Type 1 T-helper cell predominance in granulomas of Crohn's disease

Citation
T. Kakazu et al., Type 1 T-helper cell predominance in granulomas of Crohn's disease, AM J GASTRO, 94(8), 1999, pp. 2149-2155
Citations number
33
Categorie Soggetti
Gastroenerology and Hepatology
Journal title
AMERICAN JOURNAL OF GASTROENTEROLOGY
ISSN journal
00029270 → ACNP
Volume
94
Issue
8
Year of publication
1999
Pages
2149 - 2155
Database
ISI
SICI code
0002-9270(199908)94:8<2149:T1TCPI>2.0.ZU;2-U
Abstract
OBJECTIVE: The pathogenesis of Crohn's disease (CD) is thought to be associ ated with production of several cytokines, especially type-1 cytokines. To elucidate the in sial cytokine profiles in CD, cytokine-containing cells we re localized by immunohistochemistry, with special attention to noncaseatin g granulomas. The results were compared with those from studies of ulcerati ve colitis (UC). METHODS: We adopted the biotin-streptavidin-peroxidase method on frozen sec tions obtained at surgery from patients with CD or UC, and we immunohistoch emically examined the expression of several cytokines (interferon-gamma, in terleukin-2, -4, -10, and -12). RESULTS: In normal colonic tissue, expression of these cytokines was rare e xcept for interleukin-4. In actively inflamed areas of CD, increased expres sion of all cytokines by mononuclear cells was observed. In contrast, granu lomas in CD involved interferon-gamma(+) lymphocytes and interleukin-12(+) macrophage-lineage cells (epithelioid cells and multinucleated giant cells) but few interleukin-4(+) or -10(+) cells. Actively inflamed areas of UC al so showed an increase in the number of cytokine-containing cells; however, quantitative analysis revealed that there was more expression of interferon -gamma and interleukin-12, and less of interleukin-10, in CD than in UC, in dicating the presence of more type 1 T-helper cells in CD tissue than in UC . CONCLUSIONS: The findings of the present study suggest that granulomas of C D are coupled with type 1 T-helper responses; these responses may contribut e to the pathogenesis of this disease. (Am J Gastroenterol 1999;94: 2149-21 55. (C) 1999 by Am. Coll. of Gastroenterology).