Delgado V S, McLaren D J
Division of Parasitology, National Institute for Medical Research, Mill Hill, London.
Parasitology. 1989 Dec;99 Pt 3:357-64. doi: 10.1017/s0031182000059072.
Naive CBA/Ca mice and CBA/Ca mice infected 12 weeks previously with 20 normal cercariae of Schistosoma mansoni were challenged percutaneously with isotopically labelled parasites. Challenge worm migration was followed, in 5 separate experiments, by means of compressed organ autoradiography. In three experiments, 43.1% of challenge parasites did not arrive in the lungs of infected mice on day 6 as compared to 7.7% in naive controls, thereby indicating that pre-lung sites constitute the first barrier in resistance to reinfection. A further 15% of the challenge worm burden was lost in the lungs or en route to the liver in the immune animals, and portal perfusion revealed that 25.4% of the challenge was lost in the liver. Two other experiments revealed no comparable phases of pre-liver attrition however; instead resistance was only evident at final perfusion on days 28 or 35. These data reveal the variable generation of specific acquired immunity in mice harbouring a chronic schistosome infection and thus clarify current discrepancies in the literature. The results are discussed in relation to documented evidence for the nature of specific and non-specific immune mechanisms reported to operate at different sites in the infection model of schistosomiasis mansoni.
将未感染过的CBA/Ca小鼠以及12周前感染过20条曼氏血吸虫正常尾蚴的CBA/Ca小鼠,经皮用同位素标记的寄生虫进行攻击。在5个独立实验中,通过压缩器官放射自显影术追踪攻击虫体的迁移情况。在三个实验中,与未感染对照小鼠的7.7%相比,43.1%的攻击寄生虫在第6天时未抵达感染小鼠的肺部,这表明肺前部位是抵抗再感染的第一道屏障。在免疫动物中,另外15%的攻击虫体负荷在肺部或前往肝脏的途中损失,门静脉灌注显示25.4%的攻击虫体在肝脏中损失。然而,另外两个实验未发现类似的肝前损耗阶段;相反,抗性仅在第28天或35天的最终灌注时才明显。这些数据揭示了携带慢性血吸虫感染的小鼠中特异性获得性免疫的不同产生情况,从而澄清了文献中目前存在的差异。结合已记录的关于曼氏血吸虫感染模型中不同部位所报告的特异性和非特异性免疫机制性质的证据,对结果进行了讨论。