先天免疫系统
信使核糖核酸
免疫系统
体内
细胞生物学
核糖核酸
核酸
化学
生物
免疫学
生物化学
遗传学
基因
作者
Jennifer Nelson,Elizabeth W. Sorensen,Shrutika Mintri,Amy E. Rabideau,Wei Zheng,Gilles Besin,Nikhil Khatwani,Stephen Su,Edward J. Miracco,William Issa,Stephen Hoge,Matthew G. Stanton,John L. Joyal
出处
期刊:Science Advances
[American Association for the Advancement of Science (AAAS)]
日期:2020-06-24
卷期号:6 (26)
被引量:257
标识
DOI:10.1126/sciadv.aaz6893
摘要
Messenger RNA (mRNA) represents an attractive therapeutic modality for potentially a wide range of clinical indications but requires uridine chemistry modification and/or tuning of the production process to prevent activation of cellular innate immune sensors and a concomitant reduction in protein expression. To decipher the relative contributions of these factors on immune activation, here, we compared, in multiple cell and in vivo models, mRNA that encodes human erythropoietin incorporating either canonical uridine or
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