Wu Zhuanli, Zhao Chengcheng, Ai Hui, Wang Zhen, Chen Mingyue, Lyu Yanli, Tong Qi, Liu Litao, Sun Honglei, Pu Juan, Zhang Ran, Hu Xiaoxiang, Liu Jinhua, Ma Xiaowei, Sun Yipeng
National Key Laboratory of Veterinary Public Health and Safety, College of Veterinary Medicine, China Agricultural University, Beijing, 100193, China.
Key Laboratory of Animal Epidemiology of the Ministry of Agriculture and Rural Affairs, Key Laboratory for Prevention and Control of Avian Influenza and Other Major Poultry Diseases of the Ministry of Agriculture and Rural Affairs, Beijing, 100193, China.
Adv Sci (Weinh). 2025 Mar;12(9):e2414651. doi: 10.1002/advs.202414651. Epub 2025 Jan 10.
To bolster the capacity for managing potential infectious diseases in the future, it is critical to develop specific antiviral drugs that can be rapidly designed and delivered precisely. Herein, a CRISPR/Cas13d system for broad-spectrum targeting of influenza A virus (IAV) from human, avian, and swine sources is designed, incorporating Cas13d mRNA and a tandem CRISPR RNA (crRNA) specific for the highly conserved regions of viral polymerase acidic (PA), nucleoprotein (NP), and matrix (M) gene segments, respectively. Given that the virus targets cells with specific receptors but is not limited to a single organ, a Susceptible Cell Selective Delivery (SCSD) system is developed by modifying a lipid nanoparticle with a peptide mimicking the function of the hemagglutinin of influenza virus to target sialic acid receptors. The SCSD system can precisely deliver an all-RNA-based CRISPR/Cas13d system into potentially infected cells. This drug is shown to reduce the viral load in the lungs by 2.37 log TCID mL and protect 100% of mice from lethal influenza infection. The SCSD-based CRISPR/Cas13d system shows promise for the flexible and efficient therapy of infections caused by rapidly evolving and novel viruses.
为增强未来管理潜在传染病的能力,开发能够快速设计并精准递送的特定抗病毒药物至关重要。在此,设计了一种用于广谱靶向来自人类、禽类和猪源的甲型流感病毒(IAV)的CRISPR/Cas13d系统,该系统包含Cas13d mRNA以及分别针对病毒聚合酶酸性蛋白(PA)、核蛋白(NP)和基质蛋白(M)基因片段高度保守区域的串联CRISPR RNA(crRNA)。鉴于该病毒以特定受体靶向细胞,但不限于单一器官,通过用模拟流感病毒血凝素功能的肽修饰脂质纳米颗粒以靶向唾液酸受体,开发了一种易感细胞选择性递送(SCSD)系统。该SCSD系统能够将基于全RNA的CRISPR/Cas13d系统精准递送至潜在感染细胞。该药物显示可使肺部病毒载量降低2.37 log TCID/mL,并使100%的小鼠免受致命性流感感染。基于SCSD的CRISPR/Cas13d系统在灵活高效治疗由快速进化的新型病毒引起的感染方面显示出前景。