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识别曼氏血吸虫童虫和毛蚴之间共享的碳水化合物表位的IgM抗体,其可阻断体外杀伤作用。

IgM antibodies recognizing carbohydrate epitopes shared between schistosomula and miracidia of Schistosoma mansoni that block in vitro killing.

作者信息

Yi X Y, Omer-Ali P, Kelly C, Simpson A J, Smithers S R

出版信息

J Immunol. 1986 Dec 15;137(12):3946-54.

PMID:2431050
Abstract

A series of monoclonal antibodies (mAb) was raised in mice against Schistosoma mansoni, which recognized a carbohydrate determinant on a major Mr greater than 200,000 schistosomulum surface antigen. These mAb cross-reacted with the surface of cercariae and miracidia and with schistosomula of S. haematobium and S. bovis. Other mAb were generated that only recognized a Mr 20,000 schistosomulum surface antigen; they did not cross-react with eggs or miracidia and were species specific. The anti-Mr 20,000 mAb of the IgG1 isotype exhibited high levels of complement-dependent cytotoxicity to schistosomula in vitro. IgM mAb that recognized carbohydrate epitopes of the Mr greater than 200,000 surface antigen blocked the lethal activity of the anti-Mr 20,000 mAb. The IgM anti-Mr greater than 200,000 mAb also reduced complement-dependent cytotoxicity of serum from mice vaccinated with irradiated cercariae.

摘要

针对曼氏血吸虫,在小鼠体内产生了一系列单克隆抗体(mAb),这些抗体识别一种分子量大于200,000的主要尾蚴表面抗原上的碳水化合物决定簇。这些单克隆抗体与尾蚴和毛蚴的表面以及埃及血吸虫和牛血吸虫的尾蚴发生交叉反应。还产生了其他仅识别分子量为20,000的尾蚴表面抗原的单克隆抗体;它们不与虫卵或毛蚴发生交叉反应,且具有种属特异性。IgG1同种型的抗分子量20,000单克隆抗体在体外对尾蚴表现出高水平的补体依赖性细胞毒性。识别分子量大于200,000表面抗原的碳水化合物表位的IgM单克隆抗体可阻断抗分子量20,000单克隆抗体的致死活性。IgM抗分子量大于200,000单克隆抗体还降低了用辐照尾蚴免疫的小鼠血清的补体依赖性细胞毒性。

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