微泡
免疫原性
外体
信使核糖核酸
计算生物学
生物
免疫系统
细胞生物学
小RNA
免疫学
基因
生物化学
作者
Zoya Iqbal,Khurrum Rehman,Ayesha Mahmood,Maryam Shabbir,Yujie Liang,Duan Li,Hui Zeng
标识
DOI:10.1186/s12951-024-02634-x
摘要
Abstract Messenger RNA (mRNA) has emerged as a promising therapeutic molecule with numerous clinical applications in treating central nervous system disorders, tumors, COVID-19, and other diseases. mRNA therapies must be encapsulated into safe, stable, and effective delivery vehicles to preserve the cargo from degradation and prevent immunogenicity. Exosomes have gained growing attention in mRNA delivery because of their good biocompatibility, low immunogenicity, small size, unique capacity to traverse physiological barriers, and cell-specific tropism. Moreover, these exosomes can be engineered to utilize the natural carriers to target specific cells or tissues. This targeted approach will enhance the efficacy and reduce the side effects of mRNAs. However, difficulties such as a lack of consistent and reliable methods for exosome purification and the efficient encapsulation of large mRNAs into exosomes must be addressed. This article outlines current breakthroughs in cell-derived vesicle-mediated mRNA delivery and its biomedical applications. Graphical Abstract
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