a Department of immunology , Alborzi Clinical Microbiology Research Center, Shiraz University of Medical Sciences , Shiraz , Iran.
Pathog Glob Health. 2019 Feb;113(1):14-19. doi: 10.1080/20477724.2019.1568034. Epub 2019 Jan 15.
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. It could be suggested that heritage of AT genotype at position +874 of IFN-γ may predispose and TT genotype can resist individual to VL in an endemic area in the southwest of Iran.
内脏利什曼病(VL)是一种危及生命的疾病,其中调节免疫反应的各种细胞因子可以决定其结局。由于基于其在基因中的位置,一些单核苷酸多态性(SNP)可以影响其相应蛋白质的表达,本研究旨在调查 IL-10、IL-12、IFN-γ 基因中的 SNP 与 VL 易感性之间的关联。该研究在 120 名 VL 患者、67 名患者家属(家庭组)和 102 名利什曼菌素皮肤试验阳性的健康个体(阳性对照组)中进行。使用 PCR-RFLP 分析了 IL-10(-592、-819、-1082)和 IL-12(+1188)中的 SNP,并用等位基因特异性聚合酶链反应(ASPCR)分析了 IFN-γ(+874 A/T)中的 SNP。结果显示,在 IFN-γ 的+874 位,患者的 AT 基因型明显比家庭和对照组多,而 TT 基因型则明显比家庭组多。各组 IFN-γ 等位基因的分布无显著性差异。对于 IL-12 和 IL-10 基因型和等位基因,各组之间无显著性差异。尽管 IL-10 的-592、-819 和-1082 等位基因之间存在很强的连锁不平衡,但从 IL-10 等位基因重建的最常见单倍型和单倍型的分布在各组之间无显著性差异。可以认为,IFN-γ 的+874 位 AT 基因型的遗传可能使个体易患 VL,而 TT 基因型可能使其在伊朗西南部的流行地区具有抗性。