Planelles Vicente, Wolschendorf Frank, Kutsch Olaf
Department of Pathology, University of Utah, Salt Lake City, USA.
Curr HIV Res. 2011 Dec 1;9(8):568-78. doi: 10.2174/157016211798998826.
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.
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。