de Souza J B, Playfair J H
University College London Medical School, Department of Immunology, UK.
Vaccine. 1995 Oct;13(14):1316-9. doi: 10.1016/0264-410x(95)00025-v.
An effective vaccine delivery system has been developed for vaccination against a blood-stage malaria infection in mice. Subcutaneous vaccination with a semi-purified asexual blood-stage malaria antigen combined with an adjuvant formulation containing squalane, Tween 80 and pluronic L121 (AF) protected mice infected with a lethal P. yoelii infection against death and greatly reduced the severity and duration of parasitaemia. The adjuvant and the route of immunization are both clinically acceptable, thereby making this an attractive delivery system for a human malaria vaccine. Protective immunity appeared to be associated with an enhancement of both Th1 and Th2 subset cytokines.
已开发出一种有效的疫苗递送系统,用于小鼠血液期疟疾感染的疫苗接种。用半纯化的无性血液期疟疾抗原与含有角鲨烷、吐温80和普朗尼克L121(AF)的佐剂配方进行皮下接种,可保护感染致死性约氏疟原虫的小鼠免于死亡,并大大降低寄生虫血症的严重程度和持续时间。该佐剂和免疫途径在临床上都是可接受的,因此使其成为一种有吸引力的人类疟疾疫苗递送系统。保护性免疫似乎与Th1和Th2亚群细胞因子的增强有关。