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恒河猴初次感染1型登革病毒后,干扰素刺激基因发生转录激活,但细胞因子基因未发生转录激活。

Transcriptional activation of interferon-stimulated genes but not of cytokine genes after primary infection of rhesus macaques with dengue virus type 1.

作者信息

Sariol Carlos A, Muñoz-Jordán Jorge L, Abel Kristina, Rosado Lymarie C, Pantoja Petraleigh, Giavedoni Luis, Rodriguez Idia Vanessa, White Laura J, Martínez Melween, Arana Teresa, Kraiselburd Edmundo N

机构信息

Unit of Comparative Medicine, Primate Research Center, University of Puerto Rico Medical Sciences Campus, San Juan, PR 00936-5067.

出版信息

Clin Vaccine Immunol. 2007 Jun;14(6):756-66. doi: 10.1128/CVI.00052-07. Epub 2007 Apr 11.

DOI:10.1128/CVI.00052-07
PMID:17428947
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1951081/
Abstract

Macaques are the only animal model used to test dengue virus (DENV) vaccine candidates. Nevertheless, the pathogenesis of DENV in macaques is not well understood. In this work, by using Affymetrix oligonucleotide microarrays, we studied the broad transcriptional modifications and cytokine expression profile after infecting rhesus macaques with DENV serotype 1. Five days after infection, these animals produced a potent, innate antiviral immune response by inducing the transcription of signature genes from the interferon (IFN) pathway with demonstrated antiviral activity, such as myxoprotein, 2',5'-oligoadenylate synthetase, phospholipid scramblase 1, and viperin. Also, IFN regulatory element 7, IFN-stimulated gene 15, and protein ligases linked to the ISGylation process were up-regulated. Unexpectedly, no up-regulation of IFN-alpha, -beta, or -gamma genes was detected. Transcription of the genes of interleukin-10 (IL-10), IL-8, IL-6, and tumor necrosis factor alpha was neither up-regulated nor down-regulated. Results were confirmed by real-time PCR and by multiplex cytokine detection in serum samples.

摘要

猕猴是用于测试登革病毒(DENV)候选疫苗的唯一动物模型。然而,DENV在猕猴中的发病机制尚未完全了解。在这项研究中,我们使用Affymetrix寡核苷酸微阵列,研究了恒河猴感染1型DENV后广泛的转录修饰和细胞因子表达谱。感染后5天,这些动物通过诱导具有抗病毒活性的干扰素(IFN)途径的标志性基因转录,产生了强大的先天性抗病毒免疫反应,如粘蛋白、2',5'-寡腺苷酸合成酶、磷脂翻转酶1和viperin。此外,IFN调节元件7、IFN刺激基因15以及与ISGylation过程相关的蛋白连接酶均上调。出乎意料的是,未检测到IFN-α、-β或-γ基因的上调。白细胞介素-10(IL-10)、IL-8、IL-6和肿瘤坏死因子α基因的转录既未上调也未下调。实时PCR和血清样本中的多重细胞因子检测证实了结果。

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本文引用的文献

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Murine model for dengue virus-induced lethal disease with increased vascular permeability.登革病毒诱导的致死性疾病伴血管通透性增加的小鼠模型。
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