Efficient Colorectal Cancer Gene Therapy with IL-15 mRNA Nanoformulation

被引:49
|
作者
Lei, Sibei [1 ,2 ]
Zhang, Xueyan [1 ,2 ]
Men, Ke [1 ,2 ]
Gao, Yan [1 ,2 ]
Yang, Xijing [3 ]
Wu, Sisi [1 ,2 ]
Duan, Xingmei [4 ,5 ]
Wei, Yuquan [1 ,2 ]
Tong, Rongsheng [4 ,5 ]
机构
[1] Sichuan Univ, Natl Clin Res Ctr Geriatr, State Key Lab Biotherapy, West China Hosp, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Natl Clin Res Ctr Geriatr, Canc Ctr, West China Hosp, Chengdu 610041, Peoples R China
[3] Sichuan Univ, West China Hosp, Anim Expt Ctr, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Acad Med Sci, Dept Pharm, Chengdu 610072, Peoples R China
[5] Univ Elect Sci & Technol China, Sch Med, Sichuan Prov Peoples Hosp, Personalized Drug Therapy Key Lab Sichuan Prov, Chengdu 610072, Peoples R China
关键词
IVT mRNA; cancer gene therapy; IL-15; gene delivery; SYSTEMIC DELIVERY; DRUG-DELIVERY; POLYETHYLENIMINE; INTERLEUKIN-15; ENDOCYTOSIS; ACTIVATION; EFFICACY; KINASE;
D O I
10.1021/acs.molpharmaceut.0c00451
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
Immunogene therapy is a novel method for the treatment of colorectal cancer. Cytokine IL-15 has exhibited therapeutic anticancer potential due to its immune-stimulation property. However, conventional IL-15-based cancer gene therapy studies have been performed using the plasmid DNA form, which has potential shortcomings including weak delivery efficiency and backbone effect. In this study, an IL-15 immunogene therapy study for colon cancer using in vitro transcript mRNA is described. A protamine/liposome system (CLPP) is developed to provide efficient condensation and delivery capacity for in vivo mRNA transportation. They demonstrated that the prepared CLPP system could deliver the IL-15-encoding mRNA into C26 cells with high efficacy. The secretory expressed IL-15 cytokine by the C26 cells successfully produced lymphocyte stimulation and triggered anticancer cytotoxicity upon cancer cells in vitro. Local or systemic administration of the CLPP/mIL-15 complex exhibited obvious inhibition effects on multiple C26 murine colon cancer models with inhibition rates of up to 70% in the C26 abdominal cavity metastasis tumor model, 55% in the subcutaneous model, and 69% in the pulmonary metastasis model, demonstrating high efficacy and safety. These results successfully demonstrated the high therapeutic potential of the CLPP/mIL-15 complex for colorectal cancer immunogene therapy.
引用
收藏
页码:3378 / 3391
页数:14
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