Kazakova Alisa A, Leonova Elena I, Sopova Julia V, Chirinskaite Angelina V, Minskaya Ekaterina S, Kukushkin Ivan S, Ivanov Roman A, Reshetnikov Vasiliy V
Sirius University of Science and Technology, Federal Territory "Sirius", 354340, Russia.
Saint-Petersburg State University, Saint-Petersburg, 199034, Russia.
Biochemistry (Mosc). 2025 Jun;90(6):786-803. doi: 10.1134/S0006297925601212.
The worldwide number of deaths from complications caused by severe influenza and COVID-19 is about 1 million cases annually. Development of the effective antiviral therapy strategies for the disease treatment is one of the most important tasks. Use of the CRISPR/Cas13 system, which specifically degrades viral RNA and significantly reduces titer of the virus, could be a solution of this problem. Despite the fact that Cas13 nucleases have been discovered only recently, they already have shown high efficiency in suppressing viral transcripts in cell cultures. The recent advances in mRNA technology and improvements in non-viral delivery systems have made it possible to effectively use CRISPR/Cas13 in animal models as well. In this review, we analyzed experimental and studies on the use of CRISPR/Cas13 systems as an antiviral agent in cell cultures and animal models and discussed main directions for improving the CRISPR/Cas13 system. These data allow us to understand prospects and limitations of the further use of CRISPR/Cas13 in the treatment of viral diseases.
全球每年因重症流感和新冠病毒并发症导致的死亡人数约为100万例。开发有效的抗病毒治疗策略是疾病治疗的最重要任务之一。使用能特异性降解病毒RNA并显著降低病毒滴度的CRISPR/Cas13系统可能是解决这一问题的方法。尽管Cas13核酸酶最近才被发现,但它们已在细胞培养物中显示出高效抑制病毒转录本的能力。mRNA技术的最新进展和非病毒递送系统的改进也使得在动物模型中有效使用CRISPR/Cas13成为可能。在本综述中,我们分析了在细胞培养物和动物模型中使用CRISPR/Cas13系统作为抗病毒剂的实验和研究,并讨论了改进CRISPR/Cas13系统的主要方向。这些数据使我们能够了解CRISPR/Cas13在病毒疾病治疗中进一步应用的前景和局限性。