Type V Collagen Induced Tolerance Suppresses Collagen Deposition, TGF-β and Associated Transcripts in Pulmonary Fibrosis

RATIONALE: Idiopathic pulmonary fibrosis (IPF) is a fatal interstitial lung disease characterized by progressive scarring and matrix deposition. Recent reports highlight an autoimmune component in IPF pathogenesis. We have reported anti-col(V) immunity in IPF patients. The objective of our study was...

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Detalles Bibliográficos
Autores principales: Vittal, Ragini, Mickler, Elizabeth A., Fisher, Amanda J., Zhang, Chen, Rothhaar, Katia, Gu, Hongmei, Brown, Krista M., Emtiazdjoo, Amir, Lott, Jeremy M., Frye, Sarah B., Smith, Gerald N., Sandusky, George E., Cummings, Oscar W., Wilkes, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804565/
https://www.ncbi.nlm.nih.gov/pubmed/24204629
http://dx.doi.org/10.1371/journal.pone.0076451

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3804565/
https://www.ncbi.nlm.nih.gov/pubmed/24204629
http://dx.doi.org/10.1371/journal.pone.0076451

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