Increased secretion of pro-inflammatory cytokines by circulating polymorphonuclear neutrophils and regulation by interleukin 10 during intestinal inflammation
S Nikolaus
a Charité University Hospital, 4th
Medical Department, Humboldt University, Berlin, Germany, b Clinica Media I, Policlinico S. Orsola, University of Bologna,
Italy, c Charité University Hospital, 1st
Medical Department, Humboldt University, Berlin, Germany
Correspondence to: Dr S Schreiber, 1st Department of Medicine,
Christian-Albrechts-University, Schittenhelmstrasse 12, 24105 Kiel,
Germany (email: s.schreiber{at}mucosa.de). Accepted for publication 31 October 1997 Background Keywords:
granulocytes;
interleukin 1
Concentrations of pro-inflammatory
cytokines are increased in the intestinal mucosa of patients with
active inflammatory bowel disease (IBD). Polymorphonuclear neutrophil
granulocytes (PMN) are the most abundant cell type in intestinal
lesions in IBD. Interleukin 10 (IL-10) is an important
contra-inflammatory cytokine which induces downregulation of
pro-inflammatory cytokines.
Aims
To investigate whether PMN from patients with
IBD or infectious colitis, respectively, secrete increased amounts of
pro-inflammatory cytokines and can be regulated by IL-10.
Methods
Secretion (ELISA) as well as corresponding
mRNA levels (semiquantitative RT-PCR) of pro-inflammatory cytokines
(IL-1
, TNF-
) and of IL-1 receptor antagonist were assessed in
peripheral PMN.
Results
PMN from patients with IBD are primed to
secrete enhanced amounts of pro-inflammatory cytokines accompanied by
detection of corresponding mRNAs in comparison with normal controls.
This finding is not specific for IBD but rather reflects intestinal inflammation in general. IL-10 markedly inhibited pro-inflammatory cytokine secretion as well as corresponding mRNA concentrations.
Conclusions
PMN are an important source of
pro-inflammatory cytokines in patients with intestinal inflammation and
can be downregulated by IL-10.
(GUT 1998;42:470-476)
;
interleukin 10;
inflammatory bowel disease;
intestinal immunity;
inflammation;
neutrophils;
tumour necrosis factor
© 1998 by Gut
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