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用皂苷配制的类免疫刺激复合物纳米颗粒有望成为季节性流感疫苗的佐剂。

ISCOM-like Nanoparticles Formulated with Saponins Are Promising Adjuvants for Seasonal Influenza Vaccines.

作者信息

Rivera-Patron Mariana, Moreno María, Baz Mariana, Roehe Paulo M, Cibulski Samuel P, Silveira Fernando

机构信息

Departamento de Desarrollo Biotecnológico, Instituto de Higiene, Facultad de Medicina, Universidad de la República (UdelaR), Montevideo 11600, Uruguay.

Research Center in Infectious Diseases of the CHU of Québec and Université Laval, Quebec City, QC G1V 4G2, Canada.

出版信息

Vaccines (Basel). 2021 Nov 18;9(11):1350. doi: 10.3390/vaccines9111350.

Abstract

Vaccination is the most effective public health intervention to prevent influenza infections, which are responsible for an important burden of respiratory illnesses and deaths each year. Currently, licensed influenza vaccines are mostly split inactivated, although in order to achieve higher efficacy rates, some influenza vaccines contain adjuvants. Although split-inactivated vaccines induce mostly humoral responses, tailoring mucosal and cellular immune responses is crucial for preventing influenza infections. saponin-based adjuvants, including ISCOM-like nanoparticles formulated with the QB-90 saponin fraction (IQB90), have been studied in preclinical models for more than a decade and have been demonstrated to induce strong humoral and cellular immune responses towards several viral antigens. Herein, we demonstrate that a split-inactivated IQB90 adjuvanted influenza vaccine triggered a protective immune response, stronger than that induced by a commercial unadjuvanted vaccine, when applied either by the subcutaneous or the intranasal route. Moreover, we reveal that this novel adjuvant confers up to a ten-fold dose-sparing effect, which could be crucial for pandemic preparedness. Last but not least, we assessed the role of caspase-1/11 in the generation of the immune response triggered by the IQB90 adjuvanted influenza vaccine in a mouse model and found that the cellular-mediated immune response triggered by the IQB90-Flu relies, at least in part, on a mechanism involving the casp-1/11 pathway but not the humoral response elicited by this formulation.

摘要

接种疫苗是预防流感感染最有效的公共卫生干预措施,流感每年都会造成严重的呼吸道疾病负担和死亡。目前,获得许可的流感疫苗大多是裂解灭活疫苗,不过为了提高效力,一些流感疫苗含有佐剂。虽然裂解灭活疫苗主要诱导体液免疫反应,但调节黏膜和细胞免疫反应对于预防流感感染至关重要。基于皂苷的佐剂,包括用QB-90皂苷组分(IQB90)配制的类免疫刺激复合物纳米颗粒,已经在临床前模型中研究了十多年,并且已证明其能诱导针对多种病毒抗原的强烈体液和细胞免疫反应。在此,我们证明,一种裂解灭活的IQB90佐剂流感疫苗,无论是通过皮下还是鼻内途径接种,都能引发比市售无佐剂疫苗更强的保护性免疫反应。此外,我们发现这种新型佐剂具有高达10倍的剂量节省效果,这对于大流行防范可能至关重要。最后但同样重要的是,我们在小鼠模型中评估了半胱天冬酶-1/11在IQB90佐剂流感疫苗引发的免疫反应中的作用,发现IQB90-流感疫苗引发的细胞介导免疫反应至少部分依赖于一种涉及casp-1/11途径的机制,而不是该制剂引发的体液免疫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3397/8621233/838b0b04c023/vaccines-09-01350-g001.jpg

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