Jarecki-Black J C, James E R, Kirshtein J W, Kirshtein J D, Glassman A B
Am J Trop Med Hyg. 1986 Nov;35(6):1117-20. doi: 10.4269/ajtmh.1986.35.1117.
C57BL/6 mice were immunized against Leishmania donovani infection with a subcutaneous vaccination protocol. Groups received 3 injections at 4-day intervals combining glucan and killed promastigotes harvested from either logarithmic or stationary phase cultures. Controls were immunized with glucan alone, stationary or log phase promastigotes alone, or were untreated. All groups were challenged intravenously with stationary phase promastigotes at day 45 post-immunization. Results revealed that animals immunized with the glucan-killed parasite vaccine, utilizing promastigotes derived from either log (GPL) or stationary phase cultures (GPS), demonstrated significant resistance against infection as compared to controls or untreated mice. Additionally, the reduction in hepatic amastigote proliferation in mice immunized with GPS was significantly greater than in mice immunized with GPL.
采用皮下接种方案对C57BL/6小鼠进行杜氏利什曼原虫感染免疫。各实验组每隔4天接受3次注射,将葡聚糖与从对数期或稳定期培养物中收获的灭活前鞭毛体混合注射。对照组分别单独用葡聚糖、单独用稳定期或对数期前鞭毛体进行免疫,或不进行处理。所有组在免疫后第45天静脉注射稳定期前鞭毛体进行攻毒。结果显示,与对照组或未处理小鼠相比,用葡聚糖-灭活寄生虫疫苗免疫的动物(利用来自对数期(GPL)或稳定期培养物(GPS)的前鞭毛体)对感染表现出显著抗性。此外,用GPS免疫的小鼠肝脏内无鞭毛体增殖的减少显著大于用GPL免疫的小鼠。