Straight to the point: targeted mRNA-delivery to immune cells for improved vaccine design

被引:13
|
作者
Clemente, Bruna [1 ]
Denis, Maxime [1 ]
Silveira, Camila Pedroso [1 ]
Schiavetti, Francesca [1 ]
Brazzoli, Michela [1 ]
Stranges, Daniela [1 ]
机构
[1] GSK, Siena, Italy
来源
FRONTIERS IN IMMUNOLOGY | 2023年 / 14卷
关键词
mRNA vaccine; dendritic cells; targeted delivery; C-type lectins; lipid nanoparticles; C-TYPE LECTIN; HUMAN DENDRITIC CELLS; RECEPTORS DC-SIGN; LANGERHANS CELLS; ANTIGEN PRESENTATION; LIPID NANOPARTICLES; CROSS-PRESENTATION; CARBOHYDRATE-RECOGNITION; MANNOSYLATED LIPOSOMES; SURFACE-RECEPTOR;
D O I
10.3389/fimmu.2023.1294929
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
With the deepening of our understanding of adaptive immunity at the cellular and molecular level, targeting antigens directly to immune cells has proven to be a successful strategy to develop innovative and potent vaccines. Indeed, it offers the potential to increase vaccine potency and/or modulate immune response quality while reducing off-target effects. With mRNA-vaccines establishing themselves as a versatile technology for future applications, in the last years several approaches have been explored to target nanoparticles-enabled mRNA-delivery systems to immune cells, with a focus on dendritic cells. Dendritic cells (DCs) are the most potent antigen presenting cells and key mediators of B- and T-cell immunity, and therefore considered as an ideal target for cell-specific antigen delivery. Indeed, improved potency of DC-targeted vaccines has been proved in vitro and in vivo. This review discusses the potential specific targets for immune system-directed mRNA delivery, as well as the different targeting ligand classes and delivery systems used for this purpose.
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页数:16
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