da Silva L C, Vianna M R, Abrantes C P, Lima D M, Falavigna A L, Antonelli-Cardoso R H, Gallucci S D, de Brito T
Institute of Tropical Medicine of S. Paulo, Brazil.
Rev Inst Med Trop Sao Paulo. 1990 Sep-Oct;32(5):328-37. doi: 10.1590/s0036-46651990000500004.
In an attempt to be as close as possible to the infected and treated patients of the endemic areas of schistosomiasis (S. mansoni) and in order to achieve a long period of follow-up, mice were repeatedly infected with a low number of cercariae. Survival data and histological variables such as schistosomal granuloma, portal changes, hepatocellular necrosis, hepatocellular regeneration, schistosomotic pigment, periductal fibrosis and chiefly bile ducts changes were analysed in the infected treated and non treated mice. Oxamniquine chemotherapy in repeatedly infected mice prolonged survival significantly when compared to non-treated animals (chi-square 9.24, p = 0.0024), thus confirming previous results with a similar experimental model but with a shorter term follow-up. Furthermore, mortality decreased rapidly after treatment suggesting an abrupt reduction in the severity of hepatic lesions. A morphological and immunohistochemical study of the liver was carried out. Portal fibrosis, with a pattern resembling human Symmers fibrosis was present at a late phase in the infected animals. Bile duct lesions were quite close to those described in human Mansonian schistosomiasis. Schistosomal antigen was observed in one isolated altered bile duct cell. The pathogenesis of the bile duct changes and its relation to the parasite infection and/or their antigens are discussed.
为尽可能贴近血吸虫病(曼氏血吸虫)流行地区的感染和治疗患者,并为了实现长期随访,用少量尾蚴反复感染小鼠。分析了感染、治疗和未治疗小鼠的生存数据以及组织学变量,如血吸虫肉芽肿、门静脉变化、肝细胞坏死、肝细胞再生、血吸虫色素、导管周围纤维化以及主要的胆管变化。与未治疗的动物相比,反复感染小鼠的奥沙尼喹化疗显著延长了生存期(卡方值9.24,p = 0.0024),从而证实了之前在类似实验模型中但随访期较短时的结果。此外,治疗后死亡率迅速下降,表明肝脏病变的严重程度突然降低。对肝脏进行了形态学和免疫组织化学研究。感染动物在晚期出现了类似于人类Symmers纤维化模式的门静脉纤维化。胆管病变与人类曼氏血吸虫病中描述的病变非常相似。在一个孤立的改变的胆管细胞中观察到了血吸虫抗原。讨论了胆管变化的发病机制及其与寄生虫感染和/或其抗原的关系。