mRNA 疫苗和免疫疗法的临床进展。

The clinical progress of mRNA vaccines and immunotherapies.

机构信息

Translate Bio, Lexington, MA, USA.

Department of Chemical Engineering, Massachusetts Institute of Technology, Cambridge, MA, USA.

出版信息

Nat Biotechnol. 2022 Jun;40(6):840-854. doi: 10.1038/s41587-022-01294-2. Epub 2022 May 9.

Abstract

The emergency use authorizations (EUAs) of two mRNA-based severe acute respiratory syndrome coronavirus (SARS-CoV)-2 vaccines approximately 11 months after publication of the viral sequence highlights the transformative potential of this nucleic acid technology. Most clinical applications of mRNA to date have focused on vaccines for infectious disease and cancer for which low doses, low protein expression and local delivery can be effective because of the inherent immunostimulatory properties of some mRNA species and formulations. In addition, work on mRNA-encoded protein or cellular immunotherapies has also begun, for which minimal immune stimulation, high protein expression in target cells and tissues, and the need for repeated administration have led to additional manufacturing and formulation challenges for clinical translation. Building on this momentum, the past year has seen clinical progress with second-generation coronavirus disease 2019 (COVID-19) vaccines, Omicron-specific boosters and vaccines against seasonal influenza, Epstein-Barr virus, human immunodeficiency virus (HIV) and cancer. Here we review the clinical progress of mRNA therapy as well as provide an overview and future outlook of the transformative technology behind these mRNA-based drugs.

摘要

两种基于 mRNA 的严重急性呼吸综合征冠状病毒(SARS-CoV-2)疫苗的紧急使用授权(EUA)在病毒序列公布约 11 个月后获得批准,这突显了这种核酸技术的变革潜力。迄今为止,mRNA 的大多数临床应用都集中在传染病和癌症疫苗上,对于这些疫苗,由于某些 mRNA 种类和制剂的固有免疫刺激性,低剂量、低蛋白表达和局部递送就可以有效。此外,针对 mRNA 编码蛋白或细胞免疫疗法的研究也已经开始,由于需要最小的免疫刺激、目标细胞和组织中的高蛋白表达以及需要重复给药,这导致了临床转化的额外制造和制剂挑战。在此基础上,过去一年,第二代 2019 冠状病毒病(COVID-19)疫苗、针对奥密克戎的加强针以及针对季节性流感、 Epstein-Barr 病毒、人类免疫缺陷病毒(HIV)和癌症的疫苗都取得了临床进展。本文我们综述了 mRNA 疗法的临床进展,并概述了这些基于 mRNA 的药物背后变革性技术的未来展望。

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