首页> 外文期刊>Infection, Genetics and Evolution: Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases >Differential association of KIR gene loci to risk of malaria in ethnic groups of Assam, Northeast India
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Differential association of KIR gene loci to risk of malaria in ethnic groups of Assam, Northeast India

机译:印度东北部阿萨姆邦KIR基因位点与疟疾风险的差异关联

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Receptors encoded within the Natural Killer Cell (NKC) complex and Killer Immunoglobulin like (KIRs) genomic regions have been suggested to influence malaria pathogenesis and infection susceptibility. We have examined KIR locus in relation to risk of infection and disease in Tea tribes (TT) of Austro Asiatic affinity and Tibeto-Burman (TB) populations from malaria endemic regions of Assam. Consistent with differences in their genetic background, KIR gene loci frequencies differed in studied groups. Surprisingly, KIR3DS1 frequency in TT was low (17%) and comparable to that reported from African populations. KIR3DL1 frequency was positively associated with malaria severity (Pearson phi, R(2) = 0.297 p = 0.006) and logistic regression modelling predicted KIR3DL1 as a risk factor in complicated malaria [Odds Ratio (95% CI)] = [6.39 (1.34-30.60)]. An interaction between ethnicity and KIR3DL1 was also seen where higher proportion of KIR3DL1 positive and complicated malaria patients belonged to Tea tribes (p = 0.009). Notably, four activating genes protected from frequent malaria (p = 0.02) while six activating genes enhanced the risk of complicated malaria (p = 0.05). Combination of KIR2DS4, KIR2DS4del, KIR2DS5 negatively influenced disease outcome in Tea tribes (p = 0.048) but not in Tibeto-Burman. In conclusion our data indicates KIR gene loci differentially influenced malaria outcome in Tea tribes and Tibeto-Burman and that four activating genes appeared to provide optimal activation that protected from frequent episodes of malaria. Our data also indicated KIR3DS1 to be an ancestral genotype, maintained at low frequency possibly by malaria in the Austro Asiatic tribes. (C) 2011 Elsevier B.V. All rights reserved.
机译:已建议在自然杀伤细胞(NKC)复合体和杀伤免疫球蛋白样(KIRs)基因组区域内编码的受体会影响疟疾的发病机理和感染易感性。我们已经检查了与亚洲亲和力的茶部落(TT)和阿萨姆邦疟疾流行地区的藏缅人(TB)人口中的感染和疾病风险相关的KIR位点。与他们的遗传背景不同,KIR基因位点频率在研究组中也有所不同。出人意料的是,TT中的KIR3DS1频率很低(17%),与非洲人群报告的频率相当。 KIR3DL1频率与疟疾严重程度呈正相关(Pearson phi,R(2)= 0.297 p = 0.006),逻辑回归模型预测KIR3DL1是复杂疟疾的危险因素[几率(95%CI)] = [6.39(1.34- 30.60)]。在KIR3DL1阳性和复杂疟疾患者中,茶部落的比例更高,种族与KIR3DL1之间也存在相互作用(p = 0.009)。值得注意的是,四个激活基因可以预防常见的疟疾(p = 0.02),而六个激活基因则可以提高罹患复杂疟疾的风险(p = 0.05)。 KIR2DS4,KIR2DS4del和KIR2DS5的组合对茶部落的疾病结局具有负面影响(p = 0.048),而对藏缅部落则没有影响。总之,我们的数据表明,KIR基因位点在茶部落和藏缅部落中对疟疾的结局有不同的影响,并且四个激活基因似乎提供了最佳的激活作用,可以防止疟疾的频繁发作。我们的数据还表明,KIR3DS1是祖先的基因型,在亚洲的亚洲部落中可能由疟疾维持在较低的频率。 (C)2011 Elsevier B.V.保留所有权利。

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