Expression of lymphocyte-endothelial receptor-ligand pairs, alpha 4 beta 7/MAdCAM-1 and OX40/OX40 ligand in the colon and jejunum of patients with inflammatory bowel disease
Hs. Souza et al., Expression of lymphocyte-endothelial receptor-ligand pairs, alpha 4 beta 7/MAdCAM-1 and OX40/OX40 ligand in the colon and jejunum of patients with inflammatory bowel disease, GUT, 45(6), 1999, pp. 856-863
Background-The interaction between leucocytes and vascular endothelial cell
s is essential for leucocyte migration into inflammatory sites.
Aims-To study the local expression of the pairs of complementary molecules,
alpha 4 beta 7/mucosal addressin cell adhesion molecule (MAdCAM-1) and OX4
0/OX40 ligand in the lamina propria of the colon and jejunum of patients wi
th inflammatory bowel disease.
Methods-Ten patients with active ulcerative colitis (UC), nine with active
Crohn's disease (CD), and seven irritable bowel syndrome (IBS) controls wer
e submitted to endoscopic and peroral jejunal biopsies. Specimens were immu
nostained by indirect alkaline phosphatase using antibodies against: CD3, i
ntercellular adhesion molecule (ICAM) 1, alpha 4 beta 7, MAdCAM-1, and OX40
. An OX40-mouse-IgG fusion protein was used to detect OX40 ligand on frozen
sections. Immunohistological analysis was carried out by optical microscop
y using a computer assisted image analyser.
Results-Colonic lamina propria of patients with CD and UC showed increased
density of CD3+, alpha 4 beta 7+, and OX40+ cells compared with IBS control
s. ICAM-1, MAdCAM-1, and OX40 ligand positive vessels were also increased c
ompared with IBS controls. No significant difference was found in the densi
ty of any of these cells in the jejunal mucosa of patients compared with IB
S controls.
Conclusions-The expression of MAdCAM-1 and OX40 ligand on gut: endothelial
and OX40+ cells is increased in sites of mucosal inflammation in patients w
ith inflammatory bowel disease. No evidence was found for increased lamina
propria T cells or increased vascular adhesion molecule expression in the p
roximal intestine of patients with distal inflammatory bowel disease.