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首页> 外文期刊>Journal of Neuroimmune Pharmacology >Monocyte Mobilization, Activation Markers, and Unique Macrophage Populations in the Brain: Observations from SIV Infected Monkeys Are Informative with Regard to Pathogenic Mechanisms of HIV Infection in Humans
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Monocyte Mobilization, Activation Markers, and Unique Macrophage Populations in the Brain: Observations from SIV Infected Monkeys Are Informative with Regard to Pathogenic Mechanisms of HIV Infection in Humans

机译:脑中单核细胞动员,激活标记和独特的巨噬细胞群体:从人类感染艾滋病毒的猴子中观察到的信息对人类感染艾滋病毒的致病机制具有参考意义

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摘要

Non-human primate models of AIDS and neuroAIDS have been useful to study AIDS in humans in general and neuroAIDS in particular. Important information concerning target cells of infection, mechanisms of immune activation and pathology and cell traffic has been made in non-human primate models. To date observations in SIV infected monkey models have predicted or paralleled monocyte/macrophage biology with HIV infection and neuroAIDS. In this brief review we discuss a CD8+ T lymphocyte depletion model of rapid AIDS which results in a high incidence of SIV encephalitis. Specifically we review recent observations we have made using this model concerning monocyte turnover, monocyte/macrophage activation, macrophage derived biomarkers of disease and novel therapeutic approaches to AIDS and CNS pathology. Importantly, all observations made in the rapid model of AIDS discussed here are important and relevant to HIV infection of humans, even in the current era of anti-retroviral therapy that maintains HIV in plasma below the limit of detection.
机译:AIDS和NeuroAIDS的非人类灵长类动物模型对于研究普通人类尤其是NeuroAIDS的艾滋病非常有用。在非人类灵长类动物模型中已经获得了有关感染靶细胞,免疫激活机制和病理学以及细胞运输的重要信息。迄今为止,在SIV感染的猴子模型中的观察已预测单核细胞/巨噬细胞生物学与HIV感染和NeuroAIDS平行或平行。在这篇简短的综述中,我们讨论了快速艾滋病的CD8 + T淋巴细胞耗竭模型,该模型导致SIV脑炎的高发。具体而言,我们回顾了我们使用此模型所做的有关单核细胞更新,单核细胞/巨噬细胞激活,巨噬细胞衍生的疾病生物标记以及针对AIDS和CNS病理学的新型治疗方法的最新观察结果。重要的是,即使在当前将血浆中的HIV维持在检测限以下的抗逆转录病毒疗法时代,此处讨论的在AIDS快速模型中所做的所有观察也很重要且与人类HIV感染有关。

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