Alveolar macrophages are the main source for tumour necrosis factor-α in patients with sarcoidosis

被引:86
作者
Fehrenbach, H
Zissel, G
Goldmann, T
Tschernig, T
Vollmer, E
Pabst, R
Müller-Quernheim, J
机构
[1] Univ Marburg, Clin Res Grp Chron Airway Dis, Dept Internal Med Resp Med, D-35034 Marburg, Germany
[2] Med Univ Hosp, Dept Pneumol, Freiburg, Germany
[3] Hosp Med, Dept Clin & Expt Pathol, Res Ctr, Borstel, Germany
[4] Hannover Med Sch, Dept Funct & Appl Anat, D-3000 Hannover, Germany
关键词
alveolar macrophages; granuloma formation; sarcoidosis tumour necrosis factor;
D O I
10.1183/09031936.03.00083002
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
Tumour necrosis factor (TNF)-alpha is known to play a major role in the formation of noncaseating granuloma, a hallmark of sarcoidosis. The main cellular source in situ is still ambiguous. Serial sections of transbronchial biopsies from 14 patients with and 12 without sarcoidosis were studied, using immunohistochemistry (IHC), for TNF-alpha, T-cells (CD3), macrophages (CD68), and epithelial cells (MNF116). TNF-alpha spontaneously released (sr-TNF-alpha) by freshly isolated bronchoalveolar lavage cells, isolated from the same patients and cultured without any stimulus over a 24-h period was measured using an enzyme-linked immunosorbent assay. IHC revealed colocalisation of TNF-alpha with CD68 cells only. Cases with TNF-alpha tissue immunoreactivity exhibited higher sr-TNF-alpha (1,667+/-504 pg.mL(-1)) than cases without tissue immunoreactivity (211+/-60 pg.mL(-1)). In an explorative approach, a subgroup of patients could be identified and characterised by the presence of alveolar macrophage aggregates. It was found that sr-TNF-alpha was highest in this subgroup (2,700 769 pg.mL(-1)) compared with patients with normal histology (221+/-61 pg.mL(-1)) or with prominent granuloma (460 137 pg.mL(-1)), whereas in most clinical parameters this subgroup was intermediate. The findings from this study strongly corroborate the view that alveolar macrophages are the main cellular source for tumour necrosis factor-alpha in the initial phase of sarcoidosis. The authors suggest that in these patients, aggregates of alveolar macrophages may represent at least predecessors to granulomas if not granulomas in statu nascendi.
引用
收藏
页码:421 / 428
页数:8
相关论文
共 34 条
[1]   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
[2]   Inter-relationship between tumour necrosis factor-alpha (TNF-α) and TNF soluble receptors in pulmonary sarcoidosis [J].
Armstrong, L ;
Foley, NM ;
Millar, AB .
THORAX, 1999, 54 (06) :524-530
[3]  
BAUGHMAN RP, 1990, J LAB CLIN MED, V115, P36
[4]  
Baumer I, 1997, AM J RESP CELL MOL, V16, P171
[5]   Increased macrophage inflammatory protein-1α and macrophage inflammatory protein-1β levels in bronchoalveolar lavage fluid of patients affected by different stages of pulmonary sarcoidosis [J].
Capelli, A ;
Di Stefano, A ;
Lusuardi, M ;
Gnemmi, I ;
Donner, CF .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (02) :236-241
[6]   Immunological mechanisms in sarcoidosis [J].
Conron, M ;
du Bois, RM .
CLINICAL AND EXPERIMENTAL ALLERGY, 2001, 31 (04) :543-554
[7]   ATS/ERS/WASOG statement on sarcoidosis [J].
Costabel, U ;
Hunninghake, GW .
EUROPEAN RESPIRATORY JOURNAL, 1999, 14 (04) :735-737
[8]   Keratinocyte growth factor-induced hyperplasia of rat alveolar type II cells in vivo is resolved by differentiation into type I cells and by apoptosis [J].
Fehrenbach, H ;
Kasper, M ;
Tschernig, T ;
Pan, T ;
Schuh, D ;
Shannon, JM ;
Muller, M ;
Mason, RJ .
EUROPEAN RESPIRATORY JOURNAL, 1999, 14 (03) :534-544
[9]  
HOSHINO T, 1995, CLIN EXP IMMUNOL, V102, P399
[10]  
HUNNINGHAKE GW, 1984, AM REV RESPIR DIS, V129, P569