Messenger RNA (mRNA) nanoparticle tumour vaccination

被引:53
作者
Phua, Kyle K. L. [1 ]
Nair, Smita K. [2 ]
Leong, Kam W. [1 ,2 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Med Ctr, Dept Surg, Durham, NC 27708 USA
关键词
CYTOTOXIC T-LYMPHOCYTES; ANTIGEN-PRESENTING CELLS; HUMAN DENDRITIC CELLS; CLASS-II MOLECULES; MHC CLASS-I; GENE DELIVERY; PLASMID DNA; IMMUNE-RESPONSES; POLYMER NANOPARTICLES; ANTITUMOR IMMUNITY;
D O I
10.1039/c4nr01346h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Use of mRNA-based vaccines for tumour immunotherapy has gained increasing attention in recent years. A growing number of studies applying nanomedicine concepts to mRNA tumour vaccination show that the mRNA delivered in nanoparticle format can generate a more robust immune response. Advances in the past decade have deepened our understanding of gene delivery barriers, mRNA's biological stability and immunological properties, and support the notion for engineering innovations tailored towards a more efficient mRNA nanoparticle vaccine delivery system. In this review we will first examine the suitability of mRNA for engineering manipulations, followed by discussion of a model framework that highlights the barriers to a robust anti-tumour immunity mediated by mRNA encapsulated in nanoparticles. Finally, by consolidating existing literature on mRNA nanoparticle tumour vaccination within the context of this framework, we aim to identify bottlenecks that can be addressed by future nanoengineering research.
引用
收藏
页码:7715 / 7729
页数:15
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