首页> 外文期刊>Pediatric allergy and immunology: official publication of the European Society of Pediatric Allergy and Immunology >Association of TNF-alpha with severe respiratory syncytial virus infection and bronchial asthma.
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Association of TNF-alpha with severe respiratory syncytial virus infection and bronchial asthma.

机译:TNF-α与严重呼吸道合胞病毒感染和支气管哮喘的关系。

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摘要

Tumor necrosis factor (TNF-)alpha is a proinflammatory cytokine that is important in the innate host defence and thus in the defence of infectious agents. However, in excess it provokes the development of chronic inflammatory diseases. The aim of this study was to test association of TNF with severe RSV bronchiolitis as example of an infectious disease and asthma as representative for a chronic inflammatory condition. The following study populations were genotyped for 4 polymorphisms within TNF-beta (rs909253) and TNF-alpha (rs1799964, rs1799724, rs1800629): 322 asthmatic children, 151 children with severe respiratory syncytial virus (RSV) bronchiolitis and 270 controls. Furthermore, serum TNF-alpha levels were measured by a FlowCytomix Assay. Asthma showed association with two TNF-alpha polymorphisms as well as with TNF haplotypes (p = 0.0050). In contrast, RSV bronchiolitis was associated with TNF haplotypes (p < 0.00001) but not with any single polymorphism. In addition, TNF-alpha serum levels correlated with rs1799724 (p = 0.034). A genetically mediated up-regulation of TNF-alpha expression might provoke a pronounced inflammation of the airways and thus a more severe course of RSV infection as well as the onset of asthma. It remains to be elucidated whether severe RSV bronchiolitis starts TNF-alpha upregulation and is one first step in the direction to asthma later in life, or whether both diseases are independent from each other and supported by TNF-alpha upregulation.
机译:肿瘤坏死因子(TNF-α)是促炎细胞因子,在先天宿主防御中很重要,因此在传染原防御中也很重要。然而,过量地引起了慢性炎性疾病的发展。这项研究的目的是测试TNF与严重RSV细支气管炎的关系,例如感染性疾病,而哮喘则代表慢性炎症。对以下研究人群的TNF-beta(rs909253)和TNF-alpha(rs1799964,rs1799724,rs1800629)中的4个多态性进行基因分型:322例哮喘儿童,151例患有严重呼吸道合胞病毒(RSV)细支气管炎的儿童和270名对照。此外,通过FlowCytomix测定法测量血清TNF-α水平。哮喘显示与两种TNF-α多态性以及TNF单倍型相关(p = 0.0050)。相反,RSV细支气管炎与TNF单倍型相关(p <0.00001),但与任何单个多态性均不相关。此外,TNF-α血清水平与rs1799724相关(p = 0.034)。基因介导的TNF-α表达上调可能引起气道明显炎症,从而引起更严重的RSV感染过程以及哮喘发作。严重的RSV细支气管炎是否会开始TNF-α的上调,并且是朝着晚年哮喘方向迈出的第一步,或者两种疾病是否相互独立并受到TNF-α的上调支持,尚待阐明。

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