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Animal models of lung fibrosis

机译:肺纤维化的动物模型

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Interstitial lung diseases comprise a large group of pulmonary disorders characterized by lung inflammation and fibrosis. Often, these disorders are progressive leading to irreversible tissue scaring. The absence of effective and safe anti-fibrotic drugs has prompted the search for targets for intervention that could lead to new strategies for treatment. Animal models of lung fibrosis, although not resembling exactly the human condition, represent invaluable tools for the exploration of the factors and mechanisms involved in the development of lung fibrosis. In this review, we briefly discuss current concepts related to the pathogenesis of lung fibrosis followed by a more thorough discussion of currently available animal models of lung fibrosis. Experimental models induced by chemical agents, haptens, infection, genetic manipulation, and irradiation are discussed as are cell-mediated models and spontaneous models of lung fibrosis in domestic animals.
机译:间质性肺疾病包括一大批以肺部炎症和纤维化为特征的肺部疾病。通常,这些疾病是进行性的,导致不可逆的组织惊吓。缺乏有效和安全的抗纤维化药物促使人们寻找可能产生新治疗策略的干预目标。肺纤维化的动物模型虽然与人类的状况并不完全相似,但却代表了探索与肺纤维化发展有关的因素和机制的宝贵工具。在这篇综述中,我们简要讨论了与肺纤维化发病机制有关的当前概念,然后对当前可用的肺纤维化动物模型进行了更全面的讨论。讨论了由化学试剂,半抗原,感染,遗传操作和辐射诱导的实验模型,以及家畜中肺纤维化的细胞介导模型和自发模型。

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