| Literature DB >> 28440707 |
Olga Kammona1, Vassilis Bourganis2, Theodora Karamanidou2, Costas Kiparissides2,1.
Abstract
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.Entities:
Keywords: adjuvants; mucosal vaccination; nanocarriers; polymeric nanoparticles; vesicles
Mesh:
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Year: 2017 PMID: 28440707 DOI: 10.2217/nnm-2017-0015
Source DB: PubMed Journal: Nanomedicine (Lond) ISSN: 1743-5889 Impact factor: 5.307