Masihi K N, Brehmer W, Werner H
Zentralbl Bakteriol Orig A. 1979;245(3):377-86.
Toxoplasma gondii tachyzoites were disrupted in a Ribi cell fractionator and separated into cell walls and protoplasm by differential centrifugation. These products were used alone or combined with a mycobacterial glycolipid (P3) and injected either as oil-in-water emulsions or incorporated in Freund's incomplete adjuvant. Mice were vaccinated by intravenous or intradermal routes and challenged intraperitoneally with a highly virulent strain of Toxoplasma gondii. A local granuloma formation was induced after i.d. inoculation of Toxoplasma vaccines containing P3 as this glycolipid enabled an adherence of the antigens on the mineral oil droplets. The adjuvant effect of P3 on antibody formation was also observed. Most of the fractions showed a low, but statistically significant prolongation of survival time. Vaccination by the i.v. route with homologous or heterologous antigens, including Trypanosoma cruzi, were not significantly effective, with the exception of a high dose of Toxoplasma protoplasm associated with P3.
将刚地弓形虫速殖子在Ribi细胞分级分离器中破碎,并通过差速离心分离成细胞壁和原生质。这些产物单独使用或与一种分枝杆菌糖脂(P3)联合使用,以水包油乳液形式注射或掺入弗氏不完全佐剂中。通过静脉或皮内途径给小鼠接种疫苗,并腹腔注射高毒力的刚地弓形虫菌株。皮内接种含P3的弓形虫疫苗后可诱导局部肉芽肿形成,因为这种糖脂能使抗原附着在矿物油滴上。还观察到P3对抗体形成的佐剂作用。大多数组分显示存活时间有轻微但具有统计学意义的延长。静脉途径接种同源或异源抗原(包括克氏锥虫)的疫苗效果不显著,但高剂量的与P3相关的弓形虫原生质除外。