Laboratory for Molecular Design of Pharmaceutics, Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-ku, Sapporo, Hokkaido, Japan.
Laboratory of Pharmacy and Toxicology, Graduate School of Pharmaceutical Sciences, Chiba University, Chuo-ku, Chiba-Shi, Chiba, Japan.
Nanomedicine. 2018 Nov;14(8):2587-2597. doi: 10.1016/j.nano.2018.08.006. Epub 2018 Aug 29.
Cytoplasmic DNA triggers cellular immunity via activating the stimulator of interferon genes pathway. Since DNA is degradable and membrane impermeable, delivery system would permit cytoplasmic delivery by destabilizing the endosomal membrane for the use as an adjuvant. Herein, we report on the development of a plasmid DNA (pDNA)-encapsulating lipid nanoparticle (LNP). The structural components include an SS-cleavable and pH-activated lipid-like material that mounts vitamin E as a hydrophobic scaffold, and dual sensing motifs that are responsive to the intracellular environment (ssPalmE). The pDNA-encapsulating LNP (ssPalmE-LNP) induced a high interferon-β production in Raw 264.7 cells. The subcutaneous injection of ssPalmE-LNP strongly enhanced antigen-specific cytotoxic T cell activity. The ssPalmE-LNP treatment efficiently induced antitumor effects against E.G7-OVA tumor and B16-F10 melanoma metastasis. Furthermore, when combined with an anti-programmed death 1 antibody, an extensive therapeutic antitumor effect was observed. Therefore, the ssPalmE-LNP is a promising carrier of adjuvants for cancer immunotherapy.
细胞质 DNA 通过激活干扰素基因刺激物途径触发细胞免疫。由于 DNA 可降解且具有细胞膜不可透过性,因此输送系统可通过破坏内涵体膜来实现细胞质内递送来用作佐剂。本文报告了一种包裹质粒 DNA(pDNA)的脂质纳米颗粒(LNP)的开发。该结构组件包括一种 SS 可切割和 pH 激活的类脂质材料,将维生素 E 作为疏水性支架,并具有双感应基序,可响应细胞内环境(ssPalmE)。包裹 pDNA 的 LNP(ssPalmE-LNP)在 Raw 264.7 细胞中诱导产生高干扰素-β。ssPalmE-LNP 的皮下注射强烈增强了抗原特异性细胞毒性 T 细胞活性。ssPalmE-LNP 治疗有效地诱导了 E.G7-OVA 肿瘤和 B16-F10 黑色素瘤转移的抗肿瘤作用。此外,当与抗程序性死亡 1 抗体联合使用时,观察到广泛的治疗抗肿瘤作用。因此,ssPalmE-LNP 是癌症免疫治疗佐剂的一种有前途的载体。