Modern Concepts on the Role of Inflammation in Pulmonary Fibrosis

被引:5
|
作者
Homer, Robert J. [1 ]
Elias, Jack A. [2 ]
Lee, Chun Gun [3 ]
Herzog, Erica [3 ]
机构
[1] Yale Univ, Sch Med, Dept Pathol, New Haven, CT 06520 USA
[2] Yale Univ, Sch Med, Dept Internal Med, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Dept Internal Med Pulm & Crit Care, New Haven, CT 06520 USA
关键词
ALVEOLAR EPITHELIAL-CELLS; IDIOPATHIC INTERSTITIAL PNEUMONIAS; ENDOPLASMIC-RETICULUM STRESS; RECEPTOR SUBUNIT EXPRESSION; FACTOR T-BET; LUNG-DISEASE; IL-13-INDUCED INFLAMMATION; TGF-BETA; SYSTEMIC-SCLEROSIS; APOPTOTIC CELLS;
D O I
暂无
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Context.-Idiopathic pulmonary fibrosis is a uniformly lethal disease with limited biomarkers and no proven therapeutic intervention short of lung transplantation. Pulmonary fibrosis at one time was thought to be a result of inflammation in the lung. Although some forms of pulmonary fibrosis may result from inflammation, idiopathic pulmonary fibrosis is currently thought to result from cell death primarily and inflammation secondarily. Objective.-To determine the role of inflammation in pulmonary fibrosis in light of our laboratory's published and unpublished research and published literature. Data Sources.-Review based on our laboratory's published and unpublished experimental data with relevant background and clinical context provided. Conclusions.-Although cell death is central to pulmonary fibrosis, the proper cytokine environment leading to macrophage polarization is also critical. Evaluation of this environment is promising both for the development of disease biomarkers and for targets for therapeutic intervention. (Arch Pathol Lab Med. 2011;135:780-788)
引用
收藏
页码:780 / 788
页数:9
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