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人类肿瘤坏死因子-α基因启动子区域多态性与硬化性苔藓无关。

Promoter region polymorphism in the human TNF-alpha gene is not associated with lichen sclerosus.

作者信息

Clay F E, Cork M J, Wilson A G, Crane A M, Lewis F, Harrington C I, Duff G W

机构信息

Section of Molecular Medicine, Royal Hallamshire Hospital, Sheffield, UK.

出版信息

Exp Dermatol. 1996 Aug;5(4):227-9. doi: 10.1111/j.1600-0625.1996.tb00121.x.

Abstract

The pathogenesis of lichen sclerosus remains unknown. However, it has been frequently associated clinically with autoimmunity. The MHC haplotype A1, B8, DR3 is associated with many autoimmune conditions and has also been associated with the uncommon allele of the tumour necrosis factor (TNF-alpha) promoter polymorphism. This allele is also associated with higher production of TNF in vivo and in vitro, and thus it has been speculated that it is the TNF-alpha gene which underlies the genetic association of many diseases with the autoimmune haplotype. There have been many reports of HLA associations with lichen scleroses, but these have not been concordant. We therefore decided to analyse the TNF-alpha polymorphism in patients with lichen scleroses to determine if TNF-alpha was likely to play a role in susceptibility or severity of lichen scleroses. No association between alleles of the TNF-alpha polymorphism and lichen scleroses was found.

摘要

硬化性苔藓的发病机制尚不清楚。然而,临床上它常与自身免疫相关。MHC单倍型A1、B8、DR3与许多自身免疫性疾病相关,也与肿瘤坏死因子(TNF-α)启动子多态性的罕见等位基因有关。该等位基因还与体内外更高的TNF产生相关,因此有人推测,TNF-α基因是许多疾病与自身免疫单倍型遗传关联的基础。有许多关于HLA与硬化性苔藓关联的报道,但结果并不一致。因此,我们决定分析硬化性苔藓患者的TNF-α多态性,以确定TNF-α是否可能在硬化性苔藓的易感性或严重程度中起作用。未发现TNF-α多态性等位基因与硬化性苔藓之间存在关联。

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