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Type I interferon related genes are common genes on the early stage after vaccination by meta-analysis of microarray data

机译:通过基因芯片数据的荟萃分析,I型干扰素相关基因是疫苗接种后早期的常见基因。

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The objective of this study was to find common immune mechanism across different kinds of vaccines. A meta-analysis of microarray datasets was performed using publicly available microarray Gene Expression Omnibus (GEO) and Array Express data sets of vaccination records. Seven studies (out of 35) were selected for this meta-analysis. A total of 447 chips (145 pre-vaccination and 302 post-vaccination) were included. Significance analysis of microarrays (SAM) program was used for screening differentially expressed genes (DEGs). Functional pathway enrichment for the DEGs was conducted in DAVID Gene Ontology (GO) database. Twenty DEGs were identified, of which 10 up-regulated genes involved immune response. Six of which were type I interferon (IFN) related genes, including LY6E, MX1, OAS3, IFI44L, IFI6 and IFITM3. Ten down-regulated genes mainly mediated negative regulation of cell proliferation and cell motion. Results of a subgroup analysis showed that although the kinds of genes varied widely between days 3 and 7 post vaccination, the pathways between them are basically the same, such as immune response and response to viruses, etc. For an independent verification of these 6 type I IFN related genes, peripheral blood mononuclear cells (PBMCs) were collected at baseline and day 3 after the vaccination from 8 Enterovirus 71(EV71) vaccinees and were assayed by RT-PCR. Results showed that the 6 DEGs were also upregulated in EV71 vaccinees. In summary, meta-analysis methods were used to explore the immune mechanism of vaccines and results indicated that the type I IFN related genes and corresponding pathways were common in early immune responses for different kinds of vaccines.
机译:这项研究的目的是发现不同疫苗之间的共同免疫机制。使用公开可用的微阵列基因表达综合疫苗(GEO)和疫苗记录的Array Express数据集对微阵列数据集进行了荟萃分析。这项荟萃分析选择了7项研究(共35项)。总共包括447个切屑(接种前145个疫苗,接种后302个疫苗)。微阵列的重要性分析(SAM)程序用于筛选差异表达基因(DEG)。 DEG的功能途径富集在DAVID Gene Ontology(GO)数据库中进行。鉴定出二十个DEG,其中10个上调基因涉及免疫应答。其中六个与I型干扰素(IFN)相关的基因,包括LY6E,MX1,OAS3,IFI44L,IFI6和IFITM3。十个下调的基因主要介导细胞增殖和细胞运动的负调控。亚组分析的结果表明,尽管在接种后第3天到第7天基因的种类差异很大,但它们之间的途径基本相同,例如免疫应答和对病毒的应答等。对这6种类型进行独立验证在基线和接种后第3天,从8种肠病毒71(EV71)疫苗中收集I IFN相关基因,外周血单核细胞(PBMC),并通过RT-PCR进行分析。结果显示,EV71疫苗中的6个DEGs也被上调。综上所述,采用荟萃分析方法探讨了疫苗的免疫机制,结果表明,I型IFN相关基因和相应的途径在不同疫苗的早期免疫应答中很常见。

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