Dunne D W, Butterworth A E, Fulford A J, Ouma J H, Sturrock R F
Department of Pathology, University of Cambridge, UK.
Mem Inst Oswaldo Cruz. 1992;87 Suppl 4:99-103. doi: 10.1590/s0074-02761992000800014.
Schistosoma mansoni infected Kenyan patients were treated and the intensities of their reinfections were followed over the next two years. In addition, their pre- and six month post-treatment serum levels of IgG1-4, IgM, and IgE, specific for schistosomula, egg and adult worm, were measured in ELISA. No reinfection took place before six months post-treatment. Reinfection intensities varied with age; the younger children becoming reinfected at significantly higher intensities than older individuals. When antibody and reinfection levels were compared, only the six month post-treatment IgE response against adult worm correlated negatively with intensities of reinfection and, therefore, was predictive of resistance or immunity to reinfection. IgE and IgG specific Western Blots were carried out. The adult worm antigens recognized by IgE were restricted compared with the IgG responses of the same patients, although no individual antigen was uniquely recognized by the IgE isotype. A dominant 22 kDa antigen was recognized by most but not all high IgE responders. Patients with IgE responses against this antigen suffered significantly lower subsequent levels of reinfection, compared with non-responders. A monospecific rabbit antiserum against the 22 kDa adult worm antigen showed that this antigen is specifically located in the tegument of the adult worm and of 'lung' and 'liver' stage schistosomula, but is absent from the early 'skin' schistosomula. It is possible that this antigen is a target for human IgE mediated immune effector mechanisms active against the post skin stage schistosomula and that this is boosted by the death of adult worms.
对感染曼氏血吸虫的肯尼亚患者进行了治疗,并在接下来的两年中跟踪他们再次感染的强度。此外,通过酶联免疫吸附测定法(ELISA)测量了他们治疗前以及治疗后六个月针对血吸虫幼虫、虫卵和成虫的IgG1-4、IgM和IgE的血清水平。治疗后六个月内未发生再次感染。再次感染强度随年龄而异;年幼儿童再次感染的强度明显高于年龄较大者。当比较抗体水平和再次感染水平时,只有治疗后六个月针对成虫的IgE反应与再次感染强度呈负相关,因此可预测对再次感染的抵抗力或免疫力。进行了IgE和IgG特异性蛋白质印迹分析。与同一患者的IgG反应相比,IgE识别的成虫抗原受到限制,尽管没有单个抗原被IgE亚型独特识别。大多数但并非所有高IgE反应者都识别出一种主要的22 kDa抗原。与无反应者相比,对该抗原产生IgE反应的患者随后的再次感染水平明显较低。一种针对22 kDa成虫抗原的单特异性兔抗血清表明,该抗原特异性地位于成虫以及“肺”和“肝”期血吸虫幼虫的体表,但早期“皮肤”期血吸虫幼虫中不存在。这种抗原可能是人类IgE介导的针对皮肤后阶段血吸虫幼虫的免疫效应机制的靶点,并且成虫死亡会增强这种机制。