Gamaleya Research Institute for Epidemiology and Microbiology, 18, Gamaleya Street, Moscow 123098, Russia.
Antiviral Res. 2013 Mar;97(3):318-28. doi: 10.1016/j.antiviral.2012.12.021. Epub 2012 Dec 26.
One effective method for the prevention and treatment of influenza infection is passive immunization. In our study, we examined the feasibility of creating an antibody-based preparation with a prolonged protective effect against influenza virus. Single-domain antibodies (sdAbs) specific for influenza virus hemagglutinin were generated. Experiments in mouse models showed 100% survivability for both intranasal sdAbs administration 24h prior to influenza challenge and 24h after infection. sdAb-gene delivery by an adenoviral vector led to gene expression for up to 14days. Protection by a recombinant adenovirus containing the sdAb gene was observed in cases of administration prior to influenza infection (14d-24h). We also demonstrated that the single administration of a combined preparation containing sdAb DNA and protein expanded the protection time window from 14d prior to 48h after influenza infection. This approach and the application of a broad-spectrum sdAbs will allow the development of efficient drugs for the prevention and treatment of viral infections produced by pandemic virus variants and other infections.
预防和治疗流感感染的一种有效方法是被动免疫。在我们的研究中,我们研究了是否可以制备一种具有延长的抗流感病毒保护作用的抗体药物。我们生成了针对流感病毒血凝素的单域抗体(sdAb)。在小鼠模型中的实验表明,在流感病毒攻击前 24 小时和感染后 24 小时经鼻给予 sdAb,其存活率为 100%。腺病毒载体传递 sdAb 基因可导致长达 14 天的基因表达。在流感感染前(14d-24h)给予包含 sdAb 基因的重组腺病毒可观察到保护作用。我们还表明,单次给予包含 sdAb DNA 和蛋白质的联合制剂可将保护时间窗口从流感感染前 14 天扩展到感染后 48 小时。这种方法和广谱 sdAb 的应用将允许开发用于预防和治疗大流行病毒变异和其他感染产生的病毒感染的有效药物。