Barik Sailen
Center for Gene Regulation in Health and Disease, Cleveland State University, Cleveland, OH, USA.
Methods Mol Biol. 2011;721:333-8. doi: 10.1007/978-1-61779-037-9_20.
Intranasal administration of synthetic siRNA is an effective modality of RNAi delivery for the prevention and therapy of respiratory diseases, including pulmonary infections. Vehicles used for nasal siRNA delivery include established as well as novel reagents, many of which have been recently optimized. In general, they all promote significant uptake of siRNA into the lower respiratory tract, including the lung. When properly designed and optimized, these siRNAs offer significant protection against respiratory viruses such as influenza virus, parainfluenza virus and respiratory syncytial virus (RSV). Nasally administered siRNA remains within the lung and does not access systemic blood flow, as judged by its absence in other major organs such as liver, heart, kidney, and skeletal muscle. Adverse immune reaction is generally not encountered, especially when immunogenic and/or off-target siRNA sequences and toxic vehicles are avoided. In fact, siRNA against RSV has entered Phase II clinical trials in human with promising results. Here, we provide a standardized procedure for using the nose as a specific route for siRNA delivery into the lung of laboratory animals. It should be clear that this simple and efficient system has enormous potential for therapeutics.
经鼻给予合成的小干扰RNA(siRNA)是一种有效的RNA干扰(RNAi)递送方式,可用于预防和治疗包括肺部感染在内的呼吸道疾病。用于经鼻递送siRNA的载体包括已有的和新型试剂,其中许多最近已得到优化。一般来说,它们都能促进siRNA大量摄取到包括肺部在内的下呼吸道。经过合理设计和优化后,这些siRNA能为抵御流感病毒、副流感病毒和呼吸道合胞病毒(RSV)等呼吸道病毒提供显著保护。经鼻给予的siRNA会留在肺部,不会进入体循环,这可通过在肝脏、心脏、肾脏和骨骼肌等其他主要器官中未检测到它来判断。一般不会遇到不良免疫反应,尤其是当避免使用具有免疫原性和/或脱靶的siRNA序列以及有毒载体时。事实上,针对RSV的siRNA已进入人体II期临床试验,结果令人鼓舞。在此,我们提供一种标准化程序,用于将鼻子作为将siRNA递送至实验动物肺部的特定途径。应当明确的是,这种简单高效的系统在治疗方面具有巨大潜力。