共 23 条
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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