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在清除卡氏肺孢子虫肺炎期间,对卡氏肺孢子虫囊包体的独特宿主反应谱进行了表征。

Characterization of a distinct host response profile to Pneumocystis murina asci during clearance of pneumocystis pneumonia.

机构信息

Cincinnati Department of Veterans Affairs Medical Center, Cincinnati, Ohio, USA.

出版信息

Infect Immun. 2013 Mar;81(3):984-95. doi: 10.1128/IAI.01181-12. Epub 2013 Jan 14.

Abstract

Pneumocystis spp. are yeast-like fungi that cause pneumocystis pneumonia (PcP) in immunocompromised individuals and exacerbate chronic lung diseases in immunocompetent individuals. The Pneumocystis life cycle includes trophic forms and asci (cyst forms). The cell walls of Pneumocystis asci contain β-1,3-D-glucan, and treatment of PcP with β-1,3-D-glucan synthase inhibitors, such as anidulafungin, results in depletion of asci, but not trophic forms. The pulmonary host response during immune reconstitution (IR)-mediated clearance of PcP in anidulafungin-treated and untreated mice was characterized to identify ascus-specific responses. During IR, similar numbers of trophic forms were present in the anidulafungin-treated and untreated mice; however, asci were only present in the untreated mice. IR resulted in a significant reduction of trophic forms from the lungs in both groups and asci in the untreated group. The presence of asci in untreated mice correlated with increased β-glucan content in the lungs. The untreated mice mounted immune responses associated with a deleterious host inflammatory response, including increased CD8(+) T cell influx and expression of macrophage inflammatory response markers. A more robust cellular response was also observed in the untreated mice, with increased numbers of macrophages and neutrophils that were associated with greater lung damage. Markers of a Th17 response were also elevated in the untreated mice. These results suggest that the host mounts unique responses to asci and trophic forms. That these 2 life cycle stages provoked distinct host response profiles has significant implications for clearance and interpretation of the host immune responses to PcP.

摘要

卡氏肺孢子菌是一种酵母样真菌,会在免疫功能低下的个体中引起卡氏肺孢子菌肺炎(PcP),并在免疫功能正常的个体中加重慢性肺部疾病。卡氏肺孢子菌的生命周期包括滋养体形式和子囊(囊体形式)。卡氏肺孢子菌子囊的细胞壁含有β-1,3-D-葡聚糖,用β-1,3-D-葡聚糖合酶抑制剂(如安尼达弗林)治疗 PcP 会导致子囊耗尽,但不会耗尽滋养体形式。在安尼达弗林治疗和未治疗的小鼠中,通过免疫重建(IR)清除 PcP 期间,对肺部的宿主反应进行了特征描述,以确定子囊特异性反应。在 IR 期间,安尼达弗林治疗和未治疗的小鼠中存在相似数量的滋养体形式;然而,只有未治疗的小鼠中存在子囊。IR 导致两组小鼠肺部的滋养体形式和未治疗组的子囊数量显著减少。未治疗小鼠肺部的子囊存在与肺部β-葡聚糖含量增加相关。未治疗的小鼠出现了与有害宿主炎症反应相关的免疫反应,包括 CD8(+)T 细胞浸润增加和巨噬细胞炎症反应标志物的表达增加。在未治疗的小鼠中还观察到更强烈的细胞反应,巨噬细胞和中性粒细胞数量增加,与更大的肺损伤相关。未治疗小鼠的 Th17 反应标志物也升高。这些结果表明,宿主对子囊和滋养体形式都有独特的反应。这两个生命周期阶段引起了宿主反应谱的显著差异,这对清除和解释宿主对 PcP 的免疫反应具有重要意义。

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