Expression of tumor necrosis factor-alpha and nuclear factor-kappa B in childhood ulcerative colitis

OBJECTIVE: It has been proposed that aberrant immunity of local bowel mucosa may cause ulcerative colitis (UC) and the tumor necrosis factor-alpha (TNF-alpha) and nuclear factor-kappa B (NF-kappa B) may play a role in the development of this disease. To investigate the role of TNF-alpha and NF-kappa...

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Veröffentlicht in:Zhonghua er ke za zhi = Chinese journal of pediatrics. - 1960. - 41(2003), 10 vom: 19. Okt., Seite 743-6
1. Verfasser: Tang, Hong-feng (VerfasserIn)
Weitere Verfasser: Chen, Xiao-xiao, Ye, Hua-ying, Ou, Bi-you
Format: Aufsatz
Sprache:Chinese
Veröffentlicht: 2003
Zugriff auf das übergeordnete Werk:Zhonghua er ke za zhi = Chinese journal of pediatrics
Schlagworte:English Abstract Journal Article Antigens, CD Antigens, Differentiation, Myelomonocytic CD68 antigen, human NF-kappa B Tumor Necrosis Factor-alpha
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500 |a Citation Status MEDLINE 
520 |a OBJECTIVE: It has been proposed that aberrant immunity of local bowel mucosa may cause ulcerative colitis (UC) and the tumor necrosis factor-alpha (TNF-alpha) and nuclear factor-kappa B (NF-kappa B) may play a role in the development of this disease. To investigate the role of TNF-alpha and NF-kappa B in childhood UC, the expression of TNF-alpha and NF-kappa B in the bowel mucosa and their relationship were studied 
520 |a METHODS: Using anti-CD68, anti-TNF-alpha and anti-NF-kappa Bp65 antibodies, the cytokine immunoreactivities in the bowel mucosa of 39 cases of childhood UC (active UC: n = 21, non-active UC: n = 18) were detected by immunohistochemistry. The control specimens of normal bowel mucosa were collected from 7 cases with colorectal polyp or abdominal pain by sigmoidoscopy 
520 |a RESULTS: The numbers (median: interquartile range) of CD68(+) cells, TNF-alpha(+) cells and NF-kappa Bp65(+) cells were 44.0 (31.5 - 48.2), 42.7 (19.5 - 65.0) and 50.7 (30.0 - 58.0) in the active UC mucosa, and were 9.2 (7.9 - 16.6), 5.5 (2.5 - 9.1) and 4.2 (3.0 - 8.4) in non-active UC mucosa, and 5.3 (4.3 - 8.7), 3.0 (0.0 - 6.3) and 3.3 (0.0 - 4.0) in the control mucosa, respectively. The levels of CD68, TNF-alpha and NF-kappa Bp65 expressions in the active UC were significantly higher than those in the non-active UC (P < 0.001) and the controls (P < 0.001). The expression level of CD68 in non-active UC was much higher than that in the controls (P = 0.008). Using the correlation analysis, a positive correlation between TNF-alpha and NF-kappa B activation was found (r = 0.885, P < 0.001) 
520 |a CONCLUSIONS: Macrophages TNF-alpha and NF-kappa B may play an important role in the pathophysiologic mechanism of childhood active UC. The activation of NF-kappa B may be associated with the release of TNF-alpha 
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650 4 |a Journal Article 
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650 7 |a Antigens, Differentiation, Myelomonocytic  |2 NLM 
650 7 |a CD68 antigen, human  |2 NLM 
650 7 |a NF-kappa B  |2 NLM 
650 7 |a Tumor Necrosis Factor-alpha  |2 NLM 
700 1 |a Chen, Xiao-xiao  |e verfasserin  |4 aut 
700 1 |a Ye, Hua-ying  |e verfasserin  |4 aut 
700 1 |a Ou, Bi-you  |e verfasserin  |4 aut 
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