首页> 美国卫生研究院文献>Journal of the Boston Society of Medical Sciences >Respiratory reovirus 1/L induction of intraluminal fibrosis. A model for the study of bronchiolitis obliterans organizing pneumonia.
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Respiratory reovirus 1/L induction of intraluminal fibrosis. A model for the study of bronchiolitis obliterans organizing pneumonia.

机译:呼吸道呼肠孤病毒1 / L诱导腔内纤维化。研究闭塞性细支气管炎组织性肺炎的模型。

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摘要

Bronchiolitis obliterans organizing pneumonia (BOOP) is a term that was first applied in 1985 to describe a long-observed but unclassified pattern of acute lung injury. BOOP lesions are characterized by fibrous extensions into the alveolar spaces in association with a peribronchiolar organizing pneumonia. Since 1985, an increasing number of reports of BOOP have appeared in the clinical literature, and it is now accepted that BOOP is a significant pulmonary syndrome. Although BOOP can be associated with a number of documented pulmonary insults, many cases are not associated with known causes and are thus classified as idiopathic. The lack of an appropriate small animal model that closely mimics the generation of BOOP lesions has been an impediment to basic studies of the pathogenic mechanisms responsible for the generation of BOOP in humans. In this report, we describe an animal model for BOOP in which CBA/J mice infected with reovirus serotype 1/strain Lang develop BOOP lesions. These lesions closely resemble those seen in humans and occur in a well defined temporal sequence that proceeds from initial peribronchiolar inflammatory lesions to characteristic, fibrotic cellular BOOP lesions over a 3-week time course.
机译:闭塞性细支气管炎组织性肺炎(BOOP)是1985年首次使用的术语,用于描述长期观察但未分类的急性肺损伤模式。 BOOP病变的特征是与支气管周围组织性肺炎相关的纤维延伸进入肺泡腔。自1985年以来,越来越多的BOOP报告出现在临床文献中,现在人们公认BOOP是一种重要的肺部综合症。尽管BOOP可能与许多文献记载的肺损伤相关,但许多病例与已知原因无关,因此被归类为特发性。缺乏合适的小动物模型来紧密模拟BOOP病变的产生已经阻碍了对人类BOOP产生的致病机制的基础研究。在此报告中,我们描述了BOOP的动物模型,其中感染了呼肠孤病毒血清型1 / Lang株的CBA / J小鼠出现了BOOP病变。这些病变与人类中的病变非常相似,并以明确的时间顺序发生,从最初的支气管周围炎性病变发展为特征性纤维化细胞BOOP病变,历时三周。

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