T-lymphocytes and cytokines in sarcoidosis

被引:58
作者
Agostini, C [1 ]
Meneghin, A [1 ]
Semenzato, G [1 ]
机构
[1] Univ Padua, Dipartimento Med Clin & Sperimentale, Immunol Clin, Sch Med, I-35128 Padua, Italy
关键词
D O I
10.1097/00063198-200209000-00016
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
In the last few years, a number of reports have clearly shown that pulmonary T lymphocytes have evolved a number of effector mechanisms to respond to foreign antigens, ranging from direct cytotoxicity mechanisms to secretion of lymphokines, that have the ability to activate themselves or other pulmonary immunocompetent cells. Furthermore, there is also evidence that lung T cells may have a role in the immunopathogenetic mechanisms taking place in the lung of most immune-mediated diffuse lung disorders. In this paper, we will review the current concepts on the recruitment, homing, and activity of T lymphocytes in the lower respiratory tract of patients with sarcoidosis. The relevant phenotypic and functional abnormalities detected on T cells in sarcoidosis will be discussed. Furthermore, we will comment recent findings on the ability of immunomodulatory molecules, such as proinflammatory cytokines, chemokines, and other cytokines, to regulate T-cell function in immune mechanisms leading to granuloma formation and maintenance. (C) 2002 Lippincott Williams Wilkins, Inc.
引用
收藏
页码:435 / 440
页数:6
相关论文
共 37 条
[1]  
Agostini C, 1996, J IMMUNOL, V157, P910
[2]  
Agostini C, 1998, J IMMUNOL, V161, P6413
[3]   Cells and molecules involved in the development of sarcoid granuloma [J].
Agostini, C ;
Basso, U ;
Semenzato, G .
JOURNAL OF CLINICAL IMMUNOLOGY, 1998, 18 (03) :184-192
[4]   Alveolar macrophage - T cell interactions during Th1-type sarcoid inflammation [J].
Agostini, C ;
Facco, M ;
Chilosi, M ;
Semenzato, G .
MICROSCOPY RESEARCH AND TECHNIQUE, 2001, 53 (04) :278-287
[5]  
Agostini C, 2001, SARCOIDOSIS VASC DIF, V18, P18
[6]  
Agostini C, 1998, Curr Opin Pulm Med, V4, P261, DOI 10.1097/00063198-199809000-00004
[7]   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
[8]  
Baughman RP, 2001, SARCOIDOSIS VASC DIF, V18, P70
[9]  
BAUGHMAN RP, 1990, J LAB CLIN MED, V115, P36
[10]  
Baumer I, 1997, AM J RESP CELL MOL, V16, P171