Different angiogenic activity in pulmonary sarcoidosis and idiopathic pulmonary fibrosis

被引:79
作者
Antoniou, Katerina M.
Tzouvelekis, Argyris
Alexandrakis, Michael G.
Sfiridaki, Katerina
Tsiligianni, Ioanna
Rachiotis, George
Tzanakis, Nikolaos
Bouros, Demosthenes
Milic-Emili, Joseph
Siafakas, Nikolaos M.
机构
[1] Univ Crete, Dept Thorac Med, Iraklion 71110, Crete, Greece
[2] Univ Crete, Dept Hematol, Iraklion 71110, Crete, Greece
[3] Democritus Univ Thrace, Dept Pneumol, Alexandroupolis, Greece
[4] Venizele Gen Hosp, Dept Hematol, Iraklion, Greece
[5] Univ Athens, Dept Expt Pathol, Athens, Greece
[6] McGill Univ, Dept Pneumol, Montreal, PQ, Canada
关键词
angiogenesis; angiostasis; CXC chemokines; growth-related gene-alpha; interferon-gamma-inducible protein-10; interferon-gamma-inducible T-cell alpha chemoattractant; monokine induced by interferon-gamma;
D O I
10.1378/chest.130.4.982
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Background: Recent evidence has shown that several chemokines-including those involved in angiogenesis-have been implicated in the pathogenesis of idiopathic pulmonary fibrosis (IPF) and sarcoidosis. We speculated that these differences could be attributed to distinct angiogenic and angiostatic profiles. This hypothesis was investigated by estimating the levels of three angiogenic ebemokines (growth-related gene [GRO]-alpha, epithelial neutrophil-activating protein [ENA]-78, and interleukin [IL]-8), and three angiostatic chemokines (monokine induced by interferon (IFN)-gamma [MIGI, IFN-gamma-inducible protein [IP]-10, and IFN-gamma-inducible T-cell alpha chemoattractant) in serum and BAL fluid (BALF). Methods: We studied prospectively 20 patients with sarcoidosis (median age, 46 years; range, 25 to 65 years), 20 patients with IPF (median age, 68 years; range, 40 to 75 years), and 10 normal subjects (median age, 39 years; range, 26 to 60 years). Results: The GRO-a serum and BALF levels of IPF patients were found significantly increased in comparison with healthy subjects (799 pg/mL vs 294 pg/mL [p = 0.022] and 1,827 pg/mL vs 94 pg/mL [p < 0.001], respectively) and sarcoidosis patients (799 pg/mL vs 44 pg/mL [p < 0.0011 and 1,827 pg/mL vs 214 pg/mL [p < 0.001], respectively). Moreover, ENA-78 and IL-8 BALF levels in IPF patients were significantly higher compared with sarcoidosis patients (191 pg/mL vs 30 pg/mL [p < 0.0011 and 640 pg/mL vs 94 pg/mL [p = 0.031, respectively). MIG serum levels in IPF patients were found significantly upregulated in comparison with sarcoidosis patients and healthy control subjects. However, MIG and IP-10 RA-LF levels (1,136 pg/mL vs 66 pg/mL [p < 0.0011 and 112 pg/mL vs 56 pg/mL [p = 0.037], respectively) were significantly higher in sarcoidosis patients compared with IPF patients. Conclusions: Our data suggest distinct angiogenie profiles between IPF and sarcoidosis, indicating a potential different role of CXC chemokines in the local immunologic response in IPF and pulmonary sarcoidosis.
引用
收藏
页码:982 / 988
页数:7
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