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针对猿猴免疫缺陷病毒(SIV)的抗逆转录病毒药物的体外筛选。

In vitro screening for antiretroviral agents against simian immunodeficiency virus (SIV).

作者信息

Tsai C C, Follis K E, Yarnall M, Deaver L E, Benveniste R E, Sager P R

机构信息

Regional Primate Research Center, University of Washington, Seattle.

出版信息

Antiviral Res. 1990 Aug;14(2):87-98. doi: 10.1016/0166-3542(90)90046-a.

Abstract

Simian immunodeficiency virus (SIV), which causes an acquired immunodeficiency syndrome in macaques, is a lentivirus that is morphologically, antigenically, genetically, and biologically similar to the human immunodeficiency virus (HIV). Because of these similarities, the SIV model represents a unique opportunity for in vitro and in vivo testing of antiretroviral agents. Since antiretroviral agents may exhibit different properties in different cells in vitro, more than one cell line may be necessary to evaluate the efficacy and modes of action of an antiretroviral agent. Initially we tested ten cell lines for their permissiveness to five SIV isolates. One B-cell line (AA-2) and one T-cell line (HuT 78) were selected to test antiretroviral agents since both were extremely permissive for SIVmac251, an isolate with a high rate of infectivity. Using this optimized in vitro testing protocol, we screened ten antiretroviral agents for their ability to inhibit SIV replication. Six of the compounds completely inhibited SIV viral antigen expression. Based on the selectivity index, 3'-azido-3'-dideoxythymidine, 3'-azido-2',3'-dideoxyuridine, and 3'-fluoro-3'-deoxythymidine appear to be the most efficacious antiretroviral agents against SIVmac251. Several different assays for determining viral antigen inhibition were conducted and the results of these assays were comparable. Our results demonstrate that the SIV in vitro model is a valuable screening tool for determining the efficacy and toxicity of new antiretroviral agents.

摘要

猴免疫缺陷病毒(SIV)可在猕猴中引发获得性免疫缺陷综合征,它是一种慢病毒,在形态学、抗原性、遗传学和生物学特性上与人类免疫缺陷病毒(HIV)相似。由于这些相似性,SIV模型为抗逆转录病毒药物的体外和体内测试提供了独特的机会。由于抗逆转录病毒药物在体外不同细胞中可能表现出不同特性,因此可能需要不止一种细胞系来评估抗逆转录病毒药物的疗效和作用方式。最初,我们测试了十种细胞系对五种SIV分离株的易感性。选择了一种B细胞系(AA - 2)和一种T细胞系(HuT 78)来测试抗逆转录病毒药物,因为这两种细胞系对感染性很高的SIVmac251分离株都具有极高的易感性。使用这种优化的体外测试方案,我们筛选了十种抗逆转录病毒药物抑制SIV复制的能力。其中六种化合物完全抑制了SIV病毒抗原的表达。基于选择性指数,3'-叠氮基-3'-脱氧胸苷、3'-叠氮基-2',3'-二脱氧尿苷和3'-氟-3'-脱氧胸苷似乎是针对SIVmac251最有效的抗逆转录病毒药物。进行了几种不同的测定病毒抗原抑制的试验,这些试验的结果具有可比性。我们的结果表明,SIV体外模型是确定新型抗逆转录病毒药物疗效和毒性的有价值的筛选工具。

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