Circulating fibrocytes as prognostic biomarkers of autoimmune interstitial lung disease

BACKGROUND: Autoimmunity is a common cause of pulmonary fibrosis and can present either as a manifestation of an established connective tissue disease or as the recently described entity of interstitial pneumonia with autoimmune features. The rate of progression and responsiveness to immunosuppressi...

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Detalles Bibliográficos
Autores principales: Odackal, John, Yu, Victor, Gomez-Manjerres, Diana, Field, Joshua J., Burdick, Marie D., Mehrad, Borna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: European Respiratory Society 2020
Materias:
Original Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682700/
https://www.ncbi.nlm.nih.gov/pubmed/33263049
http://dx.doi.org/10.1183/23120541.00481-2020

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7682700/
https://www.ncbi.nlm.nih.gov/pubmed/33263049
http://dx.doi.org/10.1183/23120541.00481-2020

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