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2
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本文引用的文献

1
Homeostatic proliferation fails to efficiently reactivate HIV-1 latently infected central memory CD4+ T cells.稳态增殖未能有效重新激活潜伏感染的 HIV-1 中央记忆性 CD4+T 细胞。
PLoS Pathog. 2011 Oct;7(10):e1002288. doi: 10.1371/journal.ppat.1002288. Epub 2011 Oct 6.
2
HIV latency is influenced by regions of the viral genome outside of the long terminal repeats and regulatory genes.HIV 潜伏期受到病毒基因组长末端重复序列和调控基因以外的区域的影响。
Virology. 2011 Sep 1;417(2):394-9. doi: 10.1016/j.virol.2011.06.024. Epub 2011 Jul 20.
3
High-throughput screening uncovers a compound that activates latent HIV-1 and acts cooperatively with a histone deacetylase (HDAC) inhibitor.高通量筛选发现一种能激活潜伏 HIV-1 的化合物,并与组蛋白去乙酰化酶 (HDAC) 抑制剂协同作用。
J Biol Chem. 2011 Jun 17;286(24):21083-91. doi: 10.1074/jbc.M110.195537. Epub 2011 Apr 15.
4
Disulfiram reactivates latent HIV-1 in a Bcl-2-transduced primary CD4+ T cell model without inducing global T cell activation.双硫仑在转染 Bcl-2 的原代 CD4+ T 细胞模型中重新激活潜伏的 HIV-1,而不诱导全局 T 细胞激活。
J Virol. 2011 Jun;85(12):6060-4. doi: 10.1128/JVI.02033-10. Epub 2011 Apr 6.
5
Influence of host gene transcription level and orientation on HIV-1 latency in a primary-cell model.宿主基因转录水平和方向对原代细胞模型中 HIV-1 潜伏期的影响。
J Virol. 2011 Jun;85(11):5384-93. doi: 10.1128/JVI.02536-10. Epub 2011 Mar 23.
6
HIV reservoirs and latency models.HIV 储库和潜伏模型。
Virology. 2011 Mar 15;411(2):344-54. doi: 10.1016/j.virol.2010.12.041. Epub 2011 Feb 1.
7
Curing HIV: Pharmacologic approaches to target HIV-1 latency.治愈 HIV:靶向 HIV-1 潜伏期的药物治疗方法。
Annu Rev Pharmacol Toxicol. 2011;51:397-418. doi: 10.1146/annurev-pharmtox-010510-100237.
8
Studies of HIV-1 latency in an ex vivo model that uses primary central memory T cells.使用原代中枢记忆 T 细胞的体外模型研究 HIV-1 潜伏期。
Methods. 2011 Jan;53(1):54-61. doi: 10.1016/j.ymeth.2010.10.002. Epub 2010 Oct 21.
9
Hit-and-run stimulation: a novel concept to reactivate latent HIV-1 infection without cytokine gene induction.逃避刺激:一种无需细胞因子基因诱导即可重新激活潜伏 HIV-1 感染的新方法。
J Virol. 2010 Sep;84(17):8712-20. doi: 10.1128/JVI.00523-10. Epub 2010 Jun 10.
10
Establishment of HIV latency in primary CD4+ cells is due to epigenetic transcriptional silencing and P-TEFb restriction.原发性CD4+细胞中HIV潜伏期的建立是由于表观遗传转录沉默和P-TEFb限制。
J Virol. 2010 Jul;84(13):6425-37. doi: 10.1128/JVI.01519-09. Epub 2010 Apr 21.

事实与虚构:用于高通量筛选HIV-1激活药物的细胞模型

Facts and fiction: cellular models for high throughput screening for HIV-1 reactivating drugs.

作者信息

Planelles Vicente, Wolschendorf Frank, Kutsch Olaf

机构信息

Department of Pathology, University of Utah, Salt Lake City, USA.

出版信息

Curr HIV Res. 2011 Dec 1;9(8):568-78. doi: 10.2174/157016211798998826.

DOI:10.2174/157016211798998826
PMID:22211661
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3771330/
Abstract

A curative therapy for HIV-1 infection will have to include measures to eliminate the reservoir of latently HIV- 1 infected cells that allow the virus to persist despite otherwise successful therapy. To date, all efforts to deplete the latent reservoir by triggering viral reactivation have used preexisting drugs that are believed to potentially target molecular mechanisms controlling HIV-1 infection. These therapeutic attempts were not clinically successful. Only in the last few years have cellular models of latent HIV-1 infection suitable for high throughput screening been developed and concerted drug discovery efforts were initiated to discover new HIV-1 reactivating drugs. We here provide a historic overview about the development of cell models with latent HIV-1 infection that lend themselves to drug discovery. We provide an overview from the first reported latently infected cell lines to current in vitro models of latent HIV-1 infection in primary T cells, and compare their potential to be used in future large-scale drug screening efforts.

摘要

一种针对HIV-1感染的治愈性疗法必须包括采取措施,以清除潜伏感染HIV-1的细胞库,尽管治疗在其他方面取得成功,但该细胞库仍使病毒得以持续存在。迄今为止,通过触发病毒重新激活来耗尽潜伏病毒库的所有努力都使用了现有的药物,这些药物被认为可能靶向控制HIV-1感染的分子机制。这些治疗尝试在临床上并不成功。直到最近几年,才开发出适用于高通量筛选的潜伏HIV-1感染细胞模型,并启动了协同的药物发现工作,以发现新的HIV-1重新激活药物。我们在此提供有关适合药物发现的潜伏HIV-1感染细胞模型发展的历史概述。我们提供了从首次报道的潜伏感染细胞系到目前原代T细胞中潜伏HIV-1感染的体外模型的概述,并比较了它们在未来大规模药物筛选工作中使用的潜力。