Department of Critical Care Medicine, Frontiers Science Center for Disease-related Molecular Network, State Key Laboratory of Biotherapy and Cancer Center, West China Hospital, Sichuan University, Chengdu, China.
Department of Biomedical Sciences, School of Medicine and Health Sciences, University of North Dakota, Grand Forks, ND, 58203, USA.
Signal Transduct Target Ther. 2022 May 21;7(1):166. doi: 10.1038/s41392-022-01007-w.
The therapeutic use of messenger RNA (mRNA) has fueled great hope to combat a wide range of incurable diseases. Recent rapid advances in biotechnology and molecular medicine have enabled the production of almost any functional protein/peptide in the human body by introducing mRNA as a vaccine or therapeutic agent. This represents a rising precision medicine field with great promise for preventing and treating many intractable or genetic diseases. In addition, in vitro transcribed mRNA has achieved programmed production, which is more effective, faster in design and production, as well as more flexible and cost-effective than conventional approaches that may offer. Based on these extraordinary advantages, mRNA vaccines have the characteristics of the swiftest response to large-scale outbreaks of infectious diseases, such as the currently devastating pandemic COVID-19. It has always been the scientists' desire to improve the stability, immunogenicity, translation efficiency, and delivery system to achieve efficient and safe delivery of mRNA. Excitingly, these scientific dreams have gradually been realized with the rapid, amazing achievements of molecular biology, RNA technology, vaccinology, and nanotechnology. In this review, we comprehensively describe mRNA-based therapeutics, including their principles, manufacture, application, effects, and shortcomings. We also highlight the importance of mRNA optimization and delivery systems in successful mRNA therapeutics and discuss the key challenges and opportunities in developing these tools into powerful and versatile tools to combat many genetic, infectious, cancer, and other refractory diseases.
信使 RNA(mRNA)的治疗用途激发了人们战胜广泛的不治之症的巨大希望。最近生物技术和分子医学的快速发展使人们能够通过引入 mRNA 作为疫苗或治疗剂来生产人体内几乎任何功能性蛋白质/肽。这代表了一个新兴的精准医学领域,在预防和治疗许多难治性或遗传性疾病方面具有巨大的潜力。此外,体外转录的 mRNA 已实现了程序化生产,与传统方法相比,其设计和生产更快、更灵活且更具成本效益,传统方法可能具有更大的优势。基于这些非凡的优势,mRNA 疫苗具有应对传染病大爆发(如目前破坏性极强的 COVID-19 大流行)的最快反应的特点。提高 mRNA 的稳定性、免疫原性、翻译效率和递送系统以实现高效和安全的 mRNA 递送一直是科学家们的愿望。令人兴奋的是,随着分子生物学、RNA 技术、疫苗学和纳米技术的快速、惊人的成就,这些科学梦想逐渐得以实现。在这篇综述中,我们全面描述了基于 mRNA 的治疗方法,包括它们的原理、制造、应用、效果和缺点。我们还强调了 mRNA 优化和递送系统在成功的 mRNA 治疗中的重要性,并讨论了开发这些工具成为对抗许多遗传、感染、癌症和其他难治性疾病的强大和多功能工具的关键挑战和机遇。