Oliveira Cláudia, Ribeiro António J, Veiga Francisco, Silveira Isabel
J Biomed Nanotechnol. 2016 May;12(5):841-62. doi: 10.1166/jbn.2016.2245.
Delivery of nucleic acids is the most promising therapy for many diseases that remain untreatable. Therefore, many research efforts have been put on finding a safe and efficient delivery system able to provide a sustained response. Viral vectors have proved to be the most efficient for delivery of nucleic acids and, thus, stand as the foremost vector used in current clinical trials. However, safety issues arise as a main concern and mitigate their use, impelling the improvement of non-viral alternatives. This review focuses on the recent advances in pre-clinical development of non-viral polyplexes and lipoplexes for nucleic acid-based delivery, in contrast with vectors being used in present clinical trials. Nucleic acid vectors for neurodegenerative ataxias, Parkinson's disease, retinitis pigmentosa, cystic fibrosis, hemophilia, pancreatic and lung cancer, and rheumatoid arthritis are discussed to illustrate current state of pre-clinical and clinical studies. Thereby, denoting the prospects for treatment of genetic diseases and elucidating the trend in non-viral vector development and improvement which is expected to significantly increase disease rescue exceeding the modest clinical successes observed so far.
核酸递送是治疗许多目前仍无法治愈疾病最具前景的疗法。因此,许多研究致力于寻找一种能够提供持续反应的安全高效递送系统。事实证明,病毒载体是递送核酸最有效的载体,因此也是目前临床试验中使用的首要载体。然而,安全问题成为主要关注点并限制了它们的使用,促使人们改进非病毒替代方案。与目前临床试验中使用的载体相比,本综述重点关注用于基于核酸递送的非病毒多聚体和脂质体在临床前开发方面的最新进展。讨论了用于神经退行性共济失调、帕金森病、色素性视网膜炎、囊性纤维化、血友病、胰腺癌和肺癌以及类风湿性关节炎的核酸载体,以说明临床前和临床研究的现状。从而表明治疗遗传疾病的前景,并阐明非病毒载体开发和改进的趋势,预计这将显著提高疾病治疗效果,超越目前所观察到的有限临床成功。