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从曼氏血吸虫成虫中提纯的一种28000道尔顿的蛋白质可保护大鼠和小鼠免受实验性血吸虫病的侵害。

A purified 28,000 dalton protein from Schistosoma mansoni adult worms protects rats and mice against experimental schistosomiasis.

作者信息

Balloul J M, Grzych J M, Pierce R J, Capron A

出版信息

J Immunol. 1987 May 15;138(10):3448-53.

PMID:3106483
Abstract

We have purified a 28,000 dalton (P28) protein from Schistosoma mansoni adult worms and used it to immunize Fischer rats. Immunofluorescence assays demonstrated that the P28 antigen was mainly located in the parenchyma of the schistosomulum and of the adult worm, including the dorsal spines of the parasite. Western blot analysis revealed that this antigen was present in three species of schistosomes: S. mansoni, S. japonicum, and S. bovis. The antibody response raised against this protein was able to kill S. mansoni schistosomula in in vitro cytotoxicity assays in the presence of rat eosinophils. The inhibition of this cytotoxic activity by an aggregated myeloma IgG2a indicated that one of the major isotypes involved in this in vitro model is IgG2a. The passive transfer of P28 antisera induced a significant level of protection against experimental infection. Moreover, we have immunized Fischer rats and BALB/c mice with the purified 28,000 dalton protein and observed a marked decrease (up to 70%) in the parasite burden in both experimental infection models.

摘要

我们从曼氏血吸虫成虫中纯化出一种28000道尔顿(P28)的蛋白质,并用它免疫Fischer大鼠。免疫荧光分析表明,P28抗原主要位于童虫和成虫的实质组织中,包括寄生虫的背棘。蛋白质印迹分析显示,该抗原存在于三种血吸虫中:曼氏血吸虫、日本血吸虫和牛血吸虫。在大鼠嗜酸性粒细胞存在的情况下,针对该蛋白质产生的抗体反应能够在体外细胞毒性试验中杀死曼氏血吸虫童虫。聚集的骨髓瘤IgG2a对这种细胞毒性活性的抑制表明,参与该体外模型的主要同种型之一是IgG2a。P28抗血清的被动转移诱导了对实验性感染的显著保护水平。此外,我们用纯化的28000道尔顿蛋白质免疫Fischer大鼠和BALB/c小鼠,在两种实验性感染模型中均观察到寄生虫负荷显著降低(高达70%)。

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