Sarcoidosis -: Immunopathogenetic concepts

被引:73
作者
Zissel, Gernot [1 ]
Prasse, Antje [1 ]
Mueller-Quernheim, Joachim [1 ]
机构
[1] Univ Hosp Freiburg, Univ Med Ctr, Dept Pneumol, D-79106 Freiburg, Germany
关键词
sarcoidosis; granuloma; immunopathogenesis; T cells; alveolar macrophages; chemokines; cytokines;
D O I
10.1055/s-2007-970329
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Sarcoidosis is a chronic granulomatous disorder characterized by an accumulation of activated lymphocytes, predominantly T helper cells, expressing the Th1 phenotype and macrophages at sites of disease activity. Although the cause of sarcoidosis has not been elucidated, several lines of evidence suggest that granuloma formation results from exposure to one or more antigens, eliciting a T lymphocyte response. The induction and evolution of granuloma formation results from a complex interplay between diverse cell types, cytokines, and chemokines. Genetic polymorphisms may influence the clinical expression of the granuloma formation and disease outcome. This article discusses in depth the key cellular elements and signals that generate and orchestrate the sarcoid granulomatous response. The precise factors inciting the sarcoid granulomatous response have not yet been identified, but chronic exposure to microbial agents, their products, or inorganic substances may be important in the pathogenesis.
引用
收藏
页码:3 / 14
页数:12
相关论文
共 131 条
[1]   CXC chemokines IP-10 and Mig expression and direct migration of pulmonary CD8+/CXCR3+T cells in the lungs of patients with HIV infection and T-cell alveolitis [J].
Agostini, C ;
Facco, M ;
Siviero, M ;
Carollo, D ;
Galvan, S ;
Cattelan, AM ;
Zambello, R ;
Trentin, L ;
Semenzato, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (04) :1466-1473
[2]  
Agostini C, 1996, J IMMUNOL, V157, P910
[3]  
Agostini C, 1998, J IMMUNOL, V161, P6413
[4]   Regulation of alveolar macrophage-T cell interactions during Th1-type sarcoid inflammatory process [J].
Agostini, C ;
Trentin, L ;
Perin, A ;
Facco, M ;
Siviero, M ;
Piazza, F ;
Basso, U ;
Adami, F ;
Zambello, R ;
Semenzato, G .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 277 (02) :L240-L250
[5]   Expression of tumor necrosis factor receptor superfamily members by lung T lymphocytes in interstitial lung disease [J].
Agostini, C ;
Zambello, R ;
Sancetta, R ;
Cerutti, A ;
Milani, A ;
Tassinari, C ;
Facco, M ;
Cipriani, A ;
Trentin, L ;
Semenzato, G .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1996, 153 (04) :1359-1367
[6]   Expression of lymphotoxin-beta (LT-β) in chronic inflammatory conditions [J].
Agyekum, S ;
Church, A ;
Sohail, M ;
Krausz, T ;
Van Noorden, S ;
Polak, J ;
Cohen, J .
JOURNAL OF PATHOLOGY, 2003, 199 (01) :115-121
[7]  
BACHWICH PR, 1986, AM J PATHOL, V125, P421
[8]   Infliximab therapy in patients with chronic sarcoidosis and pulmonary involvement [J].
Baughman, Robert P. ;
Drent, Marjolein ;
Kavuru, Mani ;
Judson, Marc A. ;
Costabel, Ulrich ;
du Bois, Roland ;
Albera, Carlo ;
Brutsche, Martin ;
Davis, Gerald ;
Donohue, James F. ;
Mueller-Quernheim, Joachim ;
Schlenker-Herceg, Rozsa ;
Flavin, Susan ;
Lo, Kim Hung ;
Oemar, Barry ;
Barnathan, Elliot S. .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2006, 174 (07) :795-802
[9]  
BAUGHMAN RP, 1990, J LAB CLIN MED, V115, P36
[10]  
Baumer I, 1997, AM J RESP CELL MOL, V16, P171