mRNA Vaccine Nanoplatforms and Innate Immunity

被引:8
|
作者
Wei, Lai [1 ]
Dong, Chunhong [1 ]
Zhu, Wandi [1 ]
Wang, Bao-Zhong [1 ]
机构
[1] Georgia State Univ, Inst Biomed Sci, Ctr Inflammat Immun & Infect, Atlanta, GA 30303 USA
来源
VIRUSES-BASEL | 2024年 / 16卷 / 01期
基金
美国国家卫生研究院;
关键词
mRNA vaccine; innate immunity; lipid nanoparticles; polymer nanoparticles; adjuvants; LIPID NANOPARTICLES; POLYMERIC NANOPARTICLES; SYSTEMIC DELIVERY; IN-VITRO; T-CELLS; TRANSFECTION; IFN; TOLL-LIKE-RECEPTOR-7; PSEUDOURIDINE; MYOCARDITIS;
D O I
10.3390/v16010120
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
mRNA-based vaccine technology has been significantly developed and enhanced, particularly highlighted by the authorization of mRNA vaccines for addressing the COVID-19 pandemic. Various biomaterials are developed in nano-scales and applied as mRNA vaccine delivery platforms. However, how these mRNA nanoplatforms influence immune responses has not been thoroughly studied. Hence, we have reviewed the current understanding of various mRNA vaccine platforms. We discussed the possible pathways through which these platforms moderate the host's innate immunity and contribute to the development of adaptive immunity. We shed light on their development in reducing biotoxicity and enhancing antigen delivery efficiency. Beyond the built-in adjuvanticity of mRNA vaccines, we propose that supplementary adjuvants may be required to fine-tune and precisely control innate immunity and subsequent adaptive immune responses.
引用
收藏
页数:11
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