McLeod R, Estes R G, Mack D G
Trans R Soc Trop Med Hyg. 1985;79(6):800-4. doi: 10.1016/0035-9203(85)90122-1.
Toxoplasma gondii antigens and adjuvants administered parenterally and perorally were tested for their ability to produce serum antibody to T. gondii, to enhance peritoneal microbicidal capacity for T. gondii, and to prevent acquisition of infection by T. gondii ingested subsequently. N-acetylmuramyl-L-alanyl-D-isoglutamine-6-0-stearoyl (MDP) incorporated into liposomes administered intramuscularly to mice with 80 micrograms of T. gondii antigens and the synthetic adjuvant N,N-dioctadecyl-N',N'bis (2-hydroxyethyl) propanediamine (CP 20,961) administered intramuscularly to mice with 80 micrograms of T. gondii lysate antigens produced the highest titres of antibody to T. gondii in sera (i.e., the mean +/- S.D. of the log2 of the reciprocal of the antibody titre to T. gondii measured by Sabin Feldman Dye test was 9 +/- 2 in sera of mice that received T. gondii antigens plus MDP and was 8 +/- 1 in sera of mice that received T. gondii antigens plus CP 20,961). No orally administered preparation produced high titres of serum antibody to T. gondii. None of the preparations which were tested protected mice against infection with T. gondii when cysts containing the parasite were administered by mouth subsequently or enhanced macrophage microbicidal capacity between two and three weeks after the last immunizations. These experiments demonstrate that presence of Toxoplasma antibody (i.e., when log2 of the reciprocal of Toxoplasma antibody titres is 10 or less measured by Sabin Feldman dye test) does not protect mice against dissemination of ingested T. gondii from the gastrointestinal tract. The method of peroral challenge with T. gondii developed for this study is useful for examining effects of other potentially protective regimens in preventing acquisition of ingested T. gondii.
对通过肠胃外和口服方式给予的刚地弓形虫抗原和佐剂进行了测试,以检验它们产生抗刚地弓形虫血清抗体的能力、增强对刚地弓形虫的腹膜杀菌能力以及预防随后摄入的刚地弓形虫感染的能力。将80微克刚地弓形虫抗原与掺入脂质体的N - 乙酰胞壁酰 - L - 丙氨酰 - D - 异谷氨酰胺 - 6 - O - 硬脂酰(MDP)一起肌肉注射给小鼠,以及将80微克刚地弓形虫裂解物抗原与合成佐剂N,N - 二辛基 - N',N' - 双(2 - 羟乙基)丙二胺(CP 20,961)一起肌肉注射给小鼠,在血清中产生了最高滴度的抗刚地弓形虫抗体(即,通过Sabin Feldman染色试验测量的抗刚地弓形虫抗体滴度倒数的log2的平均值±标准差,在接受刚地弓形虫抗原加MDP的小鼠血清中为9±2,在接受刚地弓形虫抗原加CP 20,961的小鼠血清中为8±1)。没有口服制剂能产生高滴度的抗刚地弓形虫血清抗体。当随后经口给予含有该寄生虫的囊肿时,所测试的制剂中没有一种能保护小鼠免受刚地弓形虫感染,也没有在最后一次免疫后两到三周增强巨噬细胞杀菌能力。这些实验表明,刚地弓形虫抗体的存在(即,通过Sabin Feldman染色试验测量的刚地弓形虫抗体滴度倒数的log2为10或更低时)并不能保护小鼠免受摄入的刚地弓形虫从胃肠道扩散的影响。为本研究开发的经口用刚地弓形虫攻击的方法,对于检查其他潜在的保护性方案在预防摄入刚地弓形虫感染方面的效果很有用。