McHugh S M, Coulson P S, Wilson R A
Parasitology. 1987 Feb;94 ( Pt 1):81-91. doi: 10.1017/s0031182000053476.
The development of resistance in mice to reinfection with Schistosoma mansoni was recorded during an early chronic infection, and compared with hepatic portal pathological and vascular changes. The latter were assessed using a microsphere injection technique. The degree of acquired resistance was directly dependent on the patent worm burden and the time post-infection. Strong correlations were noted between the development of resistance and the appearance of parasite eggs in the lungs and spleens of infected hosts. Weaker associations were present between resistance and other aspects of the disease pathology, such as portal hypertension and organ weights. The appearance of injected microspheres in the lungs and spleens correlated well with the appearance of eggs in those organs and with the development of resistance. The levels of resistance had risen and microspheres were detected in the lungs, before the development of major extra-hepatic, porta-systemic collateral vessels. It is concluded that intra-hepatic vascular alterations may be a causal factor in the development of resistance, preventing the sequestration of migrating schistosomula in the liver. It is estimated that as much as 70-75% of the recorded resistance can be attributed to this immunologically non-specific mechanism.
在小鼠早期慢性感染曼氏血吸虫期间,记录了其对再次感染的抗性发展情况,并与肝门静脉病理和血管变化进行了比较。后者采用微球注射技术进行评估。获得性抗性程度直接取决于成虫虫荷和感染后的时间。抗性发展与感染宿主肺和脾中出现寄生虫卵之间存在强相关性。抗性与疾病病理的其他方面,如门静脉高压和器官重量之间的关联较弱。注入的微球在肺和脾中的出现与这些器官中卵的出现以及抗性发展密切相关。在主要肝外门体侧支血管形成之前,抗性水平已经升高,并且在肺中检测到了微球。结论是肝内血管改变可能是抗性发展的一个因果因素,阻止了移行期童虫在肝脏中的滞留。据估计,记录到的抗性中高达70 - 75%可归因于这种免疫非特异性机制。