Progress and prospects of mRNA-based drugs in pre-clinical and clinical applications

IF 52.7 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Signal Transduction and Targeted Therapy Pub Date : 2024-11-14 DOI:10.1038/s41392-024-02002-z
Yingying Shi, Meixing Shi, Yi Wang, Jian You
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Abstract

In the last decade, messenger ribonucleic acid (mRNA)-based drugs have gained great interest in both immunotherapy and non-immunogenic applications. This surge in interest can be largely attributed to the demonstration of distinct advantages offered by various mRNA molecules, alongside the rapid advancements in nucleic acid delivery systems. It is noteworthy that the immunogenicity of mRNA drugs presents a double-edged sword. In the context of immunotherapy, extra supplementation of adjuvant is generally required for induction of robust immune responses. Conversely, in non-immunotherapeutic scenarios, immune activation is unwanted considering the host tolerability and high expression demand for mRNA-encoded functional proteins. Herein, mainly focused on the linear non-replicating mRNA, we overview the preclinical and clinical progress and prospects of mRNA medicines encompassing vaccines and other therapeutics. We also highlight the importance of focusing on the host-specific variations, including age, gender, pathological condition, and concurrent medication of individual patient, for maximized efficacy and safety upon mRNA administration. Furthermore, we deliberate on the potential challenges that mRNA drugs may encounter in the realm of disease treatment, the current endeavors of improvement, as well as the application prospects for future advancements. Overall, this review aims to present a comprehensive understanding of mRNA-based therapies while illuminating the prospective development and clinical application of mRNA drugs.

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基于 mRNA 的药物在临床前和临床应用中的进展和前景
近十年来,基于信使核糖核酸(mRNA)的药物在免疫疗法和非免疫性应用领域都获得了极大的关注。这种兴趣的激增主要归功于各种 mRNA 分子所具有的独特优势,以及核酸递送系统的快速发展。值得注意的是,mRNA 药物的免疫原性是一把双刃剑。在免疫疗法中,一般需要额外补充佐剂,以诱导强大的免疫反应。相反,在非免疫治疗的情况下,考虑到宿主的耐受性和对 mRNA 编码功能蛋白的高表达需求,免疫激活是不需要的。在此,我们主要针对线性非复制 mRNA,概述了包括疫苗和其他疗法在内的 mRNA 药物的临床前和临床进展及前景。我们还强调了关注宿主特异性变化的重要性,包括患者的年龄、性别、病理状况和同时服用的药物,以最大限度地提高 mRNA 给药的疗效和安全性。此外,我们还探讨了 mRNA 药物在疾病治疗领域可能遇到的挑战、目前的改进工作以及未来的应用前景。总之,本综述旨在全面介绍基于 mRNA 的疗法,同时阐明 mRNA 药物的开发和临床应用前景。
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来源期刊
Signal Transduction and Targeted Therapy
Signal Transduction and Targeted Therapy Biochemistry, Genetics and Molecular Biology-Genetics
CiteScore
44.50
自引率
1.50%
发文量
384
审稿时长
5 weeks
期刊介绍: Signal Transduction and Targeted Therapy is an open access journal that focuses on timely publication of cutting-edge discoveries and advancements in basic science and clinical research related to signal transduction and targeted therapy. Scope: The journal covers research on major human diseases, including, but not limited to: Cancer,Cardiovascular diseases,Autoimmune diseases,Nervous system diseases.
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