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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Hlavní autoři: Groot Kormelink, Tom, Pardo, Annie, Knipping, Karen, Buendía-Roldán, Ivette, García-de-Alba, Carolina, Blokhuis, Bart R., Selman, Moises, Redegeld, Frank A.
Médium: Artigo
Jazyk:Inglês
Vydáno: Public Library of Science 2011
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Research Article
On-line přístup:https://ncbi.nlm.nih.gov/pmc/articles/PMC3182208/
https://ncbi.nlm.nih.gov/pubmed/21980441
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0025392
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