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Published on: December 15, 2011
Interferon-gamma-secreting T cells localize to the epithelium in coeliac disease
R W Olaussen1, F E Johansen, K E A Lundin
1Laboratory for Immunohistochemistry and Immunopathology, Institute of Pathology, University of Oslo, Rikshospitalet, Oslo, Norway. r.w.olaussen@labmed.uio.no
Insights
In coeliac disease (CD), interferon-gamma (IFN-gamma) secreting T cells are found in the gut epithelium. These cells are most abundant in untreated and refractory CD patients, indicating their role in the disease.
Area of Science:
- Immunology
- Gastroenterology
- Cell Biology
Background:
- Previous studies detected increased interferon-gamma (IFN-gamma) transcripts in duodenal biopsies of untreated coeliac disease (CD) patients.
- The cellular source and location of IFN-gamma production in the coeliac duodenum remained unclear.
Observation:
- This study investigated duodenal biopsy specimens from patients with untreated, treated, and refractory CD, alongside healthy controls.
- Cells spontaneously secreting IFN-gamma were identified and phenotyped using a novel fluorescence-activated cell sorter-based assay.
- IFN-gamma messenger RNA (mRNA) levels were analyzed in parallel cell suspensions.
Findings:
- Patients with untreated CD exhibited the highest proportion of IFN-gamma-secreting cells in both the epithelial (median 2.6%) and lamina propria (1.6%) compartments.
- Refractory CD also showed increased IFN-gamma+ cells compared to treated CD and controls.
- IFN-gamma-secreting intraepithelial lymphocytes were predominantly CD3+ and CD8+ T cells, while lamina propria cells included CD8- populations.
Implications:
- Spontaneously IFN-gamma-secreting T cells preferentially localize within the duodenal epithelium of patients with active and refractory CD.
- These findings highlight a specific cellular immune response in the gut mucosa of coeliac disease patients.
- Understanding the role of these IFN-gamma-producing cells may offer new therapeutic targets for CD management.
Abstract:
Increased levels of interferon-gamma (IFN-gamma) transcripts have previously been found in duodenal biopsy specimens from patients with untreated coeliac disease (CD). Such samples and duodenal control mucosa were therefore studied to locate and phenotype cells spontaneously secreting IFN-gamma. Specimens were collected from consecutively recruited patients with untreated (seven), treated (four) or refractory (three) CD and from five histologically normal controls. Morphological and immunohistochemical examinations were performed, and epithelial and lamina propria cell suspensions were prepared from parallel samples. Unstimulated viable cells secreting IFN-gamma were identified and phenotyped with a new fluorescence-activated cell sorter-based assay, and IFN-gamma messenger RNA (mRNA) was analysed in snap-frozen aliquots of the same suspensions. Untreated CD cases had the highest fraction of IFN-gamma+ cells in the epithelial compartment (median 2.6%, range 1.6-6.2%) and, less strikingly, in the lamina propria compartment (1.6%, range 0.3-3.6%), followed by refractory (1.4%, 1.0-1.9%; and 0.3%, 0.0-1.2%) and treated (0.8%, 0.5-0.9%; and 0.7%, 0.2-1.1%) disease and finally the controls (0.5%, 0.3-0.9%; and 0.2%, 0.1-0.7%). IFN-gamma mRNA data supported these findings. IFN-gamma+ intraepithelial lymphocytes were mostly CD3+ and CD8+, whereas many positive lamina propria cells were CD8-. We conclude that isolated T cells spontaneously secreting IFN-gamma localize preferentially in the epithelium of patients with classical and refractory CD.
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