Department of Microbiology and Immunology, Texas Tech University Health Sciences Center, Lubbock, TX 79430, USA.
J Infect Dis. 2011 Nov;204(9):1437-49. doi: 10.1093/infdis/jir545. Epub 2011 Sep 15.
The prophylactic efficacy of a schistosome antigen (Sm-p80) was tested in a nonhuman primate model, the baboon. Using a total of 28 baboons, different vaccination strategies were used including recombinant Sm-p80 protein formulated in Toll-like receptor 7 and Toll-like receptor 9 agonists, and DNA priming followed by boosting with protein plus adjuvants. Recombinant protein approaches provided levels of prophylactic efficacy of 52%-58%, whereas prime-boost approaches conferred 38%-47% protection in baboons. An appropriately balanced pro-inflammatory (T-helper 17 [Th17] and Th1) and anti-inflammatory (Th2) type of response was generated; the Th1 and Th17 types of immune responses appear to be indicative of increased prophylactic efficacy. Production and expression of several cytokines (interleukin 2 [IL-2], interferon γ, IL-12α, IL-1β, IL-6, and IL-22) were up-regulated in vaccinated animals. Human correlate studies revealed Sm-p80 reactivity with immunoglobulin G in human serum samples from schistosome-infected individuals. In addition, a complete lack of prevailing Sm-p80-specific immunoglobulin E in a high-risk or infected population was observed, thus minimizing the risk of hypersensitivity reaction following vaccination with Sm-p80 in humans. This study provided the proof of concept to move Sm-p80 forward into further preclinical development leading to human clinical trials.
在食源性寄生虫抗原(Sm-p80)的非人类灵长类动物模型(狒狒)中测试了其预防效果。使用总共 28 只狒狒,采用了不同的疫苗接种策略,包括用 Toll 样受体 7 和 Toll 样受体 9 激动剂配制的重组 Sm-p80 蛋白,以及 DNA 启动子后用蛋白加佐剂进行加强免疫。重组蛋白方法提供了 52%-58%的预防功效,而初免-加强方法在狒狒中提供了 38%-47%的保护。产生了适当平衡的促炎(Th17 和 Th1)和抗炎(Th2)类型的反应;Th1 和 Th17 类型的免疫反应似乎表明预防功效增加。在接种动物中,几种细胞因子(白细胞介素 2 [IL-2]、干扰素 γ、IL-12α、IL-1β、IL-6 和 IL-22)的产生和表达上调。人类相关性研究表明,Sm-p80 与感染性血吸虫病患者的人血清样本中的免疫球蛋白 G 发生反应。此外,在高危或感染人群中观察到完全缺乏流行的 Sm-p80 特异性免疫球蛋白 E,从而最大限度地降低了 Sm-p80 疫苗接种后发生过敏反应的风险。这项研究提供了将 Sm-p80 推进进一步临床前开发并进入人体临床试验的概念验证。