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Published in 2021 at "International immunopharmacology"
DOI: 10.1016/j.intimp.2021.107525
Abstract: BACKGROUND Idiopathic pulmonary fibrosis (IPF) is a chronic progressive interstitial lung disease limited to the lungs. Immunological dysregulation may significantly participate in the pathophysiology of IPF. The immunological responses to nintedanib therapy in IPF patients…
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Keywords:
antifibrotic treatment;
treatment ipf;
cell percentages;
ipf patients ... See more keywords