TY - JOUR
T1 - Colonic mucosal immune activity in irritable bowel syndrome
T2 - Comparison with healthy controls and patients with ulcerative colitis
AU - Ahn, Ji Yong
AU - Lee, Kyung Hun
AU - Choi, Chang Hwan
AU - Kim, Ju Wan
AU - Lee, Hyun Woong
AU - Kim, Jeong Wook
AU - Kim, Mi Kyung
AU - Kwon, Gui Young
AU - Han, Seungbong
AU - Kim, Seong Eun
AU - Kim, Sung Min
AU - Chang, Sae Kyung
PY - 2014/5
Y1 - 2014/5
N2 - Background and Aim: 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. Methods: 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. Results: 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. Conclusions: 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.
AB - Background and Aim: 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. Methods: 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. Results: 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. Conclusions: 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.
KW - Irritable bowel syndrome
KW - Mast cell
KW - T cell
KW - Ulcerative colitis
UR - http://www.scopus.com/inward/record.url?scp=84899905703&partnerID=8YFLogxK
U2 - 10.1007/s10620-013-2930-4
DO - 10.1007/s10620-013-2930-4
M3 - Article
C2 - 24282051
AN - SCOPUS:84899905703
SN - 0163-2116
VL - 59
SP - 1001
EP - 1011
JO - Digestive Diseases and Sciences
JF - Digestive Diseases and Sciences
IS - 5
ER -