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Increased interleukin-10 and interferon-γ levels in Plasmodium vivax malaria suggest a reciprocal regulation which is not altered by IL-10 gene promoter polymorphism

机译:间日疟原虫疟疾中白细胞介素10和干扰素-γ水平的增加表明相互调节,但IL-10基因启动子多态性不会改变

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摘要

BackgroundIn human malaria, the naturally-acquired immune response can result in either the elimination of the parasite or a persistent response mediated by cytokines that leads to immunopathology. The cytokines are responsible for all the symptoms, pathological alterations and the outcome of the infection depends on the reciprocal regulation of the pro and anti-inflammatory cytokines. IL-10 and IFN-gamma are able to mediate this process and their production can be affected by single nucleotide polymorphisms (SNPs) on gene of these cytokines. In this study, the relationship between cytokine IL-10/IFN-gamma levels, parasitaemia, and their gene polymorphisms was examined and the participation of pro-inflammatory and regulatory balance during a natural immune response in Plasmodium vivax-infected individuals was observed.MethodsThe serum levels of the cytokines IL-4, IL-12, IFN-gamma and IL-10 from 132 patients were evaluated by indirect enzyme-linked immunosorbent assays (ELISA). The polymorphism at position +874 of the IFN-gamma gene was identified by allele-specific polymerase chain reaction (ASO-PCR) method, and the polymorphism at position -1082 of the IL-10 gene was analysed by PCR-RFLP (PCR-Restriction Fragment Length Polymorphism).ResultsThe levels of a pro- (IFN-gamma) and an anti-inflammatory cytokine (IL-10) were significantly higher in P. vivax-infected individuals as compared to healthy controls. The IFN-gamma levels in primoinfected patients were significantly higher than in patients who had suffered only one and more than one previous episode. The mutant alleles of both IFN-gamma and IL-10 genes were more frequent than the wild allele. In the case of the IFNG+874 polymorphism (IFN-gamma) the frequencies of the mutant (A) and wild (T) alleles were 70.13% and 29.87%, respectively. Similar frequencies were recorded in IL-10-1082, with the mutant (A) allele returning a frequency of 70.78%, and the wild (G) allele a frequency of 29.22%. The frequencies of the alleles associated with reduced production of both IFN-gamma and IL-10 were high, but this effect was only observed in the production of IFN-gamma.ConclusionsThis study has shown evidence of reciprocal regulation of the levels of IL-10 and IFN-gamma cytokines in P. vivax malaria, which is not altered by the presence of polymorphism in the IL-10 gene.
机译:背景技术在人类疟疾中,自然获得的免疫反应可导致寄生虫的消除或由导致免疫病理的细胞因子介导的持续反应。细胞因子负责所有症状,病理改变,感染的结果取决于促炎和抗炎细胞因子的相互调节。 IL-10和IFN-γ能够介导这一过程,其产生可能受到这些细胞因子基因上的单核苷酸多态性(SNP)的影响。在这项研究中,研究了细胞因子IL-10 /IFN-γ水平,寄生虫血症及其基因多态性之间的关系,并观察了间日疟原虫感染个体在自然免疫应答过程中促炎和调节平衡的参与。通过间接酶联免疫吸附试验(ELISA)评估了132例患者的血清细胞因子IL-4,IL-12,IFN-γ和IL-10水平。通过等位基因特异性聚合酶链反应(ASO-PCR)方法鉴定了IFN-γ基因+874位的多态性,并通过PCR-RFLP(PCR-PCR)分析了IL-10基因-1082位的多态性。结果显示,感染间日疟原虫的个体中pro-(IFN-γ)和抗炎细胞因子(IL-10)的水平明显高于健康对照。原发感染患者中的IFN-γ水平明显高于仅经历过一次且多于一次的患者。 IFN-γ和IL-10基因的突变等位基因均比野生等位基因更频繁。对于IFNG + 874多态性(IFN-γ),突变(A)和野生(T)等位基因的频率分别为70.13%和29.87%。 IL-10-1082中记录了相似的频率,其中突变(A)等位基因的频率为70.78%,而野生(G)等位基因的频率为29.22%。与IFN-γ和IL-10产生减少相关的等位基因频率很高,但仅在IFN-γ产生时才观察到这种影响。结论这项研究显示了IL-10水平相互调节的证据。间日疟原虫中的IFN-γ和IFN-γ细胞因子,IL-10基因中存在多态性不会改变。

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