Tsutsumi V, Martinez-Palomo A
Section of Experimental Pathology, Centro de Investigación del I.P.N., México, D.F. Mexico.
Am J Pathol. 1988 Jan;130(1):112-9.
One of the hallmarks of tissue necrosis produced by the human protozoan parasite Entamoeba histolytica, the causative agent of human amebiasis, appeared to be the lack of inflammatory reaction to the invading trophozoites. Recent evidence suggests, however, that inflammatory cells do appear during early stages of amebic destructive lesions and that they contribute to the establishment of foci of tissue necrosis in intestinal and liver lesions. The present analysis of the fine-structural changes that take place during early stages of amebic liver abscesses induced in hamsters after the intraportal inoculation of axenic amebas has shown that large numbers of polymorphonuclear leukocytes (PMNs) are recruited around invading amebas. These leukocytes lyse as a consequence of contact-mediated damage induced by the trophozoites. Amebas were also capable of ingesting apparently intact PMNs. Macrophages and eosinophils were also recruited at the foci of inflammation. At all times examined, trophozoites of Entamoeba histolytica survived in spite of being in close contact with PMNs or degranulating eosinophils. The ultrastructural observations have also shown the lack of direct contact between amebas and liver parenchymal cells during the initial stages of the focal liver necrosis induced by the parasite, therefore supporting the view that hepatic damage may be effected indirectly through lysis of inflammatory cells. The results also provide a basis for the understanding of the induction of experimental protective immunity against invasive amebiasis, a process which seems to be mostly dependent on cellular mechanisms.
人类原生动物寄生虫溶组织内阿米巴是人类阿米巴病的病原体,其所致组织坏死的一个标志似乎是对入侵滋养体缺乏炎症反应。然而,最近的证据表明,在阿米巴破坏性病变的早期确实会出现炎症细胞,并且它们有助于在肠道和肝脏病变中形成组织坏死灶。目前对在仓鼠门静脉内接种无菌阿米巴后诱导的阿米巴肝脓肿早期阶段发生的细微结构变化的分析表明,大量多形核白细胞(PMN)在入侵的阿米巴周围募集。这些白细胞由于滋养体诱导的接触介导损伤而溶解。阿米巴也能够摄取明显完整的PMN。巨噬细胞和嗜酸性粒细胞也在炎症灶处募集。在所有检查的时间点,溶组织内阿米巴滋养体尽管与PMN或脱颗粒的嗜酸性粒细胞密切接触仍能存活。超微结构观察还表明,在寄生虫诱导的局灶性肝坏死的初始阶段,阿米巴与肝实质细胞之间缺乏直接接触,因此支持肝损伤可能通过炎症细胞溶解间接发生的观点。这些结果也为理解针对侵袭性阿米巴病的实验性保护性免疫的诱导提供了基础,这一过程似乎主要依赖于细胞机制。