Kelly C, Hagan P, Knight M, Hodgson J, Simpson A J, Hackett F, Wilkins H A, Smithers S R
Division of Parasitology, National Institute for Medical Research, Mill Hill, London.
Parasitology. 1987 Oct;95 ( Pt 2):253-66. doi: 10.1017/s0031182000057711.
Of the surface antigens identified by radio-iodination, two-dimensional gel analyses showed no similarities between those of Schistosoma haematobium and Schistosoma mansoni, thus providing a basis for the species specificity of these antigens described previously (Simpson, Knight, Hagan, Hodgson, Wilkins & Smithers (1985) Parasitology 90, 499-508). The surface antigens of S. haematobium were glycosylated and comprised an acidic polypeptide of Mr 17,000 as well as a complex set of polypeptides of approximate pI 6-7, which resolved in the Mr range 20,000-30,000. At least one of the lower Mr forms of this complex is also present in the adult worm. Limited cross-reaction was observed with S. mansoni infection sera and this may be due to a shared carbohydrate epitope. In contrast, extensive cross-reaction was observed using sera from mice immunized with S. bovis. This pattern parallels the species-specificity of vaccine-induced immunity. Extensive cross-reaction was also observed within cell-free translation products of m-RNA from adult worms of S. haematobium and S. mansoni by use of heterologous human infection sera. The few antigens which were species-specific may represent surface antigens.
在通过放射性碘化鉴定出的表面抗原中,二维凝胶分析表明埃及血吸虫和曼氏血吸虫的表面抗原没有相似之处,从而为先前描述的这些抗原的种特异性提供了依据(辛普森、奈特、哈根、霍奇森、威尔金斯和史密瑟斯(1985年),《寄生虫学》90卷,第499 - 508页)。埃及血吸虫的表面抗原是糖基化的,包括一个分子量为17,000的酸性多肽以及一组复杂的多肽,其近似等电点为6 - 7,分子量范围在20,000 - 30,000之间。该复合物中至少一种较低分子量形式在成虫中也存在。观察到与曼氏血吸虫感染血清有有限的交叉反应,这可能是由于共享的碳水化合物表位。相比之下,使用用牛血吸虫免疫的小鼠血清观察到广泛的交叉反应。这种模式与疫苗诱导免疫的种特异性相似。通过使用异源人类感染血清,在埃及血吸虫和曼氏血吸虫成虫的mRNA的无细胞翻译产物中也观察到广泛的交叉反应。少数种特异性抗原可能代表表面抗原。