期刊论文详细信息
Respiratory Research
Impact of smoking on dendritic cell phenotypes in the airway lumen of patients with COPD
Marek Lommatzsch1  J Christian Virchow1  Michael Kuepper1  Katharina Garbe1  Andrea Bier1  Kai Bratke1  Ann-Sophie Heinz1  Paul Stoll1 
[1] Department of Pneumology and Critical Care Medicine, University of Rostock, Ernst-Heydemann-Str. 6, 18057 Rostock, Germany
关键词: Airway;    Smoking;    COPD;    Dendritic cells;   
Others  :  790322
DOI  :  10.1186/1465-9921-15-48
 received in 2013-11-11, accepted in 2014-04-11,  发布年份 2014
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【 摘 要 】

Background

Myeloid dendritic cells (DCs) are increased in the airway wall of patients with chronic obstructive pulmonary disease (COPD), and postulated to play a crucial role in COPD. However, DC phenotypes in COPD are poorly understood.

Methods

Function-associated surface molecules on bronchoalveolar lavage fluid (BALF) DCs were analyzed using flow cytometry in current smokers with COPD, in former smokers with COPD and in never-smoking controls.

Results

Myeloid DCs of current smokers with COPD displayed a significantly increased expression of receptors for antigen recognition such as BDCA-1 or Langerin, as compared with never-smoking controls. In contrast, former smokers with COPD displayed a significantly decreased expression of these receptors, as compared with never-smoking controls. A significantly reduced expression of the maturation marker CD83 on myeloid DCs was found in current smokers with COPD, but not in former smokers with COPD. The chemokine receptor CCR5 on myeloid DCs, which is also important for the uptake and procession of microbial antigens, was strongly reduced in all patients with COPD, independently of the smoking status.

Conclusion

COPD is characterized by a strongly reduced CCR5 expression on myeloid DCs in the airway lumen, which might hamper DC interactions with microbial antigens. Further studies are needed to better understand the role of CCR5 in the pathophysiology and microbiology of COPD.

【 授权许可】

   
2014 Stoll et al.; licensee BioMed Central Ltd.

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