Gilboa Eli, Boczkowski David, Nair Smita K
Department of Microbiology and Immunology, Sylvester Comprehensive Cancer Center, Miller School of Medicine, University of Miami, Miami, Florida, USA.
Department of Surgery, Duke University School of Medicine, Durham, North Carolina, USA.
Nucleic Acid Ther. 2022 Dec;32(6):449-456. doi: 10.1089/nat.2021.0103. Epub 2022 Nov 7.
The success of mRNA vaccines against COVID-19 is nothing short of a medical revolution. Given its chemical lability the use of mRNA as a therapeutic has been counterintuitive and met with skepticism. The development of mRNA-based COVID-19 vaccines was the culmination of long and painstaking efforts by many investigators spanning over 30 years and culminating with the seminal studies of Kariko and Weissman. This review will describe one chapter in this saga, studies that have shown that mRNA can function as a therapeutic. It started with our seminal observation that dendritic cells (DCs) transfected with mRNA administered to mice inhibits tumor growth, and led to first-in-human clinical trials with mRNA vaccines in cancer patients. The clinical development of this patient-specific DCs-mRNA approach and use on a larger scale was hindered by the challenges associated with personalized cell therapies. Confirmed and extended by many investigators, these studies did serve as impetus and motivation that led scientists to persevere, eventually leading to the development of simple, broadly applicable, and highly effective protocols of directly injecting mRNA into patients, culminating in the COVID-19 mRNA vaccines.
针对新冠病毒的信使核糖核酸(mRNA)疫苗的成功堪称一场医学革命。鉴于其化学不稳定性,将mRNA用作治疗手段一直有悖常理且遭到质疑。基于mRNA的新冠疫苗的研发是众多研究人员历经30多年漫长而艰苦努力的成果,最终以卡里科(Kariko)和魏斯曼(Weissman)的开创性研究告终。本综述将讲述这一历程中的一个篇章,即那些表明mRNA可作为治疗手段的研究。这一历程始于我们的开创性观察,即给小鼠注射经mRNA转染的树突状细胞(DCs)可抑制肿瘤生长,并由此开启了针对癌症患者的mRNA疫苗人体首次临床试验。这种针对特定患者的DCs - mRNA方法的临床开发以及大规模应用,因个性化细胞疗法相关的挑战而受阻。这些研究得到了众多研究人员的证实和拓展,确实为科学家们提供了坚持下去的动力,最终促成了将mRNA直接注射给患者的简单、广泛适用且高效方案的开发,最终催生了新冠mRNA疫苗。