Gastric mucosal secretion of interleukin-10: Relations to histopathology, Helicobacter pylori status, and tumour necrosis factor-alpha secretion

被引:83
作者
Badger, K [1 ]
Wyatt, JI [1 ]
Heatley, RV [1 ]
机构
[1] ST JAMES UNIV HOSP,DEPT PATHOL,DIV MED,LEEDS LS9 7TF,W YORKSHIRE,ENGLAND
关键词
interleukin-10; Helicobacter pylori; tumour necrosis factor-alpha;
D O I
10.1136/gut.40.6.739
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Interleukin-10 (IL-10) is an 18 kDa peptide with a range of antiinflammatory and immunosuppressive properties, Aim-To determine whether this cytokine is involved in gastric mucosal inflammation in Helicobacter pylori infection. Methods-The production of IL-10 by antral mucosal biopsy specimens during short term in vitro culture was determined by measuring IL-10 content of supernatants by enzyme linked immunosorbant assay (ELISA). H pylori status was determined by serology and histology, with gastritis scored using the Sydney system. Tumour necrosis factor-alpha (TNF-alpha) content of supernatants was also determined in a subgroup of patients, Results-IL-10 secretion was significantly greater in patients with H pylori associated chronic gastritis than in patients who were H pylori negative with normal mucosa/reactive changes, and those with H pylori negative chronic gastritis (p < 0.01 and < 0.05 respectively). There was a significant correlation overall between IL-10 secretion and chronic inflammation score (r = 0.40). Secretion of TNF-alpha, which was significantly higher in H pylori infected patients than uninfected patients with a normal mucosa (p < 0.04), correlated with scores for chronic inflammation and activity (r = 0.39 and 0.38 respectively), but was only weakly correlated with IL-10 secretion (r = 0.22, NS). Conclusions-Gastric mucosal production of IL-10 and TNF-alpha are increased in chronic gastritis associated with H pylori infection, and mucosal cytokine secretion varies with important histopathological aspects of gastric inflammation. Whereas the secretion of IL-10 in H pylori infection may be protective, limiting tissue damage caused by inflammation, it may also contribute towards failure of the immune response to eliminate the organism.
引用
收藏
页码:739 / 744
页数:6
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