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在细胞培养物和小鼠中用吗啉代寡聚物抑制呼吸道合胞病毒感染。

Inhibition of respiratory syncytial virus infections with morpholino oligomers in cell cultures and in mice.

作者信息

Lai Shen-Hao, Stein David A, Guerrero-Plata Antonieta, Liao Sui-Ling, Ivanciuc Teodora, Hong Chao, Iversen Patrick L, Casola Antonella, Garofalo Roberto P

机构信息

Department of Pediatrics, University of Texas Medical Branch at Galveston, Galveston, Texas 77555-0369, USA.

出版信息

Mol Ther. 2008 Jun;16(6):1120-8. doi: 10.1038/mt.2008.81. Epub 2008 Apr 29.

Abstract

Respiratory syncytial virus (RSV) is a major cause of lower respiratory tract infection in infants, young children, and high-risk adults. Currently, there is no vaccine to prevent RSV infection, and the available therapeutic agents are of limited utility. Peptide-conjugated phosphorodiamidate morpholino oligomers (PPMOs) are a class of antisense agents that can enter cells readily and interfere with viral protein expression through steric blocking of complementary RNA. Two antisense PPMOs, designed to target sequence that includes the 5'-terminal region and translation start-site region of RSV L mRNA, were tested for anti-RSV activity in cultures of two human-airway cell lines. Both PPMOs showed minimal cytotoxicity and one of them, (AUG-2), reduced viral titers by >2.0 log(10). Intranasal (i.n.) treatment of BALB/c mice with AUG-2 PPMO before the RSV inoculation produced a reduction in viral titer of 1.2 log(10) in lung tissue at day 5 postinfection (p.i.), and attenuated pulmonary inflammation at day 7 postinfection. These data show that the AUG-2 PPMO possesses potent anti-RSV activity and is worthy of further investigation as a candidate for potential therapeutic application.

摘要

呼吸道合胞病毒(RSV)是引起婴幼儿和高危成人下呼吸道感染的主要原因。目前,尚无预防RSV感染的疫苗,现有的治疗药物效用有限。肽缀合的磷酰二胺吗啉代寡聚物(PPMO)是一类反义药物,能够轻易进入细胞,并通过空间位阻互补RNA来干扰病毒蛋白表达。设计了两种靶向包含RSV L mRNA 5'-末端区域和翻译起始位点区域序列的反义PPMO,在两种人气道细胞系培养物中测试其抗RSV活性。两种PPMO均显示出最小的细胞毒性,其中一种(AUG-2)使病毒滴度降低>2.0 log(10)。在RSV接种前用AUG-2 PPMO对BALB/c小鼠进行鼻内(i.n.)治疗,在感染后第5天(p.i.)肺组织中的病毒滴度降低了1.2 log(10),并在感染后第7天减轻了肺部炎症。这些数据表明,AUG-2 PPMO具有强大的抗RSV活性,作为潜在治疗应用的候选药物值得进一步研究。

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