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Spleen Selective Enhancement of Transfection Activities of Plasmid DNA Driven by Octaarginine and An Ionizable Lipid and Its Implications for Cancer Immunization

مؤلف البحث
Seigo Kimura, Ikramy A. Khalil, Yaser H.A. Elewa, Hideyoshi Harashima
قسم البحث
مجلة البحث
Journal of Controlled Release
الناشر
Elsevier
تصنيف البحث
1
عدد البحث
Vol. 313
موقع البحث
https://doi.org/10.1016/j.jconrel.2019.09.009
سنة البحث
2019
المشارك في البحث
ملخص البحث

Efficiently delivering plasmid DNA (pDNA) to the spleen is particularly significant for DNA immunization. However, increasing the efficiency of gene expression in spleen cells for achieving a therapeutic effect remains a serious challenge. An ideal spleen-targeted system should avoid liver uptake and should efficiently transfect specific functional spleen cells. Here, we report on pDNA nanocarriers with enhanced transfection in spleen cells driven by synergism between an octaarginine (R8) peptide and YSK05; a pH-responsive ionizable lipid. A double-coating design is essential for enhancing spleen selective transfection which is significantly affected by the total amount of lipid and the composition of the outer coat. The optimized R8/YSK system shows a high gene expression in the spleen with a high spleen/liver ratio and a surprising ability to target spleen B cells. Compared to other organs, the high spleen activity cannot be explained based on the amount of pDNA delivered to each organ, indicating that the system is extremely efficient in transfecting spleen cells. The system can be used in cancer immunization where a strong anti-tumor effect was observed in mice immunized with the R8/YSK system encapsulating antigen-encoding pDNA. The R8/YSK system holds great promise for future applications in the field of DNA vaccination.