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Intraepithelial lymphocytes and coeliac disease: permanent changes in CD3-/CD7+ and T cell receptor gammadelta
C Camarero1, P Eiras, A Asensio
1Department of Paediatric Gastroenterology, Hospital Ramón y Cajal, Universidad de Alcalá de Henares, Madrid, Spain. groy@hrc.insalud.es
Insights
Flow cytometry reveals distinct changes in T cell receptor gammadelta and CD3-/CD7+ intestinal lymphocytes in pediatric coeliac disease. These permanent alterations aid in diagnosing coeliac enteropathy, regardless of diet.
Area of Science:
- Immunology
- Gastroenterology
- Pediatric Medicine
Background:
- Intestinal intraepithelial lymphocytes (IELs) show altered phenotypes in coeliac disease.
- Accurate diagnosis of coeliac disease in children is crucial for timely intervention.
Purpose of the Study:
- To investigate small intestinal IELs using flow cytometry.
- To evaluate the diagnostic value of IEL subsets in coeliac disease.
Main Methods:
- Three-colour flow cytometry on epithelial cells from 117 intestinal biopsies (54 coeliac, 4 other enteropathies, 18 H. pylori gastritis, 37 controls).
- Logistic regression analysis to identify predictive IEL subsets.
Main Results:
- Coeliac patients exhibited significantly higher T cell receptor gammadelta IELs (p < 0.01) and lower CD3-/CD7+ IELs (p < 0.01) compared to controls.
- These IEL changes were independent of the patient's diet.
- Flow cytometry achieved 94.4% sensitivity and 94.9% specificity for coeliac disease diagnosis.
Conclusions:
- Specific IEL subsets (T cell receptor gammadelta and CD3-/CD7+) are persistently altered in pediatric coeliac disease.
- Flow cytometry assessment of these IELs on routine biopsies aids in characterizing coeliac enteropathy.
- This method offers a valuable diagnostic tool for identifying coeliac patients.
Unlabelled:
Permanent changes in intestinal intraepithelial lymphocytes have been observed in coeliac patients. The aim of this investigation was to study small intestinal intraepithelial lymphocytes by using flow cytometry and to evaluate its diagnostic value in coeliac disease. Three-colour flow cytometry analyses were performed on isolated epithelial cells of 117 intestinal biopsies obtained from 113 children (54 coeliac disease, 4 other enteropathies, 18 Helicobacter pylori associated gastritis and 37 normal controls). A multiple logistic regression model was developed to select the best intraepithelial lymphocytes subset predictor of coeliac disease. Coeliac patients had significant higher levels of T cell receptor gammadelta intraepithelial lymphocytes than control patients (p < 0.01), H. pylori patients (p < 0.01) and other enteropathies (p < 0.05). The density of CD3-/CD7+ intraepithelial lymphocytes, a intraepithelial lymphocyte subset poorly characterized by immunohistochemical methods, was significantly lower in coeliac patients than in the control group (p < 0.01). H. pylori group (p < 0.01) and other enteropathies (p < 0.01). Both changes remained altered independent of the coeliac patient's diet. The data were used on a logistic regression analysis in order to calculate sensitivity [94.4%; 95% confidence interval (CI) 83.7-98.6%], specificity (94.9%; 95% CI 84.9-98.7%) and likelihood ratio for a positive test 18.5 (95% CI 6.1-55.8) in the diagnosis of coeliac disease.
Conclusion:
Changes in T cell receptor gammadelta and CD3-/CD7+ intraepithelial lymphocytes subsets are permanently observed in paediatric coeliac disease. Their assessment, by three-colour flow cytometry on routine diagnostic biopsies, permits a better characterization of coeliac enteropathy and represents a valuable procedure to identify coeliac patients with different clinical presentations.
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