Kammona Olga, Bourganis Vassilis, Karamanidou Theodora, Kiparissides Costas
Chemical Process & Energy Resources Institute, Centre for Research & Technology Hellas, PO Box 60361, 57001 Thessaloniki, Greece.
Department of Chemical Engineering, Aristotle University of Thessaloniki, PO Box 472, 54124 Thessaloniki, Greece.
Nanomedicine (Lond). 2017 May;12(9):1057-1074. doi: 10.2217/nnm-2017-0015. Epub 2017 Apr 25.
To date, most of the licensed vaccines for mucosal delivery are based on live-attenuated viruses which carry the risk of regaining their pathogenicity. Therefore, the development of efficient nonviral vectors allowing the induction of potent humoral and cell-mediated immunity is regarded as an imperative scientific challenge as well as a commercial breakthrough for the pharma industries. For a successful translation to the clinic, such nanocarriers should protect the antigens from mucosal enzymes, facilitate antigen uptake by microfold cells and allow the copresentation of robust, safe for human use, mucosal adjuvants to antigen-presenting cells. Finally, the developed formulations should exhibit accuracy regarding the administered dose, a major drawback of mucosal vaccines in comparison with parenteral ones.
迄今为止,大多数已获许可的用于黏膜递送的疫苗都是基于减毒活病毒,而这些病毒存在恢复致病性的风险。因此,开发能够诱导强效体液免疫和细胞介导免疫的高效非病毒载体,被视为一项紧迫的科学挑战,也是制药行业的一个商业突破。为了成功转化至临床,此类纳米载体应保护抗原免受黏膜酶的作用,促进微褶细胞摄取抗原,并允许将对人类使用安全的强效黏膜佐剂与抗原呈递细胞共同呈递。最后,所开发的制剂应在给药剂量方面表现出准确性,这是黏膜疫苗与注射用疫苗相比的一个主要缺点。