D21 IMMUNE PATHWAYS IN ACUTE LUNG INJURY AND FIBROSIS: Lung Tissue From Patients With Idiopathic Pulmonary Fibrosis Contains A Unique Population Of C-Kit+icos+cd127int Innate Lymphoid Cells

D21 IMMUNE PATHWAYS IN ACUTE LUNG INJURY AND FIBROSIS: Lung Tissue From Patients With Idiopathic Pulmonary Fibrosis Contains A Unique Population Of C-Kit+icos+cd127int Innate Lymphoid Cells

Objectives: Idiopathic pulmonary fibrosis (IPF) is a devastating progressive lung disease that causes irreversible lung scarring and loss of pulmonary function. ILCs are primarily tissue-resident, and therefore may play a role in disease progression; however, availability of IPF lung tissue to exami...

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Veröffentlicht in:American journal of respiratory and critical care medicine 2017-01, Vol.195
Hauptverfasser: Hrusch, C L, Mohinta, S, Jaffery, M R, Blaine, K, Bonham, C, Sperling, A I
Format: Artikel
Sprache:eng
Schlagworte:
Health risk assessment
Lungs
Lymphatic system
Pulmonary fibrosis
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Zusammenfassung:Objectives: Idiopathic pulmonary fibrosis (IPF) is a devastating progressive lung disease that causes irreversible lung scarring and loss of pulmonary function. ILCs are primarily tissue-resident, and therefore may play a role in disease progression; however, availability of IPF lung tissue to examine these cells is limited.
ISSN:1073-449X
1535-4970