Simms John R, Jennings Roy, Richardson Vernon J, Heath Andrew W
Division of Genomic Medicine, Infection and Immunity, University of Sheffield Medical School, Sheffield, England, United Kingdom.
J Med Virol. 2002 Sep;68(1):82-91. doi: 10.1002/jmv.10173.
The potential of a large number of commercial and experimental adjuvant preparations to enhance the immunogenicity of an HSV-1 glycoprotein subunit vaccine was investigated. Evaluation was based on toxicity, HSV-specific antibody production, and protection against lethal challenge. All adjuvants tested increased the titer of antigen specific Ig levels when compared to subunit vaccine alone. However, following challenge, a broad range of protective responses were noted. Statistically significant correlations were observed between IgG antibody levels post immunization and the observed protection and these were particularly associated with antibodies of the IgG2a and IgG2b subclasses. The results emphasize the requirement of adjuvants for vaccine formulation when using subunit preparations, and demonstrate that the magnitude and efficacy of the induced immune response varies greatly with the choice of adjuvant.
研究了大量商业和实验性佐剂制剂增强单纯疱疹病毒1型(HSV-1)糖蛋白亚单位疫苗免疫原性的潜力。评估基于毒性、HSV特异性抗体产生以及对致死性攻击的保护作用。与单独的亚单位疫苗相比,所有测试的佐剂均提高了抗原特异性Ig水平的滴度。然而,在攻击后,观察到广泛的保护反应。免疫后IgG抗体水平与观察到的保护作用之间存在统计学上的显著相关性,这些相关性尤其与IgG2a和IgG2b亚类的抗体有关。结果强调了在使用亚单位制剂时疫苗配方中佐剂的必要性,并表明诱导的免疫反应的强度和效力随佐剂的选择而有很大差异。