| Literature DB >> 18539233 |
Alicia K Gerke1, Gary Hunninghake.
Abstract
Sarcoidosis continues to be a disease of research interest because of its complicated immune mechanisms and elusive etiology. So far, it has been established that granulomatous inflammation in sarcoidosis is predominantly a T-helper 1 immune response mediated by a complex network of lymphocytes, macrophages, and cytokines. The cause of progression to a chronic and potentially fibrotic form is unclear but may involve loss of apoptotic mechanisms, loss of regulatory response, or a persistent antigen that cannot be cleared. Recent genomic and proteomic technology has emphasized the importance of host susceptibility and gene-environment interaction in the expression of the disease.Entities:
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Year: 2008 PMID: 18539233 DOI: 10.1016/j.ccm.2008.03.014
Source DB: PubMed Journal: Clin Chest Med ISSN: 0272-5231 Impact factor: 2.878