肝素和硫酸葡聚糖在rsv感染中的作用

M. Rubio, K. Toledo, Jaqueline Calça, C. Bonfim, D. E. Gomes, E. Durigon, M. A. Fossey, P. Rahal, F. P. Souza
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引用次数: 1

摘要

呼吸道合胞病毒是婴幼儿急性下呼吸道疾病的主要病因。由于目前还没有获得许可的RSV疫苗,因此鉴定和开发RSV特异性抑制剂具有重大意义。有临床证据表明,糖胺聚糖(GAGs)是病毒感染的潜在抑制剂。本研究比较了肝素和硫酸葡聚糖两种GAGs对RSV的抗病毒和杀病毒活性。使用体外感染模型进行分析,在感染之前,用肝素或硫酸葡聚糖培养Hep-2细胞或RSV。采用逆转录-聚合酶链反应(RT-PCR)和间接免疫荧光法(IFA)分析病毒颗粒的存在。结果表明,肝素预孵育Hep-2细胞或硫酸葡聚糖预孵育病毒颗粒能更有效地抑制病毒感染。我们的研究表明,在没有细胞死亡的情况下,肝素和硫酸葡聚糖分别通过抗病毒和杀病毒的不同机制减少RSV感染。这些数据有助于最近的医学、微生物学和生化研究,这些研究表明,使用抗病毒和杀病毒化合物是控制病毒感染的更有效治疗方法。DOI: http://dx.doi.org/10.17525/vrr.v15i2.47
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Heparin and dextran sulfate: their role on rsv infectivity
Respiratory syncytial virus is the major cause of acute lower respiratory tract illness in infants and young children. Because there is currently no licensed vaccine for RSV, there is a substantial interest in the identification and development of RSV specific inhibitory agents. There are clinical evidences that glycosaminoglycans (GAGs) are potential inhibitors of viral infection. In this study, the performance of two GAGs (heparin and dextran sulfate) were compared for their antiviral and virucidal activities on RSV. Analysis was performed using an in vitro infection model where, previously to infection, Hep-2 cells or RSV were incubated with heparin or dextran sulfate. The presence of viral particles was analyzed by Reverse Transcriptase-Polimerase Chain Reaction (RT-PCR) and indirect immunofluorescence assays (IFA). The results showed that viral infection was more efficiently inhibited when Hep-2 cells were pre-incubated with heparin or, when viral particles were pre-incubated with dextran sulfate. Our study suggest that, in the absence of cellular death, heparin and dextran sulfate reduce RSV infection by different mechanisms, antiviral and virucidal ones, respectively. These data contribute for recent medical, microbiology and biochemical studies which suggest that the use of antiviral and virucidal compounds as more effective treatment to control virus infections. DOI:  http://dx.doi.org/10.17525/vrr.v15i2.47
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