Apoptosis: One of the mechanisms that maintains unresponsiveness of the intestinal mucosal immune system

被引:65
作者
Bu, P
Keshavarzian, A
Stone, DD
Liu, JZ
Le, PT
Fisher, S
Qiao, L
机构
[1] Loyola Univ, Med Ctr, Stritch Sch Med, Dept Microbiol & Immunol, Maywood, IL 60153 USA
[2] Loyola Univ, Stritch Sch Med, Dept Med, Maywood, IL 60153 USA
[3] Loyola Univ, Stritch Sch Med, Dept Cell Biol Neurobiol & Anat, Maywood, IL 60153 USA
[4] Rush Univ, Div Digest Dis, Chicago, IL 60612 USA
关键词
D O I
10.4049/jimmunol.166.10.6399
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Intestinal mucosa is constantly exposed to environmental Ags. Activation of lamina propria (LP) T cells by luminal Ags may lead to the production of inflammatory cytokines and subsequent mucosal inflammation and tissue damage. However, in normal circumstances, LP T cells do not respond to antigenic stimulation. The mechanisms of this unresponsiveness in healthy subjects are not fully understood. In this study, we found by in vivo analysis that, except for T cells in lymph nodules of the mucosa, 15% of LP T cells underwent apoptosis in normal individuals. In contrast, there was a marked reduction in apoptosis of LP T cells in patients with inflammatory bowel disease (Crohn's disease and ulcerative colitis) and those with specific colitis. Our findings suggest that apoptosis might be a mechanism that turns off mucosal T cell responses to environmental Ags in healthy subjects, and resistance to apoptosis could be an important cause of mucosal immune dysregulation and tissue inflammation in colitis.
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收藏
页码:6399 / 6403
页数:5
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