Developing mRNA for Therapy.

IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL KEIO JOURNAL OF MEDICINE Pub Date : 2022-01-01 DOI:10.2302/kjm.71-001-ABST
Katalin Karikó
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引用次数: 1

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.

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开发用于治疗的 mRNA。
信使核糖核酸(mRNA)于 1961 年被发现,直到第一个 mRNA 以 COVID-19 mRNA 疫苗的形式成为美国食品及药物管理局(FDA)批准的产品,中间经历了 60 年的时间。在这些年里,数百名科学家取得了许多进展。1978 年,首次分离出的 mRNA 进入哺乳动物细胞后产生了编码蛋白质。1984 年引入的体外转录技术使得利用噬菌体 RNA 聚合酶从编码质粒中产生任何所需的 mRNA 成为可能。90 年代初,mRNA 被用于治疗传染病和癌症,并用作疫苗。mRNA 的炎症性限制了其在体内的应用。用假尿苷取代尿苷可以使 mRNA 不产生免疫原性,更加稳定,并具有高度可翻译性。通过脂质纳米粒子输送经核苷修饰的编码病毒抗原的 mRNA 成为有效疫苗的平台。mRNA 的易变性非常适合病毒抗原的瞬时生产,从而产生有效的抗体和细胞免疫反应。mRNA 平台为提供有效、安全的疫苗、疗法和基因疗法带来了革命性的变化。
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来源期刊
KEIO JOURNAL OF MEDICINE
KEIO JOURNAL OF MEDICINE MEDICINE, RESEARCH & EXPERIMENTAL-
CiteScore
3.10
自引率
0.00%
发文量
23
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