Lapa e Silva J R, Guerreiro D, Noble B, Poulter L W, Cole P J
Department of Thoracic Medicine, National Heart and Lung Institute, Brompton Hospital, London, United Kingdom.
Am J Respir Cell Mol Biol. 1989 Oct;1(4):297-304. doi: 10.1165/ajrcmb/1.4.297.
In human bronchiectasis, the bronchial wall is the seat of abnormal mononuclear cell infiltration, which suggests the presence of a cell-mediated immune reaction. The histopathology of a recently devised animal model of experimental bronchiectasis resembles that of the human disease. We have investigated its immunohistology to validate the similarity to that of human bronchiectasis in order to provide a model for the study of cellular immune aspects of the pathogenesis of bronchiectasis. The immunohistology of the bronchial wall mononuclear cell population in experimental rat bronchiectasis was compared with that in control and normal rats. The control rats did not develop bronchiectasis, and the composition and distribution of mononuclear cells in the bronchial wall were similar to those of normal animals. In the rats developing bronchiectasis, there was infiltration of T lymphocytes, macrophages, and dendritic cells (as defined by monoclonal antibodies) in all compartments of the lung, particularly in the bronchial wall and around vessels. The bronchus-associated lymphoid tissue was disrupted by heavy infiltration of T cells, and follicular aggregates of T lymphocytes were seen deeper in the lung parenchyma. Expression of Ia antigen increased in the bronchial epithelium and in large numbers of mononuclear cells throughout the lung. These findings suggest that a cell-mediated immune response appears during the development of experimental bronchiectasis in this rat model. This cellular immune response is similar to that described in human bronchiectasis and may enable this animal model to be used in defining the role of cellular immunity in the pathogenesis of bronchiectasis.
在人类支气管扩张症中,支气管壁是异常单核细胞浸润的部位,这提示存在细胞介导的免疫反应。最近设计的实验性支气管扩张症动物模型的组织病理学与人类疾病相似。我们研究了其免疫组织学,以验证与人类支气管扩张症的相似性,从而为研究支气管扩张症发病机制的细胞免疫方面提供一个模型。将实验性大鼠支气管扩张症中支气管壁单核细胞群体的免疫组织学与对照大鼠和正常大鼠进行比较。对照大鼠未发生支气管扩张症,支气管壁单核细胞的组成和分布与正常动物相似。在发生支气管扩张症的大鼠中,肺的所有区域,特别是支气管壁和血管周围,都有T淋巴细胞、巨噬细胞和树突状细胞(由单克隆抗体定义)浸润。支气管相关淋巴组织因T细胞的大量浸润而被破坏,在肺实质深部可见T淋巴细胞的滤泡聚集。Ia抗原在支气管上皮和整个肺内的大量单核细胞中表达增加。这些发现提示,在该大鼠模型的实验性支气管扩张症发展过程中出现了细胞介导的免疫反应。这种细胞免疫反应与人类支气管扩张症中描述的相似,可能使这个动物模型能够用于确定细胞免疫在支气管扩张症发病机制中的作用。