Simpson A J, Hagan P, Hackett F, Omer Ali P, Smithers S R
Division of Parasitology, National Institute for Medical Research, The Ridgeway, Mill Hill, London.
Parasitology. 1990 Feb;100 Pt 1:73-81. doi: 10.1017/s0031182000060133.
The relationship between antigens associated with the surface of newly transformed schistosomula of Schistosoma mansoni and the tegumental surface membrane of adult S. mansoni worms has been further explored. Immunoprecipitation of detergent-solubilized 125I-tegumental surface membrane antigens of adult S. mansoni with antibodies from mice vaccinated with highly irradiated S. mansoni cercariae revealed major antigens of Mr 32, 20, 15 and 8K. The Mr 32 and 20K antigens have been previously demonstrated to be antigenically and electrophoretically identical to major antigens on the schistosomulum surface. The Mr 15 and 8K antigens, on the other hand, have not been identified by the immunoprecipitation of 125I-schistosomulum surface antigens, although a distinct schistosomulum surface antigen of Mr 15K is precipitated by antibodies from mice vaccinated with highly irradiated cercariae. Nevertheless, it was shown that antibodies to the Mr 15 and 8K antigens were specifically absorbed from vaccinated mouse serum by intact, live schistosomula, demonstrating that the Mr 15 and 8K antigens are exposed on or released from the schistosomulum surface. In contrast, absorption of the antiserum with eggs failed to remove antibody against any of the four tegumental membrane antigens examined. The Mr 15 and 8K antigens were shown to be recognized via polypeptide epitopes and not periodate-sensitive carbohydrate epitopes, further emphasizing the similarity of these to the well-characterized Mr 32 and 20K tegumental surface membrane antigens. A general relationship between schistosomulum surface, adult tegumental membrane and egg antigens was demonstrated by ELISA, using antibodies raised against the three antigenic fractions.(ABSTRACT TRUNCATED AT 250 WORDS)
曼氏血吸虫新转化的童虫表面相关抗原与曼氏血吸虫成虫体表膜之间的关系已得到进一步探究。用经高度辐照的曼氏血吸虫尾蚴免疫的小鼠产生的抗体,对成虫曼氏血吸虫去污剂可溶的¹²⁵I-体表膜抗原进行免疫沉淀,结果显示主要抗原有32K、20K、15K和8K的分子量。先前已证明,32K和20K的抗原在抗原性和电泳上与童虫表面的主要抗原相同。另一方面,尽管用经高度辐照的尾蚴免疫的小鼠产生的抗体可沉淀出一种分子量为15K的独特童虫表面抗原,但¹²⁵I-童虫表面抗原的免疫沉淀未鉴定出15K和8K的抗原。然而,研究表明,完整的活童虫可从接种疫苗的小鼠血清中特异性吸收针对15K和8K抗原的抗体,这表明15K和8K抗原暴露于童虫表面或从童虫表面释放。相比之下,用虫卵吸收抗血清未能去除针对所检测的四种体表膜抗原中任何一种的抗体。结果表明,15K和8K抗原是通过多肽表位而非对高碘酸盐敏感的碳水化合物表位被识别的,这进一步强调了它们与特征明确的32K和20K体表膜抗原的相似性。利用针对这三种抗原组分产生的抗体,通过酶联免疫吸附测定(ELISA)证明了童虫表面、成虫体表膜和虫卵抗原之间的一般关系。(摘要截短于250字)