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通过定量PCR测定rSAG-1(P30)免疫对豚鼠循环和组织寄生虫的影响。

Effect of rSAG-1(P30) immunisation on the circulating and tissue parasites in guinea pigs as determined by quantitative PCR.

作者信息

Flori Pierre, Tardy Laëtitia, Jacquet Alain, Bellete Bahrie, Hafid Jamal, Raberin Hélène, Tran Manh Sung Roger

机构信息

Laboratoire de Parasitologie-Mycologie, C.H.U. de Saint Etienne, Hôpital Nord, 42055, Saint-Etienne, cedex 2, France.

出版信息

Parasitol Res. 2006 May;98(6):511-8. doi: 10.1007/s00436-005-0074-y. Epub 2006 Jan 17.

Abstract

The efficacy of immunisation with Toxoplasma gondii recombinant protein (rSAG-1) was evaluated in the guinea pig model. For the infectious challenge, two strains, namely, strain C56 (10,000 tachyzoites) and strain 76K (100 cysts), were used to infect a group of 32 guinea pigs each. The circulating, cerebral and pulmonary parasite loads were determined with the real-time polymerase chain reaction (PCR) after immunisation. With the C56 strain, immunisation showed high activity with a reduction of greater than 1 log of the circulating and tissue parasite loads. Thus, there was a significantly lower circulating parasite load in the rSAG-1 + adjuvant group (0.5+/-1.5 Eq parasites/ml) as compared to that in the control group (67+/-110 Eq parasites/ml; p<0.05). In the same manner, the cerebral parasite load was much lower in the rSAG-1 + adjuvant group (10+/-20 Eq parasites/g) than that in the control group (339+/-291 Eq parasites/g; p<0.01). On the other hand, with the 76K strain, the effect of immunisation was much less and that only on the pulmonary parasite load [p(lung)<0.05]. This could be due to the use of different strains and stages of the parasite and/or the difference in the route of administration for challenge. The quantitative PCR technique used has shown a good correlation with animal inoculation, and when associated with the guinea pig model, it seems to be a useful and reproducible technique for future vaccine studies.

摘要

在豚鼠模型中评估了弓形虫重组蛋白(rSAG-1)免疫的效果。对于感染性攻击,使用两株菌株,即C56株(10,000个速殖子)和76K株(100个包囊)分别感染一组32只豚鼠。免疫后通过实时聚合酶链反应(PCR)测定循环、脑和肺中的寄生虫负荷。对于C56株,免疫显示出高活性,循环和组织寄生虫负荷减少超过1个对数。因此,与对照组(67±110 Eq寄生虫/ml)相比,rSAG-1+佐剂组的循环寄生虫负荷显著更低(0.5±1.5 Eq寄生虫/ml;p<0.05)。同样,rSAG-1+佐剂组的脑寄生虫负荷(10±20 Eq寄生虫/g)比对照组(339±291 Eq寄生虫/g;p<0.01)低得多。另一方面,对于76K株,免疫效果要小得多,且仅对肺寄生虫负荷有影响[p(肺)<0.05]。这可能是由于使用了不同的寄生虫菌株和阶段和/或攻击给药途径的差异。所使用的定量PCR技术已显示与动物接种有良好的相关性,并且与豚鼠模型结合时,它似乎是未来疫苗研究中一种有用且可重复的技术。

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