Advances in targeted delivery of mRNA into immune cells for enhanced cancer therapy

被引:2
|
作者
Huang, Linzhuo [1 ,2 ,3 ]
Huang, Zhiquan [1 ,2 ,3 ]
Zhang, Yuxuan [1 ,2 ,3 ]
Lin, Chunhao [1 ,2 ,3 ]
Zhao, Zixuan [4 ]
Li, Rong [4 ]
Saw, Phei Er [1 ,2 ,3 ]
Xu, Xiaoding [1 ,2 ,3 ]
机构
[1] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Med Res Ctr, Guangdong Prov Key Lab Malignant Tumor Epigenet &, Guangzhou 510120, Peoples R China
[2] Sun Yat Sen Univ, Sun Yat Sen Mem Hosp, Guangzhou Key Lab Med Nanomat, Guangzhou 510120, Peoples R China
[3] Sun Yat Sen Mem Hosp, Nanhai Translat Innovat Ctr Precis Immunol, Foshan 528200, Peoples R China
[4] Univ South China, Affiliated Hosp 2, Hengyang Med Sch, Hengyang 421001, Peoples R China
来源
THERANOSTICS | 2024年 / 14卷 / 14期
基金
中国国家自然科学基金;
关键词
Messenger RNA (mRNA); immune cells; nanoparticles (NPs); targeted delivery; cancer immunotherapy; ANTIGEN-PRESENTING CELLS; CAR T-CELLS; DENDRITIC CELLS; IN-VIVO; NEUTROPHIL RECRUITMENT; ACTIVATED MACROPHAGES; ANTITUMOR IMMUNITY; KILLER-CELLS; TUMOR-GROWTH; DC-SIGN;
D O I
10.7150/thno.93745
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Messenger RNA (mRNA) therapy has been applied to the treatment of various human diseases including malignant tumors. Increasing evidences have shown that mRNA can enhance the efficacy of cancer immunotherapy by modulating the functions of immune cells and stimulating their activity. However, mRNA is a type of negatively charged biomacromolecules that are susceptible to serum nucleases and cannot readily cross the cell membrane. In the past few decades, various nanoparticles (NPs)-based delivery systems have been rationally designed and developed to facilitate the intracellular uptake and cytosolic delivery of mRNA. More importantly, by means of the specific recognition between the targeting ligands decorated on NP surface and receptors specifically expressed on immune cells, these mRNA delivery systems could be functionalized to target immune cells to further enhance the mRNA-based cancer immunotherapy. In this review, we briefly introduced the advancements of mRNA in cancer therapy, discussed the challenges faced by mRNA delivery, and systematically summarized the recent development in NPs-based mRNA delivery systems targeting various types of immune cells for cancer immunotherapy. The future development of NPs-mediated targeted mRNA delivery and their challenges in clinical translation are also discussed.
引用
收藏
页码:5528 / 5550
页数:23
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