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慢性阻塞性肺疾病与哮喘之间的异同

Differences and similarities between chronic obstructive pulmonary disease and asthma.

作者信息

Jeffery P K

机构信息

Imperial College School of Medicine at the National Heart and Lung Institute, London, UK.

出版信息

Clin Exp Allergy. 1999 Jun;29 Suppl 2:14-26.

Abstract

Asthma and chronic obstructive pulmonary disease (COPD) are complex conditions with imprecise definitions, which make definitive morphological comparisons difficult. The airways in asthma are occluded by tenacious plugs of exudate and mucus, and there is fragility of airway surface epithelium, thickening of the reticular layer beneath the epithelial basal lamina (the last two not usually features of COPD), and bronchial vessel congestion and oedema. There is an increased inflammatory infiltrate comprising 'activated' lymphocytes and eosinophils with release of granular content in the latter, and enlargement of bronchial smooth muscle, particularly in medium-sized bronchi. CD4+ve lymphocytes predominate over CD8+ve cells and neutrophils are sparse. In contrast, three conditions contribute to COPD. In chronic bronchitis there is cough and mucous hypersecretion with enlargement of tracheobronchial submucosal glands and a disproportionate increase of mucous acini. CD8+ve lymphocytes predominate over CD4+ve cells and there are increased numbers of subepithelial macrophages and intra-epithelial neutrophils. Exacerbations of bronchitis are associated with a tissue eosinophilia, apparent absence of IL-5 protein but gene expression for IL-4 and IL-5 is present. In small or peripheral airways disease, there is inflammation of bronchioli and mucous metaplasia and hyperplasia, with increased intraluminal mucus, increased wall muscle, fibrosis, and airway stenoses (also referred to as chronic obstructive bronchiolitis). Respiratory bronchiolitis involving increased numbers of pigmented macrophages is a critically important early lesion. Increasingly severe peribronchiolitis includes infiltration of T lymphocytes in which the CD8+ subset again predominates. These inflammatory changes may predispose to the development of centrilobular emphysema and reduced FEV1 via the destruction of alveolar attachments. In emphysema there is abnormal, permanent enlargement of airspaces distal to the terminal bronchiolus (i.e. within the acinus) accompanied by destruction of alveolar walls and without obvious fibrosis. The severity of emphysema, rather than type, appears to be the most important determinant of chronic deterioration of airflow, and in this there may be significant loss of elastic recoil and microscopic emphysema prior to the observed macroscopic destruction of the acinus.

摘要

哮喘和慢性阻塞性肺疾病(COPD)是复杂的病症,定义不精确,这使得进行明确的形态学比较很困难。哮喘患者的气道被黏稠的渗出物和黏液栓阻塞,气道表面上皮脆弱,上皮基膜下网状层增厚(后两者通常不是COPD的特征),支气管血管充血和水肿。炎症浸润增加,包括“活化”淋巴细胞和嗜酸性粒细胞,后者释放颗粒内容物,支气管平滑肌增大,尤其是在中等大小的支气管中。CD4+阳性淋巴细胞多于CD8+阳性细胞,中性粒细胞稀少。相比之下,有三种情况导致COPD。在慢性支气管炎中,有咳嗽和黏液分泌过多,气管支气管黏膜下腺增大,黏液腺泡不成比例地增加。CD8+阳性淋巴细胞多于CD4+阳性细胞,上皮下巨噬细胞和上皮内中性粒细胞数量增加。支气管炎急性加重与组织嗜酸性粒细胞增多有关,IL-5蛋白明显缺乏,但存在IL-4和IL-5的基因表达。在小气道或外周气道疾病中,细支气管有炎症、黏液化生和增生,管腔内黏液增加,管壁肌肉增加、纤维化,气道狭窄(也称为慢性阻塞性细支气管炎)。涉及色素沉着巨噬细胞数量增加的呼吸性细支气管炎是一个至关重要的早期病变。越来越严重的细支气管周围炎包括T淋巴细胞浸润,其中CD8+亚群再次占主导。这些炎症变化可能通过破坏肺泡附着而导致小叶中心型肺气肿的发展和FEV1降低。在肺气肿中,终末细支气管远端(即腺泡内)的气腔异常永久性扩大,伴有肺泡壁破坏且无明显纤维化。肺气肿的严重程度而非类型似乎是气流慢性恶化的最重要决定因素,并在这方面,在观察到腺泡的宏观破坏之前可能存在显著的弹性回缩丧失和微观肺气肿。

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