Immune Inflammation and Disease Progression in Idiopathic Pulmonary Fibrosis

The clinical course in idiopathic pulmonary fibrosis (IPF) is highly heterogeneous, with some patients having a slow progression and others an accelerated clinical and functional decline. This study aims to clinically characterize the type of progression in IPF and to investigate the pathological ba...

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Veröffentlicht in:	PloS one 2016-05, Vol.11 (5), p.e0154516
Hauptverfasser:	Balestro, Elisabetta, Calabrese, Fiorella, Turato, Graziella, Lunardi, Francesca, Bazzan, Erica, Marulli, Giuseppe, Biondini, Davide, Rossi, Emanuela, Sanduzzi, Alessandro, Rea, Federico, Rigobello, Chiara, Gregori, Dario, Baraldo, Simonetta, Spagnolo, Paolo, Cosio, Manuel G, Saetta, Marina
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities Adult Aged Analysis Biological markers Biology and Life Sciences Care and treatment Chemokines Chronic obstructive pulmonary disease Data processing Development and progression Disease Progression Female Fibrosis Forced expiratory volume Gene expression Humans Identification and classification Idiopathic Pulmonary Fibrosis - immunology Idiopathic Pulmonary Fibrosis - pathology Immunoglobulins Inflammation Inflammation - immunology Inflammation - pathology Lung diseases Lung transplantation Male Measurement Medical prognosis Medicine and Health Sciences Middle Aged Pathogenesis Pathology Patients Pulmonary fibrosis Transplantation Transplants & implants
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