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Inhibition of SARS Coronavirus Infection In Vitro with Clinically Approved Antiviral Drugs

机译:临床批准的抗病毒药物对SARS冠状病毒的体外抑制作用

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摘要

Severe acute respiratory syndrome (SARS) is an infectious disease caused by a newly identified human coronavirus (SARS-CoV). Currently, no effective drug exists to treat SARS-CoV infection. In this study, we investigated whether a panel of commercially available antiviral drugs exhibit in vitro anti–SARS-CoV activity. A drug-screening assay that scores for virus-induced cytopathic effects on cultured cells was used. Tested were 19 clinically approved compounds from several major antiviral pharmacologic classes: nucleoside analogs, interferons, protease inhibitors, reverse transcriptase inhibitors, and neuraminidase inhibitors. Complete inhibition of cytopathic effects of SARS-CoV in culture was observed for interferon subtypes, β-1b, α-n1, α-n3, and human leukocyte interferon α. These findings support clinical testing of approved interferons for the treatment of SARS.
机译:严重急性呼吸系统综合症(SARS)是由新发现的人类冠状病毒(SARS-CoV)引起的传染病。当前,不存在用于治疗SARS-CoV感染的有效药物。在这项研究中,我们调查了一组可商购的抗病毒药物是否表现出体外抗SARS-CoV活性。使用对病毒诱导的对培养细胞的细胞病变作用评分的药物筛选测定法。测试了来自几种主要抗病毒药理学类别的19种临床批准的化合物:核苷类似物,干扰素,蛋白酶抑制剂,逆转录酶抑制剂和神经氨酸酶抑制剂。对于干扰素亚型β-1b,α-n1,α-n3和人白细胞干扰素α,观察到了SARS-CoV在培养物中对细胞病变作用的完全抑制。这些发现支持批准的干扰素用于治疗SARS的临床测试。

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