Univ Lyon, Université Claude Bernard Lyon 1, CNRS, LAGEPP UMR 5007, F-69100 Villeurbanne, France.
Academic Unit of Immunology and Immunotherapy, Faculty of Veterinary Medicine, Universidad de la República, Montevideo, Uruguay.
Eur J Pharm Biopharm. 2023 Nov;192:185-195. doi: 10.1016/j.ejpb.2023.09.012. Epub 2023 Sep 26.
Dogs are the main source of animal and human cystic echinococcosis caused by the Cestode parasite Echinococcus granulosus. Dog vaccination seems to be a good strategy to control this parasitic disease. Here we present the development of a polymeric nanoparticle-based oral vaccine for dogs against Echinococcus granulosus delivered in enteric-coated capsules. To achieve our target, we encapsulated two recombinant antigens into biodegradable polymeric nanoparticles in the presence of Monophosphoryl lipid A as an adjuvant to ensure efficient delivery and activation of a protective mucosal immune response. The formulated delivery system showed a nanoparticle size less than 200 nm with more than 80 % antigen encapsulation efficiency and conserved integrity and immunogenicity. The nanoparticle surface was coated with chitosan to enhance adhesion to the gut mucosa and a subsequent antigen delivery. Chitosan-coated nanoparticles showed a higher cell internalization in murine macrophages and dendritic cells as well as a higher penetration into Caco-2 cells in vitro. Antigen-loaded nanoparticles were freeze-dried and enteric-coated capsules were filled with the obtained powder. The obtained results show a promising nanoparticles delivery system for oral vaccination.
狗是由绦虫寄生虫棘球蚴引起的动物和人类包虫病的主要传染源。给狗接种疫苗似乎是控制这种寄生虫病的一种好策略。在这里,我们提出了一种基于聚合物纳米粒子的口服疫苗的发展,用于狗对抗棘球蚴,以肠溶胶囊形式给药。为了实现我们的目标,我们在单磷酰脂质 A 作为佐剂的存在下将两种重组抗原封装到可生物降解的聚合物纳米粒子中,以确保有效的传递和激活保护性黏膜免疫反应。所形成的递药系统显示纳米粒子尺寸小于 200nm,抗原包封效率超过 80%,且完整性和免疫原性得以保留。纳米粒子表面用壳聚糖进行了涂层处理,以增强对肠道黏膜的黏附性和随后的抗原传递。壳聚糖涂层的纳米粒子在小鼠巨噬细胞和树突状细胞中的细胞内化率更高,体外对 Caco-2 细胞的穿透率也更高。载抗原的纳米粒子被冷冻干燥,并将获得的粉末填充到肠溶胶囊中。所得结果表明,这是一种有前途的用于口服疫苗接种的纳米粒子递药系统。