An RNA toolbox for cancer immunotherapy

核糖核酸 RNA干扰 癌症免疫疗法 计算生物学 适体 免疫疗法 癌症 免疫系统 基因 生物 癌症研究 免疫学 遗传学
作者
Fernando Pastor,Pedro Berraondo,Iñaki Etxeberría,Josh P. Frederick,Uğur Şahin,Eli Gilboa,Ignacio Melero
出处
期刊:Nature Reviews Drug Discovery [Nature Portfolio]
卷期号:17 (10): 751-767 被引量:215
标识
DOI:10.1038/nrd.2018.132
摘要

Cancer immunotherapy has revolutionized oncology practice. However, current protein and cell therapy tools used in cancer immunotherapy are far from perfect, and there is room for improvement regarding their efficacy and safety. RNA-based structures have diverse functions, ranging from gene expression and gene regulation to pro-inflammatory effects and the ability to specifically bind different molecules. These functions make them versatile tools that may advance cancer vaccines and immunomodulation, surpassing existing approaches. These technologies should not be considered as competitors of current immunotherapies but as partners in synergistic combinations and as a clear opportunity to reach more efficient and personalized results. RNA and RNA derivatives can be exploited therapeutically as a platform to encode protein sequences, provide innate pro-inflammatory signals to the immune system (such as those denoting viral infection), control the expression of other RNAs (including key immunosuppressive factors) post-transcriptionally and conform structural scaffoldings binding proteins that control immune cells by modifying their function. Nascent RNA immunotherapeutics include RNA vaccines encoding cancer neoantigens, mRNAs encoding immunomodulatory factors, viral RNA analogues, interference RNAs and protein-binding RNA aptamers. These approaches are already in early clinical development with promising safety and efficacy results.
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