Endosomal escape: A bottleneck for LNP- mediated therapeutics

被引:168
作者
Chatterjee, Sushmita [1 ,2 ,3 ,4 ]
Kon, Edo [1 ,2 ,3 ,4 ]
Sharma, Preeti [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, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Iby & Aladar Fleischman Fac Engn, Dept Mat Sci & Engn, IL-69978 Tel Aviv, Israel
[3] Tel Aviv Univ, Ctr Nanosci & Nanotechnol, IL-69978 Tel Aviv, Israel
[4] Tel Aviv Univ, Canc Biol Res Ctr, IL-69978 Tel Aviv, Israel
基金
欧洲研究理事会;
关键词
mRNA; LNPs; endo-; lysosomes; endosomal; RNA vaccines and therapeutics; CALCIUM-PHOSPHATE NANOPARTICLES; CELL-PENETRATING PEPTIDES; MESSENGER-RNA VACCINES; FUSOGENIC LIPOSOMES; LIPID NANOPARTICLES; SIRNA DELIVERY; PROTON SPONGE; INTRACELLULAR DELIVERY; SYSTEMIC DELIVERY; TRAFFICKING;
D O I
10.1073/pnas.2307800120
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Lipid nanoparticles (LNPs) have recently emerged as a powerful and versatile clinically approved platform for nucleic acid delivery, specifically for mRNA vaccines. A major bottleneck in the field is the release of mRNALNPs from the endosomal pathways into the cytosol of cells where they can execute their encoded functions. The data regarding the mechanism of these endosomal escape processes are limited and contradicting. Despite extensive research, there is no consensus regarding the compartment of escape, the cause of the inefficient escape and are currently lacking a robust method to detect the escape. Here, we review the currently known mechanisms of endosomal escape and the available methods to study this process. We critically discuss the limitations and challenges of these methods and the possibilities to overcome these challenges. We propose that the development of currently lacking robust, quantitative high- throughput techniques to study endosomal escape is timely and essential. A better understanding of this process will enable better RNA- LNP designs with improved efficiency to unlock new therapeutic modalities.
引用
收藏
页数:9
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