Ann Intern Med. 1981 Jan;94(1):73-94. doi: 10.7326/0003-4819-94-1-73.
The alveolitis of pulmonary sarcoidosis is characterized by an intense, mononuclear cell infiltrate that probably precedes granuloma formation. Pathogenic mechanisms underlying pulmonary sarcoidosis can be shown by study of the mononuclear cells composing the alveolitis. Bronchoalveolar lavage has shown that the sarcoid lung is characterized by increased numbers of "activated" T-lymphocytes within the alveolar structures. In contrast to normal control cells, the lung T-lymphocytes of patients with sarcoid release the mediator, monocyte chemotactic factor, that probably contributes to the pathogenesis of sarcoidosis by recruiting blood monocytes to the lung, thus providing cellular building blocks for granuloma formation. Conventional monitors of the activity of pulmonary sarcoidosis, such as blood studies, pulmonary function testing, and chest roentgenograms, show little assessed by bronchoalveolar lavage or by histopathologic studies. In contrast, quantification of lavage T-lymphocyte populations and 67Ga scintigraphy of the chest provide a sensitive and specific means of assessing the activity of the alveolitis in pulmonary sarcoidosis and may provide a rational basis for therapy.
肺结节病的肺泡炎特征为强烈的单核细胞浸润,这可能先于肉芽肿形成。通过研究构成肺泡炎的单核细胞,可以揭示肺结节病的致病机制。支气管肺泡灌洗显示,结节病肺的特征是肺泡结构内“活化”T淋巴细胞数量增加。与正常对照细胞相比,结节病患者的肺T淋巴细胞释放介质单核细胞趋化因子,该因子可能通过将血液中的单核细胞募集到肺部,从而为肉芽肿形成提供细胞构建块,进而促进结节病的发病机制。传统的肺结节病活动监测指标,如血液检查、肺功能测试和胸部X线片,通过支气管肺泡灌洗或组织病理学研究评估时显示作用不大。相比之下,灌洗T淋巴细胞群体的定量分析和胸部67Ga闪烁扫描提供了一种敏感且特异的方法来评估肺结节病中肺泡炎的活动情况,并可能为治疗提供合理依据。