Development of a novel adjuvanted nasal vaccine: C48/80 associated with chitosan nanoparticles as a path to enhance mucosal immunity

被引:67
作者
Bento, D. [1 ,2 ]
Staats, H. F. [3 ]
Goncalves, T. [1 ,4 ]
Borges, O. [1 ,2 ]
机构
[1] Univ Coimbra, Ctr Neurosci & Cell Biol, P-3004504 Coimbra, Portugal
[2] Univ Coimbra, Fac Pharm, P-3000548 Coimbra, Portugal
[3] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[4] Univ Coimbra, Fac Med, Inst Microbiol, P-3004504 Coimbra, Portugal
关键词
Compound; 48/80; Chitosan; Alginate; Nanoparticles; Mast cell activator; Nasal vaccination; Mucosal immunity; Anthrax protective antigen; MAST-CELL; IN-VITRO; PROTECTIVE ANTIGEN; CLEARANCE CHARACTERISTICS; DELIVERY-SYSTEMS; DENDRITIC CELLS; TH17; CELLS; ALGINATE; RESPONSES; ACTIVATION;
D O I
10.1016/j.ejpb.2015.03.024
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In a time in which mucosal vaccines development has been delayed by the lack of safe and effective mucosal adjuvants, the combination of adjuvants has started to be explored as a strategy to obtain potent vaccine formulations. This study describes a novel adjuvant combination as an effective approach for a nasal vaccine the association of the mast cell activator compound 48/80 with chitosan based nanopartides. It was hypothesized that mucoadhesive nanoparticles would promote the cellular uptake and prolong the antigen residence time on nasal cavity. Simultaneously, mast cell activation would promote a local microenvironment favorable to the development of an immune response. To test this hypothesis, two different C48/80 loaded nanoparticles (NPs) were prepared: Chitosan-C48/80 NP (Chi-C48/80 NP) and Chitosan/Alginate-C48/80 NP (Chi/Alg-C48/80 NP). The potential as a vaccine adjuvant of the two delivery systems was evaluated and directly compared. Both formulations had a mean size near 500 nm and a positive charge; however, Chi-C48/80 NP was a more effective adjuvant delivery system when compared with Chi/Alg-C48/80 NP or C48/80 alone. Chi-C48/80 NP activated mast cells at a greater extent, were better internalized by antigen presenting cells than Chi/Alg-C48/80 NP and successfully enhanced the nasal residence time of a model antigen. Superiority of Chi-C48/80 NP as adjuvant was also observed in vivo. Therefore, nasal immunization of mice with Bacillus anthracis protective' antigen (PA) adsorbed on Chi-C48/80 NP elicited high levels of serum anti-PA neutralizing antibodies and a more balanced Th1/Th2 profile than C48/80 in solution or Chi/Alg-C48/80 NP. The incorporation of C48/80 within Chi NP also promoted a mucosal immunity greater than all the other adjuvanted groups tested, showing that the combination of a mast cell activator and chitosan NP could be a promising strategy for nasal immunization. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:149 / 164
页数:16
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