Nanocarrier design for pathogen-inspired innate immune agonist delivery

被引:1
|
作者
Kane, Griffin I. [1 ,4 ]
Brassil, Meghan L. [1 ,4 ]
Diaz-Infante, Miranda B. [1 ,4 ]
Atukorale, Prabhani U. [1 ,2 ,3 ,4 ]
机构
[1] Univ Massachusetts Amherst, Dept Biomed Engn, Amherst, MA 01003 USA
[2] Univ Massachusetts, Chan Med Sch, Dept Mol Cell & Canc Biol, Worcester, MA 01605 USA
[3] Univ Massachusetts, Chan Med Sch, Dept Med, Div Innate Immun, Worcester, MA 01605 USA
[4] Univ Massachusetts, UMass Canc Ctr, Chan Med Sch, Worcester, MA 01605 USA
关键词
NANOPARTICLES; CANCER; CELLS; ENCAPSULATION; NEOANTIGENS; CODELIVERY; MONOCYTES; TOXICITY; POTENT; NOD1;
D O I
10.1016/j.it.2024.07.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In complex diseases such as cancer, modulating cytokine signatures of disease using innate immune agonists holds therapeutic promise. Novel multi-agonist treatments offer tunable control of the immune system because they are uniquely pathogen inspired, eliciting robust antitumor responses by promoting synergistic cytokine responses. However, the chief strategic hurdle is ensuring multi-agonist delivery to the same target cells, highlighting the importance of using nanomaterial-based carriers. Here, we place nanocarriers in center stage and review the delivery hurdles related to the varying extra- and intracellular localizations of innate immune receptors. We discuss a range of nanomaterials used for multi-agonist delivery, highlighting their respective benefits and drawbacks. Our overarching stance is that rational nanocarrier design is crucial for developing pathogen-inspired multi-agonist immunotherapies.
引用
收藏
页码:678 / 692
页数:15
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