Intranasal Delivery of Quillaja brasiliensis Saponin-Based Nanoadjuvants Improve Humoral Immune Response of Influenza Vaccine in Aged Mice

被引:0
|
作者
Silveira, Fernando [1 ]
Garcia, Florencia [1 ]
Garcia, Gabriel [1 ]
Chabalgoity, Jose A. [1 ]
Rossi, Silvina [2 ]
Baz, Mariana [3 ]
机构
[1] Univ Republica, Fac Med, Dept Desarrollo Biotecnol, Inst Higiene, Ave Alfredo Navarro 3051, Montevideo 16100, Uruguay
[2] UdelaR, Fac Quim, Dept Bioquim Clin, Inst Polo Tecnol, Ramal Jose Elia Ruta 101 & 8, Canelones 91000, Uruguay
[3] Univ Laval, Fac Med, Dept Microbiol Infect Dis & Immunol, Quebec City, PQ G1V 0A6, Canada
关键词
Quillaja brasiliensis; adjuvant; nanoparticle; ISCOM matrices; IgA titers; influenza virus; delivered intranasally; viral challenge; aged mice; IMMUNOGENICITY; SAFETY;
D O I
10.3390/vaccines12080902
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Increasing the effectiveness of vaccines against respiratory viruses is particularly relevant for the elderly, since they are prone to develop serious infections due to comorbidities and the senescence of the immune system. The addition of saponin-based adjuvants is an interesting strategy to increase the effectiveness of vaccines. We have previously shown that ISCOM matrices from Q. brasiliensis (IMXQB) are a safe and potent adjuvant. In this study, we evaluated the use of IMXQB as an adjuvant for the seasonal trivalent influenza vaccine (TIV) in an aged mice model. Herein, we show that subcutaneous injection of the adjuvanted vaccine promoted higher titers of IgM, IgG (and isotypes), and serum hemagglutination inhibition titers (HAI). Notably, aged mice immunized by intranasal route also produced higher IgG (and isotypes) and IgA titers up to 120 days after priming, as well as demonstrating an improvement in the HAI antibodies against the TIV. Further, experimental infected aged mice treated once with sera from adult na & iuml;ve mice previously immunized with TIV-IMXQB subcutaneously successfully controlled the infection. Overall, TIV-IMXQB improved the immunogenicity compared to TIV by enhancing systemic and mucosal immunity in old mice conferring a faster recovery after the H1N1pdm09-like virus challenge. Thus, IMXQB nanoparticles may be a promising platform for next-generation viral vaccines.
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页数:18
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