Immunoglobulin Free Light Chains Are Increased in Hypersensitivity Pneumonitis and Idiopathic Pulmonary Fibrosis

BACKGROUND: Idiopathic pulmonary fibrosis (IPF), a devastating lung disorder of unknown aetiology, and chronic hypersensitivity pneumonitis (HP), a disease provoked by an immunopathologic reaction to inhaled antigens, are two common interstitial lung diseases with uncertain pathogenic mechanisms. Pr...

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Detalles Bibliográficos
Autores principales: Groot Kormelink, Tom, Pardo, Annie, Knipping, Karen, Buendía-Roldán, Ivette, García-de-Alba, Carolina, Blokhuis, Bart R., Selman, Moises, Redegeld, Frank A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182208/
https://www.ncbi.nlm.nih.gov/pubmed/21980441
http://dx.doi.org/10.1371/journal.pone.0025392

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3182208/
https://www.ncbi.nlm.nih.gov/pubmed/21980441
http://dx.doi.org/10.1371/journal.pone.0025392

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