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首页> 外文期刊>Pathogens and global health >Influence of genetic variants of gamma interferon, interleukins 10 and 12 on Visceral Leishmaniasis in an endemic area, Iran
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Influence of genetic variants of gamma interferon, interleukins 10 and 12 on Visceral Leishmaniasis in an endemic area, Iran

机译:γ干扰素,白细胞介素10和12遗传变异对伊朗地方地区内脏Leishmaniaisis的影响

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Visceral leishmaniasis (VL) is a life threatening disease in which a variety of cytokines regulating the immune responses can determine its outcome. As based on their region in the gene, some single nucleotide polymorphisms (SNP) can influence the expression of their corresponding proteins, this study aimed to investigate the association between SNP in the IL-10, IL-12, IFN-gamma genes and susceptibility to VL. The study was carried out on 120 patients with VL, 67 patients' families (family group), and 102 healthy individuals with positive leishmanin skin test as positive control group. SNPs in IL-10 (-592, -819, -1082), IL-12 (+1188) were analyzed using PCR-RFLP and allele specific polymerase chain reaction (ASPCR) was used to analyze SNPs in IFN-gamma (+874 A/T). The results showed that at position +874 of IFN-gamma, AT genotype was significantly more frequent in patients than that in families and controls, but TT genotype was significantly more frequent in families than in patients. Distributions of IFN-gamma alleles were not significantly different between the study groups. As for IL-12 and IL-10 genotypes and alleles, no significant difference was observed between the groups. Although a strong linkage disequilibrium was observed between alleles -592, -819 and -1082 of IL-10, distributions of the most common haplotypes and haplogenotypes reconstructed from IL-10 alleles were not significantly different between the study groups. It could be suggested that heritage of AT genotype at position +874 of IFN-gamma may predispose and TT genotype can resist individual to VL in an endemic area in the southwest of Iran.
机译:内脏LeishManiaisis(VL)是一种危及危及危及疾病,其中调节免疫应答的各种细胞因子可以确定其结果。根据基于其基因的区域,一些单一核苷酸多态性(SNP)可以影响其相应蛋白质的表达,该研究旨在研究IL-10,IL-12,IFN-γ基因和易感性SNP之间的关联到vl。该研究于120例VL,67名患者家庭(家族(家族)和102名健康个体进行的研究进行,阳性Leishmanin皮肤测试为阳性对照组。使用PCR-RFLP分析IL-10(-592,-819,-1082)中的SNP,使用PCR-RFLP和等位基因特异性聚合酶链反应(ASPCR)分析IFN-GAMMA中的SNPS(+874在)。结果表明,在IFN-Gamma的位置+874,在基因型中的患者显着更频繁,但在家庭和对照中的情况下显着更频繁,但在家庭中,TT基因型比患者在患者中经常更频繁。研究组之间IFN-γ等位基因的分布没有显着差异。至于IL-12和IL-10基因型和等位基因,在组之间没有观察到显着差异。尽管在IL-10的等位基因-59​​2,-819和-1082之间观察到强烈的连锁不平衡,但从IL-10等位基因中重建的最常见的单倍型和储备型的分布在研究组之间没有显着差异。可以建议在IFN-γ的位置+874的基因型的遗产可以易受,并且TT基因型可以将个体抵抗伊朗西南部的流行区域中的vl。

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