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Modified chitosan-based nanoadjuvants enhance immunogenicity of protein antigens after mucosal vaccination

Authors :
Genada Sinani
Melike Sessevmez
M. Koray Gök
Erdal Cevher
Saadet Özgümüş
H. Oya Alpar
Alpar, H. Oya
Sinani, Genada
Publication Year :
2019
Publisher :
Elsevier, 2019.

Abstract

OZGUMUS, SAADET/0000-0002-1793-0859; Cevher, Erdal/0000-0002-0486-2252; GOK, MEHMET KORAY/0000-0003-2497-9359 WOS:000488123900052 PubMed: 31386881 Nasal vaccination is considered to be an effective and convenient way of increasing immune responses both systemically and locally. Although various nanovaccine carriers have been introduced as potential immune adjuvants, further improvements are still needed before they can be taken to clinical usage. Chitosan-based nanovaccine carriers are one of the most widely studied adjuvants, owing to the ability of chitosan to open tight junctions between nasal epithelial cells and enhance particle uptake as well as its inherent immune activating role. In present study, bovine serum albumin (BSA) loaded nanoparticles were prepared using novel aminated (aChi) and aminated plus thiolated chitosan (atChi) polymers, to further enhance mucoadhesiveness and adjuvanticity of the vaccine system by improving electrostatic interactions of polymers with negatively charged glycoproteins. Nanocarriers with optimum size and surface charge, high encapsulation efficiency of model antigen and good stability were developed. Negligible toxicity was observed in Calu-3 and A549 cell lines. In vivo studies, revealed high levels of systemic antibodies (IgG, IgG(1) and IgG(2a)) throughout the study and presence of sIgA in vaginal washes showed that common mucosal system was successfully stimulated. Cytokine levels indicated a mixed Th1/Th2 immune response. A shift towards cellular immune responses was observed after nasal immunisation with antigen loaded nanoparticle formulations. These nanoparticles exhibit great potential for nasal application of vaccines. Scientific Research Projects Coordination Unit of Istanbul UniversityIstanbul University [36160]; Scientific and Technological Research Council of Turkey (TUBITAK)Turkiye Bilimsel ve Teknolojik Arastirma Kurumu (TUBITAK) This work was supported by Scientific Research Projects Coordination Unit of Istanbul University, No: 36160. Genada Sinani acknowledges The Scientific and Technological Research Council of Turkey (TUBITAK) for the PhD Fellowship Program.

Details

Language :
English
Database :
OpenAIRE
Accession number :
edsair.doi.dedup.....ab918c22ac65f2b3e43d20e87bba2fcd