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肥大细胞在过敏性肺炎发病机制中的作用。

Role of mast cells in the pathogenesis of hypersensitivity pneumonitis.

作者信息

Soler P, Nioche S, Valeyre D, Basset F, Benveniste J, Burtin C, Battesti J P, Georges R, Hance A J

机构信息

INSERM U82, Faculté Xavier Bichat, Paris, France.

出版信息

Thorax. 1987 Aug;42(8):565-72. doi: 10.1136/thx.42.8.565.

Abstract

To examine the possibility that mast cells have a central role in the pathogenesis of hypersensitivity pneumonitis, 20 patients with this disease were studied with the aim of seeking evidence for mast cell degranulation. The number of mast cells recovered by bronchoalveolar lavage from patients with hypersensitivity pneumonitis was more than 1,000 times greater than those recovered from normal individuals. Furthermore, discontinuation of antigen exposure resulted in an increase in the number of mast cells observed, consistent with the possibility that antigen exposure had induced mast cell degranulation. Cessation of antigen exposure also resulted in a rapid decrease in the number of neutrophils and eosinophils recovered by lavage, followed by an increase in the number of T8+ T lymphocytes present. In each case the time course of the changes was consistent with the possibility that mast cell degranulation had been important in regulating the number of the immune and inflammatory cells present in the lung. Histamine was present in lavage fluid supernatant from patients with hypersensitivity pneumonitis. The amount of histamine present was, however, closely correlated with the number of mast cells present and not with the interval since last antigen exposure. Delay in separating cells from lavage fluid supernatant resulted in an increase in histamine content. These results suggest that the free histamine in lavage fluid resulted from the degranulation of mast cells induced by the lavage procedure as histamine released in vivo has a short half life. We suggest that hypersensitivity pneumonitis results from a "late phase reaction" initiated by antigen induced mast cell degranulation.

摘要

为了研究肥大细胞在超敏性肺炎发病机制中是否起核心作用,对20例该疾病患者进行了研究,旨在寻找肥大细胞脱颗粒的证据。通过支气管肺泡灌洗从超敏性肺炎患者中回收的肥大细胞数量比从正常个体中回收的肥大细胞数量多1000倍以上。此外,停止抗原暴露导致观察到的肥大细胞数量增加,这与抗原暴露诱导肥大细胞脱颗粒的可能性一致。停止抗原暴露还导致通过灌洗回收的中性粒细胞和嗜酸性粒细胞数量迅速减少,随后出现的T8 + T淋巴细胞数量增加。在每种情况下,变化的时间进程都与肥大细胞脱颗粒在调节肺中存在的免疫和炎症细胞数量方面起重要作用的可能性一致。超敏性肺炎患者的灌洗液体上清液中存在组胺。然而,存在的组胺量与存在的肥大细胞数量密切相关,而与自上次抗原暴露以来的间隔无关。从灌洗液体上清液中分离细胞的延迟导致组胺含量增加。这些结果表明,灌洗液体中的游离组胺是由灌洗程序诱导的肥大细胞脱颗粒产生的,因为体内释放的组胺半衰期很短。我们认为超敏性肺炎是由抗原诱导的肥大细胞脱颗粒引发的“晚期反应”所致。

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