Targeting cancer with mRNA-lipid nanoparticles: key considerations and future prospects

被引:63
|
作者
Kon, Edo [1 ,2 ,3 ,4 ]
Ad-El, Nitay [1 ,2 ,3 ,4 ]
Hazan-Halevy, Inbal [1 ,2 ,3 ,4 ]
Stotsky-Oterin, Lior [1 ,2 ,3 ,4 ]
Peer, Dan [1 ,2 ,3 ,4 ]
机构
[1] Tel Aviv Univ, George S Wise Fac Life Sci, Shmunis Sch Biomed & Canc Res, Lab Precis Nanomed, Tel Aviv, Israel
[2] Tel Aviv Univ, Iby & Aladar Fleischman Fac Engn, Dept Mat Sci & Engn, Tel Aviv, Israel
[3] Tel Aviv Univ, Ctr Nanosci & Nanotechnol, Tel Aviv, Israel
[4] Tel Aviv Univ, Canc Biol Res Ctr, Tel Aviv, Israel
基金
欧洲研究理事会;
关键词
ANTI-PEG ANTIBODIES; SOLID TUMORS; CELLULAR UPTAKE; DELIVERY; INTERNALIZATION; DESIGN; IMMUNOGENICITY; EXPRESSION; VACCINES; SYSTEMS;
D O I
10.1038/s41571-023-00811-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Harnessing mRNA-lipid nanoparticles (LNPs) to treat patients with cancer has been an ongoing research area that started before these versatile nanoparticles were successfully used as COVID-19 vaccines. Currently, efforts are underway to harness this platform for oncology therapeutics, mainly focusing on cancer vaccines targeting multiple neoantigens or direct intratumoural injections of mRNA-LNPs encoding pro-inflammatory cytokines. In this Review, we describe the opportunities of using mRNA-LNPs in oncology applications and discuss the challenges for successfully translating the findings of preclinical studies of these nanoparticles into the clinic. We critically appraise the potential of various mRNA-LNP targeting and delivery strategies, considering physiological, technological and manufacturing challenges. We explore these approaches in the context of the potential clinical applications best suited to each approach and highlight the obstacles that currently need to be addressed to achieve these applications. Finally, we provide insights from preclinical and clinical studies that are leading to this powerful platform being considered the next frontier in oncology treatment. In oncology, mRNA-lipid nanoparticles (LNPs) have been used either to achieve intratumoural expression of immune-stimulating cytokine combinations or as cancer vaccines, and new strategies are in development to enable the selective delivery of payloads into cancer cells previously considered unreachable. The authors of this Review present various approaches for delivering mRNA-LNPs to tumours and discuss improvements that will improve the selective targeting of cancer cells with mRNA-LNPs.
引用
收藏
页码:739 / 754
页数:16
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