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正常受试者和间质性肺疾病患者肺泡巨噬细胞的表型分析。

Phenotypic analysis of alveolar macrophages in normal subjects and in patients with interstitial lung disease.

作者信息

Campbell D A, Poulter L W, Du Bois R M

出版信息

Thorax. 1986 Jun;41(6):429-34. doi: 10.1136/thx.41.6.429.

Abstract

Cytospin preparations of mononuclear inflammatory cells were made from bronchoalveolar lavage fluid obtained from 15 patients with interstitial lung disease (nine patients with sarcoidosis and six patients with cryptogenic fibrosing alveolitis) and six control subjects. These preparations were examined with a panel of monoclonal antibodies that have been shown to distinguish subpopulations of macrophage like cells in normal tissues. The lysosomal acid phosphatase activity of the cells was also assessed. Phenotypically distinct subpopulations of alveolar macrophages were identified in all samples studied. The results showed that all cell populations identified in bronchoalveolar lavage fluid from the groups with interstitial lung disease could be identified in the lavage fluid from normal volunteers. Some quantitative differences in the proportions of cells identified with particular reagents emerged. In each of the groups with interstitial lung disease increased proportions of cells were identified with RFD1 (interdigitating cell marker; p less than 0.01) and in the cryptogenic fibrosing alveolitis group an increased proportion of alveolar macrophages was identified with RFD7 (tissue macrophage marker; p less than 0.05). The possibility that quantitative changes in alveolar macrophage subsets observed in the interstitial lung disease groups are relevant to the pathogenesis of these conditions is discussed.

摘要

从15例间质性肺病患者(9例结节病患者和6例隐源性纤维性肺泡炎患者)及6名对照者获取支气管肺泡灌洗液体,制成单核炎性细胞的细胞离心涂片。使用一组已证实在正常组织中可区分巨噬细胞样细胞亚群的单克隆抗体对这些涂片进行检查。还评估了细胞的溶酶体酸性磷酸酶活性。在所研究的所有样本中均鉴定出表型不同的肺泡巨噬细胞亚群。结果显示,间质性肺病组支气管肺泡灌洗液体中鉴定出的所有细胞群体均可在正常志愿者的灌洗液体中找到。在用特定试剂鉴定的细胞比例方面出现了一些数量差异。在每个间质性肺病组中,用RFD1(指状突细胞标记物;p<0.01)鉴定的细胞比例增加,在隐源性纤维性肺泡炎组中,用RFD7(组织巨噬细胞标记物;p<0.05)鉴定的肺泡巨噬细胞比例增加。文中讨论了在间质性肺病组中观察到的肺泡巨噬细胞亚群数量变化与这些病症发病机制相关的可能性。

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