Extended report
Flow cytometric analysis of gut mucosal lymphocytes supports an
impaired Th1 cytokine profile in spondyloarthropathy
N Van Dammea, M De Vosb, D Baetena, P Demetterc, H Mielantsa, G Verbruggena, C Cuvelierc, E M Veysa, F De Keysera
a Department of
Rheumatology, Ghent University Hospital, De Pintelaan 185, 9000 Ghent,
Belgium, b Department of Gastroenterology, c Department of Pathology
Correspondence to: Dr N Van Damme, Ghent University Hospital, Department of Rheumatology 0K12 IB, De Pintelaan 185, 9000 Ghent, Belgium Nancy.VanDamme{at}rug.ac.be
Accepted for publication 20 October
2000
OBJECTIVE
To quantify
the fraction of gut mucosal lymphocytes expressing the T helper type 1 (Th1) cytokines, interferon
(IFN
) and interleukin (IL)2, and the
Th2 cytokines, IL4 and IL10, at the single cell level in patients with
spondyloarthropathy (SpA) in comparison with healthy controls.
METHODS
An improved
extraction protocol was used for the enrichment of intraepithelial
lymphocytes (IELs) and lamina propria lymphocytes (LPLs) from colonic
and ileal biopsy specimens obtained from patients with SpA (n=20) and
healthy controls (n=13). After stimulation with phorbol
ester/ionomycin, expression of the intracellular cytokines IFN
, IL2,
IL4, and IL10 was determined in CD3+, CD3+CD8+ and CD3+CD8
T cells
by flow cytometry.
RESULTS
In colonic
LPLs, a significant decrease in IFN
-producing CD3+ cells was
observed (p=0.02) in patients with SpA. In the CD3+CD8
subset, the
proportion of cells producing IFN
and IL2 was decreased in patients
with SpA (p=0.021 and p=0.027 respectively). In ileal LPLs, the
percentage of IL10-producing CD3+CD8
cells was significantly increased (p=0.046).
CONCLUSION
An impaired
Th1 cytokine profile is observed in gut mucosal lymphocytes from
patients with SpA. This adds to the existing evidence that the gut
mucosal immune apparatus is involved in the pathogenesis of SpA.
© 2001 by Annals of the Rheumatic Diseases
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