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本文引用的文献

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Delineating HIV-associated neurocognitive disorders using transgenic models: the neuropathogenic actions of Vpr.利用转基因模型描绘 HIV 相关神经认知障碍:Vpr 的神经致病作用。
J Neuroimmune Pharmacol. 2012 Jun;7(2):319-31. doi: 10.1007/s11481-011-9310-7. Epub 2011 Sep 15.
2
Increased neuroinflammatory and arachidonic acid cascade markers, and reduced synaptic proteins, in brain of HIV-1 transgenic rats.在 HIV-1 转基因大鼠的大脑中,神经炎症和花生四烯酸级联标志物增加,而突触蛋白减少。
J Neuroinflammation. 2011 Aug 16;8:101. doi: 10.1186/1742-2094-8-101.
3
Loss of neuronal integrity during progressive HIV-1 infection of humanized mice.在人类化小鼠进行的 HIV-1 感染的进展过程中神经元完整性的丧失。
J Neurosci. 2011 Mar 2;31(9):3148-57. doi: 10.1523/JNEUROSCI.5473-10.2011.
4
Survival after neuroAIDS: association with antiretroviral CNS Penetration-Effectiveness score.神经艾滋病后的生存:与抗逆转录病毒 CNS 穿透-疗效评分相关。
Neurology. 2011 Feb 15;76(7):644-51. doi: 10.1212/WNL.0b013e31820c3089. Epub 2011 Jan 19.
5
HIV-associated neurocognitive disorders before and during the era of combination antiretroviral therapy: differences in rates, nature, and predictors.在联合抗逆转录病毒疗法时代之前和期间与 HIV 相关的神经认知障碍:发生率、性质和预测因素的差异。
J Neurovirol. 2011 Feb;17(1):3-16. doi: 10.1007/s13365-010-0006-1. Epub 2010 Dec 21.
6
Analyses of nanoformulated antiretroviral drug charge, size, shape and content for uptake, drug release and antiviral activities in human monocyte-derived macrophages.分析纳米制剂抗逆转录病毒药物的荷电性、粒径、形态和含量,以研究其在人单核细胞衍生巨噬细胞中的摄取、药物释放和抗病毒活性。
J Control Release. 2011 Mar 10;150(2):204-11. doi: 10.1016/j.jconrel.2010.11.019. Epub 2010 Nov 23.
7
Links between progressive HIV-1 infection of humanized mice and viral neuropathogenesis.人类化小鼠中 HIV-1 感染的进展与病毒神经发病机制之间的联系。
Am J Pathol. 2010 Dec;177(6):2938-49. doi: 10.2353/ajpath.2010.100536. Epub 2010 Nov 18.
8
Brain ingress of regulatory T cells in a murine model of HIV-1 encephalitis.HIV-1 脑炎小鼠模型中调节性 T 细胞的脑内浸润。
J Neuroimmunol. 2011 Jan;230(1-2):33-41. doi: 10.1016/j.jneuroim.2010.08.014. Epub 2010 Sep 16.
9
Immunogenic profiling in mice of a HIV/AIDS vaccine candidate (MVA-B) expressing four HIV-1 antigens and potentiation by specific gene deletions.在小鼠中进行 HIV/AIDS 候选疫苗(MVA-B)的免疫原性分析,该疫苗表达四种 HIV-1 抗原,并通过特定基因缺失进行增强。
PLoS One. 2010 Aug 24;5(8):e12395. doi: 10.1371/journal.pone.0012395.
10
Identifying potential survival strategies of HIV-1 through virus-host protein interaction networks.通过病毒-宿主蛋白相互作用网络识别HIV-1的潜在生存策略。
BMC Syst Biol. 2010 Jul 15;4:96. doi: 10.1186/1752-0509-4-96.

HIV 相关神经认知障碍的啮齿动物模型。

Rodent models for HIV-associated neurocognitive disorders.

机构信息

Center for Neurodegenerative Disorders and Department of Pharmacology and Experimental Neuroscience, University of Nebraska Medical Center, Omaha, NE, USA.

出版信息

Trends Neurosci. 2012 Mar;35(3):197-208. doi: 10.1016/j.tins.2011.12.006. Epub 2012 Feb 1.

DOI:10.1016/j.tins.2011.12.006
PMID:22305769
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3294256/
Abstract

Human immunodeficiency virus (HIV)-associated neurocognitive disorders (HAND) reflect the spectrum of neural impairments seen during chronic viral infection. Current research efforts focus on improving antiretroviral and adjunctive therapies, defining disease onset and progression, facilitating drug delivery, and halting neurodegeneration and viral resistance. Because HIV is species-specific, generating disease in small-animal models has proved challenging. After two decades of research, rodent HAND models now include those containing a human immune system. Antiviral responses, neuroinflammation and immunocyte blood-brain barrier (BBB) trafficking follow HIV infection in these rodent models. We review these and other rodent models of HAND and discuss their unmet potential in reflecting human pathobiology and in facilitating disease monitoring and therapeutic discoveries.

摘要

人类免疫缺陷病毒(HIV)相关的神经认知障碍(HAND)反映了慢性病毒感染期间出现的一系列神经损伤。目前的研究重点是改善抗逆转录病毒和辅助治疗,定义疾病的起始和进展,促进药物输送,并阻止神经退行性变和病毒耐药性。由于 HIV 是种属特异性的,因此在小动物模型中产生疾病具有挑战性。经过二十年的研究,啮齿动物 HAND 模型现在包括含有人类免疫系统的模型。在这些啮齿动物模型中,抗病毒反应、神经炎症和免疫细胞血脑屏障(BBB)迁移都遵循 HIV 感染的发生。我们回顾了这些和其他啮齿动物 HAND 模型,并讨论了它们在反映人类病理生理学和促进疾病监测和治疗发现方面尚未满足的潜力。