Clinical relapse of inflammatory bowel disease is characterised by inc
reased neutrophil migration into the intestine. The site of the neutro
phil chemoattractant(s), whether luminal or mucosal, may be important
since, on contact with a chemoattractant, neutrophils cause indiscrimi
nate damage to their immediate surroundings by generating reactive oxy
gen species and by lysosomal enzyme release. If this happens within th
e mucosa, inflammation should correlate significantly with tissue dama
ge as assessed by bleeding, but if it occurs within the intestinal lum
en, the inflammation would be disproportionately greater than the blee
ding such as is seen in classical exudation. Intestinal inflammation a
nd bleeding were quantitated with the simultaneous use of indium-111 l
abelled neutrophils (four day faecal excretion of indium-111) and chro
mium-51 labelled red cells in patients with ulcerative colitis (n=12),
Crohn's disease (n=15), and NSAID induced enteropathy (n=34). Intesti
nal inflammation and blood loss correlated significantly (Spearman) in
patients with ulcerative colitis (20.3% v 6.5 ml/d (median) r: 0-85,
p<0.001) and NSAD enteropathy (1.6% v) 1.9 ml/d, r: 0.60, p<0.01) but
not in Crohn's disease (17.0% v 2.1 ml/d, r: 0-38, p>0.1). For a given
indium-111 excretion, patients with ulcerative colitis had significan
tly greater (p<0.01) blood loss than patients with Crohn's disease. Th
ese results suggest that the predominant site of neutrophil chemoattra
ctants may be within the mucosa in ulcerative colitis and NSAID entero
pathy and within the lumen in Crohn's disease.