Craig P S
Department of Parasitology, Liverpool School of Tropical Medicine, UK.
Parasite Immunol. 1988 May;10(3):243-54. doi: 10.1111/j.1365-3024.1988.tb00218.x.
125I-labelled proteins associated with the surface of the oncosphere and metacestode stages of Taenia pisiformis were investigated, together with the presence of host immunoglobulin G on the parasite surface. Rabbit IgG was detected by enzyme-linked immunosorbent assay (ELISA) in the acid washes (pH 3.0) of viable 3-week migratory metacestodes and 8-week mature cystic metacestodes from the liver and peritoneal cavity, respectively, of rabbits orally infected with eggs of T. pisiformis. However, specific anti-T. pisiformis IgG antibodies could not be detected in these washes using ELISA. When intact and washed hatch-activated oncospheres and 3-week and 8-week metacestode stages were iodinated with Bolton-Hunter 125I reagent and examined by SDS-PAGE and autoradiography, there appeared to be a marked loss and/or reduction of labelled proteins on the mature cystic metacestode compared to the oncosphere and 3-week juvenile metacestode stages. Six-week post-infection rabbit sera strongly immunoprecipitated a 43 kD iodinated protein from oncospheres together with others including a 65 kD polypeptide. Only the 65 kD polypeptide, which is the major iodinated protein on 3-week liver metacestodes, was immunoprecipitated from these juvenile or the mature metacestode stages. The results are discussed in relation to survival of metacestodes in the host, and as to how acquired resistance might result from both frequent egg challenge and concomitant immunity.
对与豆状带绦虫六钩蚴和囊尾蚴阶段表面相关的¹²⁵I标记蛋白进行了研究,并检测了寄生虫表面宿主免疫球蛋白G的存在情况。通过酶联免疫吸附测定(ELISA),在分别从经口感染豆状带绦虫卵的兔子的肝脏和腹腔中取出的存活3周的移行期囊尾蚴和8周的成熟囊状囊尾蚴的酸洗脱液(pH 3.0)中检测到兔IgG。然而,使用ELISA在这些洗脱液中未检测到特异性抗豆状带绦虫IgG抗体。当完整且洗涤后的孵化激活六钩蚴以及3周和8周的囊尾蚴阶段用博尔顿-亨特¹²⁵I试剂进行碘化,并通过SDS-PAGE和放射自显影检查时,与六钩蚴和3周龄幼年囊尾蚴阶段相比,成熟囊状囊尾蚴上标记蛋白似乎有明显损失和/或减少。感染后6周的兔血清强烈免疫沉淀了来自六钩蚴的一种43 kD碘化蛋白以及其他蛋白,包括一种65 kD多肽。从这些幼年或成熟囊尾蚴阶段仅免疫沉淀出了65 kD多肽,它是3周龄肝脏囊尾蚴上的主要碘化蛋白。结合囊尾蚴在宿主体内的存活情况以及频繁的虫卵攻击和伴随免疫如何导致获得性抗性对结果进行了讨论。