Köster B, Strand M
Department of Pharmacology and Molecular Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
Parasitology. 1994 May;108 ( Pt 4):433-46. doi: 10.1017/s0031182000075995.
We have used two monoclonal antibodies, 128C3/3 and 504B1, to immunolocalize their carbohydrate epitopes in different developmental stages of Schistosoma mansoni. Both epitopes contain fucose: mAb 128C3/3, as we have shown previously, recognizes fucose in a novel, possibly internal linkage (Levery et al. 1992) while mAb 504B1, as we show here, bound to the Le(x) epitope, which contains fucose alpha 1-->3 linked to N-acetyl-glucosamine. The tissue expression of these epitopes was strikingly different and both elicit an immune response in infected hosts. The mAb 128C3/3-defined epitope was exposed on the surface of all larval stages but not on adult worms; however, it was found in the excretory system of adult worms of both sexes. In contrast, surface expression of the Le(x) epitope was initiated after the transformation of cercariae to schistosomula and was maintained throughout the adult life in both sexes.
我们使用了两种单克隆抗体,128C3/3和504B1,来免疫定位它们在曼氏血吸虫不同发育阶段的碳水化合物表位。两种表位都含有岩藻糖:正如我们之前所表明的,单克隆抗体128C3/3识别一种新的、可能是内部连接的岩藻糖(Levery等人,1992年),而正如我们在此所展示的,单克隆抗体504B1与Le(x)表位结合,该表位含有与N-乙酰葡糖胺以α 1→3连接的岩藻糖。这些表位的组织表达显著不同,并且在受感染宿主中都引发免疫反应。单克隆抗体128C3/3定义的表位在所有幼虫阶段的表面都有暴露,但在成虫体表没有;然而,在两性成虫的排泄系统中发现了该表位。相比之下,Le(x)表位的表面表达在尾蚴转变为童虫后开始,并在两性成虫的整个生命过程中持续存在。