Department of Microbiology, Immunology and Parasitology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil; Institute for Technological Research of State of São Paulo, São Paulo, Brazil.
Department of Microbiology, Immunology and Parasitology, Escola Paulista de Medicina, Universidade Federal de São Paulo, São Paulo, Brazil.
Int J Pharm. 2019 Jun 30;565:123-132. doi: 10.1016/j.ijpharm.2019.05.013. Epub 2019 May 7.
The recognition of α-galactosylceramide (αGC), a high-affinity CD1d antigen, by the invariant Natural Killer T (iNKT) lymphocytes results in potent immunostimulatory responses that have been exploited in advanced cancer patients. Therefore, to improve αGC biological activity, several studies vectorized this agonist in PLGA and/or PEG-based nanoparticles. Despite promising findings, these approaches require several steps, from organic solvent decontamination through extrusion in membrane systems. Using a nano spray dryer, we vectorized αGC into a cationic copolymer (dimethylaminoethyl methacrylate, butyl methacrylate and methyl methacrylate - DBM) in a single step process, free of organic solvent. This methodology allowed the production of stable αGC-vectorized nanoparticles (DBM + αGC) with a more potent biological activity than the free agonist. DBM nanoparticles improved in vivo αGC loading into the CD1d molecule and induced a higher frequency of IFN-γ-expressing iNKT cells. Consequently, mice treated with DBM + αGC presented higher levels of serum IFN-γ than those treated with free agonist. Also, vectorized nanoparticles improved αGC ability to control the growth of murine lung metastatic carcinoma. Thus, this is the first study showing that nano spray dryer technology is a simple and alternative approach to enhance iNKT responses.
α-半乳糖神经酰胺(αGC)是一种高亲和力的 CD1d 抗原,其被不变自然杀伤 T(iNKT)淋巴细胞识别后会引发强烈的免疫刺激反应,这一反应已在晚期癌症患者中得到了应用。因此,为了提高 αGC 的生物活性,一些研究将该激动剂载体化为 PLGA 和/或 PEG 纳米颗粒。尽管这些方法有很有前景的发现,但它们需要经过多个步骤,包括从有机溶剂脱除到通过膜系统挤出。我们使用纳米喷雾干燥器,在不使用有机溶剂的情况下,将 αGC 一步法载体化为阳离子共聚物(二甲基氨基乙基甲基丙烯酸酯、甲基丙烯酸丁酯和甲基丙烯酸酯-DBM)。这种方法允许生产出稳定的 αGC 载体化纳米颗粒(DBM+αGC),其生物活性比游离激动剂更强。DBM 纳米颗粒提高了体内 CD1d 分子对 αGC 的摄取,并诱导产生更高频率表达 IFN-γ 的 iNKT 细胞。因此,用 DBM+αGC 治疗的小鼠血清 IFN-γ 水平高于用游离激动剂治疗的小鼠。此外,载体化纳米颗粒提高了 αGC 控制小鼠肺转移性癌生长的能力。因此,这是第一项表明纳米喷雾干燥技术是增强 iNKT 反应的一种简单替代方法的研究。