Menzies Health Institute Queensland, School of Medical Science Griffith University, Gold Coast Campus, QLD 4222, Australia.
Center for Gene Therapy, Hematological Malignancy and Stem Cell Transplantation Institute at the City of Hope and City of Hope Beckman Research Institute, 1500 E. Duarte Road, Duarte, CA 91010, USA; Irell & Manella Graduate School of Biological Sciences at the City of Hope, Duarte, CA 91010, USA.
Mol Ther. 2021 Jul 7;29(7):2219-2226. doi: 10.1016/j.ymthe.2021.05.004. Epub 2021 May 14.
Coronavirus disease 2019 (COVID-19) is caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection in humans. Despite several emerging vaccines, there remains no verifiable therapeutic targeted specifically to the virus. Here we present a highly effective small interfering RNA (siRNA) therapeutic against SARS-CoV-2 infection using a novel lipid nanoparticle (LNP) delivery system. Multiple siRNAs targeting highly conserved regions of the SARS-CoV-2 virus were screened, and three candidate siRNAs emerged that effectively inhibit the virus by greater than 90% either alone or in combination with one another. We simultaneously developed and screened two novel LNP formulations for the delivery of these candidate siRNA therapeutics to the lungs, an organ that incurs immense damage during SARS-CoV-2 infection. Encapsulation of siRNAs in these LNPs followed by in vivo injection demonstrated robust repression of virus in the lungs and a pronounced survival advantage to the treated mice. Our LNP-siRNA approaches are scalable and can be administered upon the first sign of SARS-CoV-2 infection in humans. We suggest that an siRNA-LNP therapeutic approach could prove highly useful in treating COVID-19 disease as an adjunctive therapy to current vaccine strategies.
新型冠状病毒病(COVID-19)是由人类感染严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起的。尽管出现了几种新兴疫苗,但仍然没有针对该病毒的经证实的特效治疗方法。在这里,我们使用新型脂质纳米颗粒(LNP)传递系统,展示了一种针对 SARS-CoV-2 感染的高效小干扰 RNA(siRNA)治疗方法。筛选了针对 SARS-CoV-2 病毒高度保守区域的多种 siRNA,单独或组合使用时,有三种候选 siRNA 能够有效抑制病毒超过 90%。我们同时开发并筛选了两种新型 LNP 配方,用于将这些候选 siRNA 治疗药物递送到肺部,肺部在 SARS-CoV-2 感染过程中会受到巨大损伤。将 siRNA 包封在这些 LNP 中,然后进行体内注射,证明了它们在肺部具有强大的病毒抑制作用,并显著提高了治疗小鼠的存活率。我们的 LNP-siRNA 方法具有可扩展性,可以在人类出现 SARS-CoV-2 感染的第一迹象时进行给药。我们认为,siRNA-LNP 治疗方法可能作为当前疫苗策略的辅助治疗方法,在治疗 COVID-19 疾病方面非常有用。