首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >Comparative interleukin (IL-2)/interferon IFN-gamma and IL-4/IL-10 responses during acute infection of macaques inoculated with attenuated nef-truncated or pathogenic SICmac251 virus.
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Comparative interleukin (IL-2)/interferon IFN-gamma and IL-4/IL-10 responses during acute infection of macaques inoculated with attenuated nef-truncated or pathogenic SICmac251 virus.

机译:在猕猴急性感染减毒的截短的或病原性的SICmac251病毒接种的猕猴期间比较白介素(IL-2)/干扰素IFN-γ和IL-4 / IL-10的反应。

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摘要

Comparison of immune responses to infection by a pathogenic or a nonpathogenic immunodeficiency virus in macaques may provide insights into pathogenetic events leading to simian AIDS. This work is aimed at exploring cytokine expression during infection by simian immunodeficiency virus (SIV). We used semiquantitative reverse transcription-PCR to monitor interleukin (IL)-2/interferon (IFN)-gamma (Th1-like), and IL-4/IL-10 (Th2-like) expression in unmanipulated peripheral blood mononuclear cells (PBMCs), during the acute phase of infection of eight cynomolgus macaques (Macaca fascicularis) with a pathogenic primary isolate of SIVmac251 (full-length nef), and of four other cynomolgus macaques by an attenuated molecular clone of SIVmac251 (nef-truncated). All the monkeys became infected, as clearly shown by the presence of infected PBMCs and by seroconversion. Nevertheless, PBMC-associated virus loads and p27 antigenemia in monkeys infected by the attenuated virus clone remained lower than those observed in animals infected with the pathogenic SIVmac251 isolate. A rise of IL-10 mRNA expression occurred in both groups of monkeys coincident with the peak of viral replication. In monkeys infected with the pathogenic SIVmac251, IL-2, IL-4, and IFN-gamma mRNAs were either weakly detectable or undetectable. On the contrary, animals infected by the attenuated virus exhibited an overexpression of these cytokine mRNAs during the first weeks after inoculation. The lack of expression of these cytokines in monkeys infected with the pathogenic primary isolate may reflect early immunodeficiency.
机译:比较猕猴中的致病性或非致病性免疫缺陷病毒对感染的免疫应答,可以深入了解导致猿猴AIDS的致病性事件。这项工作旨在探索猿猴免疫缺陷病毒(SIV)感染期间细胞因子的表达。我们使用半定量逆转录PCR监测未操纵的外周血单核细胞(PBMC)中的白介素(IL)-2 /干扰素(IFN)-γ(Th1样)和IL-4 / IL-10(Th2样)表达),在SIVmac251的致病性主要分离株(全长nef)感染八只食蟹猕猴(Macaca fascicularis)的急性阶段,以及SIVmac251的减毒分子克隆(nef截短)感染其他四只食蟹猕猴。如感染的PBMC的存在和血清转化清楚地表明,所有的猴子都被感染了。然而,在减毒病毒克隆感染的猴子中,PBMC相关病毒载量和p27抗原血症仍然低于在感染了病原性SIVmac251分离株的动物中观察到的水平。两组猴子中IL-10 mRNA表达的升高与病毒复制的峰值一致。在感染了病原性SIVmac251的猴子中,IL-2,IL-4和IFN-γmRNA的检测能力较弱或检测不到。相反,被减毒病毒感染的动物在接种后的最初几周内表现出这些细胞因子mRNA的过表达。这些细胞因子在感染了病原性分离株的猴子中缺乏表达可能反映了早期免疫缺陷。

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