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CD55基因的功能性变异会增加2009年甲型H1N1大流行性流感病毒感染的严重程度。

A functional variation in CD55 increases the severity of 2009 pandemic H1N1 influenza A virus infection.

作者信息

Zhou Jie, To Kelvin Kai-Wang, Dong Hui, Cheng Zhong-Shan, Lau Candy Choi-Yi, Poon Vincent K M, Fan Yan-Hui, Song You-Qiang, Tse Herman, Chan Kwok-Hung, Zheng Bo-Jian, Zhao Guo-Ping, Yuen Kwok-Yung

机构信息

Department of Microbiology, The University of Hong Kong, Queen Mary Hospital, Pokfulam Rd, Pokfulam, Hong Kong Special Administrative Region, China.

出版信息

J Infect Dis. 2012 Aug 15;206(4):495-503. doi: 10.1093/infdis/jis378. Epub 2012 Jun 12.

Abstract

Infection due to 2009 pandemic H1N1 influenza A virus (A[H1N1]pdm09) is commonly manifested as mild infection but occasionally as severe pneumonia. We hypothesized that host genetic variations may contribute to disease severity. An initially small-scale genome-wide association study guided the selection of CD55 single-nucleotide polymorphisms in 425 Chinese patients with severe (n = 177) or mild (n = 248) disease. Carriers of rs2564978 genotype T/T were significantly associated with severe infection (odds ratio, 1.75; P = .011) under a recessive model, after adjustment for clinical confounders. An allele-specific effect on CD55 expression was revealed and ascribed to a promoter indel variation, which was in complete linkage disequilibrium with rs2564978. The promoter variant with deletion exhibited significantly lower transcriptional activity. We further demonstrated that CD55 can protect respiratory epithelial cells from complement attack. Additionally, A(H1N1)pdm09 infection promoted CD55 expression. In conclusion, CD55 polymorphisms are associated with severe A(H1N1)pdm09 infection. CD55 may exert a substantial impact on the disease severity of A(H1N1)pdm09 infection.

摘要

2009年甲型H1N1流感大流行病毒(A[H1N1]pdm09)感染通常表现为轻度感染,但偶尔也会发展为重症肺炎。我们推测宿主基因变异可能与疾病严重程度有关。一项最初规模较小的全基因组关联研究指导我们在425例患有重症(n = 177)或轻症(n = 248)的中国患者中选择CD55单核苷酸多态性进行研究。在对临床混杂因素进行校正后,rs2564978基因型T/T的携带者在隐性模型下与重症感染显著相关(比值比,1.75;P = 0.011)。研究揭示了对CD55表达的等位基因特异性效应,并将其归因于启动子插入/缺失变异,该变异与rs2564978处于完全连锁不平衡状态。具有缺失的启动子变异表现出显著较低的转录活性。我们进一步证明,CD55可保护呼吸道上皮细胞免受补体攻击。此外,A(H1N1)pdm09感染可促进CD55表达。总之,CD55多态性与重症A(H1N1)pdm09感染相关。CD55可能对A(H1N1)pdm09感染的疾病严重程度产生重大影响。

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