Interstitial lung disease (ILD) is characterized by al-veolar and interstitial inflammation, followed by theprogressive derangement of alveolar architecture anddeposition of extracellular matrix components. The dis-ease is initiated by an unknown alveolar insult, whichis followed by the influx of inflammatory cells to thelung. This recruitment phase results in a several foldincrease in all cell types within the airspace, includingneutrophils, eosinophils, lymphocytes and macropha-ges. In addition, substantial interstitial inflammation isapparent, consisting predominantly of newly recruitedmonocytes and lymphocytes. Alveolar and interstitialinflammation is followed by the loss of type I epithe-lial cells and endothelial cells, proliferation of type IIcells, and expansion of the pulmonary interstitium
No takes yet. Share an insight, caveat, or question.
Keane et al. (1997) studied this question.
Synapse has enriched 5 related papers. Consider them for comparative context: