Poulter L W
Department of Immunology, Royal Free Hospital Medical School, Hampstead, London, U.K.
FEMS Microbiol Immunol. 1990 Dec;2(5-6):327-31. doi: 10.1111/j.1574-6968.1990.tb03536.x.
The alveolar macrophage pool is morphologically and phenotypically heterogeneous. Using monoclonal antibodies, homogeneous populations were isolated from broncho-alveolar lavage for functional studies. Such investigations revealed that some alveolar macrophages exhibit phagocytic and microbicidal capacity, thus being equipped to act as effector cells (MoAb RFD7+), while others exhibit the characteristics of antigen presenting cells (MoAb RFD1+) involved in the induction of acquired T cell responses. In the investigation of cells from sarcoid patients, a third population was revealed, exhibiting the phenotype RFD1+ and RFD7+. Functional studies of such cells showed them to act by suppressing T-cell responsiveness. The balance between these three populations alters in different disease processes and, in the case of sarcoidosis, is related to disease severity. It is proposed that changes in the balance of these populations may directly influence the pathogenesis of inflammatory lung disease.
肺泡巨噬细胞库在形态和表型上具有异质性。利用单克隆抗体,从支气管肺泡灌洗中分离出同质群体用于功能研究。此类研究表明,一些肺泡巨噬细胞具有吞噬和杀菌能力,因此具备作为效应细胞发挥作用的条件(单克隆抗体RFD7+),而另一些则表现出参与诱导获得性T细胞反应的抗原呈递细胞的特征(单克隆抗体RFD1+)。在对结节病患者细胞的研究中,发现了第三种群体,其表型为RFD1+和RFD7+。对此类细胞的功能研究表明它们通过抑制T细胞反应性发挥作用。这三种群体之间的平衡在不同疾病过程中会发生改变,在结节病的情况下,与疾病严重程度相关。有人提出,这些群体平衡的变化可能直接影响炎症性肺病的发病机制。