Bromelain treatment decreases secretion of pro-inflammatory cytokines and chemokines by colon biopsies in vitro

被引:71
|
作者
Onken, Jane E. [2 ]
Greer, Paula K. [1 ]
Calingaert, Brian [3 ]
Hale, Laura P.
机构
[1] Duke Univ, Med Ctr, DUMC 3712, Dept Pathol, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Div Gastroenterol, Dept Med, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Canc, Ctr Biostat, Durham, NC 27710 USA
关键词
proteinase therapy; inflammatory bowel; disease; cytokines;
D O I
10.1016/j.clim.2007.11.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oral bromelain has been anecdotally reported to decrease inflammation in ulcerative colitis (UC). Proteolytically active bromelain is known to decrease expression of mRNAs encoding pro-inflammatory cytokines by human leukocytes in vitro. To assess the effect of bromelain on mucosat secretion of cytokines in inflammatory bowel disease (IBD), endoscopic colon biopsies from patients with UC, Crohn's disease (CD), and non-IBD) controls were treated in vitro with bromelain or media, then cultured. Secretion of pro-inflammatory cytokines and chemokines was measured. Significant increases in granulocyte colony-stimulating factor (G-CSF), interferon (IFN)-gamma, interleukin (IL)-1 beta, IL-6, and tumor necrosis factor (TNF) were detected in the media from actively inflamed areas in UC and CD as compared with non-inflamed IBD tissue and non-IBD) controls. In vitro bromelain treatment decreased secretion of G-CSF, granulocyte-macrophage colony-stimulating factor (GM-CSF), IFN-gamma, CCL4/macrophage inhibitory protein (MIP)-1 beta, and TNF by inflamed tissue in IBD. Bromelain may be a novel therapy for IBD. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:345 / 352
页数:8
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