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本文引用的文献

1
Morphine exposure exacerbates HIV-1 Tat driven changes to neuroinflammatory factors in cultured astrocytes.吗啡暴露加剧了 HIV-1 Tat 驱动的培养星形胶质细胞中神经炎症因子的变化。
PLoS One. 2020 Mar 25;15(3):e0230563. doi: 10.1371/journal.pone.0230563. eCollection 2020.
2
Morphine induces the differentiation of T helper cells to Th2 effector cells via the PKC-θ-GATA3 pathway.吗啡通过蛋白激酶 C-θ- GATA3 通路诱导辅助性 T 细胞向 Th2 效应细胞分化。
Int Immunopharmacol. 2020 Mar;80:106133. doi: 10.1016/j.intimp.2019.106133. Epub 2020 Jan 20.
3
Modeling the Effects of Morphine-Altered Virus Specific Antibody Responses on HIV/SIV Dynamics.建立吗啡改变的病毒特异性抗体反应对 HIV/SIV 动力学影响的模型。
Sci Rep. 2019 Apr 1;9(1):5423. doi: 10.1038/s41598-019-41751-8.
4
A central role for glial CCR5 in directing the neuropathological interactions of HIV-1 Tat and opiates.胶质细胞 CCR5 在 HIV-1 Tat 和阿片类药物的神经病理学相互作用中的核心作用。
J Neuroinflammation. 2018 Oct 10;15(1):285. doi: 10.1186/s12974-018-1320-4.
5
Critical Role of Beclin1 in HIV Tat and Morphine-Induced Inflammation and Calcium Release in Glial Cells from Autophagy Deficient Mouse.自噬缺陷小鼠胶质细胞中 Beclin1 在 HIV Tat 和吗啡诱导的炎症及钙释放中的关键作用。
J Neuroimmune Pharmacol. 2018 Sep;13(3):355-370. doi: 10.1007/s11481-018-9788-3. Epub 2018 May 11.
6
Morphine-Mediated Brain Region-Specific Astrocytosis Involves the ER Stress-Autophagy Axis.吗啡介导的脑区特异性星形胶质细胞增生涉及内质网应激-自噬轴。
Mol Neurobiol. 2018 Aug;55(8):6713-6733. doi: 10.1007/s12035-018-0878-2. Epub 2018 Jan 17.
7
CCR5 mediates HIV-1 Tat-induced neuroinflammation and influences morphine tolerance, dependence, and reward.CCR5 介导 HIV-1 Tat 诱导的神经炎症,并影响吗啡耐受、依赖和奖赏。
Brain Behav Immun. 2018 Mar;69:124-138. doi: 10.1016/j.bbi.2017.11.006. Epub 2017 Nov 13.
8
Immunomodulatory Role of Complement Proteins in the Neuropathology Associated with Opiate Abuse and HIV-1 Co-Morbidity.补体蛋白在与阿片类药物滥用和HIV-1共病相关的神经病理学中的免疫调节作用
Immunol Invest. 2017 Nov;46(8):816-832. doi: 10.1080/08820139.2017.1371891.
9
HIV-associated synaptic degeneration.HIV 相关的突触退化。
Mol Brain. 2017 Aug 29;10(1):40. doi: 10.1186/s13041-017-0321-z.
10
Importance of Autophagy in Mediating Human Immunodeficiency Virus (HIV) and Morphine-Induced Metabolic Dysfunction and Inflammation in Human Astrocytes.自噬在介导人类免疫缺陷病毒(HIV)和吗啡诱导的人类星形胶质细胞代谢功能障碍及炎症中的重要性。
Viruses. 2017 Jul 28;9(8):201. doi: 10.3390/v9080201.

阿片类药物介导的 HIV-1 免疫发病机制。

Opioid-Mediated HIV-1 Immunopathogenesis.

机构信息

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

出版信息

J Neuroimmune Pharmacol. 2020 Dec;15(4):628-642. doi: 10.1007/s11481-020-09960-5. Epub 2020 Oct 8.

DOI:10.1007/s11481-020-09960-5
PMID:33029670
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7872067/
Abstract

Despite the ability of combination antiretroviral therapy to dramatically suppress viremia, the brain continues to be a reservoir of HIV-1 low-level replication. Adding further complexity to this is the comorbidity of drug abuse with HIV-1 associated neurocognitive disorders and neuroHIV. Among several abused drugs, the use of opiates is highly prevalent in HIV-1 infected individuals, both as an abused drug as well as for pain management. Opioids and their receptors have attained notable attention owing to their ability to modulate immune functions, in turn, impacting disease progression. Various cell culture, animal and human studies have implicated the role of opioids and their receptors in modulating viral replication and virus-mediated pathology both positively and negatively. Further, the combinatorial effects of HIV-1/HIV-1 proteins and morphine have demonstrated activation of inflammatory signaling in the host system. Herein, we summarized the current knowledge on the role of opioids on peripheral immunopathogenesis, viral immunopathogenesis, epigenetic profiles of the host and viral genome, neuropathogenesis of SIV/SHIV-infected non-human primates, blood-brain-barrier, HIV-1 viral latency, and viral rebound. Overall, this review provides recent insights into the role of opioids in HIV-1 immunopathogenesis. Graphical abstract.

摘要

尽管联合抗逆转录病毒疗法能够显著抑制病毒血症,但大脑仍然是 HIV-1 低水平复制的储存库。药物滥用与 HIV-1 相关神经认知障碍和神经 HIV 的合并症使情况更加复杂。在几种滥用药物中,阿片类药物在 HIV-1 感染个体中的使用非常普遍,既是滥用药物也是用于疼痛管理。阿片类药物及其受体因其能够调节免疫功能而引起了人们的注意,进而影响疾病的进展。各种细胞培养、动物和人体研究表明,阿片类药物及其受体在正负两方面都能调节病毒复制和病毒介导的病理学。此外,HIV-1/HIV-1 蛋白和吗啡的组合效应已证明在宿主系统中激活了炎症信号。在此,我们总结了阿片类药物在外周免疫发病机制、病毒免疫发病机制、宿主和病毒基因组的表观遗传谱、感染 SIV/SHIV 的非人类灵长类动物的神经发病机制、血脑屏障、HIV-1 病毒潜伏期和病毒反弹方面的作用的最新知识。总的来说,这篇综述提供了关于阿片类药物在 HIV-1 免疫发病机制中的作用的最新见解。