Ireland, where there is a high prevalence of FLG mutations in AD.The identification of a genetic defect as a key event in the path-ophysiology of AD and allergic sensitization has brought up many clinical questions among sufferers. On reading "Filaggrin Mutations Associated with Skin and Allergic Diseases" by Irvine, McLean, and Leung, published in 2011 The New England Journal of Medicine, a 91-year-old physician who suffered from lifelong atopic disease contacted the authors to determine whether FIG mutation could predict which of his 4 generations of family members were prone to AD or asthma and whether any environmental factors increased or decreased the risk of developing disease. Only early life cat exposure and exposure to other children have shown an additional interactive risk of AD in patients with FLG mutation.These studies were birth cohort studies, and no family pedigree study has been used to study gene-environment interactions for FLG mutation.
机译:随着蛋过敏的任何严重性,并且这些患者可以用单一剂量的IIV疫苗,而不需要通过过敏症施用,这否则对免疫的不必要的屏障并基于可用的安全性数据来证明WO新型流感疫苗未在18岁及以上患者批准鸡蛋种植;在细胞培养中繁殖的病毒制备的6种氟虫毛细血管,以及在昆虫细胞系中产生的7种重组血凝素蛋白。菲拉林是对功能性皮肤屏障的发展至关重要的表皮结构蛋白。在FLG基因中具有零突变的人们正在增加特应性皮炎(AD),花生过敏,与AD1-4的哮喘有关的哮喘,并且单一程度和0.15的一致性率为0.72至0.77的高处理发生。 Dizygotic Twin对中的0.23分.5这些研究主要是在北欧进行的,特别是在爱尔兰的大型队列中进行,在广告中的FLG突变普及。遗传缺陷作为路径中的关键事件的鉴定 - 广告和过敏性致敏的生物学在患者之间提出了许多临床问题。通过Irvine,Mclean和Leung阅读“皮肤和过敏性疾病相关的叶片突变”,于2011年发表于2011年新英格兰医学杂志,这是一个91岁的医生,遭受终身特应疾病的终身疾病,联系了作者来确定是否无花果突变可以预测他的4代家庭成员中哪一种易患广告或哮喘以及任何环境因素是否增加或减少了发展疾病的风险。只有早期生命的猫暴露和接触其他儿童都表明了FLG突变患者的额外的互动风险。这些研究是出生队列研究,并且没有用于研究FLG突变的基因环境相互作用。

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