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Cockroach allergen induced asthma: Pulmonary mechanics, inflammation and tolerance.

机译:蟑螂过敏原诱发的哮喘:肺力学,炎症和耐受性。

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摘要

Asthma is one of the most common chronic health conditions in the developed world. However, the mechanisms of this insidious disease remain poorly characterized. Animal models of allergic pulmonary inflammation can offer valuable insights into the management of human disease. Urban environments contain potent respiratory allergens and a greater incidence of new asthma diagnosis, especially in children. One particularly common urban antigen is the German cockroach allergen (CRA). The lab of Daniel G. Remick developed a model of CRA induced pulmonary inflammation in inbred BALB/c mice which closely resembles the human disease. In the current research the model was established and validated in outbred HSD-ICR mice. Outbred animals were chosen because of their genetically heterogeneous background which more closely mimics the human population. Outbred ICR mice were found to display roughly equivalent overall variability to BALB/c mice in a model of CRA induced asthma. Using equivalent overall variability to BALB/c mice in a model of CRA induced asthma. Using this model treatment with dexamethasone ameliorated respiratory distress and improved pulmonary function. The lung inflammatory response of the outbred mice was characterized at a series of early (1.5, 4, 12 hours) and late timepoints (24, 48 hours) following final allergen challenge. It was found that the airways hyperreactivity (AHR) of the experimental mice displayed a biphasic pattern. The early peak in AHR was determined to be potentiated partially by immune cell action and partially by the action of leukotrienes. The late peak of the AHR response, in contrast, was mainly dependent on cellular components of the allergic response. Finally, the establishment of oral tolerance to CRA as a method for improving lung inflammation and AHR was investigated. It was found that gastric exposure to CRA prior to CRA immunization and challenge led to significant decreases in AHR, bronchoalveolar lavage eosinophil levels and lung homogenate eosinophil specific peroxidase activity. In conclusion these studies greatly extended, characterized and induced tolerance in a highly reproducible model of CRA induced asthma in outbred mice.
机译:哮喘是发达国家中最常见的慢性健康状况之一。但是,这种隐性疾病的机制仍知之甚少。过敏性肺部炎症的动物模型可以为人类疾病的治疗提供有价值的见解。城市环境中含有强烈的呼吸道过敏原,尤其是在儿童中,新发哮喘的诊断率更高。一种特别常见的城市抗原是德国蟑螂过敏原(CRA)。丹尼尔·G·雷米克(Daniel G. Remick)的实验室开发了一种CRA诱导的近交BALB / c小鼠肺炎模型,该模型与人类疾病极为相似。在当前的研究中,该模型已在远距离HSD-ICR小鼠中建立并验证。选择近交动物是因为它们的遗传异质背景更接近于人类。在CRA诱发的哮喘模型中,发现远交ICR小鼠的总体变异性与BALB / c小鼠大致相同。在CRA诱发的哮喘模型中,使用等效于BALB / c小鼠的总体变异性。使用地塞米松治疗该模型可减轻呼吸窘迫并改善肺功能。在最后的变应原攻击后的一系列早期(1.5、4、12小时)和晚期(24、48小时),对异种小鼠的肺炎反应进行了表征。发现实验小鼠的气道高反应性(AHR)显示出双相模式。确定AHR的早期高峰部分是由于免疫细胞的作用,部分是由于白三烯的作用。相反,AHR反应的晚期峰值主要取决于过敏反应的细胞成分。最后,研究了建立对CRA的口服耐受性作为改善肺部炎症和AHR的方法。发现在CRA免疫和攻击之前,胃暴露于CRA会导致AHR,支气管肺泡灌洗嗜酸性粒细胞水平和肺匀浆嗜酸性粒细胞特异性过氧化物酶活性显着降低。总之,这些研究极大地扩展,表征和诱导了CRA诱导的近交小鼠哮喘的高度可复制模型中的耐受性。

著录项

  • 作者

    Vaickus, Louis Joseph.;

  • 作者单位

    Boston University.;

  • 授予单位 Boston University.;
  • 学科 Health Sciences Pathology.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 140 p.
  • 总页数 140
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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