Silveira Fernando, García Florencia, García Gabriel, Chabalgoity José A, Rossi Silvina, Baz Mariana
Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República, Av. Alfredo Navarro 3051, Montevideo 16100, Uruguay.
Departamento de Bioquímica Clínica, Instituto Polo Tecnológico, Facultad de Química, UdelaR, Ramal ''José D'Elía" Ruta 101 y 8, Canelones 91000, Uruguay.
Vaccines (Basel). 2024 Aug 9;12(8):902. doi: 10.3390/vaccines12080902.
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 (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 naïve 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.
提高针对呼吸道病毒疫苗的效力对老年人尤为重要,因为他们由于合并症和免疫系统衰老而容易发生严重感染。添加基于皂苷的佐剂是提高疫苗效力的一种有趣策略。我们之前已经表明,来自(IMXQB)的免疫刺激复合物基质是一种安全且有效的佐剂。在本研究中,我们在老年小鼠模型中评估了IMXQB作为季节性三价流感疫苗(TIV)佐剂的用途。在此,我们表明皮下注射佐剂疫苗可促进更高滴度的IgM、IgG(及其同种型)和血清血凝抑制滴度(HAI)。值得注意的是,通过鼻内途径免疫的老年小鼠在初次免疫后长达120天也产生了更高的IgG(及其同种型)和IgA滴度,并且针对TIV的HAI抗体也有所改善。此外,用先前皮下接种TIV-IMXQB的成年未免疫小鼠的血清单次处理的实验感染老年小鼠成功控制了感染。总体而言,与TIV相比,TIV-IMXQB通过增强老年小鼠的全身和黏膜免疫,在H1N1pdm09样病毒攻击后恢复更快,从而提高了免疫原性。因此,IMXQB纳米颗粒可能是下一代病毒疫苗的一个有前景的平台。