Morçӧl Tülin, Hurst Brett L, Tarbet E Bart
CaPtivate Pharmaceuticals LLC, Doylestown, PA, USA.
Institute for Antiviral Research, Utah State University, Logon, UT, USA.
Vaccine. 2017 Aug 16;35(35 Pt B):4569-4577. doi: 10.1016/j.vaccine.2017.07.016. Epub 2017 Jul 14.
The emergence of pandemic influenza strains, particularly the reemergence of the swine-derived influenza A (H1N1) in 2009, is reaffirmation that influenza viruses are very adaptable and influenza remains as a significant global public health treat. As recommended by the World Health Organization (WHO), the use of adjuvants is an attractive approach to improve vaccine efficacy and allow dose-sparing during an influenza emergency. In this study, we utilized CaPtivate Pharmaceutical's proprietary calcium phosphate nanoparticles (CaPNP) vaccine adjuvant and delivery platform to formulate an inactivated whole virus influenza A/CA/04/2009 (H1N1pdm) vaccine as a potential dose-sparing strategy. We evaluated the relative immunogenicity and the efficacy of the formulation in BALB/c mice following single intramuscularly administration of three different doses (0.3, 1, or 3µg based on HA content) of the vaccine in comparison to non-adjuvanted or alum-adjuvant vaccines. We showed that, addition of CaPNP in vaccine elicited significantly higher hemagglutination inhibition (HAI), virus neutralization (VN), and IgG antibody titers, at all dose levels, relative to the non-adjuvanted vaccine. In addition, the vaccine containing CaPNP provided equal protection with 1/3rd of the antigen dose as compared to the non-adjuvanted or alum-adjuvanted vaccines. Our data provided support to earlier studies indicating that CaPNP is an attractive vaccine adjuvant and delivery system and should play an important role in the development of safe and efficacious dose-sparing vaccines. Our findings also warrant further investigation to validate CaPNP's capacity as an alternative adjuvant to the ones currently licensed for influenza/pandemic influenza vaccination.
大流行性流感毒株的出现,尤其是2009年猪源甲型H1N1流感的再次出现,再次证明流感病毒具有很强的适应性,流感仍然是全球重大的公共卫生威胁。正如世界卫生组织(WHO)所建议的,使用佐剂是提高疫苗效力并在流感紧急情况下实现剂量节省的一种有吸引力的方法。在本研究中,我们利用CaPtivate制药公司专有的磷酸钙纳米颗粒(CaPNP)疫苗佐剂和递送平台,配制了一种灭活全病毒甲型流感病毒A/CA/04/2009(H1N1pdm)疫苗,作为一种潜在的剂量节省策略。我们评估了在BALB/c小鼠单次肌肉注射三种不同剂量(基于血凝素含量分别为0.3、1或3μg)的该疫苗后,与未加佐剂或铝佐剂疫苗相比,该制剂的相对免疫原性和效力。我们发现,与未加佐剂的疫苗相比,在所有剂量水平下,疫苗中添加CaPNP均能显著提高血凝抑制(HAI)、病毒中和(VN)和IgG抗体滴度。此外,与未加佐剂或铝佐剂的疫苗相比,含CaPNP的疫苗以三分之一的抗原剂量提供了同等的保护。我们的数据为早期研究提供了支持,表明CaPNP是一种有吸引力的疫苗佐剂和递送系统,应在安全有效的剂量节省疫苗的开发中发挥重要作用。我们的研究结果还需要进一步研究,以验证CaPNP作为目前已获许可用于流感/大流行性流感疫苗接种的佐剂替代品的能力。