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在激素抵抗型结节病中,肺泡巨噬细胞的肿瘤坏死因子α释放增加。

Exaggerated TNFalpha release of alveolar macrophages in corticosteroid resistant sarcoidosis.

作者信息

Ziegenhagen Manfred W, Rothe Manuela E, Zissel Gernot, Müller-Quernheim Joachim

机构信息

University Hospital Freiburg, Dep of Pneumology, Germany.

出版信息

Sarcoidosis Vasc Diffuse Lung Dis. 2002 Oct;19(3):185-90.

Abstract

BACKGROUND AND AIM OF WORK

The aim of the present study was to determine the TNFalpha release of cultured alveolar macrophages (AM) and the bronchoalveolar lavage (BAL) cellular profile in 35 patients suffering from long lasting sarcoidosis.

METHODS

The AM TNFalpha release and the BAL cellular profile of 35 patients with a mean duration of sarcoidosis of 10.4 +/- 1.3 years at the time of BAL was compared to 35 healthy controls.

RESULTS

The BAL profile of 12 sarcoid patients with a stable disease was similar to that known from acute sarcoidosis. Sarcoid patients with progressive disease (n = 12) and sarcoid patients with corticosteroid resistant disease (n = 11) were characterised by a normal CD4/CD8 ratio and a significant increase of BAL neutrophils (2.7 +/- 1.0% and 3.8 +/- 1.1%, respectively). The AM TNFalpha release of sarcoid patients with stable disease did not differ significantly from controls (523 +/- 124 pg/ml vs. 410 +/- 104 pg/ml). In contrast, we observed a significantly elevated TNFalpha release in sarcoid patients with progressive (2,124 +/- 550 pg/ml; p < 0.01) as well as in those with a corticosteroid resistant disease (1,585 +/- 520 pg/ml; p < 0.01) compared to controls.

CONCLUSION

Chronic sarcoid patients in a progressive phase of the disease and those with a corticosteroid resistant disease are characterised by a significantly increased TNFalpha release of cultured AM. Our results support the usage of chimeric anti-TNFalpha antibodies as an alternative therapeutic regimen in chronic corticosteroid resistant sarcoidosis.

摘要

工作背景与目的

本研究旨在测定35例患有长期结节病患者的培养肺泡巨噬细胞(AM)的肿瘤坏死因子α(TNFα)释放量以及支气管肺泡灌洗(BAL)细胞谱。

方法

将35例结节病患者(BAL时结节病平均病程为10.4±1.3年)的AM TNFα释放量和BAL细胞谱与35名健康对照者进行比较。

结果

12例病情稳定的结节病患者的BAL细胞谱与急性结节病时已知的情况相似。病情进展的结节病患者(n = 12)和对皮质类固醇耐药的结节病患者(n = 11)的特征是CD4/CD8比值正常,BAL中性粒细胞显著增加(分别为2.7±1.0%和3.8±1.1%)。病情稳定的结节病患者的AM TNFα释放量与对照组无显著差异(523±124 pg/ml对410±104 pg/ml)。相比之下,我们观察到病情进展的结节病患者(2,124±550 pg/ml;p < 0.01)以及对皮质类固醇耐药的患者(1,585±520 pg/ml;p < 0.01)的TNFα释放量与对照组相比显著升高。

结论

处于疾病进展期的慢性结节病患者和对皮质类固醇耐药的患者的特征是培养的AM的TNFα释放量显著增加。我们的结果支持使用嵌合抗TNFα抗体作为慢性皮质类固醇耐药结节病的替代治疗方案。

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