Tailoring mRNA Vaccine to Balance Innate/Adaptive Immune Response

被引:253
|
作者
Linares-Fernandez, Sergio [1 ]
Lacroix, Celine [1 ]
Exposito, Jean-Yves [1 ]
Verrier, Bernard [1 ]
机构
[1] Univ Claude Bernard Lyon 1, CNRS, Lab Biol Tissulaire & Ingn Therapeut, UMR 5305,Univ Lyon 1,IBCP, Lyon, France
关键词
CODON OPTIMIZATION; TRANSLATION ELONGATION; INNATE IMMUNITY; IN-VIVO; DELIVERY; IMMUNOGENICITY; ACTIVATION; VIRUS; THERAPEUTICS; RECOGNITION;
D O I
10.1016/j.molmed.2019.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
mRNA vaccine platforms present numerous advantages, such as versatility, rapid production, and induction of cellular and humoral responses. Moreover, mRNAs have inherent adjuvant properties due to their complex interaction with pattern recognition receptors (PRRs). This recognition can be either beneficial in activating antigen-presenting cells (APCs) or detrimental by indirectly blocking mRNA translation. To decipher this Janus effect, we describe the different innate response mechanisms triggered by mRNA molecules and how each element from the 50 cap to the poly-A tail interferes with innate/adaptive immune responses. Then, we emphasize the importance of some critical steps such as production, purification, and formulation as key events to further improve the quality of immune responses and balance innate and adaptive immunity.
引用
收藏
页码:311 / 323
页数:13
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