信使核糖核酸
细胞生物学
生物
化学
生物化学
基因
作者
Kevin Van der Jeught,Stefaan De Koker,Lukasz Bialkowski,Carlo Heirman,Patrick Tjok Joe,Federico Perche,Sarah Maenhout,Sanne Bevers,Katrijn Broos,Kim Deswarte,Virginie Malard,Hamida Hammad,Patrick Baril,Thierry Benvegnu,Paul‐Alain Jaffrès,Sander A.A. Kooijmans,Raymond M. Schiffelers,Stefan Lienenklaus,Patrick Midoux,Chantal Pichon,Karine Breckpot,Kris Thielemans
出处
期刊:ACS Nano
[American Chemical Society]
日期:2018-09-26
卷期号:12 (10): 9815-9829
被引量:106
标识
DOI:10.1021/acsnano.8b00966
摘要
In vitro transcribed mRNA constitutes a versatile platform to encode antigens and to evoke CD8 T-cell responses. Systemic delivery of mRNA packaged into cationic liposomes (lipoplexes) has proven particularly powerful in achieving effective antitumor immunity in animal models. Yet, T-cell responses to mRNA lipoplexes critically depend on the induction of type I interferons (IFN), potent pro-inflammatory cytokines, which inflict dose-limiting toxicities. Here, we explored an advanced hybrid lipid polymer shell mRNA nanoparticle (lipopolyplex) endowed with a trimannose sugar tree as an alternative delivery vehicle for systemic mRNA vaccination. Like mRNA lipoplexes, mRNA lipopolyplexes were extremely effective in conferring antitumor T-cell immunity upon systemic administration. Conversely to mRNA lipoplexes, mRNA lipopolyplexes did not rely on type I IFN for effective T-cell immunity. This differential mode of action of mRNA lipopolyplexes enabled the incorporation of N1 methyl pseudouridine nucleoside modified mRNA to reduce inflammatory responses without hampering T-cell immunity. This feature was attributed to mRNA lipopolyplexes, as the incorporation of thus modified mRNA into lipoplexes resulted in strongly weakened T-cell immunity. Taken together, we have identified lipopolyplexes containing N1 methyl pseudouridine nucleoside modified mRNA as potent yet low-inflammatory alternatives to the mRNA lipoplexes currently explored in early phase clinical trials.
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