Warning: Undefined variable $zfal in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525
Deprecated: str_replace(): Passing null to parameter #3 ($subject) of type array|string is deprecated in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 525

Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 530
free
Warning: Undefined variable $sterm in C:\Inetpub\vhosts\kidney.de\httpdocs\mlpefetch.php on line 531
free
free
  English Wikipedia
Nephropedia Template TP (
Twit Text
DeepDyve Pubget Overpricing |   
lüll Dendritic cells in the pathogenesis of sarcoidosis Zaba LC; Smith GP; Sanchez M; Prystowsky SDAm J Respir Cell Mol Biol 2010[Jan]; 42 (1): 32-9Sarcoidosis is a noncaseating granulomatous disease, likely of autoimmune etiology, that causes inflammation and tissue damage in multiple organs, most commonly the lung, but also skin, and lymph nodes. Reduced dendritic cell (DC) function in sarcoidosis peripheral blood compared with peripheral blood from control subjects suggests that blunted end organ cellular immunity may contribute to sarcoidosis pathogenesis. Successful treatment of sarcoidosis with tumor necrosis factor (TNF) inhibitors, which modulate DC maturation and migration, has also been reported. Together, these observations suggest that DCs may be important mediators of sarcoidosis immunology. This review focuses on the phenotype and function of DCs in the lung, skin, blood, and lymph node of patients with sarcoidosis. We conclude that DCs in end organs are phenotypically and functionally immature (anergic), while DCs in the lymph node are mature and polarize pathogenic Th1 T cells. The success of TNF inhibitors is thus likely secondary to inhibition of DC-mediated Th1 polarization in the lymph node.|Bronchoalveolar Lavage Fluid[MESH]|Cell Proliferation[MESH]|Cell Survival[MESH]|Cytokines/metabolism[MESH]|Dendritic Cells/cytology/*pathology[MESH]|Granuloma/pathology[MESH]|Humans[MESH]|Inflammation[MESH]|Lymph Nodes/pathology[MESH]|Lymphocyte Activation[MESH]|Macrophages/metabolism[MESH]|Models, Biological[MESH]|Pulmonary Alveoli/metabolism[MESH]|Sarcoidosis/*physiopathology[MESH]|Th1 Cells/cytology[MESH] |