Intrapulmonary Autoantibodies to HSP72 Are Associated with Improved Outcomes in IPF

RATIONALE: Idiopathic pulmonary fibrosis (IPF) is a progressive fibrotic interstitial lung disease, with high mortality. Currently, the aetiology and the pathology of IPF are poorly understood, with both innate and adaptive responses previously being implicated in the disease pathogenesis. Heat shoc...

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Detalles Bibliográficos
Autores principales: Mills, Ross, Mathur, Abhinav, Nicol, Lisa M., Walker, Jeremy J., Przybylski, Alexander A., Mackinnon, Alison C., Howie, Sarah E. M., Wallace, William A. H., Dransfield, Ian, Hirani, Nik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2019
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6487088/
https://www.ncbi.nlm.nih.gov/pubmed/31098385
http://dx.doi.org/10.1155/2019/1845128

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