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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干扰素白介素10和12的遗传变异对伊朗流行地区内脏利什曼病的影响

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摘要

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-γ 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-γ (+874 A/T). The results showed that at position +874 of IFN-γ, 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-γ 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.
机译:内脏利什曼病(VL)是一种危及生命的疾病,其中调节免疫应答的多种细胞因子可以决定其结局。基于基因中它们的区域,某些单核苷酸多态性(SNP)可以影响其相应蛋白的表达,本研究旨在研究IL-10,IL-12,IFN-γ基因中SNP与易感性的关系。 VL。该研究是针对120例VL患者,67例患者的家庭(家庭组)和102例利什曼宁皮肤试验阳性的健康个体作为阳性对照组进行的。使用PCR-RFLP分析IL-10(-592,-819,-1082),IL-12(+1188)中的SNP,并使用等位基因特异性聚合酶链反应(ASPCR)分析IFN-γ(+874)中的SNP在)。结果表明,在IFN-γ的+874位置,患者的AT基因型显着高于家庭和对照组,而家庭的TT基因型显着高于患者。研究组之间的IFN-γ等位基因分布没有显着差异。至于IL-12和IL-10的基因型和等位基因,两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之间观察到了强烈的连锁不平衡,但是在研究组之间,从IL-10等位基因重建的最常见单倍型和单基因型的分布没有显着差异。

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