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Development and resolution of Pneumocystis carinii pneumonia in severe combined immunodeficient mice: a morphological study of host inflammatory responses.

机译:严重合并免疫缺陷小鼠中卡氏肺孢子虫肺炎的发生和解决:宿主炎症反应的形态学研究。

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摘要

The development and resolution of naturally-acquired Pneumocystis carinii pneumonia was studied in a severe combined immunodeficient (SCID) mouse model by light and electron microscopies. Initial infection was evident in 3-week-old SCID mice and started as focal alveolar colonization in the areas near terminal airways. Pronounced pulmonary inflammation occurred in animals of 10 weeks or older and the infection intensity reached a plateau in animals 12 weeks of age. At this stage of disease, the histopathological features of P. carinii infection in SCID mice were similar to those of immunodeficient man. Reconstitution of SCID mice with immunocompetent spleen cells at day 0 induced substantial pulmonary inflammation that was evident already by day 7 and most severe and extensive by day 12. The clearance of P. carinii did not begin until after day 12 and was almost completed by day 17. Alveolar macrophages in mice killed between days 12 and 15, at the time when P. carinii are being rapidly cleared, appeared active but phagocytosis of P. carinii was not commonly observed by either light or electron microscopy. These results suggest that (1) the presence of non-lymphoid inflammatory cells in SCID mice is not sufficient to control P. carinii infection; (2) the clearance of P. carinii from the lungs of reconstituted SCID mice requires local recruitment of large numbers of inflammatory cells with an active appearance; and (3) intracellular killing of P. carinii by phagocytosis does not appear to be a major mechanism in host defences against P. carinii infection in this model.
机译:在严重的联合免疫缺陷(SCID)小鼠模型中,通过光和电子显微镜检查研究了自然获得性卡氏肺孢子虫肺炎的发生和解决。最初的感染在3周龄的SCID小鼠中很明显,并开始于末端气道附近区域的局部肺泡定植。在10周或更年长的动物中发生明显的肺部炎症,并且在12周龄的动物中感染强度达到平稳。在疾病的这个阶段,SCID小鼠中卡氏疟原虫感染的组织病理学特征与免疫缺陷人相似。在第0天用免疫能力强的脾细胞重建SCID小鼠会引起严重的肺部炎症,这在第7天就已经很明显,在第12天时最为严重和广泛。清除卡氏假单胞菌直到第12天才开始,并且几乎在第12天完成17.在迅速清除卡氏疟原虫的第12天和第15天之间杀死的小鼠中的肺泡巨噬细胞似乎活跃,但是通过光学或电子显微镜通常观察不到卡氏疟原虫的吞噬作用。这些结果表明(1)SCID小鼠中非淋巴炎性细胞的存在不足以控制卡氏疟原虫感染。 (2)从重组SCID小鼠的肺中清除卡氏疟原虫需要局部募集大量具有活跃外观的炎性细胞; (3)在该模型中,吞噬作用在细胞内杀死卡氏疟原虫似乎不是宿主对抗卡氏疟原虫感染的主要机制。

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