A Novel Insight into Adaptive Immunity in Chronic Obstructive Pulmonary Disease B Cell Activating Factor Belonging to the Tumor Necrosis Factor Family

被引:57
|
作者
Polverino, Francesca [1 ,2 ,3 ]
Baraldo, Simonetta [1 ,2 ]
Bazzan, Erica [1 ,2 ]
Agostini, Simone [1 ,2 ]
Turato, Graziella [1 ,2 ]
Lunardi, Francesca [4 ]
Balestro, Elisabetta [1 ,2 ]
Damin, Marco [1 ,2 ]
Papi, Alberto [6 ]
Maestrelli, Piero [5 ]
Calabrese, Fiorella [4 ]
Saetta, Marina [1 ,2 ]
机构
[1] Univ Padua, Dept Cardiac Thorac & Vasc Sci, I-35128 Padua, Italy
[2] Padova City Hosp, Padua, Italy
[3] Univ Messina, Dept Clin & Expt Med, Messina, Italy
[4] Univ Padua, Dept Med Diagnost Sci & Special Therapies, I-35128 Padua, Italy
[5] Univ Padua, Dept Environm Med & Publ Hlth, I-35128 Padua, Italy
[6] Univ Ferrara, Dept Clin & Expt Med, I-44100 Ferrara, Italy
关键词
inflammatory cells; lymphoid follicles; cigarette smoking; airflow limitation; CHEMOKINE RECEPTOR CXCR3; PERIPHERAL AIRWAYS; DENDRITIC CELLS; TNF FAMILY; RHEUMATOID-ARTHRITIS; LYMPHOID FOLLICLES; INDUCED EMPHYSEMA; TOBACCO SMOKING; T-LYMPHOCYTES; LIGAND BAFF;
D O I
10.1164/rccm.200911-1700OC
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Rationale: Chronic obstructive pulmonary disease (COPD) is a disorder characterized by an abnormal inflammatory response that persists even after smoking cessation, yet the underlying mechanisms are not fully understood. Objectives: To investigate the expression of B-cell activating factor of tumor necrosis factor family (BAFF), a crucial mediator in the crosstalk between innate and adaptive immune responses, in patients with COPD and to explore its correlation with disease severity. Methods: Using immunohistochemistry, expression of BAFF was examined in lung specimens from 21 smokers with COPD (FEV1 = 57 +/- 5% predicted), 14 control smokers (FEV1 = 99 +/- 2% predicted) and 8 nonsmokers (FEV1 = 104 +/- 4% predicted). BAFF was quantified in alveolar macrophages and alveolar walls, in bronchiolar and parenchymal lymphoid follicles, and in peripheral airways and pulmonary arterioles. Measurements and Main Results: In alveolar macrophages and parenchymal lymphoid follicles, BAFF expression was increased in smokers with COPD compared with control smokers and nonsmokers (P < 0.05 for all comparisons). In both compartments, BAFF was also up-regulated in control smokers as compared with nonsmokers (P = 0.03 and P = 0.01). Moreover, BAFF was overexpressed in bronchiolar lymphoid follicles, alveolar walls, peripheral airways, and pulmonary arterioles from smokers with COPD compared with nonsmokers (P < 0.05 for all). Among patients with COPD, BAFF(+) macrophages were inversely related to FEV1 (P = 0.03, Spearman's rho [r(s)] = -0.48), FEV1/FVC (P = 0.02, r(s) = -0.50), and Pa-O2 values (P = 0.01, r(s) = -0.55). Conclusions: This study demonstrated overexpression of BAFF in peripheral lung of patients with COPD, mainly in alveolar macrophages and lymphoid follicles. Moreover, BAFF expression was correlated to the degree of lung function impairment and hypoxia, suggesting that it may have a possible impact on disease severity.
引用
收藏
页码:1011 / 1019
页数:9
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