Shigeta Shiro, Yamase Toshihiro
Department of Microbiology, Fukushima Medical University, School of Medicine, Fukushima, Japan.
Antivir Chem Chemother. 2005;16(1):23-31. doi: 10.1177/095632020501600103.
Severe acute respiratory syndrome (SARS) is a disease that has newly emerged in the 21st century, and is both severe and highly contagious. SARS first surfaced in late 2002 and spread within a few months from its origin in Guandong province, China, to more than 30 countries (World Health Organization, 2003). In this review, several antiviral substances shown to be active in vitro will be introduced and summarized in the order of the virus' replication steps; that is, binding to cellular receptor, fusion and entry to the cells, viral RNA replication and transcription, protein processing and so on. The possible clinical use of several synthetic peptides, including those that mimic the S-binding domain, the HR2 fusion protein and SARS proteinase substrates, will be discussed. Monoclonal antibodies (Mabs) and established drugs, such as interferons and HIV proteinase inhibitors, are also discussed in relation to anti-SARS clinical use.
严重急性呼吸综合征(SARS)是21世纪新出现的一种疾病,病情严重且传染性极强。SARS于2002年末首次出现,并在数月内从其在中国广东省的发源地传播至30多个国家(世界卫生组织,2003年)。在本综述中,将按照病毒的复制步骤顺序介绍并总结几种在体外显示有活性的抗病毒物质;即与细胞受体结合、融合并进入细胞、病毒RNA复制和转录、蛋白质加工等。还将讨论几种合成肽(包括模拟S结合域、HR2融合蛋白和SARS蛋白酶底物的合成肽)可能的临床应用。同时也会讨论单克隆抗体(Mabs)以及已有的药物,如干扰素和HIV蛋白酶抑制剂在抗SARS临床应用方面的情况。