Rodriguez Tobias E, Falkowski Nicole R, Harkema Jack R, Huffnagle Gary B
Division of Pulmonary and Critical Care Medicine, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI 48109-0642, USA.
Infect Immun. 2007 Dec;75(12):5663-8. doi: 10.1128/IAI.01542-06. Epub 2007 Sep 17.
Acute fungal sinusitis (AFS) is a devastating disease of the paranasal sinuses afflicting immunocompromised individuals. Knowledge about this disease is limited to clinical observations because there are no animal models in which to study the pathogenesis of the infection. Our goal was to develop a murine model of AFS and examine the role of neutrophils in host defense within the nasal cavity. Female C57BL/6 mice were depleted of neutrophils using anti-Gr-1 monoclonal antibody from day -1 to day 5 postinfection to initiate a transient neutropenia within the mice. At day 0, Aspergillus fumigatus conidia were administered intranasally. The untreated Aspergillus-exposed group had significant neutrophil recruitment by day 3, but by day 7 the leukocyte numbers had returned to unexposed levels. There was not a significant influx of mononuclear cells at either time point. In contrast, beginning at day 3 postinfection and continuing through day 7, anti-Gr-1-treated mice had increased cellular recruitment consisting of banded neutrophils at day 3 and mature neutrophils at day 7. Hyphal masses developed only in the anti-Gr-1-treated mice (25 to 36%) but only during the period of treatment. When the treatment was discontinued, hyphal masses could no longer be detected in the nasal cavities of these mice. In contrast, cyclophosphamide treatment did not induce neutropenia, and the nasal cavity remained free of hyphal masses. These studies demonstrate the feasibility of using this model to study AFS and implicate neutrophils in protection of the sinuses against acute Aspergillus infection and in clearance of established hyphal masses.
急性真菌性鼻窦炎(AFS)是一种侵袭免疫功能低下个体的鼻窦毁灭性疾病。由于没有可用于研究该感染发病机制的动物模型,关于这种疾病的认知仅限于临床观察。我们的目标是建立AFS的小鼠模型,并研究中性粒细胞在鼻腔宿主防御中的作用。从感染后第 -1天至第5天,使用抗Gr-1单克隆抗体使雌性C57BL/6小鼠的中性粒细胞减少,以在小鼠体内引发短暂性中性粒细胞减少。在第0天,经鼻给予烟曲霉菌分生孢子。未治疗的烟曲霉暴露组在第3天有显著的中性粒细胞募集,但到第7天白细胞数量已恢复到未暴露水平。在这两个时间点单核细胞均无显著流入。相比之下,从感染后第3天开始并持续到第7天,抗Gr-1治疗的小鼠有增加的细胞募集,第3天为带状中性粒细胞,第7天为成熟中性粒细胞。菌丝团仅在抗Gr-1治疗的小鼠中形成(25%至36%),但仅在治疗期间形成。当停止治疗时,在这些小鼠的鼻腔中不再能检测到菌丝团。相比之下,环磷酰胺治疗未诱导中性粒细胞减少,鼻腔中也没有菌丝团。这些研究证明了使用该模型研究AFS的可行性,并表明中性粒细胞在保护鼻窦免受急性曲霉菌感染以及清除已形成的菌丝团方面发挥作用。