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基因组分析揭示恒河猴艾滋病疫苗试验中挑战前后的差异:对疫苗疗效机制的深入了解。

Genomic analysis reveals pre- and postchallenge differences in a rhesus macaque AIDS vaccine trial: insights into mechanisms of vaccine efficacy.

机构信息

Department of Microbiology, University of Washington, Box 358070, Seattle, WA 98195-8070, USA.

出版信息

J Virol. 2011 Jan;85(2):1099-116. doi: 10.1128/JVI.01522-10. Epub 2010 Nov 10.

Abstract

We have employed global transcriptional profiling of whole blood to identify biologically relevant changes in cellular gene expression in response to alternative AIDS vaccine strategies with subsequent viral challenge in a rhesus macaque vaccine model. Samples were taken at day 0 (prechallenge), day 14 (peak viremia), and week 12 (set point) from animals immunized with replicating adenovirus type 5 host range (Ad5hr) recombinant viruses expressing human immunodeficiency virus HIV(env)(89.6P), simian immunodeficiency virus SIV(gag)(239), or SIV(nef)(239) alone or in combination with two intramuscular boosts with HIV(89.6P)gp140ΔCFI protein (L. J. Patterson et al., Virology 374:322-337, 2008), and each treatment resulted in significant control of viremia following simian-human immunodeficiency virus SHIV(89.6P) challenge (six animals per group plus six controls). At day 0, 8 weeks after the last treatment, the microarray profiles revealed significant prechallenge differences between treatment groups; data from the best-protected animals led to identification of a network of genes related to B cell development and lymphocyte survival. At peak viremia, expression profiles of the immunized groups were extremely similar, and comparisons to control animals reflected immunological differences other than effector T cell functions. Suggested protective mechanisms for vaccinated animals included upregulation of interleukin-27, a cytokine known to inhibit lentivirus replication, and increased expression of complement components, which may synergize with vaccine-induced antibodies. Divergent expression profiles at set point for the immunized groups implied distinct immunological responses despite phenotypic similarities in viral load and CD4(+) T cell levels. Data for the gp140-boosted group provided evidence for antibody-dependent, cell-mediated viral control, whereas animals immunized with only the replicating Ad5hr recombinants exhibited a different evolution of the B cell compartment even at 3 months postchallenge. This study demonstrates the sensitivity and discrimination of gene expression profiling of whole blood as an analytical tool in AIDS vaccine trials, providing unique insights into in vivo mechanisms and potential correlates of protection.

摘要

我们采用全血全局转录谱分析方法,鉴定了灵长类动物艾滋病疫苗模型中针对不同艾滋病疫苗策略的细胞基因表达的生物学相关变化,随后对这些动物进行了病毒挑战。在该模型中,对用复制型腺病毒 5 型宿主范围(Ad5hr)重组病毒免疫的动物进行了研究,这些重组病毒表达人类免疫缺陷病毒(HIV)(env)(89.6P)、猴免疫缺陷病毒(SIV)(gag)(239)或 SIV(nef)(239),或单独使用这些重组病毒,或与两次肌肉内加强免疫用 HIV(89.6P)gp140ΔCFI 蛋白(L. J. Patterson 等人,《病毒学》374:322-337, 2008)联合使用,在所有处理中,在接受 SIV-人免疫缺陷病毒(SHIV)89.6P 挑战后,病毒血症都得到了显著控制(每组 6 只动物和 6 只对照)。在第 0 天,即最后一次处理后 8 周,微阵列图谱显示治疗组之间存在显著的预处理差异;来自最佳保护动物的数据导致鉴定了与 B 细胞发育和淋巴细胞存活相关的基因网络。在病毒血症高峰时,免疫组的表达谱极为相似,与对照组动物的比较反映了除效应 T 细胞功能外的免疫差异。疫苗接种动物的保护性机制包括白细胞介素 27 的上调,白细胞介素 27 是一种已知抑制慢病毒复制的细胞因子,以及补体成分的表达增加,这可能与疫苗诱导的抗体协同作用。免疫组在固定点的表达谱差异表明,尽管病毒载量和 CD4+T 细胞水平的表型相似,但存在不同的免疫反应。针对 gp140 加强免疫组的数据提供了证据表明抗体依赖性细胞介导的病毒控制,而仅用复制型 Ad5hr 重组病毒免疫的动物即使在挑战后 3 个月也表现出不同的 B 细胞区室演变。这项研究证明了全血基因表达谱分析作为艾滋病疫苗试验分析工具的敏感性和区分性,为体内机制和潜在保护相关性提供了独特的见解。

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