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化合物抗HIV活性的体外评估。

In vitro assessment of compounds for anti-HIV activity.

作者信息

Patience C, Moore J, Boyd M

机构信息

Chester Beatty Labs, Institute of Cancer Research, London, UK.

出版信息

Mol Biotechnol. 1994 Feb;1(1):49-58. doi: 10.1007/BF02821510.

Abstract

Human immunodeficiency virus types 1 and 2 (HIV-1, -2), the etiological agents of AIDS, are retroviruses that replicate in CD4+ T lymphocytes, monocytes, and macrophages. Early anti-HIV therapies were directed at the step in the virus life cycle that was considered the most readily blocked: the transcription of viral RNA into its DNA copy by the viral enzyme reverse transcriptase (RT). Unfortunately, to date, patient therapies have been relatively unsuccessful and hampered by toxicological problems. This has promoted further research into inhibitors of HIV replication, which may act at alternative stages in the viral replicative cycle as well as more effective RT inhibitors. In order to facilitate such research, simple and accurate in vitro assays are highly desirable. Here we describe such assays that measure components of the HIV replicative cycle and are suitable for use within antiviral experiments.

摘要

人类免疫缺陷病毒1型和2型(HIV-1、-2)是艾滋病的病原体,属于逆转录病毒,可在CD4+T淋巴细胞、单核细胞和巨噬细胞中复制。早期的抗HIV疗法针对的是病毒生命周期中被认为最容易阻断的步骤:通过病毒酶逆转录酶(RT)将病毒RNA转录为其DNA拷贝。不幸的是,迄今为止,患者治疗相对不太成功,且受到毒理学问题的阻碍。这促使人们进一步研究HIV复制抑制剂,这些抑制剂可能作用于病毒复制周期的其他阶段,以及更有效的RT抑制剂。为了促进此类研究,非常需要简单而准确的体外试验。在此,我们描述了此类测量HIV复制周期组成部分且适用于抗病毒实验的试验。

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