Preclinical evaluation of the saponin derivative GPI-0100 as an immunostimulating and dose-sparing adjuvant for pandemic influenza vaccines

被引:20
作者
Liu, Heng [1 ,2 ]
Bungener, Laura [1 ,2 ]
ter Veer, Wouter [1 ,2 ]
Coller, Beth-Ann [3 ]
Wilschut, Jan [1 ,2 ]
Huckriede, Anke [1 ,2 ]
机构
[1] Univ Med Ctr Groningen, Dept Med Microbiol, Mol Virol Sect, NL-9700 RB Groningen, Netherlands
[2] Univ Groningen, Groningen, Netherlands
[3] Hawaii Biotech Inc, Aiea, HI USA
关键词
Influenza; Vaccine; Adjuvant; GPI-0100; Dose-sparing; H5N1; VACCINE; VIRUS H5N1; IMMUNOGENICITY; PROTECTION; RESPONSES; ADULTS; TRIAL; MICE; MF59; IMMUNIZATION;
D O I
10.1016/j.vaccine.2011.01.012
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
With the current global influenza vaccine production capacity the large demand for vaccines in case of a pandemic can only be fulfilled when antigen dose sparing strategies are employed. Here we used a murine challenge model to evaluate the potential of GPI-0100, a semi-synthetic saponin derivative, to serve as a dose-sparing adjuvant for influenza subunit vaccine. Balb/c mice were immunized with different doses of A/PR8 (H1N1) subunit antigen alone or in combination with varying doses of GPI-0100. The addition of GPI-0100 significantly stimulated antibody and cellular immune responses, especially of the Th1 phenotype. Furthermore, virus titers detected in the lungs of mice challenged one week after the second immunization were significantly reduced among the animals that received GPI-0100-adjuvanted vaccines. Remarkably, adjuvantation of subunit vaccine with GPI-0100 allowed a 25-fold reduction in hemagglutinin dose without compromising the protective potential of the vaccine. (C) 2011 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2037 / 2043
页数:7
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