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mRNA 疗法的研发。

Developing mRNA for Therapy.

机构信息

BioNTech SE, Mainz, Germany.

University of Szeged, Szeged, Hungary.

出版信息

Keio J Med. 2022;71(1):31. doi: 10.2302/kjm.71-001-ABST.

Abstract

Messenger RNA was discovered in 1961 and it took 60 years until the first mRNA became FDA-approved product in the form of COVID-19 mRNA vaccine. During those years a lot of progress has been made by hundreds of scientists. It was 1978 when the first-time isolated mRNA delivered into mammalian cells produced the encoded protein. In vitro transcription introduced in 1984 made it possible to generate any desired mRNA from the encoding plasmid using phage RNA polymerases. In the early 90s mRNA was used for therapy as well as vaccine against infectious diseases and cancer. Inflammatory nature of the mRNAs limited their in vivo use. Replacing uridine with pseudouridine made the mRNA non-immunogenic, more stable and highly translatable. Delivery of the lipid nanoparticle-formulated nucleoside-modified mRNA encoding viral antigens became a platform for effective vaccine. Labile nature of the mRNA is ideal for transient production of the viral antigen, to generate effective antibody and cellular immune response. The mRNA platform is revolutionizing the delivery of effective and safe vaccines, therapeutics and gene therapies.

摘要

信使 RNA 于 1961 年被发现,直到 COVID-19 mRNA 疫苗成为首个获得 FDA 批准的产品,历经了 60 年。在这期间,数百位科学家取得了大量进展。1978 年,首次分离的 mRNA 被递送到哺乳动物细胞中,产生了编码蛋白。1984 年引入的体外转录技术使得可以使用噬菌体 RNA 聚合酶从编码质粒中生成任何所需的 mRNA。90 年代初,mRNA 被用于治疗传染病和癌症的疫苗。mRNA 的炎症性质限制了其在体内的应用。用假尿嘧啶替代尿嘧啶使得 mRNA 具有非免疫原性、更稳定和高度可翻译性。脂质纳米颗粒配方的核苷修饰的编码病毒抗原的 mRNA 的递送成为了有效疫苗的平台。mRNA 的不稳定性非常适合瞬时产生病毒抗原,以产生有效的抗体和细胞免疫反应。mRNA 平台正在彻底改变有效和安全疫苗、疗法和基因疗法的递药方式。

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