Research and Development, Nanotherapeutics, Inc., Alachua, FL, USA.
Research and Development, Nanotherapeutics, Inc., Alachua, FL, USA.
Vaccine. 2017 Dec 18;35(51):7121-7126. doi: 10.1016/j.vaccine.2017.10.081. Epub 2017 Nov 14.
Typhoid fever remains a serious public health problem with a high impact on toddlers and young children. Vaccines against the Vi capsular polysaccharide are efficacious against typhoid fever demonstrating that antibodies against Vi confer protection. The currently licensed Vi typhoid vaccines have however limited efficacy and are manufactured by a complex process from wild-type bacteria. Due to these inherent issues with the current vaccines, an alternative vaccine based on an O-acetylated high molecular weight (HMW) polygalacturonic acid (GelSite-OAc™) was generated. The HMW polygalacturonic acid shares the same backbone as the Vi polysaccharide of Salmonella Typhi. The GelSite-OAc™ has a high molecular weight (>1 × 10 Da) and a high degree of O-acetylation (DOAc) (>5 μmole/mg), both exceeding the potency specifications of the current Vi vaccine. Studies in Balb/c mice demonstrated that GelSite-OAc™ was highly immunogenic, inducing a strong antigen-specific antibody response in a DOAc- and dose-dependent manner which was comparable to or higher than those induced by the licensed Vi vaccine. Importantly, the GelSite-OAc™ was shown to be fully protective in mice against lethal challenge with Salmonella Typhi. Furthermore, the GelSite-OAc™ demonstrated a boosting effect or memory response, exhibiting a >2-fold increase in antibody levels upon the second immunization with either GelSite-OAc™ or the Vi vaccine. This novel boosting effect is unique among polysaccharide antigens and potentially makes GelSite-OAc™ effective in people under 2 years old. Together these results suggest that the GelSite-OAc™ could be a highly effective vaccine against Salmonella Typhi.
伤寒仍然是一个严重的公共卫生问题,对幼儿和儿童影响较大。针对 Vi 荚膜多糖的疫苗对伤寒有效,证明针对 Vi 的抗体提供了保护。然而,目前许可的 Vi 伤寒疫苗的功效有限,并且是由野生型细菌通过复杂的工艺制造的。由于目前疫苗存在这些固有问题,因此基于 O-乙酰化高分子量(HMW)聚半乳糖醛酸(GelSite-OAc™)的替代疫苗被开发出来。HMW 聚半乳糖醛酸与伤寒沙门氏菌的 Vi 多糖具有相同的骨架。GelSite-OAc™具有高分子量(>1×10 Da)和高 O-乙酰化度(DOAc)(>5 µmole/mg),均超过当前 Vi 疫苗的效力规格。在 Balb/c 小鼠中的研究表明,GelSite-OAc™具有高度的免疫原性,以 DOAc 和剂量依赖性方式诱导强烈的抗原特异性抗体反应,与许可的 Vi 疫苗诱导的反应相当或更高。重要的是,GelSite-OAc™在小鼠中显示出针对伤寒沙门氏菌致死性挑战的完全保护作用。此外,GelSite-OAc™表现出增强作用或记忆反应,在第二次用 GelSite-OAc™或 Vi 疫苗免疫时,抗体水平增加了>2 倍。这种新型增强作用是多糖抗原中独特的,并且可能使 GelSite-OAc™在 2 岁以下的人群中有效。这些结果表明,GelSite-OAc™可能是一种针对伤寒沙门氏菌的高效疫苗。