Bickle Q D, Andrews B J
London School of Hygiene and Tropical Medicine, Winches Farm Laboratories, St Albans, Herts, UK.
Parasite Immunol. 1988 Mar;10(2):151-68. doi: 10.1111/j.1365-3024.1988.tb00211.x.
We have characterized various anti-schistosomular surface MoAbs previously shown to partially block in-vitro killing of schistosomula by human sera and eosinophils (Dunne et al. 1987). Immunodiffusion analysis showed that four IgM and one IgG3 MoAbs recognized periodate sensitive epitopes on the same molecular species present in schistosomular antigen but their patterns of reactivity with soluble egg antigen demonstrated that at least three distinct epitopes were involved. SDS-PAGE analysis showed the IgMs to react with 125I-labelled surface antigens of Mr 35,000-38,000 and Mr 20,000, and the IgG3 to react with an Mr 38,000 antigen. In spite of their effect in vitro, transfer of the IgM MoAbs at the time of challenge of mice vaccinated with irradiated cercariae or of mice injected with an unrelated (anti-Mr 16,000) protective MoAb failed to produce in-vivo blocking. Similarly, injection of Schistosoma mansoni eggs, prior infection with worms of one sex, or passive transfer of serum from single-sex infected mice failed to influence the resistance conferred by vaccination with irradiated cercariae.
我们已经鉴定了多种抗血吸虫幼虫表面单克隆抗体(MoAbs),这些抗体先前已被证明可部分阻断人血清和嗜酸性粒细胞在体外对血吸虫幼虫的杀伤作用(邓恩等人,1987年)。免疫扩散分析表明,四种IgM和一种IgG3单克隆抗体识别血吸虫幼虫抗原中存在的同一分子种类上对高碘酸盐敏感的表位,但它们与可溶性虫卵抗原的反应模式表明至少涉及三个不同的表位。SDS-PAGE分析显示,IgM与分子量为35,000 - 38,000和20,000的125I标记表面抗原发生反应,而IgG3与分子量为38,000的抗原发生反应。尽管它们在体外有作用,但在用辐照尾蚴免疫的小鼠或注射无关(抗分子量16,000)保护性单克隆抗体的小鼠受到攻击时,转移IgM单克隆抗体未能产生体内阻断作用。同样,注射曼氏血吸虫虫卵、预先感染一种性别的虫体或被动转移来自单性感染小鼠的血清,均未能影响用辐照尾蚴免疫所赋予的抵抗力。