Colonic Mucosal Immune Activity in Irritable Bowel Syndrome: Comparison with Healthy Controls and Patients with Ulcerative Colitis

被引:50
作者
Ahn, Ji Yong [1 ,2 ]
Lee, Kyung Hun [1 ]
Choi, Chang Hwan [1 ]
Kim, Ju Wan [1 ]
Lee, Hyun Woong [1 ]
Kim, Jeong Wook [1 ]
Kim, Mi Kyung [3 ]
Kwon, Gui Young [3 ]
Han, Seungbong [4 ]
Kim, Seong-Eun [5 ]
Kim, Sung Min [6 ]
Chang, Sae Kyung [1 ]
机构
[1] Chung Ang Univ, Dept Internal Med, Coll Med, Seoul 156756, South Korea
[2] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Internal Med, Seoul, South Korea
[3] Chung Ang Univ, Coll Med, Dept Pathol, Seoul 156756, South Korea
[4] Univ Ulsan, Coll Med, Asan Med Ctr, Dept Clin Epidemiol & Biostat, Seoul, South Korea
[5] Ewha Womans Univ, Sch Med, Dept Internal Med, Seoul, South Korea
[6] Univ N Carolina, Ctr Funct Gastrointestinal & Motil Disorders, Chapel Hill, NC USA
关键词
Irritable bowel syndrome; Mast cell; T cell; Ulcerative colitis; QUALITY-OF-LIFE; ENTEROCHROMAFFIN CELL HYPERPLASIA; PRACTICE PARAMETERS COMMITTEE; MAST-CELLS; VISCERAL HYPERSENSITIVITY; PSYCHOLOGICAL-FACTORS; PRACTICE GUIDELINES; AMERICAN-COLLEGE; T-LYMPHOCYTES; DISEASE;
D O I
10.1007/s10620-013-2930-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Mucosal immune activity may participate in irritable bowel syndrome (IBS) pathogenesis. Mast- and T cell numbers from patients with IBS or ulcerative colitis (UC) and healthy controls were determined. Between November 2007 and May 2012, patients with diarrhea-predominant IBS (D-IBS, n = 83), 49 patients with UC, and 25 healthy controls were recruited. Of the UC group, 28 were in remission and 21 had mildly active UC. Biopsies from each colon segment were subjected to immunohistochemical analysis. The mast cells, intraepithelial lymphocytes (IELs), and lamina proprial lymphocytes (LPLs) were counted. Compared to the healthy controls, the patients with D-IBS, UC in remission, and mildly active UC had significantly higher mean colorectal mucosal mast-cell, IEL, and LPL counts. Comparison with the colon segments (ascending, transverse, descending, and sigmoid segments) that had once been involved in UC (in the patients with remission) revealed that the D-IBS colons had similar immune-cell counts. However, they had significantly fewer immune cells than the colon segments that presently showed involvement in the patients with mildly-activated UC. The mast-cell and IEL counts were similar in the D-IBS rectums and once-involved UC rectums but significantly higher in the presently-involved UC rectums. However, both the once-involved and presently-involved UC rectums had significantly higher LPL counts than the D-IBS rectums. Patients with D-IBS had significantly higher colonic mucosal immune-cell counts than healthy controls but had similar counts to patients with UC in remission. The symptoms in both conditions may originate from low-grade inflammation in the colonic mucosa.
引用
收藏
页码:1001 / 1011
页数:11
相关论文
共 48 条
[1]  
Arévalo F., 2011, Rev. gastroenterol. Perú, V31, P315
[2]   Activated mast cells in proximity to colonic nerves correlate with abdominal pain in irritable bowel syndrome [J].
Barbara, G ;
Stanghellini, V ;
De Giorgio, R ;
Cremon, C ;
Cottrell, GS ;
Santini, D ;
Pasquinelli, G ;
Morselli-Labate, AM ;
Grady, EF ;
Bunnett, NW ;
Collins, SM ;
Corinalidesi, R .
GASTROENTEROLOGY, 2004, 126 (03) :693-702
[3]   A role for inflammation in irritable bowel syndrome? [J].
Barbara, G ;
De Giorgio, R ;
Stanghellini, V ;
Cremon, C ;
Corinaldesi, R .
GUT, 2002, 51 :I41-I44
[4]   Mast cell-dependent excitation of visceral-nociceptive sensory neurons in irritable bowel syndrome [J].
Barbara, Giovanni ;
Wang, Bingxian ;
Stanghellini, Vincenzo ;
De Giorgio, Roberto ;
Cremon, Cesare ;
Di Nardo, Giovanni ;
Trevisani, Marcello ;
Campi, Barbara ;
Geppetti, Pierangelo ;
Tonini, Marcello ;
Bunnett, Nigel W. ;
Grundy, David ;
Corinaldesi, Roberto .
GASTROENTEROLOGY, 2007, 132 (01) :26-37
[5]   Cytokine gene polymorphisms are associated with irritable bowel syndrome: a systematic review and meta-analysis [J].
Bashashati, M. ;
Rezaei, N. ;
Bashashati, H. ;
Shafieyoun, A. ;
Daryani, N. E. ;
Sharkey, K. A. ;
Storr, M. .
NEUROGASTROENTEROLOGY AND MOTILITY, 2012, 24 (12) :1102-+
[6]   Is irritable bowel syndrome a low-grade inflammatory bowel disease? [J].
Bercik, P ;
Verdu, EF ;
Collins, SM .
GASTROENTEROLOGY CLINICS OF NORTH AMERICA, 2005, 34 (02) :235-+
[7]   The Manitoba Inflammatory Bowel Disease Cohort Study: Prolonged symptoms before diagnosis-how much is irritable bowel syndrome? [J].
Burgmann, Twila ;
Clara, Ian ;
Graff, Lesley ;
Walker, John ;
Lix, Lisa ;
Rawsthorne, Patricia ;
Mcphail, Cory ;
Rogala, Linda ;
Miller, Norine ;
Bernstein, Charles Noah .
CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2006, 4 (05) :614-620
[8]   Role for protease activity in visceral pain in irritable bowel syndrome [J].
Cenac, Nicolas ;
Andrews, Christopher N. ;
Holzhausen, Marinella ;
Chapman, Kevin ;
Cottrell, Graeme ;
Andrade-Gordon, Patricia ;
Steinhoff, Martin ;
Barbara, Giovanni ;
Beck, Paul ;
Bunnett, Nigel W. ;
Sharkey, Keith A. ;
Ferraz, Jose Geraldo P. ;
Shaffer, Eldon ;
Vergnolle, Nathalie .
JOURNAL OF CLINICAL INVESTIGATION, 2007, 117 (03) :636-647
[9]   Activation of the mucosal immune system in irritable bowel syndrome [J].
Chadwick, VS ;
Chen, WX ;
Shu, DR ;
Paulus, B ;
Bethwaite, P ;
Tie, A ;
Wilson, I .
GASTROENTEROLOGY, 2002, 122 (07) :1778-1783
[10]   Anxiety, Depression and Quality of Life in Patients with Irritable Bowel Syndrome [J].
Cho, Hyun Sun ;
Park, Jae Myung ;
Lim, Chul Hyun ;
Cho, Yu Kyung ;
Lee, In Seok ;
Kim, Sang Woo ;
Choi, Myung-Gyu ;
Chung, In-Sik ;
Chung, Yun Kyung .
GUT AND LIVER, 2011, 5 (01) :29-36