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一种用于治疗新冠肺炎的靶向严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的小干扰RNA纳米颗粒疗法。

A SARS-CoV-2 targeted siRNA-nanoparticle therapy for COVID-19.

作者信息

Idris Adi, Davis Alicia, Supramaniam Aroon, Acharya Dhruba, Kelly Gabrielle, Tayyar Yaman, West Nic, Zhang Ping, McMillan Christopher L D, Soemardy Citradewi, Ray Roslyn, O'Meally Denis, Scott Tristan A, McMillan Nigel A J, Morris Kevin V

出版信息

bioRxiv. 2021 Apr 19:2021.04.19.440531. doi: 10.1101/2021.04.19.440531.

Abstract

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 siRNA therapeutic against SARS-CoV-2 infection using a novel lipid nanoparticle delivery system. Multiple small-interfering RNAs (siRNAs) targeting highly conserved regions of the SARS-CoV-2 virus were screened and three candidate siRNAs emerged that effectively inhibit virus by greater than 90% either alone or in combination with one another. We simultaneously developed and screened two novel lipid nanoparticle 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 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.

摘要

2019冠状病毒病(COVID-19)是由严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染人类所致。尽管有几种新出现的疫苗,但仍然没有专门针对该病毒的可验证治疗方法。在此,我们使用一种新型脂质纳米颗粒递送系统,展示了一种针对SARS-CoV-2感染的高效小干扰RNA(siRNA)治疗方法。我们筛选了多种靶向SARS-CoV-2病毒高度保守区域的小干扰RNA(siRNAs),并筛选出三种候选siRNAs,它们单独或相互组合时能有效抑制病毒达90%以上。我们同时开发并筛选了两种新型脂质纳米颗粒制剂,用于将这些候选siRNA治疗药物递送至肺部,肺部是在SARS-CoV-2感染期间遭受巨大损伤的器官。将siRNAs封装在这些脂质纳米颗粒中,然后进行注射,结果显示对肺部病毒有强大的抑制作用,并给治疗的小鼠带来显著的生存优势。我们的脂质纳米颗粒-siRNA方法具有可扩展性,可在人类出现SARS-CoV-2感染的首个迹象时给药。我们认为,作为当前疫苗策略的辅助疗法,siRNA-脂质纳米颗粒治疗方法可能在治疗COVID-19疾病方面非常有用。

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