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艾滋病患者中Fas和FasL基因的基因组分析及其与疾病进展的无关性

Genomic analysis of Fas and FasL genes and absence of correlation with disease progression in AIDS.

作者信息

Vasilescu A, Heath S C, Diop G, Do H, Hirtzig T, Hendel H, Bertin-Maghit S, Rappaport J, Therwath A, Lathrop G M, Matsuda F, Zagury J-F

机构信息

Centre National de Génotypage, 2 rue Gaston Crémieux, 91000 Evry, France.

出版信息

Immunogenetics. 2004 Apr;56(1):56-60. doi: 10.1007/s00251-004-0664-3. Epub 2004 Mar 23.

Abstract

Apoptosis has been suggested as a major mechanism for the CD4(+) T-lymphocyte depletion observed in patients infected with human immunodeficiency virus 1 (HIV-1). To evaluate the impact of genetic variations to apoptosis during progression of acquired immunodeficiency syndrome (AIDS), we have performed an extensive genetic analysis of Fas and Fas ligand ( FasL) genes. The coding regions and promoters of these genes were resequenced in a cohort of 212 HIV-1-seropositive patients presenting extreme disease phenotypes and 155 healthy controls of Caucasian origin. Overall, 33 single nucleotide polymorphisms (SNPs) with an allele frequency >1% were identified and evaluated for their association with disease progression. Among them, 14 polymorphisms were newly characterized. We did not find any statistically significant association of Fas and FasL polymorphisms and haplotypes with AIDS progression.

摘要

细胞凋亡被认为是在感染人类免疫缺陷病毒1(HIV-1)的患者中观察到的CD4(+) T淋巴细胞耗竭的主要机制。为了评估基因变异对获得性免疫缺陷综合征(AIDS)进展过程中细胞凋亡的影响,我们对Fas和Fas配体(FasL)基因进行了广泛的基因分析。在212名呈现极端疾病表型的HIV-1血清阳性患者和155名高加索裔健康对照组成的队列中,对这些基因的编码区和启动子进行了重新测序。总体而言,鉴定出33个等位基因频率>1%的单核苷酸多态性(SNP),并评估了它们与疾病进展的关联。其中,14个多态性是新鉴定的。我们没有发现Fas和FasL多态性及单倍型与AIDS进展之间存在任何统计学上的显著关联。

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